Geographic Range
Silent dormice are found in western Africa, including southern Cameroon, Equatorial
Guinea, Gabon, and north-eastern and south-central portions of the Democratic Republic
of the Congo. The full extent of their geographic range remains unknown.
Habitat
Silent dormice prefer moist lowland forests, specifically those classified by White
(1983) as the wetter variety of the Guineo-Congolian rainforest. Only one specimen
has been found in the drier type of Guineo-Congolian rainforest. They are agile climbers
and largely arboreal.
- Habitat Regions
- tropical
- terrestrial
- Terrestrial Biomes
- rainforest
Physical Description
Silent dormice have compact bodies, and their relatively short, furred tails are frosted
brown. Their coat is short and silky. The dorsal pelage is grayish-brown and composed
of overhairs and short, fine guard hairs with no intermixed layer of underhairs. The
hairs of the ventral pelage are dark gray and tipped with a white buff. Silent dormice
have short, wide arboreal feet with six plantar pads.
Compared to other species of
Graphiurus
, silent dormice have small ears, about 5 mm shorter than those of other South African
dormice. Their faces are distinctive, with dark, mask-like markings around the muzzle
and dark rings around the eyes.
Silent dormice are not particularly sexually dimorphic. Females have four pairs of
mammae: one pectoral, one postaxillary, and two inguinal.
- Other Physical Features
- endothermic
- homoiothermic
- bilateral symmetry
- Sexual Dimorphism
- sexes alike
Reproduction
Little information is available concerning the reproductive behavior of silent dormice,
as their behavior has rarely been observed in the wild. Members of the genus
Graphiurus
, however, are territorial and solitary in general. When the summer breeding season
begins, male African dormice become highly aggressive toward other males, suggesting
polygyny.
- Mating System
- polygynous
In African dormice, most breeding occurs during the wet summer months (October through
February). Normal litter size is between 3 and 4, but female
rock dormice
and
woodland dormice
give birth to as many as 6.
Average gestation length in
woodland dormice
, the closest relative of silent dormice, is about 24 days. At birth,
woodland dormice
weigh about 3.5 g. They reach sexual maturity the summer after their first hibernation.
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- viviparous
Little information is available regarding the parental investment of silent dormice.
Newborns are altricial and, in most African dormice, they become independent after
4 to 6 weeks. Mothers provide protection and nursing in nests in shrubs and among
the branches of trees. Paternal investment of African dormice is likely low to nonexistent,
but no information is available on the subject.
- Parental Investment
- altricial
- female parental care
-
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 specifically regarding the lifespan of silent dormice
in the wild. It is likely they have a lifespan similar to that of other
dormice
, averaging just over 4 years. Silent dormice been recorded to live 5 years and 9
months in captivity.
Behavior
Silent dormice are primarily nocturnal and arboreal, although they can often be found
on the ground. In some particularly dense forests, African dormice exhibit diurnal
behavior. African dormice create globular nests in the branches of trees and shrubs
made of grass, leaves, or lichen.
No information is available regarding the specific hibernation patterns of silent
dormice. Individuals found in southern or central parts of Africa, hibernate during
the winter, but individuals collected from western Africa did not enter states of
torpor when exposed to low temperatures.
Home Range
Little information is available regarding the size of the average home range of silent
dormice. A close relative,
spectacled dormice
, occupies 13.9 hectares (males) and 8.5 hectares (females) on average. In
spectacled dormice
, adult pairs occupy the most favorable parts of the territory and their young, once
independent, disperse to the less ideal parts of the home range.
Communication and Perception
Silent dormice have excellent visual, auditory, and tactile senses. Typical vocalizations
include whistles, chirping noises, various other twittering sounds, and a "surprisingly
loud shriek" (Nowak, 1999).
Woodland dormice
, the closest relative of silent dormice, use scent marks to indicate territories
and makes warning vocalizations to defend territories. Territorial encounters between
male
spectacled dormice
involve loud vocalizations, raised claws, and threatening displays with their bushy
tails.
- Other Communication Modes
- scent marks
Food Habits
Silent dormice are omnivores. They eat grains, seeds, nuts, fruits, insects, eggs,
and even other small rodents.
- Primary Diet
- omnivore
- Animal Foods
- mammals
- eggs
- insects
- terrestrial non-insect arthropods
- Plant Foods
- leaves
- seeds, grains, and nuts
- fruit
- flowers
Predation
No information is available specifically regarding predators of silent dormice. However,
owls are the primary predators of
woodland dormice
and at least 19 species of owl are endemic in the geographic range of silent dormice.
In general, African dormice tend to have few predators because of their nocturnal
and arboreal natures.
When attacked, silent dormice bite with sharp incisors, vocalize loudly, and make
threatening displays with bushy tails.
Dormice
are able to regrow their tails when lost.
