Overview

Brief Summary

Biology

Wood mice are generally nocturnal, but males, or females suckling young may be active for short times during the day (4). They feed on seeds, invertebrates, fruits, nuts, seedlings, moss and fungi (4), and food is often stored within tunnel systems (3). All mice engage in 'refection' in order to fully digest food; they eat soft faeces that have already passed through their digestive system once, allowing carbohydrates to be fully digested the second time around (3). Breeding occurs from March/ April until October, and peaks in July and August (4). In summer, females defend breeding ranges against other females (4). Dominant males may be aggressive, and have been reported to chase and even kill juveniles (3). Before mating, males are known to produce a string of ultrasounds, which may serve to pacify the female (3). Gestation takes 25 or 26 days (3), and the litter, which consists of 2-9 young (4), is born at night within the nest (3). Nests are made in underground tunnels, inside hollow logs, bird or dormice nesting boxes or in dense vegetation (3). Between 4 and 7 litters are produced each year (4), and females are able to conceive whilst still suckling the previous litter (3). The young are fully weaned after about 18 days, and usually start to breed the year after their birth, but if they were born early in the year they may breed during the year of birth (4). Wood mice do not hibernate, but during winter males and females may group together when sleeping for extra warmth (3). The maximum life-span is 18-20 months. This species has many predators, including foxes, weasels, cats, owls and kestrels (4); the wood mouse has evolved a number of strategies to avoid these predators, it can make impressive leaps to safety, and can shed the skin of the tail if it is gripped anywhere other than its base, allowing the mouse to escape. The skin does not grow back; instead the area of the tail dies and falls off (3).
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Comprehensive Description

Description

The wood mouse is the most common native rodent in Britain (2). It has brown fur with a reddish tinge (3) and a white or greyish belly (2). The alternative common name of this species is the long-tailed field mouse, as the tail is often roughly the same size as the combined head and body length (3). This species can be distinguished from the similar yellow-necked mouse as it lacks a yellow collar that forms a bib on the chest (2).
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Distribution

Range Description

The wood mouse has a large range that extends throughout Europe (with the exception of Finland and northern parts of Scandinavia, the Baltic and Russia) and parts of North Africa (Panteleyev 1998, Montgomery 1999, Wilson and Reeder 2005).

In Europe, the species occurs from southern Europe northwards to Scandinavia; eastwards to northwest Turkey (Thrace and northwestern Anatolia), central Belarus, eastern Ukraine, and closely adjacent parts of the western Russian Federation (the easternmost limit of the species).

In Africa, it occurs in the Atlas Mountains and north of them along the entire coastal plain. It is present on the majority of offshore islands including the British Isles, Iceland and numerous Mediterranean islands: for example the Aegean islands, Greece, some islands in the Tuscan Archipelago, Sardinia and Corsica, Italy.

It occurs from sea level to 3,300 m in the High Atlas mountains.
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Geographic Range

Apodemus sylvaticus is found throughout Europe, except northern Scandinavia and Finland, east to the Altai and Himalayan mountains. It is also found in parts of central and southwestern Asia, Himalayas, northwestern Africa, British Isles and nearby islands. (Fact-File 1991, Nowak 1991)

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Range

Widespread and common throughout Britain and continental Europe, reaching as far north as southern Scandinavia (4). It is not present on many of the smaller British islands, but where it does occur on islands it is often the result of introductions (4).
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Physical Description

Morphology

Physical Description

Head and body length of Apodemus sylvaticus is 60-150mm, tail length is 70-145 mm. The fur is soft, and the tail is only moderately hairy. Coloration on the dorsal area is grayish buff, grayish brown, brown with yellow or red mixed in, or pale sand color. The underparts are white or light gray, often with yellow tinges and an oblong yellow spot on the throat. The feet are white. The tail is not prehensile. Females have six or eight nipples. The eyes and ears are large, allowing good vision at night and predator avoidance. The sense of smell is highly developed, and these rodents can detect the exact location of buried seeds without having to dig at random in a general area.

Like other members of the subfamily Murinae, these mice have moderately low crowned cheek teeth, with an arrangement of cusps which results in the formation of three longitudinal rows on the biting surface. The incisors are ever-growing self sharpening. There is a layer of enamel on only the front and sides of the teeth, resulting in the back part of the tooth wearing away during normal gnawing behavior so as to form a chisel-like edge.

(Fact-File 1991; Macdonald 1985; Nowak 1991; Parker 1990)

Average mass: 23.4 g.

Average basal metabolic rate: 0.264 W.

