Tupaia (mammal)

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Tupaia
Pygmy treeshrew
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Scandentia
Family: Tupaiidae
Genus: Tupaia
Raffles
, 1821
Type species
Tupaia ferruginea [1]

Raffles, 1821
Species

See text.

Synonyms
  • Chladobates Schinz, 1824
  • Cladobates F. Cuvier, 1825
  • Gladobates Schinz, 1824
  • Glipora Jentink, 1888
  • Glirisorex Scudder, 1882
  • Glisorex Desmarest, 1822
  • Glisosorex Giebel, 1855
  • Hylogale Temminck, 1827
  • Hylogalea Schlegel and Mueller, 1843
  • Lyonogale Conisbee, 1953
  • Palaeotupaia Chopra and Vasishat, 1979
  • Sorex-glis É. Geoffroy and F. Cuvier, 1822
  • Tana Lyon, 1913
  • Tapaia Gray, 1860
  • Tupaja Haeckel, 1866
  • Tupaya É. Geoffroy and F. Cuvier, 1822

Tupaia is a

Thomas Stamford Raffles in 1821.[1][2] The name of this genus derives from the Malay word tupai meaning squirrel or small animal resembling a squirrel.[3]

Characteristics

Raffles described the genus as having an elongated snout, eight to 10 incisors, well-developed limbs, five-toed naked feet, and the sole furnished with projecting pads and sharp claws, with a habit and tail of a squirrel.[2]

premolars. The size of head, body, and tail varies between species.[4]

One outstanding characteristic of Tupaia species is their color vision. They have rod and cone visual receptors similar to humans and other primates.[5]

Classification and taxonomic history

When

Urogale, disbanding the latter, based on a 2011 molecular phylogeny.[7]

The following species are in the genus Tupaia:[1]

In the past, various authors proposed to place treeshrews in the

Scandentia.[24][25][26]

Distribution and habitat

Tupaia species range from

Celebes, nor on islands to the east of Java, with the possible exception of Bali.[4]

They inhabit the dense undergrowth of tropical forests. With the exception of T. minor, they are primarily terrestrial and forage on the forest floor, usually below 1.5 m (4 ft 11 in). Since they are rarely seen crossing wide roads, populations likely are negatively affected by fragmentation of forests caused by logging operations.[27]

Ecology and behaviour

Early naturalists described wild-caught captive Tupaia specimens as restless, nervous, and rapidly reacting to sounds and movements.[4] Their auditory sensitivity is highly developed as the broad frequency range of their hearing reaches far into the ultrasonic.[28]

The shape of the cheek-teeth of Tupaia species indicate they are foremost

intestines and rudimentary ceca.[29]

The well-developed

Observations of Tupaia species in their natural habitats suggest they usually form

monogamous pairs. Social behaviour differs between species and the available food resources in their territories. Where food is adequate and sufficient, they tolerate conspecifics without engaging in territorial disputes.[27] Common treeshrews observed in the Bukit Timah Nature Reserve defended diminishing food resources by chasing away residents of adjacent areas.[31]

Birds of prey, snakes, and small carnivores are known to hunt treeshrews. Humans have no interest in killing them for food because of their unpleasant taste, and they are rarely seen as pests.[32]

Reproduction and development

Treeshrews share more similarity with rodents and squirrels than with primates in regards to their reproduction and development. In contrast to primates, which produce one baby with longer gestation periods, treeshrews generally have litters of two or three young and are only in utero about 45 days. Female treeshrews give birth in nests made of many dry leaves, and are known to leave the young unattended while returning occasionally to give them milk. Parental care of Tupaia is relatively limited.[33]

The young remain in the nest for 33 days on average, developing gradually before they exit the nest. Ten identified embryonic developmental stages are seen in Tupaia species.[34] Baby treeshrews are sexually immature until about 90 days after birth.[25]

Medical research

Their close relationship to primates makes treeshrews important model organisms in human medical research. A study investigating the effects of the

Borna disease virus on treeshrews has given new insight into neurological disease.[35]

Since Tupaia species share so many similarities with primates, yet are more abundant and have more plentiful

progeny than them, interest is increasing in using them as an alternative model for use in human medical research. Successful psychosocial studies were carried out, and dramatic behavioral, neuroendocrinal, and physiological changes occurred in subordinate males of Tupaia, similar to depressed human patients. Their susceptibility to viruses has also piqued interest in using them to study immune responses to infections such as hepatitis B.[36]
Tupaia species have been used to overcome the limitations of using rodent models in the study of human biology and disease mechanisms, as well as the development of new drugs and diagnostic tools. Recent studies have used treeshrews to study infectious, metabolic, neurological, and psychiatric diseases, as well as cancers.[37]

In 2013, the

H1N1 influenza virus. This was advantageous because other possible candidates such as guinea pigs, rats, mice, and other rodents leave gaps in the information, especially regarding clinical symptoms and transmission. Tupaia, though, displays moderate systemic and respiratory symptoms, as well as pathological changes in the respiratory tract, supporting its use as a beneficial model in H1N1 research.[38]

References

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  2. ^ a b c Raffles, T. S. (1821). "Descriptive Catalogue of a Zoological Collection made on account of the Honourable East India Company, in the Island of Sumatra and its Vicinity, under the Direction of Sir Thomas Stamford Raffles, Lieutenant-Governor of Fort Marlborough; with additional Notices illustrative of the Natural History of those Countries". The Transactions of the Linnean Society of London. XIII. Linnean Society of London: 239–340.
  3. ^ Wilkinson, R. J. (1901). A Malay-English dictionary Kelly & Walsh Limited, Hongkong, Shanghai and Yokohama.
  4. ^ a b c d e Lyon, M. W., Jr. (1913). Tree shrews: An account of the mammalian family Tupaiidae. Proceedings of the United States National Museum, 45:1–188.
  5. ^ Shriver, J .G., Noback, C. R. (1967). Color Vision in the Tree Shrew (Tupaia glis). Folia Primatologia 6: 161−169.
  6. ^ a b Diard, P.M., Duvaucel, A. (1820). "Sur une nouvelle espèce de Sorex — Sorex Glis". Asiatick researches, or, Transactions of the society instituted in Bengal, for inquiring into the history and antiquities, the arts, sciences, and literature of Asia, Volume 14: 470–475.
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  9. ^ Miller, G. S. Jr. (1903). Seventy New Malayan Mammals. Smithsonian Miscellaneous Collections 45: 1–73.
  10. ^ Lyon Jr, M. W. (1906). "Mammals of Banka, Mendanau, and Billiton Islands, between Sumatra and Borneo". Proceedings of the United States National Museum. 1906.
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  19. ^ Zelebor, J. (1868). Cladobates Nicobaricus. In: Reise der österreichischen Fregatte Novara um die Erde. Zoologischer Theil, Band 1 Säugethiere. Wien: Kaiserliche Akademie der Wissenschaften. Pp. 17–19.
  20. ^ Thomas, O. (1894). On the Palawan Representative of Tupaia ferruginea. The Annals and Magazine of Natural History 6 (13): 367.
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