|At Heidelberg Zoo, Germany|
Sciurus degus Molina, 1782
The common degu (Octodon degus; //), or, historically, the degu, is a small hystricomorpha rodent endemic to the Chilean matorral ecoregion of central Chile. The name degu on its own indicates either the entire genus Octodon or, more commonly, just the common degu. Common degus belong to the parvorder Caviomorpha of the infraorder Hystricognathi, along with the chinchilla and guinea pig. The word degu comes from the indigenous language of Chile, Mapudungun, and the word dewü, meaning 'mouse' or 'rat'.
The common degu is a small animal with a body length of 25.0 to 31.0 cm (9.8–12.2 in) and a weight of 170 to 400 g (6.0 to 14.1 oz). It has yellow-brown fur above and creamy-yellow below, with yellow around the eyes and a paler band around the neck. It has a long, thin tail with a tufted, black tip, dark sparsely furred ears, and pale grey toes. Its fifth toe is small with a nail, rather than a claw, on the fore feet. Its hind feet are bristled. Its cheek teeth are shaped like figures-of-eight, hence the degu's genus name Octodon.
Common 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.
Common degus exhibit a wide array of communication techniques. They have an elaborate vocal repertoire comprising up to 15 different sounds, 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, although in males the hormone testosterone may suppress their sense of smell somewhat.
Common degus are seasonal breeders; the breeding season for wild degus begins in the Chilean autumn when day and night are roughly equal, with pups born in early to mid-spring. Female degus are pregnant for approximately ninety days, having a comparatively long gestation period compared to other non-caviomorph rodents. Female pregnant weight varies over the course of gestation and according to litter size; litters contain an average of six pups, but size can range from one or two up to twelve young. Common degu pups are born relatively precocial, fully furred and with eyes open, and their auditory and visual systems are functional at birth. Unlike most other rodents, male common degus also take part in protecting and raising their pups until they are old enough to leave the family.
Unlike some other octodontids, common degus are diurnal (active during the day), and they have good vision. Their retinas include rod cells and two types of cone cells, corresponding to peak sensitivity in the green and ultraviolet regions 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.
Common degus are strictly herbivorous, in the wild feeding on grasses and browsing the leaves of shrubs, though they will also take seeds. Throughout much of the year forage is dried and so common degus are specially adapted to a very high fibre intake, and this varies between food types and environmental conditions. Like some other herbivores such as rabbits, they perform coprophagy (faecal reingestion) so as to extract more nutrition from their diet. 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 instead emerge to forage in the mornings and evenings.
Perhaps the most remarkable feature of common degu physiology is their intolerance of dietary sugar. Common degus have been found to have a divergent insulin structure (one of the hormones that regulate blood glucose level) and so are highly susceptible to developing diabetes mellitus when fed regularly on a diet containing free sugars. This is thought to be due to evolutionary pressure arising from the lack of availability of free sugars in the degu's natural environment. Because of this, the ingredients of non-degu-specific hard feed formulations given to captive common degus should be checked for sugar-laden ingredients, such as molasses, honey, and glucose syrup.
Common degus entered the research spotlight due to their unique relationship with sugar and diabetes, but are also studied for a wide variety of other reasons. Neuroscientists at the Riken Institute in Tokyo, Japan, used common degus for research into tool use in animals with good eye-and-paw coordination, in which they spontaneously learned to use a tiny rake to retrieve out-of-reach seeds. Common degus have also been found to spontaneously stack objects in order of decreasing size. In both cases it is the first time these behaviours have been recorded in animals other than apes and birds. [Dubious.]
Another interesting area of common degu research is circadian rhythm function, i.e. the ability of the brain to tell what time of day it is. Degus have the ability to show both diurnal and nocturnal rhythms if the environment permits, allowing a unique opportunity for study. Common degus can take cues that do not relate to day length, such as temperature, melatonin levels and even scents from other degus to adjust their rhythms.
Common degus are also invaluable in development and aging studies. Research has shown that separation anxiety caused by separating pups from their mother from an early age for periods of half an hour or more can cause developmental and behavioural changes in later life, similar to ADHD in humans. In elderly common degus, neural markers have been discovered which are remarkably similar to those in humans with Alzheimer's disease, which is the first time this has been seen in a wild-type rodent.
