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Euchoreutes naso
long-eared jerboa


By Nicole Swanson

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Rodentia
Family: Dipodidae
Genus: Euchoreutes
Species: Euchoreutes naso

Geographic Range

Long-eared jerboas are found in the Palearctic region. They occur from southernmost Mongolia into the Takla-Makan Desert, Mengxin, Aerijin Mountain, and Qing-Zang Plateau regions of north western China. (Rogovin and Shenbrot, 1995; Wilson and Reeder, 2005; Xiang, et al., 2004)

Biogeographic Regions
palearctic (Native )

Habitat

Specimens of long-eared jerboas have been collected in sandy valleys that are covered with low growing bushes. Their range includes the Mengxin and Aerjin Mountain regions, which are arid and classified as desert or semi desert. Their range also extends into the Qing-Zang Plateau region, a cold, high elevation desert area. Plant diversity is low in these areas, Haloxylon ammodendron is a low-growing shrub that has been documented at some capture sites. (Nowak, 1999; Rogovin and Shenbrot, 1995)

Habitat Regions
temperate ; terrestrial

Terrestrial Biomes
desert or dune

Physical Description

Range length
70 to 90 mm
(2.76 to 3.54 in)

Long-eared jerboa tail length is 150 to 162 mm, body length is from 70 to 90 mm. The tail is covered with short hairs that are similar in color to the rest of the body except for the terminal tuft, which is white and black. Upper parts are reddish yellow to a light russet color. The belly is white. The hind foot is 40 to 46 mm in length, with five digits. The two lateral digits are shorter than the three central ones. The central metatarsals are fused for a small distance. The feet are covered with tufts of bristly hairs. Long-eared jerboas have ears that are 1/3 longer than their heads. The incisors are thin and white. A small premolar can be found on each side of the upper jaw. Females have eight mammae. (Nowak, 1999)

Other Physical Features
endothermic ; heterothermic ; bilateral symmetry

Sexual Dimorphism
sexes alike

Reproduction

Mating systems for long-eared jerboas are not known. However, mating systems of closely related species in the family Dipodidae suggest that they may be polygynous. (Heske, et al., 1995)

Breeding interval
Breeding can occur twice each season.

Breeding season
Breeding begins shortly after awaking from hibernation.

Range number of offspring
2 to 6

Range gestation period
25 to 35 days

For some closely related jerboa species mating usually happens a short time after awaking from winter hibernation. A female will breed twice during the summer season and raise between 2 to 6 young. Gestation time is between 25 and 35 days. (Macdonald, 1999)

Key Reproductive Features
iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); viviparous

Little is known about parental investment in long-eared jerboas. Like most mammals, females nurse and care for their young at least until they are weaned.

Parental Investment
pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Female)

Lifespan/Longevity

The longevity of long-eared jerboas is not known. However, average longevity of jerboas is 2 to 3 years. (Macdonald, 1999)

Behavior

Long-eared jerboas are presumed to be mainly nocturnal, as are other jerboas. Related jerboas often create four different types of burrows. A temporary, summer day burrow is used for cover while hunting during the daylight. They will have a second, temporary burrow used for hunting at night. They will also have two permanent burrows one for summer and one for winter. The permanent summer burrow is actively used throughout the summer and the young are raised there. Jerboas hibernate during the winter and use the permanent winter burrow for this. Temporary burrows are shorter in length than permanent burrows. (Macdonald, 1999; Shenbrot, et al., 1999)

Key Behaviors
terricolous; fossorial ; saltatorial ; nocturnal ; sedentary ; hibernation

Home Range

Home ranges of long-eared jerboas are not known.

Communication and Perception

Exact forms of communication in long-eared jerboas are not known. However, many species within the family Dipodidae participate in dust bathing. Dust bathing is often a way to use chemical communication. Their keen hearing suggests they may use sounds or vibrations to communicate. (Ebensperger, 2000)

Long-eared jerboas eat flying insects, using sound to locate insects and capture them by performing fast leaps into the air. (Nowak, 1999)

Communication Channels
acoustic ; chemical

Other Communication Modes
scent marks

Perception Channels
visual ; acoustic

Food Habits

Long-eared jerboas are insectivorous. They often eat flying insects by using sound to locate them and then capturing them by performing fast leaps into the air. (Kelt, et al., 1999; Kelt, et al., 1996; Shenbrot, et al., 1999)

Animal Foods
insects

Predation

Known Predators


Little owls (Athene noctua) are predators of some species in the family Dipodidae in central Asia. Most species in this family take advantage of their excellent hearing to avoid predation by nocturnal predators. Jerboas are also cryptically colored. (Lay, 1974)

Anti-predator Adaptations
cryptic

Ecosystem Roles

Long-eared jerboas are insectivorous, impacting insect populations within their range. (Shenbrot, et al., 1999)

Commensal/Parasitic Species

Economic Importance for Humans: Positive

Long-eared jerboas are important members of their native ecosystems.

