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[[pl:Koszatniczka]]
[[pl:Koszatniczka]]
[[pt:Octodon degus]]
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[[ru:Дегу]]
[[sk:Degu čilský]]
[[sk:Degu čilský]]
[[fi:Degu]]
[[fi:Degu]]

Revision as of 21:46, 1 January 2010

Degu
Octodon degus
Scientific classification
Kingdom:
Animalia
Phylum:
Chordata
Class:
Mammalia
Order:
Rodentia
Family:
Octodontidae
Genus:
Octodon
Species:
O. degus
Binomial name
Octodon degus
(Molina, 1782)
Synonyms
  • Sciurus degus Molina 1782
  • Octodon degus: Waterhouse 1848

The Degu (Octodon degus; /'deɪgu:/) is a small caviomorph rodent that is endemic to Chile. It is sometimes referred to as the Brush-Tailed Rat (although not closely related to the rats) 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 the parvorder Caviomorpha of the infraorder Hystricognathi.

Description

The Degu is a small rodent with a body length of 2.50 to 3.10 centimetres (0.98–1.22 in) and a weight of 170 to 300 grams. It has yellow-brown fur above and creamy-yellow below, with yellow about 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 forefeet. Its hindfeet are bristled. Its cheek teeth are shaped like figures-of-eight, hence the Degus's generic name "Octodon".[2]

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.[3] Degus digging together coordinate their activities, forming digging chains.[4] Females living in the same group have been shown to spontaneously nest communally;[5][6] they nurse one another's young. They spend a large amount of time on the surface, where they forage for food.[4] When foraging, their ability to detect predators is increased in larger groups,[7] and each animal needs to spend less time in vigilance. Degus exhibit a wide array of communication techniques. They have an elaborate vocal repertoire comprising up to 15 unique sounds,[8] and the young need to be able to hear their mother's calls if the emotional systems in their brains are to develop properly.[9] They use their urine to scent mark,[10] and experiments have shown that they react to one another's marks,[11] although in males the hormone testosterone may suppress their sense of smell somewhat.[12]

Degus are seasonal breeders; the breeding season for wild degus begins in the Chilean autumn when there is roughly 12 hours light:12 hours darkness,[13] with pups born in early to mid spring.[14] Female degus are pregnant for approximately ninety days,[15][2] 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;[16] litters contain an average of six pups,[5] but size can range from one or two up to twelve young.[16] Degu pups are born relatively precocial, fully furred and with eyes open, and their auditory and visual systems are functional at birth.[17]

Unlike some other octodontids, degus are diurnal[18] (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.[19] 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.[20]

Diet

Degus use their forepaws to hold food whilst eating

Degus are strictly herbivorous, in the wild feeding on grasses and browsing the leaves of shrubs, though they will also take seeds.[21] Throughout much of the year forage is dried[18] and so degus are specially adapted to a very high fibre intake,[22] and this varies between food types and environmental conditions.[23] Like some other herbivores such as rabbits, they perform coprophagy (faecal reingestion) so as to extract more nutrition from their diet.[24] This also serves to maintain healthy gut function during times when food is scarce.[24] Although they are active by day, in high summer they do not leave their burrows in the middle of the day[18] and instead emerge to forage in the mornings and evenings.

Perhaps the most remarkable feature of degu physiology is their intolerance of dietary sugar. Degus have been found to have a divergent insulin structure (one of the hormones that regulates blood glucose level) and so are highly susceptible to developing diabetes mellitus when fed regularly on a diet containing free sugars.[25] This is thought to be due to evolutionary pressure arising from the lack of availability of free sugars in the degu's natural environment.[26]

Research subjects

Degus are extremely intelligent and have a good ability to solve problems[citation needed]

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 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.[27] Degus have also been found to spontaneously stack objects in order of decreasing size.[28] In both cases it is the first time these behaviours have been recorded in animals other than apes and birds.

Another interesting area of 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,[29] allowing a unique opportunity for study. Degus can take cues that do not relate to day length, such as temperature,[30] melatonin levels[31] and even scents from other degus[32] to adjust their rhythms.

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.[33] In elderly degus, neural markers have been discovered which are remarkably similar to those in humans with Alzheimer's disease,[34] which is the first time this has been seen in a non-human mammal.

