By Whitney Wiest
Geographic Range
Jaculus orientalis (greater Egyptian jerboa) can be found across North Africa in Morocco, Algeria, Tunisia, Libya, and Egypt. The species is especially common in Egypt and extends east through Sinai and into southern parts of Israel; formerly, the species inhabitated areas of Saudi Arabia. (Aulagnier, 2004)
Habitat
Jaculus orientalis lives in humid coastal and salt semi-deserts and in subtropical shrubland, including rocky valleys and meadows. They are also found in barley fields of the semi-nomadic Bedouin tribes. (Aulagnier, 2004; Kirmiz, 1962)
Habitat Regions
temperate
; terrestrial ![]()
Terrestrial Biomes
desert or dune
; savanna or grassland
; scrub forest ![]()
Physical Description
139.1 g
(4.90 oz)
9.5 to 16 cm
(3.74 to 6.30 in)
Jaculus orientalis is covered in white fur ventrally and pale, yellowish-dark, sandy fur dorsally. Inner and outer ear areas are covered with thin hair. Eyelashes and sensory hairs are black, while the whiskers are a grey-white. The long tail is also covered with thin, short hair and ends in a tuft of black and white hair; the tail length averages 12.8 to 25 cm (5-9.8 inches). When standing, J. orientalis rests its tail in a curved position, providing support and balance. Males are slightly larger than females; average body mass is 139.1 g. ("Family: Birch mice, jumping mice, and jerboas", 2003; Nowak, 1991; "Family: Birch mice, jumping mice, and jerboas", 2003; Hooper and El Hilali, 1972; Kirmiz, 1962; Nowak, 1991)
The body is very compact with a large head and limbs adapted for saltatorial locomotion. The hindlimbs are roughly four times as long as the forelimbs and are used for leverage when the animal jumps great distances. The metatarsal bones of the hind feet are fused together into a 'cannon bone,' and the first and fifth digits are missing, leaving three long, flattened toes. Hair on the sides and bottom of toes increase the surface area of the foot and aid in locomotion on sand. (Kirmiz, 1962; Vaughan, et al., 2000)
Average basal metabolic rate is 3.649 kcal/kg/h and body temperature is 37.0 degrees Celcius. (El Hilali and Veillat, 1975; Kirmiz, 1962)
Reproduction
There is limited information regarding the reproduction of J. orientalis primarily because of its nocturnal and burrowing behavior. Other members of the genus Jaculus display a particular courting behavior that involves the male standing upright in front of a female. He then lowers himself to the height of the prospective mate and slaps her regularly with his front limbs. It is believed that most desert jerboa species have a polygynous mating system. (Happold, 1967; Happold, 1967)
Greater Egyptian jerboas breed once a year.
Greater Egyptian jerboas breed from February to July.