Economic Importance for Humans: Negative

Helicobacter species were found in the feces of long-eared jerboas, suggesting they could carry and transmit this disease. (Kazuo, et al., 2004)

Negative Impacts
injures humans (carries human disease)

Conservation Status

IUCN Red List [Link]
Endangered

US Federal List [Link]
No special status

CITES [Link]
No special status

State of Michigan List [Link]
No special status

The major threat to long-eared jerboas, according to IUCN, is ongoing human disturbance. The IUCN states that the population has undergone an observed or probable reduction of at least eighty percent over the last ten years due to either a decline in area of occupancy, extent of occurrence, and/or quality of their habitat. (Baillie, 2006)

For More Information

Find Euchoreutes naso information at

Contributors

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

Nicole Swanson (author), University of Wisconsin Stevens Point, Chris Yahnke (editor, instructor), University of Wisconsin Stevens Point.

References

Baillie, J. 2006. "IUCN Red List of Threatened Species" (On-line). Accessed November 18, 2006 at http://www.iucnredlist.org/search/details.php/8162/summ.

Ebensperger, L. 2000. Dustbathing and intra-sexual communication of social degus, Octodon. Revista chilena de historia natural, 73: 2. Accessed November 20, 2006 at http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-078X2000000200011&lng=es&nrm=i&tlng=en.

Heske, E., G. Shenbrot, K. Rogovin. 1995. Spatial Oraganization of Stylodipus telum (Dipodidae, Rodentia) in Dagestan, Russia. Journal of Mammalogy, 76: 800-808. Accessed November 20, 2006 at http://www.jstor.org/cgi-bin/jstor/printpage/00222372/ap050308/05a00120/0.pdf?backcontext=page&dowhat=Acrobat&config=jstor&userID=8fec23ca@uwsp.edu/01cc99331400501b2be7a&0.pdf.

Kazuo, G., J. Wei, Z. Qiang, O. Yuzaburo, K. Haruo, I. Toshio, I. Mamoru. 2004. Epidemiology of Helicobacter Infection in Wild Rodents in the Xinjiang-Uygur Autonomous Region of China. Current Microbiology, 49: 221-223. Accessed November 20, 2006 at http://www.springerlink.com/content/g0v87fn0l9n4rg1n/.

Kelt, D., J. Brown, E. Heske, P. Marquet, S. Morton, J. Reid, K. Rogovin, G. Shenbrot. 1996. Community Structure of Desert Small Mammals: Comparisons Across Four Continents. Ecology, 77/3: 746-761. Accessed September 12, 2006 at http://links.jstor.org/sici?sici=0012-9658%28199604%2977%3A3%3C746%3ACSODSM%3E2.0.CO%3B2-Y.

Kelt, D., K. Rogovin, G. Shenbrot, J. Brown. 1999. Patterns in the Structure of Asian and North American Desert Small Mammal Communities. Journal of Biogeography, 26/4: 825-841. Accessed September 12, 2006 at http://links.jstor.org/sici?sici=0305-0270%28199907%2926%3A4%3C825%3APITSOA%3E2.0.CO%3B2-N.

Lay, D. 1974. Differential Predation on Gerbils (Meriones) by the Little Owl, Athene brahma. Journal of Mammalogy, 55: 608-614. Accessed November 16, 2006 at http://links.jstor.org/sici?sici=0022.

Macdonald, D. 1999. The Encyclopedia of Mammals. New York, New York: Facts On File Inc..

Nowak, R. 1999. Walker's Mammals of the World. Baltimore and London: The Johnson Hopkins University Press.

Rogovin, K., G. Shenbrot. 1995. Geographical Ecology of Mongolian Deset Rodent Communities. Journal of Biogeography, Vol. 22: 111-128. Accessed September 12, 2006 at http://links.jstor.org/sici=0305-0270%28199501%2922%3A1%3C111%3AGEOMDR%E2.0.CO%3B2-4.

Shenbrot, G., B. Krasnov, K. Rogovin. 1999. Spatial Ecology of Deser Rodent Communities. Journal of Mammalogy, 081/04: 1177-1179. Accessed October 01, 2006 at http://www.bioone.org/perlserv/?request=get-document&issn=0022-2372&volume=081&issue=04&page=1177.

Wilson, D., D. Reeder. 2005. Mammal Species of the World. Baltimore: The Johns Hopkins University Press.

Xiang, Z., X. Liang, S. Huo, S. Ma. 2004. Quantitative Analysis of Land Mammal Zoogeographical Regions in China and Adjacent Regions. Zoological Studies, 43(1): 142-160. Accessed October 01, 2006 at http://zoolstud.sinica.edu.tw/Journals/43.1/142.pdf.

To cite this page: Swanson, N. 2007. "Euchoreutes naso" (On-line), Animal Diversity Web. Accessed February 12, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Euchoreutes_naso.html

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