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Home -> Kingdom Animalia -> Phylum Chordata -> Subphylum Vertebrata -> Class Mammalia -> Order Lagomorpha -> Family Ochotonidae -> Species Ochotona curzoniae

Ochotona curzoniae
black-lipped pika



2009/11/22 03:59:06.653 US/Eastern

By Cara Ocobock

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Lagomorpha
Family: Ochotonidae
Genus: Ochotona
Species: Ochotona curzoniae

Geographic Range

Black-lipped pikas are found in the Alpine meadows and steppes of the Tibetan plateau in the Chang Taung region of the People’s Republic of China. (Schaller, 1998)

Biogeographic Regions:
palearctic (native ).

Habitat

Elevation
5300 m (high)
(17384 ft)


Ochotona curzoniae prefers to make burrows in flat to gently sloping terrain and silty to sandy-soiled meadow lands with few rocks and good drainage at elevations up to 5300 meters. (Schaller, 1998)

These animals are found in the following types of habitat:
temperate ; terrestrial .

Physical Description

Mass
0.10 to 0.20 kg
(0.22 to 0.44 lbs)


Black-lipped pikas are small, chunky, and lack a conspicuous tail. They have characteristic black lips and thick fur which is brown to reddish tan on the dorsal side and light gray on the ventral side. There is no sexual dimorphism in size or coloration and it is difficult to determine males from females by the external genitalia. (Dobson, Smith, and Gao, 2000; Schaller, 1998)

Some key physical features:
endothermic ; homoiothermic; bilateral symmetry .

Reproduction

Breeding interval
Breeding can occur every three weeks during the summer months.

Breeding season
The female is in estrous for one day during the week that copulation occurs.

Number of offspring
1 to 8; avg. 4.80

Gestation period
21 to 24 days; avg. 22.50 days

Time to weaning
21 days (average)

Time to independence
3 weeks (average)

Black-lipped pikas employ several mating systems. Most commonly, black-lipped pikas live in monogamous family groups made up of and adult male and female, juveniles, and younger animals. Both polygamy and polyandry have been recorded among O. curzoniae; this most commonly happens when an adult black-lipped pika dies and its mate joins another family group. Promiscuity has also been observed, though it is not common. (Dobson, Smith, and Gao, 1998; Dobson, Smith, and Gao, 2000; Smith and Gao, 1991; Smith, 1988)

Mating systems:
monogamous ; polyandrous ; polygynous .

Female black-lipped pikas breed and produce litters every three weeks during summer months. As the summer continues, more food becomes available and each successive litter becomes larger throughout the summer. During the mating season, there is intense male-male competition for females. Once family groups are formed, intergroup aggression keeps families together. Also, social interaction via grooming, boxing, communication and other contact helps to maintain social relationships. Communication reaches its peak during the weaning period of a new litter so that juveniles maintain strong social bonds with each other and their parents. Female O. curzoniae can, and often do, breed within the same summer of their own birth.

It was once thought that black-lipped pikas practiced a great deal of inbreeding to maintain family ties. However, it has since been discovered that roughly 97% of males leave their family range during the spring just before mating season. These males usually move to neighboring family groups. Some females also disperse from their natal family groups to join neighboring ones. This behavior helps to reduce the negative effects of inbreeding; however, the most successful matings usually occur between family members. (Dobson, Smith, and Gao, 1998; Dobson, Smith, and Gao, 2000; Schaller, 1998; Smith and Gao, 1991; Smith, 1988)

Key reproductive features:
iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; viviparous .

One unusual feature about O. curzoniae is that males invest heavily in offspring. Their behaviors consist of vigilance and awareness of the surroundings. They look out for potential predators as well as help maintain home range boundaries. The majority of juvenile-adult interactions occur with adult males rather than the females.

Females have limited interactions with offspring outside of nursing. A mother spends the majority of her time foraging so that she can provide enough energy to feed her young and prepare for the next litter, which quickly follows.

After three weeks, the offspring are weaned and go through a period of learning, generally with an adult male. The litters usually remain with their family for the first winter and disperse in spring before the reproductive season. (Dobson, Smith, and Gao, 1998; Dobson, Smith, and Gao, 2000; Smith and Gao, 1991; Smith, 1988)

Parental investment:
altricial ; pre-fertilization (provisioning, protecting: female); pre-hatching/birth (provisioning: female, protecting: female); pre-weaning/fledging (provisioning: female, protecting: male); pre-independence (protecting: male); post-independence association with parents; extended period of juvenile learning.

Lifespan/Longevity

Average lifespan (wild)
119.90 days

Extreme lifespan (wild)
957 days (high)

Average lifespan (wild)
119.90 days

The life expectancy of O. curzoniae is short because this species faces harsh winters and high parasitosis. Few members of each family group survive to the next spring. About 15.7% survive to breed during first year after birth, and only 1.5% survive to breed during their second year. (Smith and Gao, 1991; Wang and Dai, 1989)

Behavior

Territory Size
1000 m^2 (average)

Black-lipped pika families usually consist of one adult male, one adult female and 5-10 juveniles from at least 2 litters. They live in burrows comprising several tunnels and entrances. These allow a wide foraging area and quick access to protection from predators. Burrows also have many openings to above ground latrines. Tunnels can stretch for over 800 cm and are generally 20-40 cm below the turf.

Burrow and family structures are more cohesive on the plateau meadow lands than they are on the plateau desert. It is suggested that the greater abundance of food on the meadow makes it easier for a large family to live together without competing for resources. Families are generally territorial, and males chase off members of other families.