After initial interest into common degus as research subjects, they have become popular as pets, though until recently[when?] 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 lifespan: they are reported to live up to 13 years under ideal circumstances (though a poor gene pool or genetic background often reduces a pet degu's lifespan significantly). The average lifespan of a common degu in captivity is typically around six to eight years of age.
One disadvantage of the common degu as a pet is their predisposition to chewing, due to their continually growing incisor and molar teeth. For this reason, common degus cannot be housed in plastic-bottomed cages typically found in pet stores. A metal cage with multiple levels made for rats and secured double latches works best. It is important to line the levels with grass mats or a soft fabric so that the common degus do not get bumblefoot.
Untamed common degus, as with some other small animals kept as pets, can be prone to biting, but their intelligence makes them easy to tame. Regular non-predatory handling and food offerings help with this transition. It is important to never try to catch a common degu by the tail because the skin and tuft at the end is easily "shed" (pulled off). This helps common degus in the wild elude capture by predators, but it is painful to the creature and the tail end will not grow back. When tail shedding occurs, common degus will chew off the damaged portion. This can reduce the chances of infection.
Common degus often "groom" their human owners with a gentle nibbling action, and readily bond with any person spending time with them. Common degus need regular sand baths, like Chinchillas need dust baths, to keep their coats healthy and free from grease. Chinchilla sand is ideal for this. They should have access to these baths regularly, preferably two or three times a week for half an hour at a time. However, too frequently, daily sand bathing can make their coats soiled.
Some jurisdictions consider common degus as a potential invasive species and forbid owning them as a pet.
In Canada, they are illegal to own in Newfoundland and Labrador.
- Ojeda, R.; Bidau, C. (2013). "Octodon degus". IUCN Red List of Threatened Species. 2013: e.T15088A22240077. doi:10.2305/IUCN.UK.2013-2.RLTS.T15088A22240077.en.
- C. Michael Hogan & World Wildlife Fund. 2013. Chilean Matorral. Ed. Mark McGinley. Encyclopedia of Earth. National Council for Science and the Environment. Washington DC
- Muñoz Urrutia, Rafael, ed. (2006), Diccionario Mapuche: Mapudungun/Español, Español/Mapudungun (in Spanish) (2nd ed.), Santiago, Chile: Editorial Centro Gráfico, pp. 104, 105, 141, ISBN 978-956-8287-99-3
- Woods, C.; Boraker, D. (21 November 1975), "Octodon degus" (PDF), Mammalian Species, 67 (67): 1–5, doi:10.2307/3503820, JSTOR 3503820
- Ebensperger, L. A.; Bozinovic, F. (2000), "Communal burrowing in the hystricognath rodent, Octodon degus: A benefit of sociality?", Behavioural and Ecological Sociobiology, 47 (5): 365–369, doi:10.1007/s002650050678, ISSN 0340-5443
- Ebensperger, L. A.; Bozinovic, F. (2000b), "Energetics and burrowing behaviour in the semifossorial degu Octodon degus (Rodentia: Octodontidae)", Journal of Zoology, 252 (2): 179–186, doi:10.1111/j.1469-7998.2000.tb00613.x
- Ebensperger, L.A.; Veloso, C.; Wallem, P. (2002), "Do female degus communally nest and nurse their pups?", Journal of Ethology, 20 (2): 143–146, doi:10.1007/s10164-002-0063-x, ISSN 0289-0771
- Ebensperger, L.A.; Hurtado, M.; Lacey, E.; Chang, A.; Chang, AT (2004), "Communal nesting and kinship in degus (Octodon degus)", Naturwissenschaften, 91 (8): 391–395, doi:10.1007/s00114-004-0545-5, ISSN 0028-1042, PMID 15309311
- Quirici, V.; Castro, R.A.; Oyarzun, J.; Ebensperger, L.A. (2008), "Female degus (Octodon degus) monitor their environment while foraging socially", Anim Cogn, 11 (3): 441–448, doi:10.1007/s10071-007-0134-z, ISSN 1435-9448, PMID 18214556
