By Mary Hejna
Geographic Range
Octodon degus is generally considered endemic to west central Chile, where it inhabits the lower slopes of the Andes. Although some have argued that its range may extend north into Peru, this is not well supported. It is common in the international pet trade, however, and is often used in laboratory studies outside of its native range. (Contreras, Torres-Mura, and Yanez, 1987; Woods and Boraker, 1975)
Biogeographic Regions:
neotropical
(native
).
Habitat
(3936 ft)
Octodon degus inhabits a mediterranean-type semi-arid shrubland ecosystem called "matorral", which is found on the western slopes of the Andes between 28 and 35 degrees south latitude. Further north the climate becomes too arid to support this plant community, and further south it is too wet. Degus appear to be limited to elevations below 1200 meters, both by the distribution of their habitat and by their intolerance of low oxygen partial pressure. Degus are well able to inhabit lands influenced by cattle grazing, and are agricultural pests in some areas. (Contreras, Torres-Mura, and Yanez, 1987; Fulk, 1976)
These animals are found in the following types of habitat:
temperate
; terrestrial
.
Terrestrial Biomes:
chaparral
.
Other:
agricultural
.
Physical Description
(5.98 to 10.56 oz)
(12.8 to 17.32 in)
Octodon degus superficially resembles a gerbil, but is much larger. Degus typically weigh between 170 and 300 g, and measure between 325 and 440 mm in length, including the tail. The fur is yellow-brown on the back and head, and the underparts and feet are cream colored. There is a pale band around the eye and, in some individuals, the neck. The tail is moderately long and conspicuously tufted. The ears are large and darkly pigmented. The fifth digit is reduced, and on the forefeet it has a nail instead of a claw. The cheekteeth are hypsodont and their biting surfaces resemble a figure of eight. Sexes are difficult to distinguish, but males tend to be about 10% larger than females. Pups are born furred and able to see, and begin exploring within hours of birth. Octodon degus can be distinguished from the two other members of the genus Octodon by slight differences in dental morphology. It is also smaller than its relatives and its tail is said to be more noticeably tufted. (Fulk, 1976; Lee, 2004)
Some key physical features:
endothermic
; homoiothermic; bilateral symmetry
.
Sexual dimorphism:
male larger.
Reproduction
Degus breed once a year.
Wild degus breed in September and October.
During the annual breeding season, male-male aggression temporarily increases. Males exclude other males from their burrow and monopolize the females (usually 2 to 4) who live there. Dustbathing and urine marking may be used in the defense of territory by both sexes, but these behaviors particularly increase in the male during the breeding season. Courting males often engage in mutual grooming with females, and frequently perform a courtship ritual which involves wagging of the tail and trembling of the body. The male then raises a hind leg and sprays urine onto the female. This may serve to familiarize her with his scent and perhaps make her more receptive to his advances in the future. Receptive females may sometimes enurinate males in a similar fashion. Related female degus may nurse each other's young. (Ebensperger and Caiozzi, 2002; Fulk, 1976; Kleiman, 1974; Soto-Gamboa, 2005)
Mating systems:
polygynous
; cooperative breeder
.
In the wild degus tend to breed once per year. The breeding season usually begins in late May (autumn in Chile), and the young are conceived in late winter to early spring (September to October). In wet years, degus may produce second litters. It has been suggested that degus may be induced ovulators, but this has not been established for certain. There is also some evidence that male reproductive organs may be sensitive to changes in photoperiod. The gestation period is 90 days, and litter size is typically 4-6 pups. The young are precocial. They are born with fur and teeth; their eyes are open and they are able to move about the nest on their own. Pups are weaned at 4 to 5 weeks, and become sexually mature between 12 and 16 weeks of age. Degus do not reach adult size until about 6 months of age, however, and they generally live in same-sex social groups until they are about 9 months old and their first breeding season occurs. It has been reported that pups raised in isolation in the laboratory experience severe neural and behavioral abnormalities. (Ebensperger and Hurtado, 2005b; Lee, 2004; Woods and Boraker, 1975)
Key reproductive features:
iteroparous
; seasonal breeding
; gonochoric/gonochoristic/dioecious (sexes separate); sexual
; viviparous
; post-partum estrous.
Before conception can occur, the male degu must invest considerable energy in the defense of his territory and harem from other males. The female subsequently expends considerable energy in gestation and lactation. The pregnancy is relatively long for a rodent, and the young are born well developed. After birth, both parents protect and provision the pups. Degus nest communally, and groups of related females nurse one another's young. In the laboratory, the female remains close to the pups until two weeks after birth, and males have been observed to huddle with the young during this period without instances of infanticide. In the wild, male degus may spend as much time feeding and huddling with the young as females do. Pups begin to eat solid food at about two weeks of age, and venture out of the burrow at three weeks. Upon weaning at four to six weeks, the pups are able to live independently of the parents and form same-sex social groups until their first breeding season. (Ebensperger and Hurtado, 2005b; Fulk, 1976; Lee, 2004; Woods and Boraker, 1975)
Parental investment:
precocial
; pre-fertilization (provisioning, protecting: female); pre-hatching/birth (provisioning: female, protecting: male, female); pre-weaning/fledging (provisioning: male, female, protecting: male, female); pre-independence (protecting: male, female).
Lifespan/Longevity
In laboratory conditions, degus typically live five to eight years.
