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Home -> Kingdom Animalia -> Phylum Chordata -> Subphylum Vertebrata -> Class Mammalia -> Order Rodentia -> Suborder Myomorpha -> Family Spalacidae -> Subfamily Tachyoryctinae

Subfamily Tachyoryctinae
East African mole rats



2008/10/12 08:49:33.748 GMT-4

By Allison Poor

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Mammalia
Order: Rodentia
Suborder: Myomorpha
Family: Spalacidae
Subfamily: Tachyoryctinae
Members of this Subfamily

Diversity

Tachyoryctinae, the east African mole rats, is a small Old World family of fossorial muroid rodents. There is one mole rat genus, Tachyoryctes, and 13 species. (Musser and Carleton, 2005)

Geographic Range

Tachyoryctine mole rats are native to east Africa, from northern Tanzania and the eastern part of the Democratic Republic of the Congo, north to Ethiopia and Somalia. (Carleton and Musser, 1984)

Biogeographic Regions:
ethiopian (native ).

Habitat

Tachyoryctines inhabit areas that receive more than 500 mm of annual rainfall, including grasslands, woodlands, savannah, and agricultural areas. They have been found at elevations of up to 4,150 meters. (Nowak, 1999)

These animals are found in the following types of habitat:
tropical ; terrestrial .

Terrestrial Biomes:
savanna or grassland ; forest ; mountains .

Other:
agricultural .

Systematic and Taxonomic History

Tachyoryctines, along with rhizomyines, have often been placed in a family separate from Spalacidae, the Rhizomyidae (Miller and Gidley 1918; Ellerman 1940, 1941; Simpson 1945; Chaline et al. 1977, Flynn 1990). Molecular evidence now lends support to the classification proposed by Tullberg in 1899: rhizomyines, spalacines, tachyoryctines, and myospalacines form a monophyletic group, and all belong to the family Spalacidae (Michaux et al. 2001, Jansa and Weksler 2004, Norris et al. 2004, Steppan et al. 2004).

Another point of contention is whether Tachyoryctes is a rhizomyine genus or whether it warrants placement in its own subfamily, Tachyoryctinae. Most authors have favored the former scenario (Carleton and Musser 1984, Musser and Carleton 1993, Potapova and Vorontsov 2004), but Flynn (1990) recognized separate tachyoryctine and rhizomyine clades based on a number of morphological characteristics. This is the taxonomy employed here. It is estimated from fossil evidence that rhizomyines and tachyoryctines diverged about 17 million years ago, in the Miocene.

Finally, it is uncertain just how many Tachyoryctes species exist. Musser and Carleton (1993) listed 11 species, but noted that Allen (1939) and Ellerman (1941) had listed 14, and this number was reduced to just two by Misonne (1974) and Corbert and Hill (1991). Musser and Carleton (1993) contend that the recognition of just two tachyoryctine species was not based on a careful survey of morphological variation among forms and recognized 13 species. (Allen, 1939; Carleton and Musser, 1984; Chaline, Mein, and Petter, 1977; Corbert and Hill, 1991; Ellerman, 1940; Ellerman, 1941; Flynn, 1990; Jansa and Weksler, 2004; Michaux, Reyes, and Catzeflis, 2001; Miller and Gidley, 1918; Misonne, 1974; Musser and Carleton, 1993; Musser and Carleton, 2005; Nevo, 1999; Norris et al., 2004; Nowak, 1999; Potapova and Vorontsov, 2004; Simpson, 1945; Steppan, Adkins, and Anderson, 2004; Tullberg, 1899)

Synonyms
  • Tachyoryctini
Synapomorphies
  • ventral part of infraorbital foramen is reduced, but not absent
  • bony palate has posterior invaginations and median keel
  • reduced incisive foramena
  • lower masseteric crest locally inflated beneath 2nd lower molar and extends anteriorly beneath first molar, beyond upper masseteric crest
  • lateral masseter has origin on premaxilla, instead of on zygomatic plate
  • constricted interorbital region
  • greatly compressed frontals
  • hypsodont, planar molars
  • infraorbital foramen contains nasolacrimal canal
  • no stapedial or sphenofrontal foramina
  • foramen ovale coalesced with middle lacerate foramen
  • no accessory foramen ovale
  • deeply recessed and wholly ossified pterygoid fossa
  • separate masticatory and buccinator foramina
  • tubular external auditory meatus
  • moderately inflated tympanic bullae
  • perpendicular malleus
  • no entepicondylar foramen
  • two circumvallate papillae on tongue
  • pelvis modified for digging, with five sacral vertebrae and reduced symphyis
  • Nucleotide characters in a suite of genes including: Lechitin cholesterol acetyltransferase (LCAT), von Willebrand’s factor (vWF), interphotoreceptor retinoid binding protein (IRBP), growth hormone receptor (GHR), breast cancer 1 (BRCA1), recombination activating gene 1 (RAG1), and the c-myc oncogene.

