Overview

Brief Summary

Biology

Bank voles are active during both the day and night, although they become increasingly nocturnal during the summer (4). They do not hibernate in winter, but are active throughout the year (4). They have a broad diet, which is mainly herbivorous, including fruit, soft seeds, leaves, fungi, roots, grass, buds and moss. They may also occasionally take invertebrate food such as snails, worms and insects (4), and the odd bird egg may be eaten (2). Breeding typically takes place between April and October, but when conditions are suitable, births may occur throughout the year (4). Ovulation by the female is stimulated by the presence of a male, possibly via certain scents that males produce (5). Gestation takes around 21 days, but may be a short as 17 days in this species if conditions are optimal (5). Between 4 and 5 litters are produced in a year, each one consisting of 3-5 young (4). Females are able to conceive again whilst still suckling the previous litter; under these circumstances the gestation period will be longer, up to 24 days (5). The young voles are born in a nest, which is usually located underground (5). Males do not assist with rearing the offspring. Females are very protective of the litter; if any young leave the nest the female locates them and carries them back to the nest (5). The young become sexually mature at around 4.5 weeks of age, however those born later in the year will not start to breed until the next spring (4). Predators such as owls, kestrels, foxes and weasels take their toll on vole populations; the maximum life span for this species is 18 months. The numbers of bank voles varies greatly throughout the year, being high towards the end of summer and plummeting through the winter to a low in April (4).
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Comprehensive Description

Description

The bank vole has a small, stocky body and a blunt, rounded muzzle (2). The upperparts may be yellowish, reddish or brown in colour, the flanks are greyish and the rump is whitish-grey (2). The short tail is usually slightly bushy at the tip (2).
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Distribution

Range Description

The bank vole, Myodes glareolus has a wide range in the Palaearctic which stretches from the British Isles through continental Europe and Russia to Lake Baikal. In the north, its range extends beyond the Arctic circle, and in the south it reaches northern Turkey and northern Kazakhstan (Shenbrot and Krasnov 2005). It is widespread in Europe, although it is absent from southern Iberia and the Mediterranean islands. It is found from sea level to 2,400 m (Spitzenberger 1999).
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Geographic Range

Palearctic: Myodes glareolus is found from Europe through Central Asia (Macdonald 2001; Jonsson et al. 2000). Populations have frequently been recorded in Finland (Oksanen et al. 2001; Yoccoz et al. 2001; Oksanen et al. 1999; Prevot-Julliard et al. 1999; Horne and Ylonen 1996, 1998; Koskela et al. 1998; Koskela et al. 1997) and the United Kingdom (Bellamy et al. 2000; Flowerdew and Gardner 1978).

Biogeographic Regions: palearctic (Native )

  • Macdonald, D. 2001. The Encyclopedia of Mammals. United Kingdom: Andromeda Oxford Limited.
  • Bellamy, P., R. Shore, D. Ardeshir, J. Treweek, T. Sparks. 2000. Road verges as habitat for small mammals in Britain. Mammal Review, 30: 131-139.
  • Flowerdew, J., G. Gardner. 1978. Small rodent populations and food supply in a Derbyshire Ahswood. Journal of Animal Ecology, 47: 725-740.
  • Horne, T., H. Ylonen. 1998. Heritabilities of dominance-related traits in male bank voles (*Clethrionomys glareolus*). Evolution, 52: 894-899.
  • Horne, T., H. Ylonen. 1996. Female bank voles (*Clethrionomys glareolus*) prefer dominant males; but what if there is no choice. Behavioral Ecology and Sociobiology, 38: 401-405.
  • Jonsson, P., E. Koskela, T. Mappes. 2000. Does risk of predation by mammalian predators affect the spacing behavior of rodents? Two large-scale experiments. Oecologia, 122: 4877-492.
  • Koskela, E., P. Jonsson, T. Hartikainen, T. Mappes. 1998. Limitation of reproductive success by food availability and litter size in the bank vole, *Clethrionomys glareolus*. Proceedings of the Royal Society, London B, 265: 1129-1134.
  • Koskela, E., T. Mappes, H. Ylonen. 1997. Territorial behaviour and reproductive success of bank vole *Clethrionomys glareolus* females. Journal of Animal Ecology, 66: 341-349.
  • Oksanen, T., P. Jonsson, E. Koskela, T. Mappes. 2001. Optimal allocation of reproductive effort: manipulation of offspring number and size in the bank vole. Proceedings of the Royal Society, London B, 268: 661-666.
  • Oksanen, T., R. Alatalo, T. Horne, E. Koskela, J. Mappes. 1999. Maternal effort and male quality in the bank vole, *Clethrionomys glareolus*. Proceedings of the Royal Society, London B, 266: 1495-1499.
  • Prevot-Julliard, A., H. Henttonen, N. Yoccoz, N. Stenseth. 1999. Delayed maturation in female bank voles: optimal decision or social constraint. Journal of Animal Ecology, 68: 684-697.
  • Yoccoz, N., N. Stenseth, H. Henttonen, A. Prevot-Julliard. 2001. Effects of food addition on the seasonal density-dependent structure of bank vole, *Clethrionomys glareolus*, populations. Journal of Animal Ecology, 70: 713-720.
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occurs (regularly, as a native taxon) in multiple nations

