Diversity
Delanymyinae is an Old World nesomyid subfamily consisting of just a single genus
and species, Delany's swamp mice (
Delanymys brooksi
).
Geographic Range
Delany's swamp mice are native to east central Africa, including southwestern Uganda,
Zaire, Rwanda, and the eastern portion of the Democratic Republic of the Congo.
Habitat
The preferred habitat of Delany's swamp mice is sedge marsh in montane and bamboo
forests, at elevations from 1,700 to 2,625 meters.
- Habitat Regions
- tropical
- terrestrial
- Wetlands
- marsh
Physical Description
Delany's swamp mice are small nesomyid rodents. The head and body length ranges from 50 to 63 mm, the tail length ranges from 87 to 111 mm, and the body weight is about 6 grams. The tail is about twice as long as the head and body. Delany's swamp mice have delicate, gracile bodies with long hind feet and digits. The tail is semiprehensile, and the fifth toe is semiopposable. Four of the digits on the front feet bear claws, and the hind feet have claws on all five digits. The fur on the back is russet, the chin is whitish, and the belly is a warm, buff color. The bases of the hairs are grayish. The coat is thick, soft, and woolly. The scaly, bicolored tail is covered in thin hairs, and the soles of the feet lack fur except near the bases.
The delanymyine dental formula is 1/1, 0/0, 0/0, 3/3 = 16. The upper
incisors
are orthodont and the upper
molars
lie in parallel rows. The
brachydont
molars have three roots in the upper jaw and two roots in the lower jaw. The first
two molars are about the same size, and the third molar is about a third the size
of the others. The molar surface is marked by a series of alternating cusps, and
the anterior crests of the first upper molars are large and not bicuspid. The first
and second upper molars have distinct
mesolophs and mesostyles
. There is a labial cusp on the
cingulum
of the first and second molars of the lower jaw, and there is no posterior cingulum
of the molars of the upper jaw. The small
mandible
has thin
coronoid processes
. The
rostrum
is short, and the delicate skull has a high, rounded braincase. The area between
the orbits is narrow to moderately wide and has smooth edges. There are no temporal
ridges. The
zygomatic arches
are narrow and delicate, and the
infraorbital foramina
are relatively large. The
zygomatic plates
are narrow and do not extend anterior to the dorsal zygomatic roots. The
incisive foramina
terminate before the anterior borders of the molar rows, and the bony palate terminates
in a deep V-shape before the posterior borders of the molar rows. The mesopterygoid
fossa is narrow and the anterior portion is constricted, and the
pterygoid fossae
are long, wide, and almost flat. There are small sphenopalatine vacuities. The middle
lacerate foramina are small. There is no
alisphenoid
strut, and the
accessory foramen ovale
, masticatory foramen, and buccinator foramen are all merged into a single opening.
There is no stapedial foramen, and the internal maxillary artery is a branch of the
internal carotid artery. The
auditory bullae
are relatively inflated, and there is a large opening in the lateral surface of each
mastoid bulla. The soft palate has three ridges in the premolar region and four ridges
in the molar region.
- Other Physical Features
- endothermic
- homoiothermic
- bilateral symmetry
Reproduction
The mating system of Delany's swamp mice has not been reported.
Not much information is available on reproduction in Delanymyinae. Two females were
collected with three embryos each, and a nest was found containing four young.
- Key Reproductive Features
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- fertilization
- viviparous
Delany's swamp mice rear their young inside of globular nests that they make out of
grass and place in low shrubs. Being mammals, females nurse their offspring, but
no further information is available on the investment of these mice in their young.
- Parental Investment
-
pre-fertilization
- provisioning
-
protecting
- female
-
pre-hatching/birth
-
provisioning
- female
-
protecting
- female
-
provisioning
-
pre-weaning/fledging
-
provisioning
- female
-
protecting
- female
-
provisioning
Lifespan/Longevity
No information is available on the lifespan of delanymyines.
Behavior
Delany's swamp mice build small, round nests out of grass. Each nest has one or two
entrances and is situated in a low shrub. They are nocturnal, and, as their common
name would suggest, they are well-adapted for climbing, with semi-prehensile tails,
long digits, and semi-opposable toes.
Communication and Perception
Delanymyines have eyes and ears, so they no doubt perceive the world through vision and hearing. They probably also receive tactile and chemical signals, as do all mammals. No information is available on how these rodents communicate.
Food Habits
Predation
There have been no reports of predation on delanymyines, nor have any anti-predator adaptations been reported. However, these mice probably remain vigilant and use their agility to escape predation. Likely predators include raptors , snakes , and small to medium-sized mammalian carnivores .
Ecosystem Roles
Delanymyines are primary consumers, and they are no doubt consumed by other animals, although no one has reported predation on climbing swamp mice.
Economic Importance for Humans: Positive
There are no known positive impacts of these rodents on humans, although these mice are undoubtedly integral parts of healthy ecosystems in areas they inhabit.
Economic Importance for Humans: Negative
There are no known negative impacts of these rodents on humans.
Conservation Status
Delanymys brooksi
is listed as endangered by the IUCN due to the destruction of habitat in its already
small geographic range.
Additional Links
Contributors
Tanya Dewey (editor), Animal Diversity Web.
Allison Poor (author), University of Michigan-Ann Arbor.
- Ethiopian
-
living in sub-Saharan Africa (south of 30 degrees north) and Madagascar.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- tropical
-
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
- terrestrial
-
Living on the ground.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- mountains
-
This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.
- marsh
-
marshes are wetland areas often dominated by grasses and reeds.
- endothermic
-
animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.
- bilateral symmetry
-
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- fertilization
-
union of egg and spermatozoan
- internal fertilization
-
fertilization takes place within the female's body
- viviparous
-
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
- arboreal
-
Referring to an animal that lives in trees; tree-climbing.
- nocturnal
-
active during the night
- motile
-
having the capacity to move from one place to another.
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
- herbivore
-
An animal that eats mainly plants or parts of plants.
- granivore
-
an animal that mainly eats seeds
References
Carleton, M., G. Musser. 1984. Muroid rodents. Pp. 289-379 in Orders and Families of Recent Mammals of the World . New York: John Wiley and Sons.
Hayman, R. 1962. A new genus and species of African rodent. Revue de Zoologie et de Botanique Africaines , 65: 129-138.
IUCN, 2004. "2004 IUCN Red List of Threatened Species" (On-line). Accessed June 02, 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.
Musser, G., M. Carleton. 1993. Family Muridae. Pp. 501-753 in Mammal Species of the World . Washington, D.C.: Smithsonian Institution Press.
Musser, G., M. Carleton. 2005. Family Muridae. Mammal Species of the World . Washington, D.C.: Smithsonian Institution Press.
Nowak, R. 1999. Walker's Mammals of the World, vol. 2 . Baltimore and London: The Johns Hopkins University Press.
Petter, F. 1967. Particularities dentaires des Petromyscinae Roberts 1951 (Rongeurs, Cricetides). Mammalia , 31: 217-224.
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.