Behavior
Degus are social and tend to live in groups of one to two males and two to five related females. Females participate in rearing on another's young. Groups maintain territories throughout much of the year. Degus are semi-fossorial, digging extensive communal burrow systems. These burrows are often shared by Bennett's chinchilla rat (Abrocoma bennettii). Degus feed exclusively above ground, however, and have been observed climbing into the low branches of shrubs while foraging. Dustbathing is an important social behavior among degus. Groups repeatedly mark favorite wallows with urine and anal gland secretions. This may help the group identify each other by scent as well as delineating territorial boundaries. Degus are mainly diurnal, and are most active during the morning and evening. (Ebensperger et al., 2004; Fulk, 1976; Woods and Boraker, 1975)
Home Range
Fulk (1976) estimated that social groups of degus occupy home areas of roughly 200 square meters, and that their density is about 75 degus per hectare. This may be an underestimate, however, due to the trapping methods used. (Fulk, 1976)
Key behaviors:
terricolous; fossorial
; saltatorial
; diurnal
; crepuscular
; motile
; sedentary
; territorial
; social
.
Communication and Perception
Degus have well-developed sight, smell, and hearing. They are highly vocal and use various calls to communicate with one another, including alarm calls, mating calls, and communication between parents and young. Vision is very important in avoidance of predators and in foraging. It has been shown that degus are able to see ultraviolet wavelengths, and that their urine reflects in the UV range when fresh. It has therefore been suggested that degus' urine scent marks are also visual cues. These scent marks are also used as dust wallows, allowing members of a social group to identify each other by scent. (Chavez et al., 2003; Fulk, 1976; Woods and Boraker, 1975)
Other communication keywords:
scent marks
.
Food Habits
Degus are generalist herbivores. They feed on the leaves, bark, and seeds of shrubs and forbs. Among their favorite foods are the bark of Cestrum palqui and Mimosa cavenia, leaves and bark of Proustia cuneifolia, Atriplex repunda, and Acacia caven, annuals such as Erodium cicutarum when in season, green grasses, and thistle seeds. Degus choose food items that reduce fiber and increase nitrogen and moisture in the diet, and thus prefer young leaves and avoid woodier shrubs. Degus rely on microbial fermentation in their enlarged cecum (they are "hindgut fermenters") to digest their food. They reingest a large percentage of their feces, usually during the night. This allows them to maximize their digestion. Degus store food in the winter, and it has been reported that they occasionally eat meat in old age. (Gutierrez and Bozinovic, 1998; Kenagy, Veloso, and Bozinovic, 1999; Veloso and Kenagy, 2005; Woods and Boraker, 1975)
Primary Diet:
herbivore
(folivore
, granivore
, lignivore); coprophage
.
Plant Foods:
leaves; wood, bark, or stems; seeds, grains, and nuts.
Other Foods:
dung.
Foraging Behaviors:
stores or caches food
.
Predation
- barn owls (Tyto alba)
- short-eared owls (Asio flammeus)
- black-chested buzzard eagles (Geranoaetus melanoleucus)
- culpeo foxes (Lycalopex culpaeus)
Octodon degus is subject to predation by larger mammals such as culpeo foxes (Lycalopex culpaeus), and from the air by raptors such as barn owls (Tyto alba), short-eared owls (Asio flammeus), and black-chested buzzard eagles (Geranoaetus melanoleucus). Degus use vigilance and cover to avoid predators. Their pelage is also counter-shaded and matches the soil color, which reduces visibility to predators. Degus live socially and use alarm calls to warn others of danger. When a predator is spotted, they take cover in shrubby areas and may retreat to the communal burrow. (Ebensperger and Wallem, 2002; Woods and Boraker, 1975)
Anti-predator adaptations::
cryptic
.
Ecosystem Roles
Octodon degus affects the plant community in its habitat by selective browsing. Degus behaviorally reduce the fiber content of their diet, preferrentially eating shrubs such as Adesmia bedwellii, Baccharis paniculata, and Chenopodium petioare, which are less fibrous and less thorny than others. These species have been shown to increase their foliage area upon exclusion of degus. As degus are very common, they are themselves an important food source for their predators. (Gutierrez and Bozinovic, 1998)
Degus often live in association with Bennett's chinchilla rats (Abrocoma bennettii). The two species are known to share burrow systems and have even been observed in the same chamber within a burrow. This is believed to be a mutualistic relationship, but it is not well understood. (Fulk, 1976; Woods and Boraker, 1975)
Key ways these animals impact their ecosystem:
creates habitat.
- Abrocoma benettii (Bennett's chinchilla rat)
Economic Importance for Humans: Negative
Degus are significant agricultural pests in some areas. They take advantage of cultivated prickly pear cactus, wheat, vineyards, and orchards as abundant food sources, and can do considerable damage. They are also known to host three species of parasites that can infect humans. (Fulk, 1976)
Ways that these animals might be a problem for humans:
injures humans (carries human disease); crop pest.
Economic Importance for Humans: Positive
Degus are frequently kept as pets, and are used extensively in laboratory research. Because they are largely diurnal, they are useful in research on circadian rhythms, and their intolerance of sugars makes them ideal models for diabetes research. (Lee, 2004)
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.
State of Michigan List: [link]:
No special status.
Octodon degus is considered the most common mammal in its range, and is not considered threatened or endangered. (Ebensperger and Wallem, 2002; Woods and Boraker, 1975)
Contributors
Tanya Dewey (editor), Animal Diversity Web, University of Michigan Museum of Zoology.
Mary Hejna (author), University of Michigan. Phil Myers (editor, instructor), Museum of Zoology, University of Michigan.