Ecosystem Roles
Given their dietary habits, silent dormice likely function as seed dispersers. They
also probably play an important role in insect population dynamics and perhaps in
owl population dynamics, if owls are in fact the primary predator of silent dormice
as they are for the woodland dormice. Silent dormice are primary, secondary, and sometimes
even higher-level consumers.
- Ecosystem Impact
- disperses seeds
Economic Importance for Humans: Positive
Because of their small size, African dormice in general have a relatively minor economic
impact on humans. However, the human consumption of dormice for food is well-documented
in Africa.
- Positive Impacts
- food
Economic Importance for Humans: Negative
Dormice
sometimes make themselves a nuisance by raiding poultry yards for food. African dormice
can sometimes be found living in human habitations, especially in the upholstery of
old furniture, but this occurs less frequently now because of competition with introduced
rats
.
Woodland dormice
are vectors for bubonic plague and monkeypox. Given the extremely close relationship
between woodland dormice and silent dormice, it seems likely that silent dormice may
also be carriers of those diseases.
- Negative Impacts
-
injures humans
- carries human disease
- crop pest
- household pest
Conservation Status
Not enough data are available to assign
G. surdus
a conservation status, they are considered data deficient according to the IUCN Red
List.
Other Comments
Silent dormice are not actually silent, they make quite a few vocalizations. When
Dollman discovered the species in 1912, he chose the name to emphasize the small size
of its ears.
Although Dollman (1912) and Allen (1939) listed silent dormice as their own species,
Misonne (1974) combined
Graphiurus surdus
and
Graphiurus murinus
into a single species. In 1981 Robbins and Schlitter (1981) listed
Graphiurus surdus
as its own species once again in a report on Cameroonian dormice, and Holden (1996)
revised
Graphiurus surdus
in a report on Sub-Saharan dormice.
Additional Links
Contributors
Thomas Berry (author), Yale University, Eric Sargis (editor), Yale University, Rachel Racicot (editor), Yale University, Tanya Dewey (editor), 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.
- rainforest
-
rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.
- 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.
- polygynous
-
having more than one female as a mate at one time
- iteroparous
-
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
- seasonal breeding
-
breeding is confined to a particular season
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- viviparous
-
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
- altricial
-
young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.
- female parental care
-
parental care is carried out by females
- 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.
- sedentary
-
remains in the same area
- solitary
-
lives alone
- territorial
-
defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement
- visual
-
uses sight to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
- scent marks
-
communicates by producing scents from special gland(s) and placing them on a surface whether others can smell or taste them
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
- food
-
A substance that provides both nutrients and energy to a living thing.
- omnivore
-
an animal that mainly eats all kinds of things, including plants and animals
References
Allen, G. 1939. A checklist of African mammals. Bulletin of the Museum of Comparative Zoology , 83: 1-763.
Dollman, J. 1912. Seven new African dormice. Journal of Natural History , 9(51): 312-320.
Fenton, M., T. Fleming. 1976. Ecological Interactions between Bats and Nocturnal Birds. Biotropica , 8(2): 104-110.
Grzimek, B. 2004. Grzimek's Encyclopedia of Mammals . Farmington Hills, MI: Gale.
Holden, M. 1996. Systematic Revision of Sub-Saharan African Dormice (Rodentia: Myoxidae: Graphiurus) Part 1: An Introduction to the Generic Revision, and a Revision of Graphiurus Surdus. American Museum Novitates , 3157: 1-44.
Lodel, J. 2011. "Graphiurus murinus" (On-line). Animal Diversity Web. Accessed April 30, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Graphiurus%20murinus.html .
Misonne, X. 1974. Part 6: Order Rodentia. Pp. 1-39 in The Mammals of African: An Identification Manual . Washington, D.C.: Smithsonian Institution Press.
Nowak, R. 1999. Walker's Mammals of the World . Baltimore, MD: The Johns Hopkins University Press.
Robbins, L., D. Schlitter. 1981. Systematic status of dormice (Rodentia: Gliridae) from southern Cameroon, Africa. Annals of Carnegie Museum , 50: 271-288.
Schlitter, D. 2008. "Graphiurus surdus" (On-line). IUCN Red List of Threatened Species. Version 2011.2. Accessed February 15, 2012 at www.iucnredlist.org .
Stuart, C., T. Stuart. 2001. Field Guide to Mammals of Southern Africa . Cape Town, South Africa: Struik.
Vaughan, T., J. Ryan, N. Czaplewski. 2000. Mammalogy . Stamford, CT: Thomson Learning, Inc.
Webb, P., J. Skinner. 1994. The Dormice (Myoxidae) of southern Africa. Hystrix, the Italian Journal of Mammalogy , 6: 287-293.
White, F. 1983. The vegetation of Africa, a descriptive memoir to accompany the UNESCO/AETFAT/UNSO vexation map of Africa. UNESCO, Natural Resour. Res. , 20: 1-356.