Geographic Range
Japanese hares are endemic to Japan. They are commonly found on the mainland islands
of Honshu, Shikoku and Kyushu and most of the surrounding Japanese islands, excluding
Hokkaido. There are four subspecies of the Japanese hare found in different geographical
regions.
Lepus brachyurus angustidens
is found in northern Honshu,
L. b. lyoni
is found on Sado Island,
L. b. brachyurus
is found in southern Honshu, and
L. b. okiensis
is found on the Oki Islands.
- Other Geographic Terms
- island endemic
Habitat
Japanese hares can be found throughout Japan in urban, rural and forest settings,
but the vast majority are found in rural areas. They are typically found in areas
with dense shrub-like vegetation and a low tree canopy, often near the edge of forests.
Japanese hares are predominant in young, Japanese cedar plantations where there is
plenty of incoming light and an abundance of vegetation. Japanese hares are also found
near and around rivers or streams. They range from sea level to 2700 m. Japanese hares
do not inhabit mountainous areas.
- Habitat Regions
- temperate
- terrestrial
- Terrestrial Biomes
- savanna or grassland
- forest
- scrub forest
- Other Habitat Features
- urban
- suburban
- agricultural
Physical Description
Adult Japanese hares are mid-size mammals with body masses ranging from 1.3 to 2.5
kg. There are variations in color from a dark brown to a red brown with areas of white.
All four subspecies are brownish in the summer, but
L. brachyurus angustidens
and
L.b.lyoni
change their coat colors to white in the winter.
Like all members of the Order
Lagomorpha
, Japanese hares have a second set of incisors, or peg teeth, behind their first upper
incisors. All hares have dental formula of i 2/1, c 0/0, p 3/2, m 3/3.
There are variations between Japanese hare subspecies found on the main island and
those found on surrounding islands. The dimensions of a mainland female Japanese hare
described in 1905 were 505 mm head and body length, 40 mm tail length, 135 mm hindfoot
length and 78 mm ear length. Measurements from a female Japanese hare from Oki Island
were a 506 mm head and body length, a 54 mm tail, a 138 mm hind foot and a 78 mm ear.
The subspecies found on the smaller islands appear to have sexual dimorphism, with
the vast majority of skull characteristics being smaller in males than in females.
On the main island, the only feature that is not equal in size is the width of the
palate. In general, the subspecies on the small islands are often larger in mass,
length of head, and length of body. The subspecies on the main island have larger
ears, hind feet length and skull size compared to those on the islands. It has been
suggested that this variation is not due to insular variation, but that the island
forms are actually closer to the ancestral form and the main island subspecies has
evolved and adapted to a changing environment.
- Other Physical Features
- endothermic
- homoiothermic
- bilateral symmetry
- Sexual Dimorphism
- sexes alike
- female larger
Reproduction
Nothing is known about Japanese hare mating systems. There is, however, generalizable
information regarding other species of
hares
. Aside from
arctic hares
, which pair each breeding season, most male and female hares are promiscuous. Male
and female hares come together during the breeding season and males sometimes display
aggressive behavior, such as boxing, in order to compete for mates.
- Mating System
- polygynous
- polygynandrous (promiscuous)
Japanese hares have a long breeding season, beginning in early January and ending
in August. The number of litters per season ranges from 4 to 5. The average litter
size ranges from one to four, with 1.6 babies being the average and the average weight
of the young at birth is 132 g. There is a 1:1 ratio of males to females born in each
litter. Within one breeding season, a typical female will average 7.4 young. The weaning
period typically takes place 2 to 3 weeks after birth.
Female hares become sexually mature at ten months old. The gestation period ranges
from 43 to 45 days and the period between births ranges from 33 to 109 days. An interbirth
period shorter than the gestation period suggests the possibility of superfoetation.
This is further supported by the occurrence of postcoital ovulation in Japanese hares.
At the other end of the spectrum, there can also be delays between birth and the next
copulation. Sometimes female Japanese hares will chase away males with whom they do
not want to copulate.
There is some variability in breeding patterns between northern and southern Japanese
hares as breeding appears to be affected by temperature, photoperiod, and precipitation.
Environments in higher latitudes have decreased temperature and photoperiods throughout
the majority of the year and studies of captive animals have found that with increasing
latitude, the breeding season, gestation period and litter size decreases.
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- viviparous
- post-partum estrous
Nothing is known about parental care in Japanese hares, however the young of other
hares are precocial and have limited parental care and this can be inferred for Japanese
hares.
- Parental Investment
- precocial
-
pre-hatching/birth
-
provisioning
- female
-
protecting
- female
-
provisioning
-
pre-weaning/fledging
-
provisioning
- female
-
provisioning
Lifespan/Longevity
Behavior
Japanese hares are solitary and nocturnal. They do not burrow, but will hide in the
scrub or brush during the daytime. When they are active at night, they can travel
about 1000 m in a single night in forested areas and can cover approximately 6 hectares.
