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Home -> Kingdom Animalia -> Phylum Chordata -> Subphylum Vertebrata -> Class Mammalia -> Order Rodentia -> Suborder Myomorpha -> Family Cricetidae -> Subfamily Cricetinae -> Species Phodopus campbelli

Phodopus campbelli
Campbell's hamster



2009/11/29 04:24:35.137 US/Eastern

By Nora Cothran

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Rodentia
Suborder: Myomorpha
Family: Cricetidae
Subfamily: Cricetinae
Genus: Phodopus
Species: Phodopus campbelli

Geographic Range

Originally identified by O. Thomas in 1905, Phodopus campbelli, commonly known as Campbell’s hamsters or Djungarian hamsters, is a native inhabitant of the steppes and deserts of inner Mongolia and northeastern China.

Heavily inhabited areas of Mongolia include, but are not limited to; the Altai Mountains, Transbaikalia, Nei Mongol, and Tuvinskaya (Tuva) Autonomous Region. Bordering territories in northern China, the Heilungkiang and Hebei provinces more specifically, also maintain dense populations of Phodopus campbelli. (Thomas, 1905)

Biogeographic Regions:
palearctic (native ).

Habitat

Depth
1 m (high); avg. 0 m
(3.28 ft; avg. 0 ft)


Phodopus campbelli, like fellow members of the subfamily Cricetinae, creates and dwells within a system of subterranean tunnels. The burrow of a Campbell’s hamster is usually composed of four to six main tunnels, with both horizontal and vertical orientation. A nest is often constructed at the end of a tunnel and comprised of dry and insulating materials including but not limited to; grasses, feathers and wool. Seeds and nuts are, more often than none, cached in extremely close proximity to the nesting area.

Additionally, several region-dependant variations in Phodopus campbelli habitat preference have been documented. In the Barga and Great Kingan Regions of Manchuria, Campbell’s hamsters are known to share tunnels and burrows with several species of pikas, Ochotona dauria and Ochotona mantchuria. Moreover, Phodopus campbelli residing on the Mongolian Plateau do not dig their own burrows, but instead share the burrows of several species of Meriones, more commonly known as jirds or gerbils. (Allen, 1938)

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

Physical Description

Mass
23.40 g (average)
(0.82 oz)


Length
80 to 103 mm; avg. 102 mm
(3.15 to 4.06 in; avg. 4.02 in)


Basal Metabolic Rate
1.63 +/- 0.38 to 1.88 +/- 0.57 cm^3 oxygen/hour

Phodopus campbelli is very small in size and the pelage is short and silky. The underside of the animal is covered in soft, buff, light grey fur and the dorsal portions, including the head, are woody brown in color. The underfur is quite short and is a dark slate grey. A defined charcoal stripe runs from between the ears to the tail. The pads of all digits, and the small tail, are covered in silky white fur. Additionally, Campbell’s hamsters, like other members of the subfamily Cricetinae, possess large internal cheek pouches that terminate above the scapula. Males are larger than females. (Thomas, 1905)

Phodopus campbelli is often confused with Phodopus sungorus, Siberian hamsters. However, there are several physical characteristics that distinguish the two species. The ears of Phodopus campbelli are generally smaller than those of Phodopus sungorus. The mid-dorsal stripe of the Campbell’s hamster is both thin and defined and the area where the dorsal fur meets the ventral fur is a creamy light yellow. Moreover, the underfur of Phodopus campbelli is dark grey, whereas that of Phodopus sungorus is white. (Allen, 1938; Hollister, 1912)

Documentations of region-dependant color variations have been collected from several populations of Phodopus campbelli native to the Chuisaya Steppes. Campbell’s hamsters from this area are slightly greyer in color and possess a shorter mid-dorsal stripe. (Hollister, 1912)

Some key physical features:
endothermic ; bilateral symmetry .

Reproduction

Breeding interval
Wild Phodopus campbelli breed 3-5 times per year, whereas captive Phodopus campbelli breed year-round.

Breeding season
The breeding of the Campbell’s hamster varies by geographic location. Breeding begins in April and May, in the Tuva and Transbaikalia regions of Mongolia, respectively, and ends in late September or early October.

Number of offspring
1 to 12; avg. 8.20

Gestation period
13.50 to 22 days; avg. 17.50 days

Time to weaning
17 days (average)

Time to independence
23 days (average)

Age at sexual or reproductive maturity (female)
48 days (average)

Age at sexual or reproductive maturity (male)
23 days (average)

These hamsters are promiscuous.