- Long, C.V. (2007), "Vocalisations of the degu (Octodon degus), a social caviomorph rodent", Bioacoustics, 16 (3): 223–244, doi:10.1080/09524622.2007.9753579, ISSN 0952-4622
- Ziabreva, I.; Schnabel, R.; Poeggel, G.; Braun, K. (2003), "Mother's voice "buffers" separation-induced receptor changes in the prefrontal cortex of Octodon degus", Neuroscience, 119 (2): 433–441, doi:10.1016/S0306-4522(03)00123-4, PMID 12770557
- Kleiman, D.G. (1974), "Patterns of behaviour in hystricomorph rodents", in Rowlands, I. W.; Weir, B. J. (eds.), The Biology of Hystricomorph Rodents, London: Academic Press
- Fischer, R.; Meunier, G. (1985), "Responses to conspecifics' urine by the degu Octodon degus", Physiological Behaviour, 34 (6): 999–1001, doi:10.1016/0031-9384(85)90027-7, PMID 4059390
- Jechura, T.; Walsh, J.; Lee, T. (2003), "Testosterone suppresses circadian responsiveness to social cues in the diurnal rodent Octodon degus", Journal of Biological Rhythms, 18 (1): 43–50, doi:10.1177/0748730402239675, PMID 12568243
- Ebensperger, L.A.; Caiozzi, A. (2002), "Male degus, Octodon degus, modify their dustbathing behaviour in response to social familiarity of previous dustbathing marks", Revista Chilena de Historia Natural, 75: 157–163, doi:10.4067/S0716-078X2002000100015, ISSN 0716-078X
- Bozinovic, F.; Bacigalupe, L.; Vasquez, R.; Visser, H.; Veloso, C.; Kenagy, G. (2004), "Cost of living in free-ranging degus (Octodon degus): Seasonal dynamics of energy expenditure", Comparative Biochemistry and Physiology A, 137 (3): 597–604, doi:10.1016/j.cbpb.2003.11.014, PMID 15123196
- Brown, C.; Donnelly, T. (2001), "Cataracts and reduced fertility in degus (Octodon degus): Contracts secondary to diabetes mellitus", Lab Animal, 30: 25–26, ISSN 0093-7355
- Long, C.V.; Ebensperger, L.A. (2009), "Pup growth rates and breeding female weight changes in two populations of captive bred degus (Octodon degus), a precocial caviomorph rodent", Reprod Domest Anim., 45 (6): 975–82, doi:10.1111/j.1439-0531.2009.01470.x, ISSN 0936-6768, PMID 19497026
- Reynolds, T.; Wright, J. (1979), "Early postnatal physical and behavioural development of degus (Octodon degus)", Lab Animal, 13 (2): 93–9, doi:10.1258/002367779780943576, PMID 480906
- "Breeding Degus". Exoticnutrition.com. Retrieved 20 May 2019.
- Kenagy, G.; Nespolo, R.; Vasquez, R.; Bozinovic, F. (2002), "Daily and seasonal limits of time and temperature to activity of degus", Revista Chilena de Historia Natural, 75 (3): 567–581, doi:10.4067/S0716-078X2002000300008, ISSN 0716-078X
- Cha'vez, A.; Bozinovic, F.; Peich, F.; Palacios, A. (2003), "Retinal spectral sensitivity, fur coloration and urine reflectance in the genus Octodon (Rodentia): Implications for visual ecology", Investigative Ophthalmology & Visual Science, 44 (5): 2290–2296, doi:10.1167/iovs.02-0670, PMID 12714673
- Palacios, A.; Bozinovic, F. (2003), "An "enactive" approach to ingtegrative and comparative biology: Thoughts on the table", Biol. Res., 36 (1): 101–105, doi:10.4067/S0716-97602003000100008, ISSN 0716-9760, PMID 12795209
- Bozinovic, F.; Gallardo, P.A.; Visser, G.H.; Cortés, A. (2003), "Seasonal acclimatization in water flux rate, urine osmolality and kidney water channels in free-living degus: Molecular mechanisms, physiological processes and ecological implications", J Exp Biol, 206 (Pt 17): 2959–2966, doi:10.1242/jeb.00509, PMID 12878664
- Langer, P. (2002), "The digestive tract and life history of small mammals", Mammal Review, 32 (2): 107–131, doi:10.1046/j.1365-2907.2002.00101.x
- Gutiérrez, J.; Bozinovic, F. (1998), "Diet selection in captivity by a generalist herbivorous rodent (Octodon degus) from the Chilean coastal desert", Journal of Arid Environments, 39 (4): 601–607, doi:10.1006/jare.1998.0412
- Kenagy, G.; 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 (1): 78–86, doi:10.1086/316644, PMID 9882606
- Opazo, J.C.; Soto-Gamboa, M.; Bozinovic, F. (2004). "Blood glucose concentration in caviomorph rodents". Comp. Biochem. Physiol. A. 137: 57–64. doi:10.1016/j.cbpb.2003.09.007. PMID 14720591.