Pets

Captive degus need plenty of space to exhibit a full range of normal behaviours

After initial interest into degus as research subjects, 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 reported 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 typically around 6-8 years of age. One disadvantage of the degu as a pet is their predisposition to chewing, due to their continually growing incisor and molar teeth.[2] For this reason degus cannot be housed in 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, and readily bond with any person spending time with them.

  • Octodon degus in captivity.
    Octodon degus in captivity.
  • Two degus outside.
    Two degus outside.
  • Baby degus nursing.
    Baby degus nursing.
  • Baby degu wrapped in a sock.
    Baby degu wrapped in a sock.
  • Adult degu on a perch.
    Adult degu on a perch.
  • Two degus.
    Two degus.
  • Degu scratching.
    Degu scratching.
  • Three degu pups, eight days old.
    Three degu pups, eight days old.

References

  1. ^ Template:IUCN2008
  2. ^ a b c Woods, C.; Boraker, D. (21 November 1975), "Octodon degus" (PDF), Mammalian Species, 67: 1–5
  3. ^ Ebensperger, L.A; Bozinovic, F. (2000), "Communal burrowing in the hystricognath rodent, Octodon degus: A benefit of sociality?", Behavioural and Ecological Sociobiology, 47: 365–369, doi:10.1007/s002650050678, ISSN (Print) 1432-0762 (Online) 0340-5443 (Print) 1432-0762 (Online) {{citation}}: Check |issn= value (help)
  4. ^ a b Ebensperger, L.A.; Bozinovic, F. (2000b), "Energetics and burrowing behaviour in the semifossorial degu Octodon degus (Rodentia: Octodontidae)", Journal of Zoology, 252: 179–186, doi:10.1111/j.1469-7998.2000.tb00613.x
  5. ^ a b Ebensperger, L.A.; Veloso, C.; Wallem, P. (2002), "Do female degus communally nest and nurse their pups?", Journal of Ethology, 20: 143–146, doi:10.1007/s10164-002-0063-x, ISSN (Print) 1439-5444 (Online) 0289-0771 (Print) 1439-5444 (Online) {{citation}}: Check |issn= value (help)
  6. ^ Ebensperger, L.A.; Hurtado, M.; Lacey, E.; Chang, A. (2004), "Communal nesting and kinship in degus (Octodon degus)", Naturwissenschaften, 91: 391–395, doi:10.1007/s00114-004-0545-5, ISSN (Print) 1432-1904 (Online) 0028-1042 (Print) 1432-1904 (Online) {{citation}}: Check |issn= value (help)'
  7. ^ Quirici, V.; Castro, R.A.; Oyarzun, J.; Ebensperger, L.A. (2008), "Female degus (Octodon degus) monitor their environment while foraging socially", Anim Cogn., 11: 441–448, doi:10.1007/s10071-007-0134-z, ISSN (Print) 1435-9456 (Online) 1435-9448 (Print) 1435-9456 (Online) {{citation}}: Check |issn= value (help)
  8. ^ Long, C.V. (2007). "Vocalisations of the degu (Octodon degus), a social caviomorph rodent". Bioacoustics. 16: 223–244. ISSN 0952-4622.
  9. ^ 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: 433–441. doi:10.1016/S0306-4522(03)00123-4.
  10. ^ Kleiman, D.G. (1974). Patterns of behaviour in hystricomorph rodents. Symp Zool Soc Lond., 34: 171-209. In: The Biology of Hystricomorph Rodents (1974; Rowlands, I. W. and Weir, B. J. eds.). London: Academic Press Inc.
  11. ^ Fischer, R.; Meunier, G. (1985), "Responses to conspecifics' urine by the degu Octodon degus", Physiological Behaviour, 34: 999–1001, doi:10.1016/0031-9384(85)90027-7
  12. ^ Jechura, T.; Walsh, J. last3=Lee (2003), "Testosterone suppresses circadian responsiveness to social cues in the diurnal rodent Octodon degus", Journal of Biological Rhythms, 18: 43–50, doi:10.1177/0748730402239675 {{citation}}: |first3= missing |last3= (help); Missing pipe in: |first2= (help)CS1 maint: numeric names: authors list (link)
  13. ^ Ebensperger, L.A.; Caiozzi, A. (2002), "Male degus, Octodon degus, modify their dustbathing behviour 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
