The Damaraland mole-rat, Damara mole rat, or Damaraland blesmol (Fukomys damarensis) is a burrowing rodent found in southern Africa. Along with the smaller, less hairy, naked mole rat, it is one of only two known eusocial mammals.
Like other blesmols, the Damaraland mole-rat has a cylindrical body with short, stout limbs, large feet, and a conical head. It is also similar in size to most other African mole-rats, having a head-body length of 14 to 20 cm (5.5 to 7.9 in), with a short, 2 to 3 cm (0.79 to 1.18 in), tail, and weighing between 100 and 280 grams (3.5 and 9.9 oz). There are no external ears, and the blue-coloured eyes are tiny with thick eyelids. The incisor teeth are large and prominent, with flaps of skin behind them to prevent soil from falling into the throat while the animal is using them to dig.
The fur is short and thick, and varies from fawn to almost black, with shades of brown being most common. There is always a white patch on the top of the head, although its exact shape varies, and there may also be additional blotches of white fur elsewhere on the body. Longer sensory hairs project above the fur over much of the body, with the facial whiskers being particularly long. Females have six teats.
Distribution and habitat
Although named specifically for Damaraland, the mole-rats are found across much of southern Africa, including Botswana, Namibia, South Africa, Zambia, and Zimbabwe. They inhabit warm, semi-arid environments dominated by savannah scrubland or sandy grasslands. They are most commonly associated with red Kalahari psamments, and are found only where there is a sufficient supply of plants with subterranean storage organs.
Damaraland mole-rats are herbivorous, feeding solely on tubers, corms, and bulbs. Favoured foods include such plants as Acanthosicyos, Star-of-Bethlehem, Ledebouria, and Talinum. Their natural predators include mole snakes, and occasionally other local snakes, such as cobras. They do not drink, obtaining all their water from their food, which is also an important source of minerals. Unlike most other mammals, they can effectively metabolise these minerals without access to vitamin D, which they lack because they are normally never exposed to sunlight. The basal metabolic rate of Damaraland mole rats is also unusually low for mammals of their size, at just 0.66 cm3 O2 / g · h.
Despite living in an entirely subterranean environment, Damaraland mole-rats exhibit circadian rhythms, and are active primarily during the day. Their levels of the hormone melatonin can be altered by artificially changing the length of apparent daylight, suggesting that they are at least able to distinguish light from dark, although their eyesight may otherwise be very poor.
Damaraland mole-rats live in networks of underground tunnels, which they dig with their front teeth. The tunnels are 65 to 75 mm (2.6 to 3.0 in) in diameter, and may stretch for up to 1 km (0.62 mi) below the ground. They have no connection to the surface, although their presence can be inferred from dome-shaped molehills of excavated earth pushed up to the surface. As a result, the tunnels develop their own microclimate, containing warm, moist air, with low oxygen levels. Most digging occurs after rainfall, since dry soil is too difficult to excavate. Because they live in arid environments, this means that Damaraland mole-rats can be extremely active over short periods; a typical colony has been estimated to excavate three tons of soil over a two-week period.
The burrow system consists primarily of foraging tunnels, which the rats dig in search of food. While particularly large tubers and bulbs are at least partially eaten where they are found, smaller ones are dragged to food storage chambers beneath the foraging tunnels. The foraging tunnels are typically only 5 to 25 cm (2.0 to 9.8 in) beneath the soil, but are connected to a smaller number of deep tunnels that lead down to the storage chambers, latrines, and a central nest that may be as much as 2.5 m (8 ft 2 in) underground.
Each burrow system is inhabited by a single colony of mole rats, typically with about twelve members, although colonies can range from as little as two to as many as forty members. The colony is eusocial, consisting of a single breeding pair and their non-reproductive offspring. The non-reproductive members of the colony spend their time foraging and maintaining the tunnel system, in particular closing any breaches that may occur. Intruders from other colonies are generally rejected, although DNA paternity studies show that at least some non-reproductive members of a colony may have been fathered by outsiders. The colony has a clearly defined hierarchy, with the breeding male dominant, followed by the breeding female, then non-reproductive males, and finally non-reproductive females.
Colonies fragment if the breeding female dies, with most surviving members dispersing to new locations. Particularly large individuals may also leave the colony to establish a new burrow system. In such cases, dispersal usually only occurs during rainy weather, ensuring that digging will be relatively easy once a suitable location has been found. New colonies are established by unrelated males and females, which become the new breeding pair. Dispersing individuals travel above ground, and are therefore vulnerable to predation from a wide range of animals; some studies have shown that only around 10% of dispersing individuals are later found in new colonies. For example, while small groups of siblings may sometimes leave a burrow system at the same time, normally only one survives to found a new colony.
The Damarland mole-rat is less vocal than the naked mole-rat, making only some birdlike chirps.
As eusocial animals, only the breeding pair within a colony is capable of reproduction. Non-reproductive individuals are not truly sterile, however, and become capable of reproduction if they establish a colony of their own. The reproductive systems of non-reproductive females are underdeveloped, with small, unvascularised uteri and tiny ovaries that contain undeveloped germ cells, but which are incapable of ovulation. Non-reproductive males have smaller testes than their reproductive counterparts and produce little, if any, viable sperm. The non-reproductive status of other adults is maintained by the presence of the breeding female. While her removal causes previously non-reproductive females to become fully fertile, they will only mate with unrelated males, thus avoiding incest within the colony.