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National Distribution

Canada

Origin: Exotic

Regularity: Regularly occurring

Currently: Present

Confidence: Confident

Type of Residency: Year-round

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Global Range: (>2,500,000 square km (greater than 1,000,000 square miles)) Europe, parts of Asia Minor, and central Asia (Nowak 1991). Introduced and established in Ireland (Nowak 1991) and Newfoundland (Joe Brazil, pers. comm., 2000). Brazil last checked the population on Yellow Fox Island, Notre Dame Bay, Newfoundland, in 1986. Specimens from that survey are in the National Museum in Ottawa, the Newfoundland Museum in St. John's, and in Brazil's possession. This vole was introduced to this small island in the mid- to late 1960s by Dr. Bill Pruitt and/or one of his students. The island is not large, less than a square kilometer. Brazil stated he had no reason to believe that the voles are not still thiving on the island. They have no competitors and few if any predators.

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Range

Common in Britain, including a number of the islands. On Skomer Island off the Pembrokeshire coast of Wales, there is a subspecies known as the Skomer vole (Clethrionomys glareolus skomerensis). The bank vole is also common throughout much of western and central Europe (4).
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Physical Description

Morphology

Physical Description

Adult bank voles reach a head-body length of 10-11cm and a weight of 17-20g, with males and females being approximately the same size. The tail is less than body length and reaches a length of 3-4cm. Bank voles are small with small eyes and ears. Their body is covered by thick fur in shades of brown or gray. Their muzzle is blunt and rounded. Relative to body size, M. glareolus has a small brain. Teeth are prismatic and are characterized by flat crowns, which are adapted for their herbivorous diet (Macdonald 2001).

Range mass: 17 to 20 g.

Range length: 10 to 11 cm.

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Type Information

Type for Myodes glareolus
Collection: Smithsonian Institution, National Museum of Natural History, Department of Vertebrate Zoology, Division of Mammals
Sex/Stage: Female;
Preparation: Skin; Skull
Collector(s): T. Stejneger
Year Collected: 1898
Locality: Bergen, Bergen Municipality, Hordaland, Norway, Europe
  • Type:
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Type for Myodes glareolus
Collection: Smithsonian Institution, National Museum of Natural History, Department of Vertebrate Zoology, Division of Mammals
Sex/Stage: Male;
Preparation: Skin; Skull
Collector(s): R. Young
Year Collected: 1899
Locality: Montrejeau, Haute-Garonne Department, Midi-Pyrenees, France, Europe
  • Type:
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Type for Myodes glareolus
Collection: Smithsonian Institution, National Museum of Natural History, Department of Vertebrate Zoology, Division of Mammals
Sex/Stage: Female;
Preparation: Skin; Skull
Collector(s): J. Loring
Year Collected: 1898
Locality: Uppsala, Uppsala Municipality, Sweden, Europe
  • Type:
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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
It inhabits all kinds of woodland, preferring densely-vegetated clearings, woodland edge, and river and stream banks in forests. It is also found in scrub, parkland, and hedges (Viro and Niethammer 1982, Spitzenberger 1999).