  14. ^ 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: 597–604, doi:10.1016/j.cbpb.2003.11.014
  15. ^ Brown, C.; Donnelly, T. (2001), "Cataracts and reduced fertility in degus (Octodon degus): Contracts secondary to diabetes mellitus", Lab Animal (NY), 30: 25–26, ISSN 0093-7355.
  16. ^ a b 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.: pp. 8, doi:10.1111/j.1439-0531.2009.01470.x, ISSN 0936-6768. {{citation}}: |pages= has extra text (help); Check |issn= value (help)
  17. ^ Reynolds, T.; Wright, J. (1979), "Early postnatal physical and behavioural development of degus (Octodon degus)", Lab Animal (NY), 13: 93–9, doi:doi:10.1258/002367779780943576 {{citation}}: Check |doi= value (help)
  18. ^ a b c 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: 567–581, doi:10.4067/S0716-078X2002000300008, ISSN 0716-078X
  19. ^ 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", IOVS, 44: 2290–2296, doi:10.1167/iovs.02-0670
  20. ^ Palacios, A.; Bozinovic, F. (2003), "An "enactive" approach to ingtegrative and comparative biology: Thoughts on the table", Biol Res., 36: 101–105, doi:10.4067/S0716-97602003000100008, ISSN 0716-9760 ISSN 0716-9760 {{citation}}: Check |issn= value (help)
  21. ^ 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: 2959–2966, doi:10.1242/jeb.00509
  22. ^ Langer, P. (2002), "The digestive tract and life history of small mammals", Mammal Review, 32: 107–131, doi:10.1046/j.1365-2907.2002.00101.x
  23. ^ Gutiérrez, J.; Bozinovic, F. (1998), "Diet selection in captivity by a generalist herbivorous rodent (Octodon degus) from the Chilean costal desert", Journal of Arid Environments, 39: 601–607, doi:10.1006/jare.1998.0412
  24. ^ a b 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: 78–86, doi:10.1086/316644
  25. ^ 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
  26. ^ 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: 1192–8, doi:10.1210/mend-4-8-1192
  27. ^ Okanoya, K.; Tokimoto, N.; Kumazawa, N.; Hihara, S.; Iriki, A. (2008), "Tool-Use Training in a Species of Rodent: The Emergence of an Optimal Motor Strategy and Functional Understanding", PLoS One, 3: e1860, doi:10.1371/journal.pone.0001860{{citation}}: CS1 maint: unflagged free DOI (link)
  28. ^ Tokimoto, N.; Okanoya, K. (2004), "Spontaneous construction of "Chinese boxes" by degus (Octodon degus): A rudiment of recursive intelligence?", Japanese Psychological Research, 46: 255–261, doi:10.1111/j.1468-5584.2004.00257.x
  29. ^ Edgar, D.M. (2000), "Photic phase response curve in Octodon degus: Assessment as a function of activity phase preference", American Journal of Physiology, 277: R1385-1389, ISSN 0363-6119/00 {{citation}}: Check |issn= value (help)
  30. ^ Kas, M.J.; Edgar, D.M. (1998), "Crepuscular rhythms of EEG sleep-wake in a hystricomorph rodent, Octodon degus", J Biol Rhythms., 13: 9–17, doi:10.1177/074873098128999871
  31. ^ Morris, L.G.; Tate, B.L. (2007), "Phase response curve to melatonin in a putatively diurnal rodent, Octodon degus", Chronobiol Int., 24: 407–411, doi:10.1080/07420520701420352
  32. ^ 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: R1808-1816, doi:10.1152/ajpregu.00005.2006, ISSN 0363-6119/06 {{citation}}: Check |issn= value (help)
  33. ^ 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: 1891–1900, doi:10.1002/dneu.20543
  34. ^ Inestrosa, N.C.; Reyes, A.E.; Chacon, M.A.; Cerpa, W.; Villalon, A.; Montiel, J.; Merabachvili, G.; Aldunate, R.; Bozinovic, F.; Aboitiz, F. (2004), "Human-like rodent amyloid-beta-peptide determines Alzheimer pathology in aged wild-type Octodon degus", Neurobiol Aging., 26: 1023–8, doi:10.1016/j.neurobiolaging.2004.09.016
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