|Scientific Name:||Eptesicus serotinus|
|Species Authority:||Schreber, 1774|
Eptesicus isabellinus Temminck, 1840
|Taxonomic Notes:||The North African population has been named as a subspecies (E. s. isabellinus) and is considered by some authors to be a separate species (e.g., Mayer et al. 2007). This may or may not be conspecific with the population in southern Iberia. Until this is resolved they are all treated as E. serotinus.|
|Red List Category & Criteria:||Least Concern ver 3.1|
|Assessor(s):||Hutson, A.M., Spitzenberger, F., Aulagnier, S., Alcaldé, J.T., Csorba, G., Bumrungsri, S., Francis, C., Bates, P., Gumal, M., Kingston, T. & Benda, P.|
|Reviewer(s):||Hutson, A.M., Racey, P.A. (Chiroptera Red List Authority) & Temple, H. (Global Mammal Assessment Team)|
A very widespread and abundant species. Global and regional population trends are difficult to determine, as the species is decreasing in some range states (sometimes dramatically) whilst increasing in others. Overall, it is not believed to approach the threshold for the population decline criterion of the IUCN Red List (i.e. declining more than 30% in ten years or three generations). For these reasons, it is evaluated as Least Concern.
|Range Description:||Eptesicus serotinus is widely distributed through the Palaearctic from the Atlantic to the Pacific seaboards, across the Mediterranean from Portugal eastwards to Turkey, and is marginal to North Africa. It occurs north to about 57ºN in Denmark, south-west to North Africa (found in Morocca, Algeria, Tunisia, and to western Libya), and east into northern parts of the Indian subcontinent and south-east Asia. In the Middle East it is recorded from Syria and Lebanon. Records from the Canary Islands (Lanzarote) refer to a single vagrant that died shortly after arrival (Trujillo 1991). Its altitudinal range is from sea level to to 1,440 m in the Alps (Spitzenberger 2002).|
Native:Afghanistan; Albania; Algeria; Andorra; Armenia (Armenia); Austria; Azerbaijan; Belarus; Belgium; Bosnia and Herzegovina; Bulgaria; China; Cyprus; Czech Republic; Denmark; France; Georgia; Germany; Gibraltar; Greece (Kriti); Holy See (Vatican City State); Hungary; India; Iran, Islamic Republic of; Israel; Italy (Sicilia); Korea, Democratic People's Republic of; Lao People's Democratic Republic; Latvia; Lebanon; Libya; Liechtenstein; Lithuania; Luxembourg; Macedonia, the former Yugoslav Republic of; Malta; Moldova; Monaco; Mongolia; Montenegro; Morocco; Nepal; Netherlands; Pakistan; Poland; Portugal; Romania; Russian Federation; San Marino; Serbia (Serbia); Slovakia; Slovenia; Spain (Baleares, Canary Is. - Regionally Extinct); Sweden; Switzerland; Syrian Arab Republic; Taiwan, Province of China; Thailand; Tunisia; Turkey; Turkmenistan; Ukraine; United Kingdom; Uzbekistan; Viet Nam
|Range Map:||Click here to open the map viewer and explore range.|
A very widespread and abundant species, with decreases recorded in some areas and increases in others. It may be increasing in some parts of northern Europe (e.g. Denmark) and decreasing in others, slightly (e.g. UK), or severely (e.g. Austria). In Austria, a 70% decline has been recorded in the eastern part of the country (the former stronghold) over the last 15 years, and the species is now absent from lowland regions with bare arable land (F. Spitzenberger pers. comm. 2006). It is suspected to be declining in the rest of Pannonian basin. It is known from a single locality in European Turkey, and the total population in Turkey is small (A. Karatas pers. comm. 2005). In Iran it is at the edge of the its range, the species occurs in low numbers (M. Sharifi pers. comm. 2005). There is a large North African population: it is the most common bat species in northwest Algeria and Libya.
Summer maternity colony size is generally 10-50 females (occasionally up to 300). It winters singly or in small groups.
|Habitat and Ecology:||
Found in a variety of habitats across its wide range including semi-desert, temperate and subtropical dry forest, Mediterranean-type shrubland, farmland and suburban areas. Favoured feeding areas include pasture, parkland, open woodland edge, tall hedgerows, gardens, and forested regions. Feeds on larger beetles, moths and flies.
Most summer (maternity) colonies are in buildings and occasionally tree holes or rock fissures.
In winter it roosts singly or in small numbers in buildings and rock crevices, or often in underground habitats in north central Europe. Winter roosts are usually in fairly cold, dry sites. It is a largely sedentary species, with movements to 330 km recorded (Havekost 1960 in Hutterer et al. 2005).
|Major Threat(s):||In some areas it is affected by habitat loss and disturbance and destruction of colonies in houses. Population decline in Austria might be related to food reduction due to large scale mosquito control with the bacterium Bacillus thuringiensis, used in the Danube and Moravia regions (F. Spitzenberger and I. Coroiu pers. comm. 2006). The species is a host of the rabies-related virus EBLV1. There is increasing interest in the occurrence, risk to humans and epidemiology of this virus (e.g. Stantic-Pavlinic 2005), which could have an effect on the public image of this house-dependent bat.|
|Conservation Actions:||It is protected by national legislation in most range states. There are also international legal obligations for its protection through the Bonn Convention (Eurobats) and Bern Convention in parts of range where these apply. It is included in Annex IV of EU Habitats and Species Directive, and there is some habitat protection through Natura 2000. No specific conservation actions known in North Africa or South Asia.|
|Citation:||Hutson, A.M., Spitzenberger, F., Aulagnier, S., Alcaldé, J.T., Csorba, G., Bumrungsri, S., Francis, C., Bates, P., Gumal, M., Kingston, T. & Benda, P. 2008. Eptesicus serotinus. The IUCN Red List of Threatened Species. Version 2014.3. <www.iucnredlist.org>. Downloaded on 19 December 2014.|
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