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Degu
Octodon degus
Conservation status
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Rodentia
Family: Octodontidae
Genus: Octodon
Species: O. degus
Binomial name
Octodon degus
(Molina, 1782)

The Degu (Octodon degus; pronounced DAY-goo) is a small caviomorph rodent that is native to Chile. It is sometimes referred to as the Brush-Tailed Rat (although not closely related to the rat family) and is also called the Common Degu, to distinguish it from the other members of the genus Octodon. Other members are also called degus, but they are distinguished by additional names. The name "degu" on its own, however, indicates either the genus Octodon or, more usually, O. degus. Degus are closely related to the chinchilla and guinea pig, also placed in parvorder Caviomorpha.

Contents

[edit] Social behavior

Degus are highly social. They live in burrows, and, by digging communally, they are able to construct larger and more elaborate burrows than they could on their own. Degus digging together coordinate their activities, forming digging chains. Females living in the same group have been shown to spontaneously nest communally; they nurse one another's young. They spend a large amount of time on the surface, where they forage for food. When foraging, their ability to detect predators is increased in larger groups, and each animal needs to spend less time in vigilance. Degus exhibit a wide array of communication techniques. They have an elaborate vocal repertoire, and the young need to be able to hear their mother's calls if the emotional systems in their brains are to develop properly. They use their urine to scent mark, and experiments have shown that they react to one another's marks. Degus' urine turns white when dry. Many degus bite when coming in contact with an unfamiliar scent.

Degus are seasonal breeders; the breeding season for wild degus begins in the Chilean winter, with pups born mid-late spring. It is also speculated that female degus are induced ovulators. Female degus are pregnant for approximately ninety days, having a long gestation period compared to other squirrels and even rodents such as hamsters. Litters usually contain four to seven pups, but size can range from one or two up to fifteen young. Degu pups are born relatively precocial, fully furred and with eyes open, and their auditory and visual systems are functional at birth.

Unlike other octodontids, degus are diurnal, and they have good vision. Their retinas include rod cells and two types of cone cells, one of which has its peak sensitivity in the ultraviolet region of the spectrum. Behavioral experiments have shown that degus are able to discriminate ultraviolet light from the wavelengths visible to humans. It is likely that this ultraviolet sensitivity has a social function, since both their ventral (stomach) fur and their urine are highly UV reflective.

[edit] Diet

Degu after dust bath

Degus are herbivores, feeding on grasses and browsing the leaves of shrubs, though they will also take seeds. Their feeding rate is constrained by the rate at which they can digest this relatively low quality food, and this varies between food types and environmental conditions, and like some other herbivores such as rabbits, they show coprophagy, chewing their own feces so as to extract more nutrition from them. This also serves to maintain healthy gut function during times when food is scarce. Although they are active by day, in high summer they do not leave their burrows in the middle of the day, and in hot conditions they forage as quickly as possible instead of maximizing the quality of their food. They tend to forage in shaded areas, though this tendency is reduced in the absence of predators. In open areas they spend more time being vigilant, so their effectiveness as foragers is reduced. Degus have a significant impact on the vegetation in areas where they live, and as the only rodent foraging by day, their numbers influence the food supply available to the more numerous nocturnal. However, numbers of all species of degu have been declining over recent decades, most likely due to human disturbance. Degus should not be fed a diet full of sugar, because due to their body's inability to process sugar, it will cause diabetes to develop.

[edit] As pets and research subjects

Degus are prone to diabetes due to their divergent insulin structure. For this reason, they are used frequently for research in this field. The degu's popularity as a pet was influenced by this research, as animals were imported into various countries for research and study.

Degus are also used extensively as laboratory animals.[2] Neuroscientists at the Riken Institute in Tokyo, Japan, used degus in research on tool-using in animals with good eye-and-paw coordination, in which the rodents were trained over a period of two months to use a tiny rake to retrieve out-of-reach seeds.[3]

Degus have become popular as pets, though until very recently they were seldom found in pet shops. Their advantages over traditional small pets are their diurnal habits, bubbly personalities, the haired tail (as compared to rats and mice) and their lifetime: they are said to live up to 13 years under ideal circumstances (though a poor gene pool/genetic background often reduces a pet degu's lifespan significantly). The average lifespan of a degu in captivity is said to be around 5-8 years of age. One disadvantage of the degu as a pet is that they gnaw much more than most other common rodent pets, especially through plastic-bottomed cages typically found in pet stores. Untamed degus, as with most small animals, can be prone to biting, but their intelligence makes them easy to tame. Degus often 'groom' their human owners, by a gentle nibbling action, but they can give a defensive bite if they feel threatened.

Degus are mainly known for their brown fur, but through genetic mutations and intentional inbreeding, there are degus with white, cream, black, blue, tan, and even patched fur.

[edit] Gallery

[edit] External links

[edit] References

  1. ^ Lessa, E., Ojeda, R. & Bidau, C. (2008). Octodon degus. In: IUCN 2008. IUCN Red List of Threatened Species. Downloaded on 5 January 2009.
  2. ^ Hejna, M. and P. Myers (2006). Octodon degus. Animal Diversity Web. http://animaldiversity.ummz.umich.edu/site/accounts/information/Octodon_degus.html. Retrieved 2008-04-09. 
  3. ^ "What a Rodent Can Do With a Rake in Its Paw". New York Times. 2008-03-26. http://www.nytimes.com/2008/03/26/science/26rodentw.html. Retrieved 2008-04-08. 