2 to 8
3
40 days
Although captive breeding has been unsuccessful, it is known that J. orientalis breeds once a year. The breeding season is typically 5-6 months, starting in February and culminating in July. Females average 3 offspring per litter, but may have anywhere from 2-8 young each season. The gestation period is roughly 40 days long. ("Family: Birch mice, jumping mice, and jerboas", 2003; Aulagnier, 2004)
When a young J. orientalis is born, its forelimbs and hindlimbs are the same length, the tail is short, fur is absent, and the eyes and ears are closed. For the first 4 weeks, pups move by crawling with their forelimbs, dragging their body and hindlimbs along. After 4 weeks, quadruped locomotion emerges, and after about 47 days old they are capable of bipedal locomotion. In other members of Jaculus, particularly J. jaculus, offspring are born naked with short vibrissae, and relatively short hindlimbs and tail. They crawl with their forelimbs in the same fashion as J. orientalis. Jaculus jaculus young open their eyes after 5 weeks and eat solid food at 6 weeks. They are independent at 8-10 weeks and sexually mature at 8 to 12 months. ("BBC- Science & Nature- Wildfacts", 2002; Eilam and Shefer, 1997; Happold, 1967)
Key Reproductive Features
iteroparous
; seasonal breeding
; gonochoric/gonochoristic/dioecious (sexes separate); fertilization
; viviparous ![]()
After birth, the mother stays with the young in her burrow during the breeding and suckling season until the altricial offspring are self-sufficient. She provides the young with food and resources as well as the protection and shelter of the burrow. In addition, it is assumed that the mother teaches locomotion and survival skills until independence is reached, about the time of weaning. It is unknown if the male has a role in parental investment. (Kirmiz, 1962)
Parental Investment
altricial
; pre-fertilization (Provisioning, Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Female)
Lifespan/Longevity
Status: captivity
6 (high) years
The lifespan of J. orientalis in the wild is unknown; however, the offspring of a pregnant female captured for a study lived for over six years in captivity. (Kirmiz, 1962)
Behavior
Jaculus orientalis is nocturnal. These jerboas emerge from their burrows during late dusk and retreat at dawn. Related jerboas begin their nocturnal activities with a sand bath, removing oils and fat from their fur. They groom themselves with their paws and teeth each night. When in the burrow, they sleep most of the time or rest in a crouching position. If in a group, jerboas like to sleep on top of one another, helping to retain body heat in the winter months. They are social and play with each other; Bedouins have reported that the jerboas congregate in large burrows for "play" on some nights. (Ferguson, 2002; Hooper and El Hilali, 1972; Kirmiz, 1962)
Greater Egyptian jerboas dig burrows into desert sand and clay by brushing away, pushing, or beating the soil. Burrows can range from 0.75 m to 1.75 m in depth and 1 to 2.5 m long. All burrows have a main chamber where the jerboa lives and most have an emergency exit tunnel as well. The nest is frequently lined with camel hair, dry shredded vegetation, and plant wool to keep the inhabitant warm. In rainy winters burrows are made on the sides of hills to avoid flooding, and the entrance is usually left open. In the summertime, burrows are usually on less elevated areas near vegetation; the entry hole is plugged with soil, possibly to prevent snakes and warm air from entering. (Kirmiz, 1962; Nowak, 1991)
Earlier studies observed neither hypothermia nor temperature-induced torpor in Jaculus, suggesting that J. orientalis neither hibernated nor aestivated and was active year-round. However, Jaculus does not store food or have cheek pouches, and reports by Bedouins suggest that these animals disappear in the winter, implying extended below ground occupancy of burrows. This might be in response to extremely cold temperatures or food shortages. Later investigations supported this hypothesis and have depicted J. orientalis as an ideal model for deep hibernation. It has been found that during cold periods J. orientalis accumulates lipid reserves, developing a seasonal obesity. Following this accumulation, the jerboa's body temperature decreases to around 9.8°C and the heart frequency drops to about 9.3 beats/min; an active jerboa maintains a 37°C body temperature with a heart rhythm around 300 beats/min. (El Hilali and Veillat, 1975; Hooper and El Hilali, 1972; Kirmiz, 1962)
Home Range
Since J. orientalis is nocturnal, it is difficult to assess their home range; however, during a field survey, 1 to over 50 individuals were counted over a distance of 0.8 km. (Nowak, 1991)
Communication and Perception
