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Northern bat
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| Northern bat | |
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| A northern bat, crawling on a wooden surface | |
Scientific classification 
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| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Mammalia |
| Order: | Chiroptera |
| Family: | Vespertilionidae |
| Genus: | Eptesicus |
| Species: | E. nilssonii
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| Binomial name | |
| Eptesicus nilssonii (Keyserling et Blasius, 1839)
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The northern bat (Eptesicus nilssonii) is the most abundant species of bat in northern Eurasia occurring from France to Hokkaidō and south to Kazakhstan.[2]
Description
[edit]The northern bat is dark brown or black with some gold touched at the tip of the hairs in the head and back region. Its nose, ears, tail and wings are black or blackish brown. The coat on the ventral side is yellowish brown. It has short and rounded ears. It body length is 54–64 mm (2.1–2.5 in) with a wing span of 240–280 mm (9.4–11.0 in), and it weighs 8–16 g (0.28–0.56 oz) depending on the season.[2]
Distribution and habitat
[edit]
The northern bat is widespread throughout Eurasia, and is the most common bat in the northern part of the continent. It occurs from northern Scandinavia beyond the Arctic Circle to northern Italy, and eastern England to northern Japan.[1] It favours forest uplands at elevations of 200–2,000 m (660–6,560 ft).[3]
Behaviour and ecology
[edit]Northern bat colonies have moved as far as 450 km (280 mi) over a period of several years.[1] It breeds in late autumn, and the females stores the male sperm over the winter. Hibernation begins in November to December and lasts until April. Females become pregnant in spring and give birth 50–60 days later. In summer, males dwell alone. Females form a colony of 10–80 adults in early summer, which they disband in August, when young bats are able to fly. Winter colonies are often found in houses, and natural or artificial underground habitats.[2]
Hunting
[edit]Northern bats are nocturnal and fast flying, adapted to hunting airborne insects using echolocation.[1] For example, northern bats commonly hunt ghost moths while the moths are hovering above ground to attract a mate. The species hunts in open spaces at a speed of 5–6 m/s. The sound pulse consists of 10-13 ms in normal foraging habitats, sometimes up to 18 ms of steeply frequency-modulated (FM) component (about 40–30 kHz). The bats send out the pulse approximately once every 200 ms, and the steep FM are used to locate obstacles or targets, allowing them to fly indoors.[2] In high latitude areas, female northern bats fly during daytime because of the short nights, but their foraging peaks after dusk and sometime before dawn. Females select small feeding territories where their food source is abundant, and sometimes can be used by the same individual over a period of years.[2]
Genetics
[edit]The northern bat is closely related to the serotine bat (Eptesicus serotinus). They are distinguishable by appearance but the genetic difference between the two species is an intraspecific variation.[4]
References
[edit]- ^ a b c d Coroiu, I. (2016). "Eptesicus nilssonii". IUCN Red List of Threatened Species. 2016 e.T7910A22116204. doi:10.2305/IUCN.UK.2016-2.RLTS.T7910A22116204.en. Retrieved 19 November 2021.
- ^ a b c d e Rydell, J. (1993). "Eptesicus nilssonii". Mammalian Species (430): 1–7. doi:10.2307/3504128. JSTOR 3504128. S2CID 253944821.
- ^ Hanak, V. & Gaisler, J. (1971). "The status of Eptesicus ogveni bobrinskii, 1918 and remarks on some other species of this genus (Mammalia: Chiroptera)". Vestnik Ceskoslovenske Spolecnosti Zoologicke. 35: 11–24.
- ^ Mayer, F. & von Helversen, O. (2001). "Cryptic diversity in European bats". Proceedings of the Royal Society of London. Series B: Biological Sciences. 268 (1478): 1825–1832. doi:10.1098/rspb.2001.1744. PMC 1088815. PMID 11522202.