- Nishi, M.; Steiner, D. (2003). "Cloning of complementary DNA's encoding islet amyloid polypeptide, insulin, and glucagon precursors from a New World rodent, the degu, Octodon degus". Molecular Endocrinology. 4 (8): 1192–8. doi:10.1210/mend-4-8-1192. PMID 2293024.
- Okanoya, K.; Tokimoto, N.; Kumazawa, N.; Hihara, S.; Iriki, A.; Ferrari, Pier Francesco (2008), Ferrari, Pier Francesco (ed.), "Tool-Use Training in a Species of Rodent: The Emergence of an Optimal Motor Strategy and Functional Understanding", PLOS ONE, 3 (3): e1860, doi:10.1371/journal.pone.0001860, PMC 2268009, PMID 18365015
- Tokimoto, N.; Okanoya, K. (2004), "Spontaneous construction of "Chinese boxes" by degus (Octodon degus): A rudiment of recursive intelligence?", Japanese Psychological Research, 46 (3): 255–261, doi:10.1111/j.1468-5584.2004.00257.x
- Kas, M. J. H.; Edgar, D. M. (2000), "Photic phase response curve in Octodon degus: Assessment as a function of activity phase preference", American Journal of Physiology, 278 (5): R1385–1389, doi:10.1152/ajpregu.2000.278.5.R1385, PMID 10801311, S2CID 18503215
- Kas, M.J.; Edgar, D.M. (1998), "Crepuscular rhythms of EEG sleep-wake in a hystricomorph rodent, Octodon degus", J. Biol. Rhythms, 13 (1): 9–17, doi:10.1177/074873098128999871, PMID 9486839
- Morris, L.G.; Tate, B.L. (2007), "Phase response curve to melatonin in a putatively diurnal rodent, Octodon degus", Chronobiol. Int., 24 (3): 407–411, doi:10.1080/07420520701420352, PMID 17612940
- Jechura, T.J.; Mahoney, M.M.; Stimpson, C.D.; Lee, T.M. (2006), "Odor-specific effects on reentrainment following phase advances in the diurnal rodent, Octodon degus", Am. J. Physiol. Regul. Integr. Comp. Physiol., 291 (6): R1808–1816, doi:10.1152/ajpregu.00005.2006, ISSN 0363-6119, PMID 16840658, S2CID 7354002
- Zehle, S.; Bock, J.; Jezierski, G.; Gruss, M.; Braun, K. (2007), "Methylphenidate treatment recovers stress-induced elevated dendritic spine densities in the rodent dorsal anterior cingulate cortex", Dev. Neurobiol., 67 (14): 1891–1900, doi:10.1002/dneu.20543, PMID 17874461
- Inestrosa, N.C.; Reyes, A.E.; Chacon, M.A.; Cerpa, W.; Villalon, A.; Montiel, J.; Merabachvili, G.; Aldunate, R.; et al. (2004), "Human-like rodent amyloid-beta-peptide determines Alzheimer pathology in aged wild-type Octodon degus", Neurobiol. Aging, 26 (7): 1023–8, doi:10.1016/j.neurobiolaging.2004.09.016, PMID 15748782
- CDFW, California Department of Fish and Wildlife (2018). "Why can't I have a [...] in California?". Wildlife.ca.gov. Retrieved 2019-04-11.
- "UT Admin Code R657-3. Collection, Importation, Transportation, and Possession of Animals. April 1, 2019". Rules.utah.gov. Retrieved 20 May 2019.
- "Regulations of Connecticut State Agencies : TITLE 26. Fisheries & Game". Eregulations.ct.gov. Retrieved 20 May 2019.
- "10 Facts That Make Degus The Coolest Pet Ever!". Animalhub.com. 6 March 2016. Retrieved 20 May 2019.
|Wikimedia Commons has media related to Octodon degus.|
|Wikispecies has information related to Octodon degus|