Jaculus orientalis is a social species, so different forms of communication are likely. However, only observations based on captive animals are available. Captive jerboas make sounds to display their anger or annoyance with other jerboas. They have also been observed rhythmically tapping and scratching the floor of their cages. The action gives the impression of communication; however, the animal might only be imitating digging movements used to create burrows in the wild. Communication with scent marking or pheromones is highly likely. (Kirmiz, 1962)
The related desert jerboa, J. jaculus, seems to recognize one another by smell when in captivity. Individuals close their eyes, come together until their noses touch, and remain in contact this way for 1 to 5 seconds. (Happold, 1967)
Jerboas have keen hearing and eyesight, being well-adapted to their nocturnal habits. They also perceive chemical cues and vibrations. (Nowak, 1991; Vaughan, et al., 2000)
Communication Channels
tactile
; acoustic
; chemical ![]()
Food Habits
Jaculus orientalis feeds primarily on succulent roots, sprouts, seeds, grains, a few cultivated vegetables, and occasional insects. They use their front paws to sift through sand and loose soil looking for seeds, to handle food, and to climb plants. Jaculus orientalis derives water from green vegetation and can live without drinking free-standing water for long periods of time. When related desert jerboa species do drink from a body of water, they dip their front paws in the water and then lick them, instead of drinking directly from the source. ("Family: Birch mice, jumping mice, and jerboas", 2003; Ferguson, 2002; Kirmiz, 1962; Nowak, 1991)
Animal Foods
insects
Plant Foods
leaves; roots and tubers; seeds, grains, and nuts
Predation
- snakes (Serpentes)
- Rüppel's foxes (Vulpes rueppellii)
- fennecs (Vulpes zerda)
- owls (Strigiformes)
- humans (Homo sapiens)
Jaculus orientalis is highly nocturnal and stays in the safety of its burrow during the day. However, if the animal feels threatened while inside, it can escape through an emergency exit tunnel. When alarmed at night, J. orientalis takes off towards its burrow or another safe, sheltered area. Its normal bipedal walking/running gait turns into great leaps as it flees a predator. These leaps have been measured at 1.5 to 3 m long and 1 m high. This is the animal's only mechanism of defense, and generally it cannot get away from a predator once captured. Common predators of J. orientalis include snakes, Rüppel's foxes, fennecs, owls, and humans. (Ferguson, 2002; Kirmiz, 1962)
Ecosystem Roles
The herbaceous food habits and subsequent foraging behavior of J. orientalis influences its ecological community. When the animal sifts through the soil searching for seeds and other plant matter, it disperses seeds, particularly those too hard to eat, and aerates the soil. This can promote new plant growth and enhance water movement in the soil. Likewise, J. orientalis serves as a food source for carnivorous and omnivorous species in the ecosystem. (Ferguson, 2002)
The burrow of J. orientalis may be used as a home by conspecifics when the homeowner dies, or by other rodent species. It is possible that even insects such as scorpions and spiders will make use of abandoned burrows. In addition, tiny ticks, mites, and lice live in the fur of jerboas. (Happold, 1967)
Economic Importance for Humans: Positive
Jaculus orientalis is hunted by Bedouin peoples for its meat, and sometimes its fur, used as trim. The Bedouin have three strategies for capturing jerboas. They pour water into burrows, forcing the animals to run out, they dig up burrows, or they set traps by burrow openings. In addition, J. orientalis is occasionally found on the pet trade due to its tame disposition and manageable size. (Kirmiz, 1962)
Economic Importance for Humans: Negative
Jaculus orientalis has been known to eat barley and ripe from Bedioun agricultural fields, damaging the crop harvest. This negative impact often leads the Bedouin to intensify their hunting of the species. (Kirmiz, 1962)
Negative Impacts
crop pest
Conservation Status
IUCN Red List [Link]
Least Concern
US Federal List [Link]
No special status
CITES [Link]
No special status
State of Michigan List [Link]
No special status
In 1996, J. orientalis was designated as 'Lower Risk/Near Threatened' on the IUCN Red List of Threatened Species. In 2004, the species was re-assessed and its status improved to 'Least Concern,' where it now currently resides. This means the species is widespread and abundant. (Aulagnier, 2004)
For More Information
Find Jaculus orientalis information at
Contributors
Tanya Dewey (editor), Animal Diversity Web, University of Michigan Museum of Zoology.
Whitney Wiest (author), University of Michigan, Phil Myers (editor, instructor), Museum of Zoology, University of Michigan.