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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
It is a very adaptable species, inhabiting a wide variety of semi-natural habitats including all types of woodland, moorland, steppe, arid Mediterranean shrubland, and sand dunes. It is also found in many man-made habitats including suburban and urban parks, gardens and wasteland, pastures and arable fields, and forestry plantations. It has an omnivorous diet including seeds and invertebrates. Although it can cause occasional damage, it is not generally considered an agricultural pest (Montgomery 1999).

Systems
  • Terrestrial
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Habitat

These mice like grassy fields, cultivated areas, woodlands and forests, although they will live anywhere they can find adequate shelter. They may move into human habitations in the fall and winter but usually dig deep burrows and build a nest of shredded grass and leaves at the end of a tunnel. (Fact-File 1990;Nowak 1991; Parker 1990)

Terrestrial Biomes: savanna or grassland

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Habitat

A highly adaptable species, the wood mouse exploits a wide range of habitats, providing that they are not overly wet (4).
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Trophic Strategy

Food Habits

The diet of the Wood Mouse consists of roots, grains, seeds, berries, nuts, grasses, grain kernels, fruits and insects. (Nowak 1991;Parker 1990)

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Associations

Associations

Animal / parasite / ectoparasite / blood sucker
Amalaraeus penicilliger mustelae sucks the blood of Apodemus sylvaticus

In Great Britain and/or Ireland:
Animal / parasite / endoparasite
Capillaria hepatica endoparasitises patchily yellow liver of Apodemus sylvaticus

Animal / parasite / endoparasite
Capillaria muris sylvatici endoparasitises intestine of Apodemus sylvaticus

Animal / parasite / endoparasite
Chilomastix bettencourti endoparasitises caecum of Apodemus sylvaticus

Animal / parasite / endoparasite
fluke of Corrigia vitta endoparasitises pancreas (interlobary canals) of Apodemus sylvaticus

Animal / parasite / ectoparasite / blood sucker
Ctenophthalmus nobilis nobilis sucks the blood of skin of Apodemus sylvaticus

Animal / parasite / ectoparasite / blood sucker
Ctenophthalmus nobilis vulgaris sucks the blood of skin of Apodemus sylvaticus

Animal / rests in
Entamoeba muris rests inside large intestine of Apodemus sylvaticus

Animal / parasite / endoparasite
Giardia muris endoparasitises small intestine of Apodemus sylvaticus

Animal / parasite / endoparasite
Grahamella endoparasitises red blood cells of Apodemus sylvaticus

Animal / parasite / endoparasite
Hepatozoon sylvaticae endoparasitises white blood cells of Apodemus sylvaticus

Animal / parasite / endoparasite
Hexamita muris endoparasitises caecum of Apodemus sylvaticus

Animal / parasite / ectoparasite / blood sucker
Hystrichopsylla talpae talpae sucks the blood of skin of Apodemus sylvaticus
Other: major host/prey

Animal / parasite / ectoparasite / blood sucker
nymph of Ixodes ricinus sucks the blood of skin of Apodemus sylvaticus

Animal / parasite / ectoparasite / blood sucker
nymph of Ixodes trianguliceps sucks the blood of ear of Apodemus sylvaticus

Animal / associate
Leptinus testaceus is associated with nest of Apodemus sylvaticus

Animal / vector
Leptospira is spread by Apodemus sylvaticus

Animal / parasite / ectoparasite / blood sucker
Megabothris turbidus sucks the blood of skin of Apodemus sylvaticus

Animal / parasite / endoparasite
Mycoplasma endoparasitises red blood cells of Apodemus sylvaticus

Animal / parasite / endoparasite
spirally coiled worm of Nematospiroides dubius endoparasitises duodenum of Apodemus sylvaticus

Animal / parasite / endoparasite
preadult of Pelodera strongyloides endoparasitises tears of Apodemus sylvaticus
Other: minor host/prey

Animal / associate
Rhadinopsylla pentacantha is associated with nest of Apodemus sylvaticus

Animal / rests in
intestine of Syphacia stroma rests inside Apodemus sylvaticus

Animal / parasite / endoparasite
Trichomonas microti endoparasitises gut of Apodemus sylvaticus

Animal / parasite / endoparasite
Trichomonas muris endoparasitises caecum of Apodemus sylvaticus

Animal / parasite / endoparasite
Trichomonas sylvaticus endoparasitises gut of Apodemus sylvaticus

Animal / parasite / endoparasite
Trypanosoma grosi endoparasitises blood plasma of Apodemus sylvaticus
Other: sole host/prey

Animal / parasite / ectoparasite / blood sucker
Typhloceras poppei poppei sucks the blood of skin of Apodemus sylvaticus

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Life History and Behavior

Life Expectancy

Lifespan/Longevity

Average lifespan

Status: captivity:
4.0 years.