External links
[edit]
Media related to Eptesicus nilssonii at Wikimedia Commons- Eptesicus nilssonii - Science for Nature Foundation
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Northern bat
View on Grokipediafrom Grokipedia
Taxonomy and description
Taxonomy
The Northern bat, Eptesicus nilssonii (Keyserling & Blasius, 1839), belongs to the order Chiroptera, suborder Yangochiroptera, family Vespertilionidae, subfamily Vespertilioninae, and genus Eptesicus within the tribe Eptesicini.[2] The genus Eptesicus comprises approximately 21 species of vespertilionid bats, characterized by their robust build and echolocation capabilities.[6] The specific epithet nilssonii honors the Swedish zoologist Sven Nilsson (1787–1883), who contributed to early studies of Scandinavian fauna; the genus name derives from Greek roots meaning "house flier" or "able to fly."[7] Historical synonyms include Vespertilio nilssonii Keyserling and Blasius, 1839, and Eptesicus nilssoni (Keyserling and Blasius, 1839), reflecting initial placements in the genus Vespertilio before taxonomic revisions in the 19th century.[8] Eptesicus parvus Kishida, 1932, is recognized as the Asian subspecies E. n. parvus based on morphological and genetic evidence.[9] Phylogenetically, E. nilssonii is the closest relative of the serotine bat (E. serotinus), forming a sister species pair within the Old World Eptesicus clade, with evidence of ancient hybridization and mitochondrial DNA (mtDNA) introgression.[10] Genetic studies using mtDNA (e.g., ND1 and cytochrome b genes) reveal very low divergence between the two species, approximately 1.7% in cytochrome b sequences, comparable to intraspecific levels and indicative of recent divergence likely in the late Pleistocene.[11][12] Nuclear DNA (nuDNA) analyses, however, show greater separation, supporting distinct species status despite shared mtDNA haplotypes in some E. serotinus populations, possibly due to secondary contact and gene flow.[10] Intraspecific genetic variation in E. nilssonii is low across its Eurasian range, with mitochondrial and nuclear markers indicating shallow phylogeographic structure and a subtle east-west split between European and Asian populations, likely shaped by postglacial recolonization.[13] Studies of cytochrome b and other loci reveal minimal differentiation (e.g., <1% mtDNA divergence between western and eastern clades), suggesting high gene flow and adaptation to diverse habitats without strong barriers to dispersal.[14] This low variation contrasts with higher diversity in southern Palearctic congeners and underscores the species' resilience to Pleistocene climatic fluctuations.[3]Description
The Northern bat (Eptesicus nilssonii) is a medium-sized vespertilionid bat characterized by a head-body length of 54–64 mm, a forearm length of 40–46 mm, a wingspan of 240–280 mm, and a body weight of 8–16 g.[5][9] These measurements position it as the smallest species within the genus Eptesicus in Europe, facilitating identification in field surveys.[5] Its pelage features long dorsal fur that ranges from dark brown to black, with distinctive gold-tipped hairs prominently on the head and back, creating a subtle golden sheen; the ventral fur is lighter, appearing yellowish-brown.[15] The ears are short and rounded, measuring approximately 15 mm in length, with a short, rounded tragus that bends slightly inward and five transverse folds along the edge; the ears are broadest near the base and covered in dark brownish-black skin.[6] The wings exhibit a broad, rounded structure with an unspecialized form, including a wing area of about 112 cm², an aspect ratio of approximately 6.6, and a wing loading of around 8.1 N/m², supporting agile maneuverability in cluttered environments.[6] The dental formula is I 2/3, C 1/1, P 1/2, M 3/3 (total 32), typical of the genus Eptesicus, with the upper second premolar (P²) often rudimentary in some individuals.[6][16] Sexual dimorphism is present, with females slightly larger than males in body size and mass.[17] Overall, these traits distinguish the Northern bat from congeners like the serotine bat, to which it bears superficial resemblance but differs in scale.[6]Distribution and habitat
Geographic distribution
The Northern bat (Eptesicus nilssonii) exhibits a broad Palearctic distribution across Eurasia, ranging from western Europe—where it occurs in France, northern Italy, and Norway—through northern and central Europe, Siberia, and Asia, extending eastward to Japan including Hokkaido and northwest China, and southward to Kazakhstan, northern Mongolia, Iraq, and Iran.[5][6][1] This transcontinental range follows a latitudinal band suited to boreal and temperate climates, remaining largely continuous across Siberia.[18] The species reaches its northernmost limit at approximately 70°N in Scandinavia and Russia, supporting reproductive colonies farther north than any other bat species.[3][1] It inhabits elevations from sea level to 2,000 m, with highest concentrations in boreal forests and montane zones.[6] In southern areas, populations become fragmented, appearing as isolated groups in montane regions including the Carpathians, Sudeten Mountains, and Alps.[19] Recent surveys underscore the ongoing documentation of its range, including passive acoustic monitoring that detected individuals across Latvia in 2023, field records from multiple sites in Romania during 2015, and monitoring programs in Sweden around 2020.[20][21][22]Habitat preferences