Systems
  • Terrestrial
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Habitat

Bank voles are found in a wide variety of habitats, including forests, scrub forests, hedges, banks, and swamps (Macdonald 2001; Bellamy et al. 2000). They appear to prefer deciduous, coniferous, and taiga forests (Yoccoz et al. 2001; Prevot-Julliard et al. 1999; Koskela et al. 1998; Koskela et al. 1997; Ostfeld 1985).

Habitat Regions: temperate ; terrestrial

Terrestrial Biomes: taiga ; forest

Wetlands: swamp

Other Habitat Features: agricultural ; riparian

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Habitat

This adaptable species (2) inhabits broadleaved woodlands, scrub, parks, hedgerows and banks where there is plenty of herbaceous cover (4).
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Trophic Strategy

Food Habits

Myodes glareolus have been characterized as omnivorous (Ostfeld 1985) and herbivorous (Macdonald 2001). When eating grass, M. glareolus clip the stalks and lays the clippings in piles. Food is obtained in the winter by burrowing underground. In the summer and fall food is cached. Diet changes with season and location but includes green parts of plants (Macdonald 2001), fruits and seeds from available trees, such as the European ash tree (Fraxinus excelsior) (Flowerdew and Gardner 1978) and grass (Macdonald 2001).

Plant Foods: leaves; seeds, grains, and nuts; fruit

Foraging Behavior: stores or caches food

Primary Diet: herbivore (Folivore , Frugivore , Granivore )

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Associations

Ecosystem Roles

Bank voles are important as a prey base for many small avian and mammalian predators and snakes. They are often abundant and can form the main component of the diet of these predators. They may also help in recycling and redistributing nutrients in the ecosystems in which they live through herbivory.

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Predation

Many small predators rely on bank voles as prey. Bank voles partially escape predation by remaining under cover in underground tunnels or runways in grass and vegetation. I is thought that avian predators use the ultraviolet reflections of scent marks to locate their prey (Koivula et al. 1999).

Known Predators:

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Known predators

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Associations

Animal / parasite / ectoparasite / blood sucker
Amalaraeus penicilliger mustelae sucks the blood of Clethrionomys glareolus

In Great Britain and/or Ireland:
Animal / parasite / endoparasite
Babesia microti endoparasitises red blood cells of Clethrionomys glareolus

Animal / parasite / endoparasite
Capillaria hepatica endoparasitises patchily yellow liver of Clethrionomys glareolus

Animal / parasite / endoparasite
Capillaria muris sylvatici endoparasitises intestine of Clethrionomys glareolus

Animal / parasite / endoparasite
tapeworm of Catenotaenia lobata endoparasitises small intestine of Clethrionomys glareolus

Animal / parasite / endoparasite
tapeworm of Catenotaenia pusilla endoparasitises small intestine (middle part) of Clethrionomys glareolus

Animal / parasite / endoparasite
fluke of Corrigia vitta endoparasitises pancreas (interlobary canals) of Clethrionomys glareolus

Animal / parasite / endoparasite
Eimeria endoparasitises rectum of Clethrionomys glareolus

Animal / rests in
Entamoeba muris rests inside large intestine of Clethrionomys glareolus

Animal / parasite / endoparasite
Frenkelia glareoli endoparasitises brain of Clethrionomys glareolus

Animal / parasite / endoparasite
Giardia microti endoparasitises small intestine of Clethrionomys glareolus

Animal / parasite / endoparasite
schizont of Hepatozoon erhardovae endoparasitises lung of Clethrionomys glareolus

Animal / parasite / endoparasite
Hexamita muris endoparasitises caecum of Clethrionomys glareolus

Animal / parasite / ectoparasite / blood sucker
Hystrichopsylla talpae talpae sucks the blood of Clethrionomys glareolus
Other: minor host/prey