Physical Description

EXTERNAL CHARACTERISTICS

Tachyoryctines are stocky, mole-like animals. Their head and body length ranges from 160 to 313 mm, tail length ranges from 50 to 95 mm. They weigh 160 to 930 grams. Males tend to be noticeably larger than females. Their tails are about twice the length of the hind feet and are usually covered in fur. The fur on the body is soft and thick and comes in a variety of colors, including black, pale gray, brown, and cinnamon. Albino individuals with white fur are also relatively common. In general, the belly is slightly paler than the upper parts and has a silvery sheen. The eyes are small but visible and functional, and the ears are small as well. There are stiff tactile hairs on the face. East African mole rats have thick, projecting, orange pigmented incisors, with which they dig; small claws; and short, powerful legs.

INTERNAL CHARACTERISTICS

The tachyoryctine dental formula is 1/1, 0/0, 0/0, 3/3 = 16. The molars are hypsodont, hypertrophied, and the alveoli project into the orbit. The molar rows converge anteriorly. The bony palate has posterior furrows and a keel running down its midline. The heavy mandible has prominent coronoid and capsular processes. The incisive foramena are short. Tachyoryctines have flaring zygomatic arches and prominent sagittal and lambdoidal crests, which provide the broad attachment surfaces for the powerful head and neck muscles necessary for digging with their jaws. Due to the reduction of the ventral portion of the infraorbital foramen, the zygomatic plate is poorly demarcated. The infraorbital foramen contains the nasolacrimal canal. The anterior portion of the lateral masseter muscle has a broad origin on the side of the short rostrum, instead of on the zygomatic plate. The area between the orbits is constricted and the frontals are compressed. There are no sphenofrontal, stalacerate, or entepicondylar foramena, and no accessory foramen ovale. The buccinator and masticatory foramena are separate. The pterygoid fossa is deep and well-ossified. The external auditory meatus is tubular in shape, the auditory bullae are moderately inflated, and the malleus is constructed perpendicularly. The interparietal bone is tiny. The tachyoryctine stomach has two chambers, and the cecum has a spiral valve. There is no stapedial artery, and the internal carotid artery provides circulation to the orbits. (Carleton and Musser, 1984; Nevo, 1999; Nowak, 1999)

Some key physical features:
endothermic ; homoiothermic; bilateral symmetry .

Reproduction

Male and female tachyoryctines only associate for the short time necessary for mating to take place. Mating is initiated when a male visits a female's burrow at night. (Flynn, 1990)

Mating systems:
polygynous .

Tachyoryctines breed year round, but they concentrate most of their reproduction during the wet season. Conflicting information is available on how often females bear litters. Females are either polyestrous and conceive a second litter while they are nursing the first, presumably due to a postpartum estrous (Nowak 1999), or they only breed once every six months (Flynn 1990). Gestation lasts 37 to 49 days and litter sizes range from one to four, although litters of one and two young are most common. The young nurse until they are between 28 and 50 days old, and leave their mother's burrow about a month later, when their black juvenile pelage assumes the adult coloration. The young reach sexual maturity when they are four to six months old. (Flynn, 1990; Nowak, 1999)

Key reproductive features:
iteroparous ; year-round breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; fertilization (internal ); viviparous ; post-partum estrous.

Female tachyoryctines build underground nests in which they raise their altricial young. They nurse their young for up to 50 days, and the young stay with their mother for another month, even though they can eat solid food. There is no male parental care known in this group. (Flynn, 1990; Nowak, 1999)

Parental investment:
altricial ; pre-fertilization (provisioning, protecting: female); pre-hatching/birth (provisioning: female, protecting: female); pre-weaning/fledging (provisioning: female, protecting: female); pre-independence (provisioning: female, protecting: female).

