By Allison Poor
Diversity
Otomyinae is one of the smaller subfamilies of muroid rodents, with 23 species in 3 genera: Myotomys, Otomys, and Parotomys. This Old World subfamily includes the vlei rats, whistling rats, and karoo rats. ()
Geographic Range
Otomyines are native to southern and east central Africa, with an isolated population in Cameroon and Nigeria (Otomys occidentalis). ()
Habitat
Otomyines live in deserts, veldts, grasslands, savannahs, swamps, marshes, stream borders, alpine meadows, and areas of brushy secondary growth. They are found at elevations up to 4,000 meters. ()
These animals are found in the following types of habitat:
temperate
; tropical
; terrestrial
.
Terrestrial Biomes:
desert or dune
; savanna or grassland
; mountains
.
Other:
riparian
.
Systematic and Taxonomic History
Otomyinae was given status as a subfamily by Thomas in 1896, and since then, there has been disagreement over whether the subfamily belongs in Muridae (Tullberg 1899, Miller and Gidley 1918, Simpson 1945), Cricetidae (Misonne 1971), or Nesomyidae (Chaline et al. 1977), or whether Otomyidae should be recognized as its own family (Roberts 1951). Most recent fossil discoveries and analyses of morphological characteristics link otomyines closely with murines (see summary in Carleton and Musser 1984). In fact, molecular studies based on LCAT and vWF genes (Michaux et al. 2001), IRBP gene sequences (Jansa and Weksler 2004), and GHR, BRCA1, RAG1, and c-myc genes (Steppan et al. 2004) actually show that otomyines fall within the murine clade. For now, however, Musser and Carleton (2005) classify Otomyinae as a separate murid subfamily, in recognition of the unique shared traits of its members.
Another point of contention is just how many genera should be recognized in the subfamily. The number has ranged from five (Roberts 1951) to one (Bohmann 1953), with most authorities recognizing just two, Otomys and Parotomys (Ellerman 1941, Corbert and Hill 1980, Carleton and Musser 1984, Musser and Carleton 1993). However, as Musser and Carleton (2005) note, an analysis of morphological and molecular features suggests that Otomys, as traditionally defined, is polyphyletic, and that two of the species in this genus are actually more similar to Parotomys than to other Otomys, yet they lack certain skull characteristics of Parotomys. Thus, they provisionally place these two species in a separate genus, Myotomys. ()
- Otomyini
- Otomyidae
- high-crowned
molars with pronounced laminate configuration - third upper molar longer than first two molars
- molar rows converge anteriorly and slant outward
- moderately or strongly developed
zygomatic notch and spine - robust
zygomatic arches with expanded middle portion - narrow bony palate with deep furrows and median keel
- moderately or deeply excavated
pterygoid fossa - large sphenopalatine vacuities
- no sphenofrontal foramen or squamosoalisphenoid groove
- large
postglenoid foramen
- hourglass-shaped interorbital area with beaded edges
- globular
tympanic bullae
- orbicular apophysis small or absent
-
manubrium intermediate between perpendicular and parallel angle -
dentary with deep mandibular ramus, small
coronoid process, shallow sigmoid notch - 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
Otomyines are medium-sized, volelike muroid rodents with stocky bodies, rounded profiles, short hind feet, small eyes, and small ears. Their head and body length ranges from 124 to 217 mm, their tails range from 55 to 150 mm, and they weigh 60 to 255 grams. Otomyines have long, dense, soft fur that varies in color from pale buff to brown to reddish to rusty-yellow with black or brown streaks. The underparts and sides of the body tend to be paler, and are white, grayish white, cream, buff, brown, or gray.
The otomyine dental formula is 1/1, 0/0, 0/0, 3/3 = 16. They have wide, opisthodont
incisors. The
molars are rooted, and the crowns consist of transverse crests of enamel, with no individually demarcated cusps. The first upper molars each have three of these crests, while the second upper and second and third lower molars each have two. The third upper molars and first lower molars have a variable number of crests.
Skull features include a large
interparietal bone; somewhat enlarged
mastoid bullae; a narrow mesopterygoid fossa that extends between the third molars; long, narrow
incisive foramina; a separation of the masticatory foramen and accessory
foramen ovale by a strut of the
alisphenoid bone; and the presence of an
accessory tympanum. Otomyines have single-chambered stomachs and complex ceca. ()
Some key physical features:
endothermic
; homoiothermic; bilateral symmetry
.
Reproduction
The mating system of otomyines has not been explicitly studied, and it may vary substantially by species. Some species do not breed in captivity when housed as male/female pairs (Davis 1972), but others do (Pillay 2001). ()
Otomyines reproduce year round, although in some areas breeding peaks during the wet season. Females produce up to five litters per year. Gestation lasts about 40 days. Litters consist of one to five, usually two to three, relatively precocial young. The young develop quickly. They gain the ability to smell at birth or a few days afterward, and some are born well-furred with functional eyes and ears. By the second week, they have been observed running around and carrying objects in their mouths, presumably in play (Davis 1972). Young otomyines commonly practice allogrooming by day 14, by which time they are also weaned. They become sexually mature at 5 to 13 weeks, with females maturing a few weeks earlier than males. ()
Key reproductive features:
iteroparous
; year-round breeding
; gonochoric/gonochoristic/dioecious (sexes separate); sexual
; viviparous
.