Females spend over 62% of their time foraging to maintain the high energy level necessary for almost constant gestation and lactation. Once weaning occurs, it is the males that interact with the juveniles during the learning process leading up to adulthood. Males also protect and maintain the burrow and home range of the family.

Ochotona curzoniae does not hibernate even during harsh winters. Foraging activity usually begins at sunrise and. Black-lipped pikas remain active periodically throughout much of the day. (Dobson, Smith, and Gao, 1998; Schaller, 1998; Smith and Gao, 1991; Smith, 1988)

Home Range

Ochotona curzoniae average adult home range is about 1000 square meters with the juvenile range about 900 square meters. (Smith and Gao, 1991)

Key behaviors:
terricolous; fossorial ; diurnal ; motile ; sedentary ; territorial ; social .

Communication and Perception

Black-lipped pikas communicate with family members by grooming, boxing and other contact to maintain social bonds. There is also frequent vocal communication informing the family of potential threats. (Dobson, Smith, and Gao, 1998; Smith and Gao, 1991; Smith, 1988)

Communicates with:
tactile ; acoustic .

Perception channels:
tactile ; acoustic ; chemical .

Food Habits

Black-lipped pikas spend the majority of their time foraging for food. Those that live in meadows can store large amounts of forage in hay piles, for later consumption. Desert dwelling O. curzoniae cannot easily create hay stores because high winds blow it away, and less cohesive social structures make it more difficult to protect caches. (Schaller, 1998; Smith and Gao, 1991; Smith, 1988)

Primary Diet:
herbivore (folivore , granivore ).

Plant Foods:
leaves; seeds, grains, and nuts; flowers.

Foraging Behaviors:
stores or caches food .

Predation

Known predators

Ochotona curzoniae are preyed upon by birds of prey, including common kestrels (Falco tinnunculus), black kites (Milvus lineatus), upland buzzards (Buteo hemilasius), and weasels and polecats (Mustela). They avoid predation primarily through their vigilance, cryptic coloration, and tendency to remain under cover of foliage or rocks when active. (Lai and Smith, 2003; Schaller, 1998)

Anti-predator adaptations::
cryptic .

Ecosystem Roles

Black-lipped pikas feed on seeds, and they disperse those seeds to some extent. However, since they have a limited home range, the seeds are not dispersed far from where they were collected. They are reservoirs for parasitic species such as fleas. Poisoning of Ochotona curzoniae by local people to reduce the destruction created by burrows has lead to the death of several bird species, for example Montifringilla and Pyrgilauda as well as Pseudopodoces humilis>. These birds are known to nest in black-lipped pika burrows and are harmed by the poison used to cull the pika population. (Lai and Smith, 2003; Schaller, 1998)

Key ways these animals impact their ecosystem:
disperses seeds; parasite .

Commensal or parasitic species (or larger taxonomic groups) that use this species as a host

Economic Importance for Humans: Negative

Black-lipped pikas have been blamed for soil erosion caused by burrowing and also for eating the vegetation normally fed upon by livestock. Generally, soil erosion is present before burrows have been created. At high densities, O. curzoniae populations do compete with livestock for vegetation. (Schaller, 1998)

Economic Importance for Humans: Positive

Ochotona curzoniae in low densities eat the foods untouched by livestock, and their excrement fertilizes the plants that livestock do eat. (Schaller, 1998)

Ways that people benefit from these animals:
produces fertilizer.

Conservation Status

IUCN Red List: [link]:
Lower Risk - Least Concern.

US Federal List: [link]:
No special status.

CITES: [link]:
No special status.

State of Michigan List: [link]:
No special status.

Pastoralists have used zinc phosphate to poison black-lipped pikas in hopes of reducing competition with livestock for vegetation. These pikas are not currently threatened, but further persecution and habitat changes may threaten populations in the future. (Schaller, 1998)

For More Information

Find Ochotona curzoniae information at

Contributors

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

Cara Ocobock (author), University of Michigan. Phil Myers (editor, instructor), Museum of Zoology, University of Michigan.

References

Dobson, F., A. Smith, W. Gao. 1998. Social and ecological influences on dispersal and philopatry in the plateau pika (Ochotona curzoniae). Behavioral Ecology, 9: 622-635.

Dobson, F., A. Smith, W. Gao. 2000. The mating system and gene dynamics of plateau pikas. Behavioural Processes, 51: 101-110.

Lai, C., A. Smith. 2003. Keystone status of plateau pikas (Ochotona curzoniae): effect of control on biodiversity of native birds. Biodiversity and Conservation, 12(9): 1901-1912.

Schaller, G. 1998. Wildlife of the Tibetan Steppe. Chicago: University of Chicago Press.

Smith, A., W. Gao. 1991. Social Relationships of Adult Black-Lipped pikas (Ochotona curzoniae). Journal of Mammalogy, 72: 231-247.

Smith, A. 1988. Patterns of Pika (Genus Ochotona) Life History Variation. Pp. 233-256 in M. Boyce, ed. Evolution of Life Histories of Mammals Theory and Pattern. New Haven: Yale University Press.

Wang, G., K. Dai. 1989. Natural Longevity of Plateau Pika. Acta Theriologica Sinica, 9: 56-62.

Yu, N., C. Zheng, L. Shi. 1997. Variation in Mitochondrial DNA and Phylogny of Six Species of Pikas (Ochotona). Jourmal of Mammalogy, 78: 387-396.

2009/11/22 03:59:08.587 US/Eastern

To cite this page: Ocobock, C. and P. Myers. 2006. "Ochotona curzoniae" (On-line), Animal Diversity Web. Accessed November 23, 2009 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Ochotona_curzoniae.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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