Lifespan/Longevity

East African mole rats have an average life expectancy of about one year, and their maximum lifespan is about three years. (Flynn, 1990; Nowak, 1999)

Behavior

East African mole rats, like all spalacids, are fossorial creatures. They construct underground nest chambers consisting of food stores, latrines, and nests which they line with grasses. Foraging tunnels 15 to 30 cm deep and up to 52 meters long radiate outward from each mole rat's nest chamber. Mole rats incorporate deep bolt holes into their burrow systems, into which they can make a quick getaway if a predator attacks. They dig with their incisors, pushing back soil with their forefeet, kicking it behind them with their hindfeet, and using their heads to push it out of their tunnels when too much accumulates. Mounds of soil form where mole rats are active; these can be anywhere from 15 cm wide and 7 cm high to 18 m wide and 2 m high near territory centers. Although they are primarily fossorial, tachyoryctines do forage above ground and spend over 5% of the day doing so. They are known to sit just inside their burrow entrances and grab whatever plants they can reach without having to venture too far. Tachyoryctines are diurnal and active year round, but they become less active during the dry season and burrow deeper--up to one meter below the surface. They can survive cold temperatures at high elevations because fermenting feces and nest material in their burrows raises the temperature in their underground chambers. East African mole rats are solitary--just one individual occupies each burrow system--and they are territorial. (Flynn, 1990; Nevo, 1999; Nowak, 1999)

Communication and Perception

East African mole rats perceive the world using vision, touch, smell, taste, and hearing. Given their small eyes and the fact that they spend most of their lives underground in complete darkness, vision is probably the least important of these senses. On the other hand, the tactile bristles that tachyoryctines have on the sides of the face imply that touch is especially significant. East African mole rats are known to rap on the ground with their upper incisors, which may be a way to communicate territory ownership. Also, males have large sex-pheromone producing glands between each eye and ear and on the penis. (Flynn, 1990)

Communicates with:
acoustic ; chemical .

Other communication keywords:
pheromones .

Perception channels:
visual ; tactile ; acoustic ; chemical .

Food Habits

Tachyoryctines are herbivores that feed on roots, rhizomes, bulbs, tubers, and grass. They store excess food in underground chambers in their burrow systems. (Nowak, 1999)

Primary Diet:
herbivore (folivore ).

Predation

Known predators

East African mole rats fall prey to a variety of hawks, owls, and small mammalian carnivores. Their predators include: Simian jackals (Canis simensis), servals (Leptailurus serval), African striped weasels (Poecilogale albinucha), striped polecats (Ictonyx striatus), Abyssinian owls (Asio abyssinicus), Cape eagle-owls (Bubo capensis), Verreaux's eagle-owls (Bubo lacteus), barn owls (Tyto alba), jackal buzzards (Buteo rufofuscus), and lammergeiers (Gypaetus barbatus). They probably avoid predation to some degree by staying hidden underground. Tachyoryctines incorporate bolt holes into their burrow systems into which they can make a quick escape if caught out in the open. If cornered, they can be vicious and do not hesitate to rush at their attacker and attempt to bite. (Flynn, 1990; Nowak, 1999)

Ecosystem Roles

Because of their fossorial lifestyle, tachyoryctines probably help to aerate the soil. They are important consumers of a variety of plant species, and they are prey for many avian and mammalian predators. (Flynn, 1990)

Key ways these animals impact their ecosystem:
soil aeration .

Economic Importance for Humans: Negative

East African mole rats are agricultural pests on peas, beans, corn, sweet potatoes, and various root crops. (Nowak, 1999)

Ways that these animals might be a problem for humans:
crop pest.

Economic Importance for Humans: Positive

Tachyoryctines are hunted for food and their skins are used as charms by native tribes. (Nowak, 1999)

Ways that people benefit from these animals:
food ; body parts are source of valuable material.

Conservation

Three tachyoryctine species are on the IUCN's Red List of Threatened Species. Tachyoryctes annectens and Tachyoryctes storeyi are listed as having deficient data, because it is unclear whether they actually are real species, or whether they are subspecies of a tachyoryctine with a wider distribution. Research is needed to clarify their taxonomic relationships with other tachyoryctines and to assess their population status. The third species on the list, T. macrocephalus, is considered vulnerable because it is only known from one location. Fortunately, that location mostly falls within a national park, but illegal grazing still threatens the population there. (IUCN, 2004)

Contributors

Allison Poor (author), University of Michigan.
Tanya Dewey (editor), Animal Diversity Web, University of Michigan Museum of Zoology.