Young otomyines are relatively precocial. They have their incisors at birth and they cling tenaciously to their mothers' nipples for the first 7 days or so. Females of some species may drag their young around with them while foraging. Some female otomyines do not carry their babies in their mouths, as the young are highly mobile fairly early in life. Also, mothers do not groom their offspring as much as do some other rodents, because the young can groom themselves after just a few days. After a couple of weeks, they can groom their mothers. When the young begin eating solid food, 6 or 7 days after birth, they may squabble over food items with their mothers, threatening them as they would threaten intruders as adults, their mothers seem to ignore these threats. ()
Parental investment:
precocial
; pre-fertilization (provisioning, protecting: female); pre-hatching/birth (provisioning: female, protecting: female); pre-weaning/fledging (provisioning: female, protecting: female); pre-independence (protecting: female).
Lifespan/Longevity
Deomyines live two to four years in captivity; lifespan in the wild is undoubtedly shorter. ()
Behavior
Otomyines are terrestrial rodents. They are often described as being wary and quick to seek shelter at the slightest hint of danger. Some species are diurnal, and others are nocturnal, crepuscular, or active both day and night. They are active year round.
Some otomyine species construct nests out of sticks and other plant material and place these in burrows, on the ground surface, or in low shrubs above the entrances to burrows. Others do not build nests at all. Burrows may be complex systems of underground tunnels with multiple entrances or simple holes in the ground. Otomyines often make networks of above-ground runways through the grass, which radiate outward from a burrow or surface nest. These runways are sometimes marked by small piles of grass clippings left behind during their construction.
Otomyines are generally cursorial, but they are known to swim and dive to escape predators. Most are sedentary, but those that live near water may migrate during the wet season to avoid being flooded out.
These rodents range in social habits from gregarious, living in pairs or small family groups, to solitary, aggressive, and territorial. They seem to have well-defined home ranges, but these home ranges may overlap with one another. In one study, males were noted to be dominant over females, and heavier animals were dominant over lighter animals (Davis 1972). Also, males and females housed in pairs became mutually tolerant, whereas intrasex pairs always fought. ()
Key behaviors:
cursorial; terricolous; fossorial
; diurnal
; nocturnal
; crepuscular
; motile
; migratory
; sedentary
; solitary
; territorial
; social
; dominance hierarchies
.
Communication and Perception
Otomyines perceive their world through vision, hearing, olfaction, taste, and touch. Of these, vision may be less important, whereas hearing and olfaction seem quite keen (Davis 1972). Among Otomys irroratus, Davis (1972) noted that individuals confronted by new objects or environments spent a long time sniffing their unfamiliar surroundings and touching unfamiliar objects with their vibrissae.
Otomyines use visual, auditory, and olfactory signals to communicate with one another. Individuals sniff one another's noses upon meeting, and during social conflicts, they often utter a metallic-sounding chirp. Body posturing also plays a role in social interactions; in one study on O. irroratus, dominant individuals were seen to approach subordinate individuals in a flattened crouch, whereas subordinate individuals adopted an upright posture (Davis 1972). They were also seen to vibrate their tails quickly back and forth as a sign of aggression. Otomyines mark their territories with urine and with secretions from their anal glands. Young otomyines that have been separated from their mothers squeak loudly so that she can locate them, and mothers seem to recognize their offpring by scent. Some species make whistling noises and/or stamp their hind feet when alarmed. ()
Other communication keywords:
scent marks
.
Food Habits
Otomyines are primarily herbivorous. They eat grasses, roots, shoots, bark, forbs, seeds, and berries, and sometimes insects. Otomyines have been known to practice coprophagy, especially during times of food shortage. ()
Primary Diet:
carnivore
(insectivore
); herbivore
(folivore
, frugivore
, granivore
, lignivore); omnivore
; coprophage
.
Predation
- carnivores (Carnivora)
- snakes (Serpentes)
- hawks (Accipitridae)
- owls (Strigiformes)
Small mammalian carnivores, snakes, and birds of prey including hawks and owls prey upon otomyines. No doubt their vigilance, agility, and cryptic coloration help them to avoid predation. ()
Anti-predator adaptations::
cryptic
.
Ecosystem Roles
In general, otomyines are primary consumers. They, in turn, are preyed upon by a number of secondary consumers. In addition, otomyines are parasitized by several flea species, including Dinopsyllus titan, D. longifrons, Ctenopthalmus evidens, and C. cophurus. ()
- Dinopsyllus titan
- Dinopsyllus longifrons
- Ctenopthalmus evidens
- Ctenopthalmus cophurus
Economic Importance for Humans: Negative
Otomyines may carry plague in some locations. In addition, these rodents are known to damage trees in nurseries by gnawing the bark. ()
Ways that these animals might be a problem for humans:
injures humans (carries human disease); crop pest.
Economic Importance for Humans: Positive
There are no known positive effects of otomyines on humans.
Conservation
Currently, the IUCN considers three otomyine species to be endangered (Barbour's vlei rats, Otomys barbouri, Mt. Elgon vlei rats, Otomys jacksoni, and Uzungwe vlei rats, Otomys uzungwensis), three to be vulnerable (Burton's vlei rats, Otomys burtoni, Ruwenzori vlei rats, Otomys dartmouthi, and western vlei rats, Otomys occidentalis), and two to be near threatened (Dent's vlei rats, Otomys denti and Tanzanian vlei rats, Otomys lacustris). Another two lack sufficient data to be assessed (Afroalpine vlei rats, Otomys orestes and Dollman's vlei rats, Otomys dollmani). The species that are on the IUCN's list are there because their ranges are very small, highly fragmented, or both. Preserves have been established that may slow the decline of some species, but research is still needed that will allow the creation of comprehensive management plans. ()
Contributors
Allison Poor (author), University of Michigan.
Tanya Dewey (editor), Animal Diversity Web, University of Michigan Museum of Zoology.