The breeding female initiates courtship by calling and drumming with her hind feet. The pair then chase each other in a right circle before mating. Mating occurs frequently over a ten-day period, and gestation lasts 78 to 92 days. Females can produce up to three litters of one to six pups per year. The pups are initially hairless, with closed eyes, and only weigh 8 or 9 grams. They are weaned after 28 days, and reach adult size after around 14 months.
- Maree, S. & Faulkes, C. (2008). Cryptomys damarensis. In: IUCN 2008. IUCN Red List of Threatened Species. Retrieved 5 January 2009.
- Kock, D.; et al. (2006). "On the nomenclature of Bathyergidae and Fukomys n. gen. (Mammalia: Rodentia)" (PDF). Zootaxa. 1142: 51–55.
- Woods, C.A.; Kilpatrick, C.W. (2005). "Infraorder Hystricognathi". In Wilson, D.E.; Reeder, D.M. Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. p. 1540. ISBN 978-0-8018-8221-0. OCLC 62265494.
- Bennett, N.C.; Jarvis, J.U.M. (2004). "Cryptomys damarensis". Mammalian Species: Number 756: pp. 1–5. doi:10.1644/756.
- Skinner, D.C.; et al. (1991). "Is vitamin D3 essential for mineral metabolism in the Damara mole-rat (Cryptomys damarensis)?". General and Comparative Endocrinology. 81 (3): 500–505. doi:10.1016/0016-6480(91)90178-9.
- Oosthuizen, M.K.; et al. (2003). "Circadian rhythms of locomotor activity in solitary and social species of African mole-rats (family Bathyergidae)". Journal of Biological Rhythms. 18 (6): 481–490. doi:10.1177/0748730403259109.
- Richter, T.A.; et al. (2006). "Melatonin secretion in a strictly subterranean mammal, the Damaraland mole-rat (Cryptomys damarensis)". Journal of Zoology. 261 (3): 313–319. doi:10.1017/S0952836903004254.
- Naked and Not: Science News Online, June 24, 2006
- Lovegrove, B.G.; Painting, S. (1987). "Variations in the foraging behaviour and burrow structures of the Damara mole-rat Cryptomys damarensis (Bathyergidae) in the Kalahari Gemsbok National Park". Koedoe. 30 (1): 149–163. doi:10.4102/koedoe.v30i1.508.
- Roper, T.J.; et al. (2001). "Environmental conditions in burrows of two species of African mole-rat, Georychus capensis and Cryptomys damarensis". Journal of Zoology. 254 (1): 101–107. doi:10.1017/S0952836901000590.
- Jarvis, J.U.M.; et al. (1998). "Food availability and foraging in wild colonies of Damaraland mole-rats, Cryptomys damarensis: implications for sociality". Oecologia. 113 (2): 290–298. doi:10.1007/s004420050380.
- Burland, T.M.; et al. (2004). "Colony structure and parentage in wild colonies of co-operatively breeding Damaraland mole-rats suggest incest avoidance alone may not maintain reproductive skew". Molecular Ecology. 13 (8): 2371–2379. doi:10.1111/j.1365-294X.2004.02233.x.
- Jacobs, D.S.; et al. (1991). "The colony structure and dominance hierarchy of the Damaraland mole-rat, Cryptomys damarensis (Rodentia: Bathyergidae) from Namibia". Journal of Zoology. 224 (4): 553–576. doi:10.1111/j.1469-7998.1991.tb03785.x.
- Molteno, A.J.; Bennett, N.C. (2002). "Rainfall, dispersal and reproductive inhibition in eusocial Damaraland mole-rats (Cryptomys damarensis)". Journal of Zoology. 256 (4): 445–448. doi:10.1017/S0952836902000481.
- Jarvis, J.U.M.; Bennett, N.C. (1993). "Eusociality has evolved independently in two genera of bathyergid mole-rats but occurs in no other subterranean mammal". Behavioral Ecology and Sociobiology. 33 (4): 253–360. doi:10.1007/BF02027122.
- Maswanganye, K.A.; et al. (1999). "Oligospermia and azoospermia in non-reproductive male Damaraland mole-rats". Journal of Zoology. 248 (3): 411–418. doi:10.1111/j.1469-7998.1999.tb01039.x.
- Bennett, N.C.; et al. (1996). "Reproductive suppression in subordinate, non-breeding female Damaraland mole-rats: two components to a lifetime of socially-induced infertility". Proceedings of the Royal Society B. 263 (11): 1599–1603. doi:10.1098/rspb.1996.0234.
- Rickard, C.A.; Bennett, N.C. (1997). "Recrudescence of sexual activity in a reproductively quiescent colony of the Damaraland mole-rat by the introduction of a genetically unrelated male—a case of incest avoidance in "queenless" colonies". Journal of Zoology. 241 (1): 185–202. doi:10.1111/j.1469-7998.1997.tb05508.x.
- Bennett, N.C.; Jarvis, J.U.M. (1988). "The social structure and reproductive biology of colonies of the Damaraland mole-rat, Cryptomys damarensis (Rodentia, Bathyergidae)". Journal of Mammalogy. 69 (2): 293–302. doi:10.2307/1381379.