References

Allen, G. 1939. A checklist of African mammals. Bulletin of the Museum of Comparative Zoology at Harvard College, 83: 1-763.

Carleton, M., G. Musser. 1984. Muroid rodents. Pp. 289-379 in S. Anderson, J. K. Jones Jr., eds. Orders and Families of Recent Mammals of the World. New York: John Wiley and Sons.

Chaline, J., P. Mein, F. Petter. 1977. Les grandes lignes d'une classification évolutive des Muroidea. Mammalia, 41: 245-252.

Corbert, G., J. Hill. 1991. A world list of mammalian species. London: British Museum (Natural History).

Ellerman, J. 1940. The Families and Genera of Living Rodents, vol. I. London: British Museum (Natural History).

Ellerman, J. 1941. The Families and Genera of Living Rodents, vol. II. London: British Museum (Natural History).

Flynn, L. 1990. The natural history of rhizomyid rodents. Pp. 155-183 in E. Nevo, O. A. Reig, eds. Evolution of Subterranean Mammals at the Organismal and Molecular Levels. New York: Wiley-Liss.

IUCN, 2004. "2004 IUCN Red List of Threatened Species" (On-line). Accessed May 20, 2005 at www.redlist.org.

Jansa, S., M. Weksler. 2004. Phylogeny of muroid rodents: relationships within and among major lineages as determined by IRBP gene sequences. Molecular Phylogenetics and Evolution, 31: 256-276.

Michaux, J., A. Reyes, F. Catzeflis. 2001. Evolutionary history of the most speciose mammals: Molecular phylogeny of muroid rodents. Molecular Biology and Evolution, 18(11): 2017-2031.

Miller, G., J. Gidley. 1918. Synopsis of supergeneric groups of rodents. Journal of the Washington Academy of Science, 8: 431-448.

Misonne, X. 1974. Order Rodentia. Pp. 1-39 in J. Meester, H. W. H. W. Setzer, eds. The mammals of Africa: An identification manual. Washington, D. C.: Smithsonian Institution Press.

Musser, G., M. Carleton. 1993. Family Muridae. Pp. 501-753 in D. E. Wilson, D. M. Reeder, eds. Mammal Species of the World. Washington, D.C.: Smithsonian Institution Press.

Musser, G., M. Carleton. 2005. Superfamily Muroidea. D. E. Wilson, D. M. Reeder, eds. Mammal Species of the World. Washington, D.C.: Smithsonian Institution Press.

Nevo, E. 1999. Mosaic Evolution of Subterranean Mammals. Oxford: Oxford University Press.

Norris, R., K. Zhou, C. Zhou, G. Yang, C. Kilpatrick, R. Honeycutt. 2004. The phylogenetic position of the zokors (Myospalacinae) and comments on the families of muroids (Rodentia). Molecular Phylogenetics and Evolution, 31: 972-978.

Nowak, R. 1999. Walker's Mammals of the World, vol. 2. Baltimore and London: The Johns Hopkins University Press.

Potapova, E., N. Vorontsov. 2004. Taxonomic position of the genus Tachyoryctes and mutual relations between Rhizomyidae and Spalacidae families (Rodentia). Zoologicheskii Zhurnal, 83(8): 1044-1058.

Simpson, G. 1945. The principles of classification and a classification of mammals. Bulletin of the American Museum of Natural History, 85: 1-350.

Steppan, S., R. Adkins, J. Anderson. 2004. Phylogeny and divergence-date estimates of rapid radiations in muroid rodents based on multiple nuclear genes. Systematic Biology, 53(4): 533-553.

Tullberg, T. 1899. Uber das system der nagethiere: eine phylogenetische studie. Nova Acta Regiae Societatis Scientiarum Upsaliensis, 3: 1-514.

2008/10/12 08:49:36.875 GMT-4

To cite this page: Poor, A. 2005. "Tachyoryctinae" (On-line), Animal Diversity Web. Accessed October 12, 2008 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Tachyoryctinae.html.

Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college students. ADW doesn't cover all species in the world, nor does it include all the latest scientific information about organisms we describe. Though we edit our accounts for accuracy, we cannot guarantee all information in those accounts. While ADW staff and contributors provide references to books and websites that we believe are reputable, we cannot necessarily endorse the contents of references beyond our control.

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