Wild Phodopus campbelli breed 3-5 times per year, whereas captive Phodopus campbelli breed year-round. The breeding of the Campbell’s hamster varies by geographic location. Breeding begins in April and May, in the Tuva and Transbaikalia regions of Mongolia, respectively, and ends in late September or early October. (Ross, 1995)

Key reproductive features:
iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; viviparous ; sperm-storing ; post-partum estrous.

At birth, Phodopus campbelli are completely helpless and hairless. Incisors and small claws are present, but the ears and eyes are both sealed. The young depend on parental investment, until weaned approximately 17 days after birth. Prior to a study published in 2000 (Jones, 2000), it was widely held that female hamsters were primarily responsible for care of the young. However, recent evidence suggests that male hamsters may assist in the delivery process by consuming both amniotic fluid, placenta and fetal membranes. (Jones, 2000; McMillan, 1999)

Parental investment:
altricial ; pre-hatching/birth (protecting: male, female); pre-weaning/fledging (protecting: male, female); pre-independence (protecting: male, female).

Lifespan/Longevity

Typical lifespan (captivity)


Minimal documentation exists regarding the lifespan of wild Phodopus campbelli. However, captive Phodopus campbelli have been extensively studied in various laboratory settings and their average lifespan ranges anywhere from 1.5 - 3 years.

Behavior

Territory Size
3.50 km^2 (average)

Phodopus campbelli is generally classified as a solitary species. However, in captivity, Phodopus campbelli exhibits a high tolerance for other species members when sharing territory. Campbell’s hamsters, like other members of the subfamily Cricetinae, are nocturnal. But captive specimens exhibit sporadic adherence to the cyclical sleep and wake patterns of wild specimens.

Phodopus campbelli scuttles when moving quickly. In order to avoid predators the Campbell’s hamster often moves both abruptly and quickly. The maximum documented running speed of Phodopus campbelli is 6.5 km/hr. (Wynne-Edwards, Surov, and Telitzina, 1992)

Home Range

Aside from burrow dimensions, very few documented accounts investigate the overall territory size of Phodopus campbelli. However, in 1992 a survey of the home ranges of several female Campbell's hamsters was conducted in the Lake Tere Xol region of Mongolia. (Wynne-Edwards, Surov, and Telitzina, 1992)

Key behaviors:
fossorial ; nocturnal ; motile ; solitary ; territorial .

Communication and Perception

Of all the senses, Phodopus campbelli relies primarily on smell. Wild Campbell’s hamsters, both male and female, utilize urine and feces to identify territory. Additionally, secretions originating from both the ventral sebaceous glands and the Harderian glands, located behind the animal’s ears, are utilized not only for territory identification, but also for communication. The oral sebaceous glands of Phodopus campbelli also serve to mark all of the contents that enter or leave the animal’s cheek pouches. (Tikhonova, Tikhonov, and Surov, 1999; Wynne-Edwards, Surov, and Telitzina, 1992)

Communicates with:
chemical .

Other communication keywords:
scent marks .

Perception channels:
visual ; tactile ; acoustic ; chemical .

Food Habits

The diet of wild Phodopus campbelli is primarily composed of a wide variety of seeds, nuts and vegetation, including Stipa capillata, Iris ruthenia and Iris flavisima. Additionally, the diet may be supplemented with small invertebrates and insects. (Ross, 1995)

Captive Phodopus campbelli will welcome almost any commercially prepared hamster food, traditionally composed of an extensive assortment of corn, oats, sunflower, peanuts, dried fruits and dehydrated vegetables. The latter diet is often supplemented with alfalfa and minerals or salts.

Primary Diet:
herbivore (folivore , granivore ).

Animal Foods:
insects; terrestrial non-insect arthropods; mollusks.

Plant Foods:
leaves; wood, bark, or stems; seeds, grains, and nuts; fruit; flowers.

Foraging Behaviors:
stores or caches food .

Predation

Known predators

Known predators of tsaker falcon this species are corsac foxes (Vulpes corsac), eagle owls (Bubo bubo), steppe eagles (Aquila nipalensis), kestrels (Falco tinnunculus) and saker falcons (Falco cherrug).

Ecosystem Roles

Phodopus campbelli disperses the seeds of numerous plant species. Their burrows are not particularly destructive to the environment. They serve as a primary food source for corsac foxes (Vulpes corsac).

Key ways these animals impact their ecosystem:
disperses seeds.

Species (or larger taxonomic groups) that are mutualists with this species
  • Ochotona dauria
  • Ochotona mantchuria

Economic Importance for Humans: Negative

Because the natural habitat of Phodopus campbelli is large, undeveloped expanses of desert, steppe and mountain terrain, the Campbell’s hamster is not responsible for any documented significant negative economic impact.