Animal / parasite / ectoparasite / blood sucker
Ixodes trianguliceps sucks the blood of skin of Clethrionomys glareolus

Animal / parasite / endoparasite
spirally coiled worm of Nematospiroides dubius endoparasitises duodenum of Clethrionomys glareolus

Animal / parasite / endoparasite
preadult of Pelodera strongyloides endoparasitises tears of Clethrionomys glareolus
Other: major host/prey

Animal / rests in
posterior intestine of Syphacia obvelata rests inside Clethrionomys glareolus

Animal / parasite / endoparasite
Cystocercus larva of Taenia taeniaeformis endoparasitises liver of Clethrionomys glareolus

Animal / parasite / endoparasite
Trichomonas muris endoparasitises caecum of Clethrionomys glareolus

Animal / parasite / endoparasite
Trypanosoma evotomys endoparasitises blood plasma of Clethrionomys glareolus
Other: sole host/prey

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Life History and Behavior

Life Expectancy

Lifespan/Longevity

The lifespan of M. glareolus is very short. Average lifespan is 0.5-2 years, with most individuals not lasting more than one breeding season (Macdonald 2001; Ostfeld 1985). Bank voles mature quickly with females maturing at 2-3 weeks and males maturing at 6-8 weeks (Macdonald 2001).

Range lifespan

Status: wild:
0.5 to 2 years.

Typical lifespan

Status: wild:
0.5 to 2 years.

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Lifespan, longevity, and ageing

Maximum longevity: 4.9 years (captivity)
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Reproduction

Reproduction

The mating system of M. glareolus can be described as polygamous (Macdonald 2001), and possibly promiscuous (Horne and Ylonen 1998). While females defend territories that may overlap with other females, males defend larger territories that overlap with the territories of several females. Females appear to prefer dominant males and may affect which males get the chance to mate by running away from subordinate males (Horne and Ylonen 1998). As parturition nears, females become more aggressive and each female's territory decreases in size. The home range becomes smaller and the central ranges of different territories become farther from each other (Koskela et al. 1997).

Mating System: polygynous ; polygynandrous (promiscuous)

The estrous cycle of M. glareolus lasts four days (Oksanen et al. 1999). The breeding season is from late April to September (Oksanen et al. 2001). Copulation is characterized by a series of intromissions followed by ejaculation (Horne and Ylonen 1996).  Gestation lasts from 17 days with optimal nutrition, to 24 days if the female becomes pregnant while lactating during postpartum estrus (Macdonald 2001; Koskela et al. 1998). The average gestation length is 21 days (Macdonald 2001). From 1 to 10 pups are born per litter with approximately 4 litters born per breeding season (Macdonald 2001; Oksanen et al. 2001). The average number of pups per litter is 4-8 (Oksanen et al. 2001). Pups weigh 1-10g at birth, which makes up a total of 22-28% of the female’s weight. During pregnancy and lactation, females require 30-130% more energy (Ostfeld 1985). Infanticide occurs in males and females. Females will kill the pups of their female neighbors and males will kill pups as a mating tactic (Koskela et al. 1998; Koskela et al. 1997; Horne and Ylonen 1996).

Breeding season: Breeding occurs from April to September.

Range number of offspring: 1 to 10.

Average number of offspring: 4-8.

Range gestation period: 17 to 24 days.

Average gestation period: 21 days.

Range weaning age: 20 to 25 days.

Range age at sexual or reproductive maturity (female): 2 to 8 weeks.

Average age at sexual or reproductive maturity (female): 3-6 weeks.

Range age at sexual or reproductive maturity (male): 2 to 8 weeks.

Average age at sexual or reproductive maturity (male): 3-6 weeks.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); viviparous

Pups are born blind and helpless in an underground nest lined with grass and other vegetation. The female is the sole provider of parental care (Macdonald 2001). The pups are weaned at the age of 20-25 days (Macdonald 2001; Oksanen et al. 2001; Oksanen et al. 1999; Horne and Ylonen 1998).