Average lifespan

Status: wild:
1.0 years.

Average lifespan

Status: captivity:
4.4 years.

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The average life expectancy of Apodemus sylvaticus in the wild is 12 to 15 months (Jenrich, Löhr, Müller 2010).
  • JENRICH, J., LÖHR, P.-W. & MÜLLER, F. (2010). Kleinsäuger, Körper- und Schädelmerkmale, Ökologie. Fulda, Michael Imhof Verlag.
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Lifespan, longevity, and ageing

Maximum longevity: 6.3 years (captivity) Observations: One wild born specimen was about 6.3 years of age when it died in captivity (Richard Weigl 2005).
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Reproduction

Reproduction

The breeding season of Apodemys sylvaticus is from March through early winter. Females produce up to four litters annually, with four to seven young each litter after a gestation period of 21-26 days. The young are altricial, weighing a mere 2.5g. They are born with a thin coat of dark fur and open their eyes after 13 days. They are weaned at three weeks and reach sexual maturity at two months. Females of this age usually weigh around 14 grams, while males weigh approximately 25 g. (Fact-File 1991; Nowak 1991)

Average birth mass: 1.5 g.

Average gestation period: 23 days.

Average number of offspring: 5.2.

Average age at sexual or reproductive maturity (male)

Sex: male:
65 days.

Average age at sexual or reproductive maturity (female)

Sex: female:
71 days.

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Molecular Biology and Genetics

Molecular Biology

Statistics of barcoding coverage: Apodemus sylvaticus

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 0
Species: 7
Species With Barcodes: 1

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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
LC
Least Concern

Red List Criteria

Version
3.1

Year Assessed
2008

Assessor/s
Schlitter, D., van der Straeten, E., Amori, G., Hutterer, R., Kryštufek, B., Yigit, N. & Mitsain, G.

Reviewer/s
Amori, G. (Small Nonvolant Mammal Red List Authority) & Temple, H. (Global Mammal Assessment Team)

Justification
Listed as Least Concern because, it is a very common and widespread species. It is commensal with people and is sometimes considered to be a pest.

History
  • 2004
    Least Concern
  • 1996
    Lower Risk/least concern
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Conservation Status

This species is the most common mouse throughout its range. It is not under any threat. (Fact-File 1990)

IUCN Red List of Threatened Species: least concern

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Status

No legal protection (2).
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Population

Population
It is widespread and abundant throughout much of its range, and populations appear to be stable. Population density may fluctuate more than tenfold between years of maximum and minimum abundance, but there are no regular cycles (Montgomery 1999). It is very abundant and in places it is considered to be a pest species.

Population Trend
Stable
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Threats

Threats

Major Threats
There are no major threats to this species, although pollution by lead and agrochemicals may have localised negative impacts.
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Threats

Although this species is not threatened at present, loss of woodlands, hedgerows and changes in agriculture may all negatively affect wood mice. Chemicals used in agriculture may also pose a threat, either directly, or via contamination of food sources (4).
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Management

Conservation Actions

Conservation Actions
It occurs in many protected areas within its range. No specific conservation actions are needed.
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Conservation

No conservation measures or legal protection is in place for this common species, which is an important source of food for many carnivores and owls (2).
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Relevance to Humans and Ecosystems

Benefits

Economic Importance for Humans: Positive

Apodemus sylvaticus are important agents for the transportation and burying of tree seeds. Their impact on the forests has both a positive and a negative aspect, and their role in the health of woodland is currently under study. (Nowak 1991)

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Economic Importance for Humans: Negative

The wood mouse is seen as a pest, inflicting serious damage to vegetable gardens and farmland, digging up seeds before they can germinate, and eating crop grasses down to the ground. These mice are also responsible for damage to seedlings in wooded areas of their range. (Fact-File 1990; Nowak 1991)

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Wikipedia

Wood mouse

The wood mouse (Apodemus sylvaticus) is a common murid rodent from Europe and northwestern Africa. It is closely related to the yellow-necked mouse (Apodemus flavicollis) but differs in that it has no band of yellow fur around the neck, has slightly smaller ears, and is usually slightly smaller overall: around 90 mm (3.54") in length. It is found across most of Europe and is a very common and widespread species, is commensal with people and is sometimes considered a pest.[1] Other common names are long-tailed field mouse, field mouse, common field mouse, and European wood mouse.[2]

Contents

Habitat

Wood mice inhabit forests, grasslands, and cultivated fields. Almost entirely nocturnal and terrestrial, wood mice burrow extensively, build nests of plants and live in buildings during harsh seasons. It is one of the most intensively studied species in the genus. In Europe it ranges north to Scandinavia and east to Ukraine. The wood mouse is also found in northwestern Africa and on many Mediterranean islands.[3]

Behaviour

A Cherry stone hoard.

