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Home -> Kingdom Animalia -> Phylum Chordata -> Subphylum Vertebrata -> Class Mammalia -> Order Rodentia -> Suborder Myomorpha -> Family Muridae -> Subfamily Gerbillinae -> Species Meriones crassus

Meriones crassus
Sundevall's jird



2010/02/07 03:43:42.413 US/Eastern

By Sean Maher

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Rodentia
Suborder: Myomorpha
Family: Muridae
Subfamily: Gerbillinae
Genus: Meriones
Species: Meriones crassus

Geographic Range

Extends fromnorthwest Africa above 20 degrees north, through the Middle East and into Central Asia (Koffler, 1972). Parts of Egypt, Libya, northern Tunisia, northern Algeria, and northern Morocco are not inhabited by the species.

Biogeographic Regions:
palearctic (native ).

Habitat

They live in sandy soil in hot and dry environments (Koffler, 1972). Burrow locations are not necessarily dependent on vegetation proximity. They have been found in rocky environments as well. They live in complex burrows, sometimes with multiple exits and several chambers (Harrison et al., 1991).

These animals are found in the following types of habitat:
tropical .

Terrestrial Biomes:
desert or dune .

Physical Description

Mass
29 to 110 g; avg. 69.50 g
(1.02 to 3.87 oz; avg. 2.45 oz)


Length
205 to 290 mm; avg. 251.20 mm
(8.07 to 11.42 in; avg. 9.89 in)


They are small in body size, but comparatively large compared to some other gerbils. The fur is soft and dense. It shows a pattern of counter-shading coloration, with a sandy color and black spots on the dorsal side and solid white on the ventral side (Harrison et al., 1991). The claws are ivory-white. The upper lip, inside of the limbs, and the bottoms of the feet, are white as well. The tail has a black tip (Harrison et al., 1991) and is about the length of the body (Koffler, 1972). Females have four pairs of mammae (Harrison et al., 1991).

Some key physical features:
endothermic ; bilateral symmetry .

Reproduction

Breeding season
All year

Number of offspring
1 to 8; avg. 3.50

Gestation period
21 to 31 days; avg. 26 days

Birth Mass
3.35 g (average)
(0.12 oz)
[External Source: AnAge]


Time to weaning
1 months (average)

Age at sexual or reproductive maturity (female)
53 days (low)

Age at sexual or reproductive maturity (male)
53 days (low)

Pairs mate during the night, for the period of about two hours with quick copulations and repetition (Koffler, 1972). The mating behavior includes tail beats by the male during mounting; and foot-stomping takes place during courtship. Between mounts, the female grooms the male (Koffler, 1972).

Individuals are able to breed at an early age, and do so throughout the year (Koffler, 1972). The estrus cycle lasts 4.5 days on average and is negatively affected by poor food intake (Khokhlova et al., 2000). Litter size varies from one to eight newborns, averaging 3.5 individuals (Hayssen, 1993). Gestation usually lasts about 21 (Hayssen, 1993) to 26 (Koffler, 1972) days, although it takes longer if the mother is nursing young. Newborns weigh 2.5g to 4.5g at birth.

Key reproductive features:
year-round breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; fertilization (internal ); viviparous .

Newborns do not have hair. Hair growth begins after six to nine days, with a full coat complete after two weeks (Koffler, 1972). Weaning is complete after one month and sexual maturity can occur within two months after birth.

The female alone cares for the young until weaning (about one month) (Koffler, 1972).

Parental investment:
altricial ; female parental care .

Lifespan/Longevity

Extreme lifespan (captivity)
5.58 years (high)

Average lifespan (captivity)
5.60 years
[External Source: Max Planck Institute for Demographic Research]


There have been no recent studies on this subject with only one note of lifespan (Nowak, 1991).

Behavior

Individuals ususally do not leave a burrow until evening hours, presumably to avoid the high heat of day (Gould et al., 1998) and diurnal predators. They have specific physiological adaptations for water conservation, including highly efficient kidneys and te production of unusually dry fecal matter.

These jirds live in small colonies of upwards to 10 individuals (Harrison et al., 1991). The colonies occupy complex burrow structures (Harrison et al., 1991), individual burrow design varies (Nowak, 1991).

Key behaviors:
nocturnal ; motile ; colonial .