Phodopus campbelli are inquisitive by nature, and individuals kept as pets have been known to nip humans when startled. However, the bite is primarily a reaction mechanism and nips rarely extend beyond the outermost, dermal, layer of tissue.

Ways that these animals might be a problem for humans:
injures humans (bites or stings).

Economic Importance for Humans: Positive

Phodopus campbelli, Phodopus roborovskii (desert hamsters) and Phodopus sungorus (Dzhungarian or Siberian hamsters) were collectively introduced to the American pet industry as “dwarf hamsters” in the mid-1990s. The small size, mild temperament and inexpensive maintenance of Phodopus campbelli make it both a novel pet for first-time pet owners and a particularly ideal pet for young children. Moreover, unlike larger species of the subfamily Cricetinae, Phodopus campbelli will contentedly cohabitate with one another.

The same characteristics that make the Campbell’s hamster an attractive pet also make it an ideal animal model for scientific study. Phodopus campbelli has been utilized in numerous cytogenetic and cancer investigations. (Pogosianz, 1975)

Ways that people benefit from these animals:
pet trade ; research and education.

Conservation Status

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

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

CITES: [link]:
No special status.

The natural habitat of Phodopus campbelli is an extremely dry, harsh and undeveloped environment. The Campbell’s hamster is not considered an endangered species and probably does not face extinction anytime in the near future.

For More Information

Find Phodopus campbelli information at

Contributors

Matthew Wund (editor), University of Michigan.

Nora Cothran (author), University of Michigan. Phil Myers (editor, instructor), Museum of Zoology, University of Michigan.

References

Allen, G. 1938. The Mammals of China and Mongolia. New York, New York: The American Museum of Natural History.

Hollister, N. 1912. New mammals from the highlands of Siberia. Smithsonian Miscellaneous Collections, 60/14: 1-6.

Jones, J. 2000. Paternal hamsters mechanically assist the delivery, consume amniotic fluid and placenta, remove fetal membranes, and provide parental care during the birth process. Hormones & Behavior, 37/2: 116-125.

Lai, S. 1994. Individual odors in Djungarian hamsters (Phodopus campbelli). Ethology, 96/2: 117-126.

McMillan, H. 1999. Divergent reproductive endocrinology of the estrous cycle and pregnancy in dwarf hamsters (Phodopus). Comparative Biochemistry & Physiology, 124/1: 53-67.

Pogosianz, H. 1975. Djungarian hamster, a suitable tool for cancer research and cytogenetic studies. Journal of the National Cancer Institute, 54: 659-664.

Robinson, T. 1993. Cross-species discrimination of individual odors by hamsters (Muridae: Mesocricetus auratus, Phodopus campbelli). Ethology, 94/4: 317-325.

Ross, P. 1995. Phodopus campbelli. Mammalian Species, 0/503: 1-7. Accessed November 01, 2004 at http://www.science.smith.edu/departments/Biology/VHAYSSEN/msi/default.html.

Sokolov, V., N. Vasil'ev. 1993. Behavior of Phodopus campbelli Thomas, 1905 in nature: Confirmation of the social biological field theory. Doklady Akademii Nauk, 332/5: 667-670.

Sokolov, V., N. Vasil'ev. 1993. Hybridological analysis confirms species independence of Phodopus sungorus (Pallas, 1973) and Phodopus campbelli (Thomas, 1905). Doklady Akademii Nauk, 332/1: 120-123.

Thomas, O. 1905. A new Cricetulus from Mongolia. Annals and Magazine of Natural History, 6: 322-323.

Tikhonova, G., I. Tikhonov, A. Surov. 1999. Comparative analysis of sensory information in dwarf hamsters (Rodentia, Cricetidae). Zoologicheskii Zhurnal, 78/2: 253-259.

Wynne-Edwards, K. 1987. Evidence for Obligate Monogamy in the Djungarian hamster Phodopus-Campbelli. Behavioral Ecology & Sociobiology, 20/6: 427-438.

Wynne-Edwards, K., A. Surov, A. Telitzina. 1992. Field Studies of Chemical Signaling: Direct Observations of Dwarf Hamsters in Soviet Asia. New York, New York: Plenum Press.

2009/11/29 04:24:37.473 US/Eastern

To cite this page: Cothran, N. and P. Myers. 2004. "Phodopus campbelli" (On-line), Animal Diversity Web. Accessed December 02, 2009 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Phodopus_campbelli.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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