Parental Investment: altricial ; female parental care

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Molecular Biology and Genetics

Molecular Biology

Statistics of barcoding coverage: Myodes glareolus

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 0
Species: 251
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
Amori, G., Hutterer, R., Kryštufek, B., Yigit, N., Mitsain, G., Palomo, L.J., Henttonen, H., Vohralík, V., Zagorodnyuk, I., Juškaitis, R., Meinig, H. & Bertolino, S.

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

Contributor/s

Justification
A widespread and common species with no major threats.

History
  • 1996
    Lower Risk/least concern
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Conservation Status

Bank voles are widely distributed and often abundant, they are not threatened.

US Federal List: no special status

CITES: no special status

IUCN Red List of Threatened Species: least concern

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National NatureServe Conservation Status

Canada

Rounded National Status Rank: NNA - Not Applicable

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NatureServe Conservation Status

Rounded Global Status Rank: G5 - Secure

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Status

Not legally protected in the UK. No conservation designations (3).
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Population

Population
It is very common throughout much of its European range, with typical densities varying between approximately 6-12 individuals per hectare and 50-100 individuals per hectare (Spitzenberger 1999). Populations densities fluctuate from year to year. The long-term trend appears stable.

Population Trend
Stable
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Threats

Threats

Major Threats
There are no major threats to this species at present.
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Threats

Where they occur in close proximity to roads, bank voles may be at risk from lead exposure. In agricultural areas, pesticide drift, and exposure to molluscicides and rodenticides may all pose threats. The fragmentation of woodlands, removal of hedgerows and overgrazing of herbaceous ground cover by deer reduce the chances of bank voles persisting in an area (4).
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Management

Conservation Actions

Conservation Actions
It occurs in a number of protected areas throughout its wide range. No specific conservation actions are recommended.
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Conservation

There is no conservation action targeted at this species.
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Relevance to Humans and Ecosystems

Benefits

Economic Importance for Humans: Negative

Myodes glareolus have been found to spread hantavirus. In temperate climates, they are also crop pests (Macdonald 2001).

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Economic Importance for Humans: Positive

Humans benefit from bank voles through their beneficial ecosystem roles.

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Wikipedia

Bank Vole

The bank vole (Myodes glareolus; formerly Clethrionomys glareolus) is a small vole with red-brown fur and some grey patches, with a tail about half as long as its body. A rodent, it lives in woodland areas and is around 100 millimetres (3.9 in) in length. The bank vole is found in western Europe and northern Asia. It is native to Great Britain but not to Ireland, where it has been accidentally introduced, and has now colonised much of the south and southwest; concerns have recently been expressed that it may be replacing the native wood mouse.

The bank vole lives in woodland, hedgerows and other dense vegetation such as bracken and bramble. Its underground chamber is lined with moss, feathers and vegetable fibre and contains a store of food. It can live for 18 months and is omnivorous, eating insects, leaves and fruits such as raspberries and hazel nuts. It readily climbs into scrub and low branches of trees.

In areas such as Great Britain, where the only other small vole is the short-tailed vole (Microtus agrestis), the bank vole is distinguished by its more prominent ears, chestnut-brown fur and longer tail.

Young bank voles in their nest beneath a wood pile

References

  1. ^ Amori, G., Hutterer, R., Kryštufek, B., Yigit, N., Mitsain, G., Muñoz, L.J.P., Henttonen, H., Vohralík, V., Zagorodnyuk, I., Juškaitis, R., Meinig, H. & Bertolino, S. (2008). Myodes glareolus. In: IUCN 2008. IUCN Red List of Threatened Species. Downloaded on 30 June 2009. Database entry includes a brief justification of why this species is of least concern.
  • Musser, G. G. and M. D. Carleton. 2005. Superfamily Muroidea. pp. 894–1531 in Mammal Species of the World: A Taxonomic and Geographic Reference. D. E. Wilson and D. M. Reeder, eds., Johns Hopkins University Press, Baltimore.
  • Ferris-Khan, R. (Ed.). 1995. The Ecology of Woodland Creation. John Wiley & Sons, Chichester.



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