Wood mice are primarily seed eaters,[4] particularly seeds of trees such as oak, beech, ash, lime, hawthorn and sycamore. If there is a plentiful amount of seeds on the ground, they carry them back to their nests/burrows for storage. They may eat small invertebrates such as snails and insects, particularly in late spring and early summer when seeds are least available. They also consume berries, fruits and roots. During the colder months wood mice do not hibernate; however, during severe winter seasons they fall into a sort of torpor, a decrease in physiological activity. They are mainly active during the dark, and are very good climbers. While foraging, wood mice pick up and distribute visually conspicuous objects, such as leaves and twigs, which they then use as landmarks during exploration.[5] If a wood mouse is caught by its tail, it can quickly shed the end of it, which may never regrow.[6] Despite its name, it prefers hedgerows to woodland. In order to prevent predation, wood mice tend to forage in covered microsites.[7]

Reproduction

Wood mouse

The wood mouse has a breeding season from February to October in which multiple matings occur between males and females resulting in scramble competition. Such behavioral characteristics result in sperm competition and multiple paternity litters. The society is polygynous with copulation resulting from scramble competition during reproductive periods. Males possess a sac known as the cauda epididymus which stores sperm and lies underneath the scrotum protrusion. Temperature regulation ensures maximum sperm output.

One interesting observation about the species, in particular the males, is the morphology of the spermatozoa. They develop falciform (sickle shaped) heads after meiosis and before spermiation (release during ejaculation). The hook located at the tip of the head adheres to the surface of the head prior to deployment. Propidium iodide staining revealed that only the basal surface of the hook is of nuclear origin.[8] These apical hooks are deployed in female reproductive tract (mechanism responsible involved the remodeling of actin filaments in the hook).[8] Deployed apical hooks combine with apical hooks and flagella of other spermatozoa. The aggregates of spermatozoa that result form "mobile trains", which have experimentally been determined to possess better motility in the female reproductive tract.[8] The mobility of these mobile trains was also found to be influenced by premature acrosome reactions, altruistic acts performed by some spermatozoa for the benefit of other genetically similar gametocytes. This altruism follows a "green beard" mechanism in which spermatozoa discern the genetic similarity of surrounding gametocytes (such mechanisms are rare because they must code for a recognizable phenotype as well as response mechanisms). Once spermatozoa of similar genotypes are identified, altruism genes are turned on to elicit a response that seeks to conserve the genes present in the other cell, even if it results in the destruction of the cell performing the action.

The gestation period of wood mice is of 25–26 days and each female produces on average five young. The offspring become independent after about three weeks and become sexually active after two months.

References

  1. ^ Schlitter & Van der Straeten (2004). Apodemus sylvaticus. 2006. IUCN Red List of Threatened Species. IUCN 2006. www.iucnredlist.org. Retrieved on 11 May 2006. Database entry includes a brief justification of why this species is of least concern
  2. ^ Murray Wrobel: Elsevier’s Dictionary of Mammals. Elsevier 2006, ISBN 978-0-444-51877-4.
  3. ^ Encyclopædia Britannica. 2008. http://www.britannica.com/EBchecked/topic/206303/wood-mouse
  4. ^ Fedriani J. M. 2005. Do frugivorous mice choose where or what to feed? Journal of Mammalogy 86:576-586.
  5. ^ Stopka, P.; et al. (April 2003). "Way-marking behaviour: an aid to spatial navigation in the wood mouse (Apodemus sylvaticus)". BMC Ecology 3: 3. doi:10.1186/1472-6785-3-3. http://www.biomedcentral.com/1472-6785/3/3. 
  6. ^ Goaman, K., Amery, H. (1983). Mysteries & Marvels of the Animal World: pg.15
  7. ^ Fedriani J. M. 2005.
  8. ^ a b c Moore, Harry; et al. (2002). "Exceptional sperm cooperation in the wood mouse". Nature 418 (6894): 174–177. doi:10.1038/nature00832. PMID 12110888. 
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