Overview
Distribution
Range Description
In the Mediterranean, occurs in Italy (including an isolated population in the south), Slovenia, Croatia, Bosnia and Herzegovenia, Montenegro, Albania, Serbia, Macedonia, Greece, Bulgaria, Turkey, Syria, Israel. Its vertical range is from sea level to 2,300 m (Kryštufek 1999).
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Geographic Range
Forest dormice (Dryomys nitedula) occur in the Palearctic region. They are present throughout Europe and range as far south as northern Africa and as far east as Japan.
Biogeographic Regions: palearctic (Native )
- Haberl, W. 1999. "The Dormouse Hollow: Dryomys" (On-line ). The Dormouse Hollow. Accessed 10/20/2002 at http://www.gliratium.org/dormouse.
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Physical Description
Morphology
Physical Description
Head and body length of forest dormice ranges from 80 to 130 mm. Tail length ranges from 60 to 113 mm. Body weights range from 18 to 34 g. Dryomys is considered to be very similar to Eliomys, but is smaller. The braincase of forest dormice is more rounded and the auditory bullae are smaller when compared with Eliomys.
Forest dormice are squirrel-like in appearance, with a grayish brown to yellowish-brown dorsum and buff white underside. They have a flat and bushy tail that is more uniform in color than Eliomys.
Range mass: 18 to 34 g.
Range length: 80 to 130 mm.
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Ecology
Habitat
Habitat and Ecology
Systems
- Terrestrial
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Habitat
Forest dormice are found in dense forests, usually deciduous and mixed forests, as well as thickets at elevations of up to 3500 m. Forest dormice utilize cultivated areas such as gardens and also rocky meadows. They choose dense shrubbery or lower branches of trees in which to make a nest.
Range elevation: 3,500 (high) m.
Habitat Regions: temperate ; terrestrial
Terrestrial Biomes: forest
Other Habitat Features: agricultural
- Kashtalian, A. 1999. Dormice of Belarus: ecology, distribution and history of study. IVth International Conference on Dormice (Rodentia, Gliridae). Accessed November 01, 2002 at http://www.trakya.edu.tr/conference/df6.htm.
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Trophic Strategy
Food Habits
Forest dormice are omnivores. They eat leaves as well as choice flowers, fruits, and nuts. They also eat arthropods, eggs, and young birds. Animal matter is observed to be preferred dietary item during the summer.
Animal Foods: birds; eggs; insects; terrestrial non-insect arthropods
Plant Foods: leaves; seeds, grains, and nuts; fruit
Primary Diet: omnivore
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Associations
Ecosystem Roles
Forest dormice may play a role in controlling poulations of arthropods that make up a significant part of their diet. They also eat seeds and fruits, and therefore may aid in the dispersal of seeds. Because this species provides food for predators such as owls, forest dormice may have some positive impact on populations of these predators.
Ecosystem Impact: disperses seeds
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Predation
Dryomys nitedula is nocturnal, occurs at low densities, and individuals are very careful to not travel away from brushy cover. These behaviors make these animals difficult prey to find. Remains of forest dormice have been found in the pellets of owl such as Strix aluco and Bubo bubo in eastern Europe.
Known Predators:
- tawny owls (Strix aluco)
- Eurasian eagle-owls (Bubo bubo)
- Obuch, J. 1999. Dormice in the diet of owls in the Middle East. IVth International Conference on Dormice (Rodentia, Gliridae). Accessed 11/01/02 at http://www.trakya.edu.tr/conference/d21.htm.
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Known prey organisms
Arthropoda
Insecta
Aves
This list may not be complete but is based on published studies.
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Known predators
Bubo bubo
Strix aluco
This list may not be complete but is based on published studies.
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Life History and Behavior
Behavior
Communication and Perception
Dryomys has been observed to emit a variety of vocalizations. Most notable of those is a delicate, melodious squeak that appears to function as an alarm call. Research on captive individuals has demonstrated that D. nitedula has the ability to emit repeated series of ultrasounds. The signals were given off by both sexes in situations suggesting a social character of the communication. These communications were entirely inaudible to the human ear.
Although not specifically reported for this species, it is likely that tactile, chemical, and visual signals are part of the repetoir of communication. Mammals typically use tactile communication during mating, conflict, and rearing of young. Chemical communication can be important in individual identification, as well as in reproductive contexts. Visual signals are often given, by means of body posturing, to indicate hostile or friendly intent.
Communication Channels: visual ; tactile ; acoustic ; chemical
Perception Channels: visual ; ultrasound
- Boratynski, P., A. Rachwald, W. Nowakowski. 1999. Ultrasound communication calls in Forest Dormouse (*Dryomys nitedula*). IVth International Conference on Dormice (Rodentia, Gliridae). Accessed 11/01/02 at http://www.trakya.edu.tr/conference/d13.htm.
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Life Expectancy
Lifespan/Longevity
Dryomys nitedula can be expected to live up to 5.5 years in the wild.
Average lifespan
Status: wild: 5.5 years.
Average lifespan
Status: wild: 4.0 years.