- Key Behaviors
- terricolous
- saltatorial
- nocturnal
- motile
- sedentary
- solitary
Home Range
The home ranges of Japanese hares are 10 to 30 hectares in size.
Communication and Perception
While nothing is known about communication between Japanese hares, information may
be inferred from other hare species. There appears to be various types of vocalizations,
mostly high-pitched, that occur when hares are confronted with uncomfortable or frightening
situations. Like other hares, hearing is an important mode of perception.
- Communication Channels
- acoustic
Food Habits
Japanese hares are opportunistic herbivores that typically eat newly planted grasses,
grasses at plantations, and young trees and shrubs. Saito and Koike (2009) determined
that their main source of food during the summer comes from the Family
Gramineae
, which includes the grasses and many commercial crops. In northern Japan, when these
grasses are unavailable due to winter snow cover, Japanese hares eat the buds and
seedlings of young trees, often found in plantations. Tori and Suzuki (1996) examined
which trees were favored in the winter and concluded that the vast majority of trees
were
Phyllostachys praecox
, a bamboo which is high in crude protein content. Other popular winter trees include
Acer
,
Paulownia
,
Acanthopanax
,
Aralia
and
Leguminosae
. The trees and shrubs chosen by Japanese hares often have increased amounts of branches
and stems, which are typically found in young forests. Most of the trees that are
consumed have high protein content.
Japanese hares also engage in coprophagy, or the reingestion of feces. While coprophagy
is common in most hares, what is unique in
L. brachyurus
is that it reingests both soft and hard feces, as they are observed simply swallowing
soft feces and chewing hard feces. Coprophagy is done to extract as many nutrients
as possible from their difficult to digest plant food. There is also a positive relationship
with the lack of available food and an increased occurrence of consuming hard feces.
- Plant Foods
- leaves
- wood, bark, or stems
- Other Foods
- dung
Predation
Japanese hares are readily preyed on by red foxes (
Vulpes vulpes
), golden eagles (
Aquila chrysaetos
) and Japanese martens (
Martes melampus
). The color change in the northern subspecies of Japanese hares, from brown to white
in the winter, is likely a cryptic color change to blend into their surrounding environment
and avoid predation.
- Anti-predator Adaptations
- cryptic
Ecosystem Roles
Due to the large population sizes of Japanese hares, they are extremely important
in the food web. They are prey for larger mammals and they impact the vegetation on
which they feed. They can cause damage to woody trees and plants when they are foraging
for buds in the winter.
Economic Importance for Humans: Positive
Japanese hares are important economically to humans as a source of food and fur.
- Positive Impacts
- food
- body parts are source of valuable material
Economic Importance for Humans: Negative
Japanese hares can cause damage to agricultural crops both by eating the crops and
by trampling them. They are also considered to be pests because they damage the forest
plantations which they inhabit.
Japanese hares are sources of and can transmit several diseases that affect humans.
Tularemia, a bacterial disease caused by
Francisella tularensis
can be transmitted to humans by contact with
L. brachyurus
and if not treated quickly, can be lethal. Since 1960, approximately 1400 cases have
been reported. Another disease, Q fever, which is caused by the transmission of bacterial
Coxiella burnetii
, induces fever-like symptoms and can later cause organ problems, can be transmitted
from infected hares and other Japanese mammals.
- Negative Impacts
- injures humans
- crop pest
Conservation Status
Japanese hares are considered least concern by the IUCN (2013). Although populations
are considered stable, there have been suggestions on actions to maintain this stability.
Saito and Koike (2009; 2013) stress the importance of forest regrowth and decreased
deforestation to ensure there is no habitat loss for these hares.
Other Comments
Lepus brachyurus
has been divided into two clades and four subspecies. The two clades are found in
southern and northern Japan and appear to be the result of these groups evolving differently
in these different regions approximately 1.24 million years ago.
Additional Links
Contributors
Jennifer Holmberg (author), University of Manitoba, Jane Waterman (editor), University of Manitoba, Tanya Dewey (editor), University of Michigan-Ann Arbor.
- oriental
-
found in the oriental region of the world. In other words, India and southeast Asia.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- island endemic
-
animals that live only on an island or set of islands.
- 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.
- tropical savanna and grassland
-
A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.
- savanna
-
A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.
- temperate grassland
-
A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- scrub forest
-
scrub forests develop in areas that experience dry seasons.
- urban
-
living in cities and large towns, landscapes dominated by human structures and activity.
- suburban
-
living in residential areas on the outskirts of large cities or towns.
- 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.
- polygynous
-
having more than one female as a mate at one time
- polygynandrous
-
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
- 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
- viviparous
-
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
- young precocial
-
young are relatively well-developed when born
- saltatorial
-
specialized for leaping or bounding locomotion; jumps or hops.