[edit] Further reading

  • Bacigalupe, L. D., Rezende, E. L., Kenagy, G. J., & Bozinovic, F. (2003). Activity and space use by degu: a trade-off between thermal conditions and food availability? Journal of Mammalogy, 84, 311-318.
  • Bozinovic, E., & Vasquez, R. A. (1999). Patch use in a diurnal rodent: handling and searching under thermoregulatory costs. Functional Ecology, 13, 602-610.
  • Bozinovic, F., & Torres-Contreras, H. (1998). Does digestion rate affect diet selection? A study in Octodon degu, a generalist herbivorous rodent. Acta Theriologica, 43, 205-212.
  • Chavez AE, Bozinovic F, Peichl L, Palacios AG. (2003) Retinal spectral sensitivity, fur coloration, and urine reflectance in the genus octodon (rodentia): implications for visual ecology. Invest Ophthalmol Vis Sci. May;44(5):2290-6.
  • Delgado LM; Vielma AH; Palacios AG; Schmachtenberg O. (2009) The GABAergic system in the retina of neonate and adult Octodon degus, studied by immunohistochemistry and electroretinography J Comp Neurol. 514(5):459-472.
  • Ebensperger, L. A., & Bozinovic, F. (2000). Communal burrowing in the hystricognath rodent, Octodon degu: a benefit of sociality? Behavioral Ecology and Sociobiology, 47, 365-369.
  • Ebensperger, L. A., & Caiozzi, A. (2002). Male degu, Octodon degu, modify their dustbathing behavior in response to social familiarity of previous dustbathing marks. Revista Chilena De Historia Natural, 75, 157-163.
  • Ebensperger, L. A., Veloso, C., & Wallem, P. K. (2002). Do female degu communally nest and nurse their pups? Journal of Ethology, 20, 143-146.
  • Ebensperger, L. A., & Wallem, P. K. (2002). Grouping increases the ability of the social rodent, Octodon degu, to detect predators when using exposed microhabitats. Oikos, 98, 491-497.
  • Gutierrez, J. R., Meserve, P. L., Herrera, S., Contreras, L. C., & Jaksic, F. M. (1997). Effects of small mammals and vertebrate predators on vegetation in the Chilean semiarid zone. Oecologia, 109, 398-406.
  • Helmeke, C., Poeggel, G., & Braun, K. (2001). Differential emotional experience induces elevated spine densities on basal dendrites of pyramidal neurons in the anterior cingulate cortex of Octodon degu. Neuroscience, 104, 927-931.
  • Jacobs, G. H., Calderone, J. B., Fenwick, J. A., Krogh, K., & Williams, G. A. (2003). Visual adaptations in a diurnal rodent, Octodon degu. Journal of Comparative Physiology A: Neuroethology Sensory Neural and Behavioral Physiology, 189, 347-361.
  • Kenagy, G. J., Veloso, C., & Bozinovic, F. (1999). Daily rhythms of food intake and feces reingestion in the degu, an herbivorous Chilean rodent: optimizing digestion through coprophagy. Physiological and Biochemical Zoology, 72, 78-86.
  • Lagos, V. O., Contreras, L. C., Meserve, P. L., Gutierrez, J. R., & Jaksic, F. M (1995). Effects of predation risk on space use by small mammals: a field experiment with a neotropical rodent. Oikos, 74, 259-264.
  • Ocampo-Garcés, A.,Hernández, F., Mena, W., Palacios, A.(2005). Wheel-running and rest activity pattern interaction in two octodontids (Octodon degus, Octodon bridgesi). Biological Research, 38, 299-305.
  • Ocampo-Garcés A, Mena W, Hernández F, Cortés N, Palacios AG. (2006). Circadian chronotypes among wild captured west-andean octodontids. Biological Research 39:209-20.
  • Opazo, J. C. (2005). A molecular timescale for caviomorph rodents (Mammalia, Hystricognathi). Molecular Phylogenetics and Evolution, 37, 932-937.
  • Ovtscharoff, W., & Braun, K. (2001). Maternal separation and social isolation modulate the postnatal development of synaptic composition in the infralimbic cortex of Octodon degu. Neuroscience, 104, 33-40.
  • Palacios, A., L. Peichl et F. Bozinovic (2004) La vision ultraviolette du rat degus. Pour la Science Cerveau & Psycho 5:92-95.
  • Vasquez, R. A., Ebensperger, L. A., & Bozinovic, F. (2002). The influence of habitat on travel speed, intermittent locomotion, and vigilance in a diurnal rodent. Behavioral Ecology, 13, 182-187.
  • Yunger, J. A., Meserve, P. L., & Gutierrez, J. R. (2002). Small-mammal foraging behavior: mechanisms for coexistence and implication for population dynamics. Ecological Monographs, 72, 561-577.
  • Ziabreva, I., Schnabel, R., Poeggel, G., & Braun, K. (2003). Mother's voice "buffers" separation-induced receptor changes in the prefrontal cortex of Octodon degu. Neuroscience, 119, 433-441.



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