Food Habits

The jird is able to exploit low quality roughage and has a low energy requirement (Choshniak et al., 1987). The long period in which food stays within the lower digestive tract may add to this ability (Yahav et al., 1990). The diet shifts from mainly seeds in the summer to more green vegetation in the winter, possibly to increase water consumption (Degen et al., 1997). Change in the amount of food consumption has been linked to change in circadian rhythm, which is related to seasonal light changes (Haim et al., 1990). Jirds have also been known to eat locusts and other insects (Harrison et al., 1991). Sexual dimorphism also leads to different food intake and food selection, as the larger males tend to be less selective (Khokhlova et al., 1995). Food is stored in the burrows, and jirds normally return from foraging before eating (Koffler, 1972).

Foods eaten include: seeds, grassy vegetation, twigs and insects.

Primary Diet:
herbivore (folivore , granivore ).

Animal Foods:
insects.

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

Foraging Behaviors:
stores or caches food .

Predation

Known predators

Nocturnal activity allows individuals to avoid many day predators, and quick movements back to the burrow are used to escape (Gould et al., 1998). Coloration of the fur may also be an adaptive trait to avoid being seen by predators.

Ecosystem Roles

Jirds probably help disperse seeds when eating and foraging, since they moves food back to the burrow (Roberts, 1997). A number of other animal species have been found inside jird burrows, including tenebrionid beetles, scorpions, riddled hillcocks, and other kinds of gerbils (Koffler, 1972). They have a similar role as Gervillus cheesmani, Jaculus blanfordi, Allactage elater, and Meriones libycus in other areas (Roberts, 1997).

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

Economic Importance for Humans: Negative

They are sometimes seen as pests because they cause damage to agriculture, irrigation structures, and may even spread disease (Nowak, 1991). The pet trade may also lead to feral populations.

Ways that these animals might be a problem for humans:
crop pest; causes or carries domestic animal disease .

Economic Importance for Humans: Positive

They are used as pets and in medical research.

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

Conservation Status

IUCN Red List: [link]:
Least Concern.

US Migratory Bird Act: [link]:
No special status.

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

CITES: [link]:
No special status.

We have no text on this topic for this species. Look to the sidebar on the right for some limited information.

For More Information

Find Meriones crassus information at

Contributors

Sean Maher (author), University of Michigan.
Ondrej Podlaha (editor), University of Michigan.

References

Choshniak, I., S. Yahav. 1987. Can desert rodents better utilize low quality roughage than their non-desert kindred?. Journal of Arid Environment, 12: 241-246.

Degen, A., I. Khokhlova, M. Kam, K. Nagy. 1997. Body size, granivory and seasonal dietary shifts in desert gerbilline rodents. Functional Ecology, 11: 53-59.

Gould, E., G. McKay. 1998. Encyclopedia of Mammals. San Diego, CA: Academic Press.

Haim, A., G. Levi. 1990. Role of Body Temperature is Seasonal Acclimation: Photoperiod-Induced Rhythms and Heat Production in Meriones crassus. Journal of Experimental Zoology, 256: 237-241.

Harrison, D., P. Bates. 1991. The Mammals of Arabia. Kent, Engalnd: Harrison Zoological Museum.

Hayssen, V., A. Van Tienhoven, A. Van Tienhoven. 1993. Asdell's Patterns of Mammalian Reproduction; A Compendium of Species-Species Data. Ithaca, NY: Comstock Publishing.

Khokhlova, I., A. Degen, M. Kam. 1995. Body size, gender, seed husking and energy requirements in two species of desert gerbilline rodents, Meriones crassus and Gerbillus henleyi. Functional Ecology, 9: 720-724.

Khokhlova, I., M. Kam, S. Gonen, A. Degen. 2000. Level of Energy Intake Affects the Estrous Cycle in Sundevall's Jird (Meriones crassus). Physiological and Biochemical Zoology, 73 (3): 257-263.

Koffler, B. 1972. Meriones crassus. Mammalian Species, 9: 1-4.

Nowak, R. 1991. Walker's Mammals of the World. Baltimore, MD: The Johns Hopkins University Press.

Roberts, T. 1997. The Mammals of Pakistan. New York: Oxford University Press.

Yahav, S., I. Choshniak. 1990. Response of the digestive tract to low quality dry food in the fat jird (Meriones crassus) and the levant vole (Microtus guentheri). Journal of Arid Environment, 19: 209-215.

2010/02/07 03:43:43.881 US/Eastern

To cite this page: Maher, S. 2002. "Meriones crassus" (On-line), Animal Diversity Web. Accessed February 10, 2010 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Meriones_crassus.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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