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Lifespan, longevity, and ageing
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Reproduction
Reproduction
Not much information is available on the mating system of this species.
The breeding season for forest dormice varies throughout the species' range. In Israel, the breeding season extends from March to December. On average, each female gives birth 2 to 3 times a year. In Europe, the breeding season lasts from May to August, and usually just one litter occurs each year. The gestation period is between 21 and 30 days. Usually 2 to 5 individuals are born per litter, although occassionally up to 7 may be possible.
Each offspring weighs approximately 2 g at birth. Eyes do not open until around day 16 of life, and independence from the mother is not achieved until the young are 4 to 5 weeks of age. In Europe the young will wait until after their first winter to mate.
Breeding interval: In Israel the species will breed 2 to 3 times per year. In Europe the species breeds only once per year.
Breeding season: In Israel, the mating season extends from March to December. In Europe the mating season occurs from May to August.
Range number of offspring: 2 to 7.
Range gestation period: 21 to 30 days.
Range time to independence: 4 to 5 weeks.
Average age at sexual or reproductive maturity (female): 1 years.
Average age at sexual or reproductive maturity (male): 1 years.
Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); fertilization ; viviparous
Average birth mass: 1.73 g.
Average number of offspring: 3.
There is little information available on the parental care of this speices. Neonates are altricial, and do not open their eyes until they are about 16 days old. Young are dependent upon their mother until they are 4 to 5 weeks of age. Until they are independent, it is likely that the mother provides them with food (milk), grooming, and protection. Male parental care has not been reported, but cannot be ruled out, either.
Parental Investment: no parental involvement; altricial ; pre-fertilization (Protecting: Female); pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Female); pre-independence (Provisioning: Female, Protecting: Female)
- Nowak, R. 1999. Walker's Mammals of the World, Sixth Edition. Baltimore and London: The Johns Hopkins University Press.
- Haberl, W. 1999. "The Dormouse Hollow: Dryomys" (On-line ). The Dormouse Hollow. Accessed 10/20/2002 at http://www.gliratium.org/dormouse.
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Molecular Biology and Genetics
Molecular Biology
Statistics of barcoding coverage: Dryomys nitedula
Public Records: 0
Species: 1
Species With Barcodes: 1
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Conservation
Conservation Status
IUCN Red List Assessment
Red List Category
Red List Criteria
Version
Year Assessed
Assessor/s
Reviewer/s
Contributor/s
Justification
History
- 1996Lower Risk/near threatened
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Conservation Status
Dryomys nitedula is regarded as endangered in the Czech Republic and as rare in most other European countries. IUCN designated forest dormice as lower risk, but the species is not listed by CITES. The threat to the population stems mainly from the destruction of forest habitat throughout their range.
The UK has developed a National Dormouse Monitoring Programme, which exists primarily to monitor hazel dormice. Hazel dormice are a cherished child storybook star in England and Wales, but the program elements are a standard for all species of dormice. Researchers have placed dormouse nest boxes on trees in woodland areas where dormice have been known to occur, and return to those boxes to count, sex, and weigh the dormice. Research is done in order to form a database for the species and monitor the health of the population.
English Nature has been running a reintroduction program that has been reintroducing captive-bred dormice since 1994 to areas where populations were at one time plentiful. Also the English government has begun to award farmers incentives to replant hedgerows which are very important to the habitat of forest dormice. Such conservation efforts would also be helpful in maintaining populations of other species of dormice, such as D. nitedula.
US Federal List: no special status
CITES: no special status
IUCN Red List of Threatened Species: least concern
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Trends
Population
In Europe west of Russia it is generally rare, although in some southeastern areas (e.g. Bulgaria, Turkish Thrace, Moldova) it is locally common, reaching densities of 23-25 individuals per hectare in Moldova (Kryštufek 1999). At the western border of its distribution, populations have declined due to deforestation. There is only one population remaining in Switzerland (Tester and Müller 2000), and the German population has not been surveyed in over 30 years (H. Meinig pers. comm. 2006). However, there have been no reports of declines elsewhere in Europe as yet (Kryštufek 1999, EMA Workshop 2006).
This species is widespread and common in mountainous areas of Azerbaijan and is widespread in Turkey. In Israel in 1961 only 35 animals were observed during 350 hours of field surveys (Harrison and Bates 1991). Reported as quite common in Syria in evergreen forests and orchards (Shehad et al. 2003).
In Mongolia, a survey along the Bulgan River drainage basin estimated there to be 20 individuals per hectare (Stubbe and Chotolchu, 1968). In 1988, only a few old nests were found in the vicinity of Bag Shar Bolog, although the population is believed to be fairly stable (M. Stubbe pers. comm.).
Population Trend
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Threats
Threats
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Management
Conservation Actions
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Relevance to Humans and Ecosystems
Benefits
Economic Importance for Humans: Negative
Populations of D. nitedula have been known to cause economic damage by raiding fruit orchards and gnawing at the bark of coniferous trees.
Negative Impacts: crop pest
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Economic Importance for Humans: Positive
There was no specific data on the positive economic significance for humans of D. nitedula.
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