- nocturnal
-
active during the night
- motile
-
having the capacity to move from one place to another.
- sedentary
-
remains in the same area
- solitary
-
lives alone
- acoustic
-
uses sound to communicate
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
- cryptic
-
having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.
- food
-
A substance that provides both nutrients and energy to a living thing.
- causes disease in humans
-
an animal which directly causes disease in humans. For example, diseases caused by infection of filarial nematodes (elephantiasis and river blindness).
- herbivore
-
An animal that eats mainly plants or parts of plants.
- folivore
-
an animal that mainly eats leaves.
References
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Chapman, J., J. Flux. 1990. Introduction and Overview of the Order Lagomorpha. Pp. 1-6 in Rabbits, Hares, and Pikas: Status Survey and Conservation Action Plan . Glan, Switzerland: IUCN.
Ejercito, C., L. Cai, K. Htwe, M. Taki, Y. Inoshima, T. Kondo, C. Kano, S. Abe, K. Shirota, T. Sugimoto, T. Yamaguchi, H. Fukushi, N. Minamoto, T. Kinjo, E. Isogai, K. Hirai. 1993. Serological Evidence of Coxiella burnetii Infection in Wild Animals in Japan. Journal of Wildlife Diseases , 29: 481-484.
Enari, H., H. Sakamaki. 2012. Landscape-scale evaluation of habitat uses by sympatric mammals foraging for bark and buds in a heavy snowfall area of Northern Japan. Acta Theriologica , 57: 173-183.
Hirakawa, H., T. Kuwahata, Y. Shibata, E. Yamada. 1992. Insular Variation of the Japanese Hare ( Lepus brachyurus ) on the Oki Islands, Japan. Journal of Mammalogy , 73(3): 672-679.
Hirakawa, H. 1994. Coprophagy in the Japanese hare ( Lepus brachyurus ): reingestion of all the hard and soft faeces during the daytime stay in the form. Journal of Zoology , 232: 447-456.
Honda, T., Y. Miyagawa, H. Ueda, M. Inoue. 2009. Effectiveness of Newly-Designed Electric Fences in Reducing Crop Damage by Medium and Large Mammals. Mammal Study , 34: 13-17.
IUCN, 2013. "IUCN Red List of Threatened Species. Version 2013.1" (On-line). Accessed October 27, 2013 at www.iucnredlist.org .
Lumpkin, S., J. Seidensticker. 2011. Rabbits: The Animal Answer Guide . Baltimore, Maryland: The John Hopkins University Press.
Murray, D. 2003. Snowshow hare and other hares ( Lepus americanus and Allies). Pp. 126-146 in Wild Mammals of North America: Biology, Management and Conservation . Baltimore, Maryland: The John Hopkins University Press.
Numone, M., H. Torii, R. Matsuki, G. Kinoshita, H. Suzuki. 2010. The Influence of Pleistocene Refugia on the Evolutionary History of the Japanese Hare, Lepus brachyurus . Zoological Science , 27: 746-754.
Park, C., A. Nakansishi, H. Hatai, D. Kojima, T. Oyamada, H. Sato, N. Kudo, J. Shindo, O. Fujita, A. Hotta, S. Inoue, K. Tanabayashi. 2009. Pathological and Microbiological Studies of Japanese Hares ( Lepus brachyurus angustidens ) Naturally Infected with Francisella tularensis subsp. holarctica . Journal of Veterinary Medical Science , 71: 1629-1635.
Saito, M., F. Koike. 2013. Distribution of Wild Mammal Assemblages along an Urban-Rural-Forest Landscape Gradient in Warm-Temperature East Asia.. PLOS1 , 8: e65464.
Saito, M., F. Koike. 2009. The importance of past and present landscape for Japanese hares Lepus brachyurus along a rural-urban gradient. Acta Theriologica , 54: 363-370.
Shimano, K., H. Yatake, M. Nashimoto, S. Shiraki, R. Matsuki. 2006. Habitat Availability and Density Estimates for the Japanese Hare by Fecal Pellet Counting. The Journal of Wildlife Management , 70: 1650-1658.
Shimizu, R., K. Shimano. 2010.
Takeda, Y., H. Torii, S. Aiko. 1994. Reproductive Traits of Captive Japanese Hares Lepus brachyurus in Central Japan. Journal of Mammal Society Japan , 19: 83-88.
Thomas, O. 1905. The Duke of Bedford's zoological expedition in eastern Asia. 1. List of mammals obtained by Mr. M. P. Anderson in Japan.. Proceedings of the Zoological Society of London , 2: 331-363.
Torii, H., H. Suzuki. 1996. Winter Food Selection by Japanese Hares in the Western Slope of Mt. Fuji, Central Japan. Journal of Wildlife Research , 1: 95-98.