The Northern bat (Eptesicus nilssonii) primarily inhabits boreal and hemiboreal forests dominated by coniferous species such as pine, spruce, and birch, as well as mixed hardwood stands, with a strong preference for mature forest uplands that provide suitable roosting opportunities.[23][24] These environments are often found across its Eurasian range at elevations from sea level to 2,000 m, extending into lowlands, foothills, and occasionally more open or altered landscapes near water bodies.[6][25] During the summer breeding season, females form small maternity colonies of 10–80 individuals in tree hollows, building attics, or rock crevices, selecting sites that offer seclusion and thermal stability.[6] These roosts are typically located in upland forest areas, with microhabitat features including proximity to water sources, open areas for flight, and built structures—all within approximately 200 m—to facilitate access and energy efficiency.[26] In winter, the species shifts to lower elevations for hibernation in underground sites such as mines, caves, or cellars, where cooler, stable conditions prevail, often in small clusters or solitary.[6] In its northernmost ranges, the Northern bat adapts to high-latitude challenges by increasingly utilizing artificial structures like buildings for roosting, which provide essential warmth during short summers and extended cold periods.[23] This flexibility allows persistence in hemiboreal zones where natural cavities may be limited by harsh climates.[27]Behavior and ecology
Reproduction and social behavior
Mating in the northern bat (Eptesicus nilssonii) occurs primarily during late autumn swarming aggregations at hibernation sites, where males and females gather in large numbers.[28] Females store sperm in their reproductive tracts throughout the winter hibernation period, with fertilization delayed until spring upon emergence from hibernation.[29] This strategy allows synchronization of birth with optimal summer conditions in northern latitudes. Gestation lasts approximately 32 days on average (ranging from 23.6 to 40.4 days) from the female's arrival at maternity sites in spring to parturition, though periods of torpor induced by cold weather can prolong this phase.[29] Births typically occur between early June and late July, aligning with peak insect availability.[30] Litter size is usually one pup per female in northern populations such as Scandinavia, although twins are more common in southern ranges.[31] Pups are born relatively large, with a forearm length of about 41% of the mother's at birth, and exhibit rapid postnatal development adapted to the short northern breeding season.[29] Eyes open around 4 days postpartum, and young become volant (capable of flight) by 13–19 days (mean 15.3 days), roughly 3 weeks after birth.[30] Maternal care is intensive during this period, with pups dependent on lactation until becoming independent foragers by August, approximately 6–8 weeks post-birth.[32] This care occurs within maternity colonies comprising 10–80 adult females.[29] Social structure is sexually segregated, with females forming stable maternity colonies for reproduction and pup-rearing, exhibiting high philopatry to specific sites across years.[29] Males remain solitary or in small, loose groups outside the breeding season, without forming large harems. Colonies display fission-fusion dynamics, where individuals temporarily split and rejoin subgroups for roosting and foraging, facilitating information sharing on resources.[33] In the wild, northern bats can live up to 20 years, with documented recaptures after 12 years indicating strong site fidelity and longevity.[34] Annual adult survival rates are estimated at 60–70%, supporting population persistence despite low reproductive output.[35]Foraging and diet
The Northern bat (Eptesicus nilssonii) is primarily an insectivore, feeding on airborne arthropods such as moths (including ghost moths Hepialus humuli), beetles, and flies (particularly small dipterans like midges).[5][36][37] Its diet appears unselective and opportunistic, incorporating other flying insects such as caddisflies, lacewings, and mayflies near water bodies, as well as dung beetles in open habitats.[37][6] This species employs a nocturnal aerial-hawking strategy, pursuing prey in continuous flight through open areas at speeds of approximately 5–6 m/s.[38][39] It relies on frequency-modulated echolocation pulses, typically sweeping from 40 kHz down to 30 kHz over durations of 10–18 ms, which enable effective prey detection and clutter rejection in vegetated or forested environments.[40][41][42] Foraging typically occurs 1–5 km from roosts, though distances can extend up to 20 km depending on prey availability and season, with individuals covering home ranges as small as 20 ha.[36] In high-latitude populations above 60°N, females may hunt both day and night during periods of midnight sun to maximize limited seasonal foraging opportunities.[44][3] Insectivory peaks during summer when prey abundance is highest, supporting high energy demands for reproduction, while foraging activity declines in poor weather conditions that reduce insect flight.[6][45] Overall activity is confined to brief summer periods in northern regions, lasting about 2.5 months, after which bats enter hibernation as insect availability drops.[44]Migration and hibernation
The northern bat (Eptesicus nilssonii) undertakes short- to medium-distance migrations, typically up to 450 km, from summer breeding sites to hibernation roosts in autumn.[1][9] These movements are not strictly seasonal but occur occasionally, with ring recoveries indicating distances of 100–450 km across Europe.[1] In northern populations, such migrations are limited by the species' sedentary nature and local hibernation availability, allowing bats to remain relatively close to breeding areas.[46] Hibernation lasts from November to April, spanning up to 9.5 months in northern latitudes where prey availability is severely restricted by cold.[3] During this period, body temperature drops to 2–5°C, closely tracking ambient conditions through thermoconformity, enabling energy conservation without increased metabolic costs even at near-freezing levels (as low as 1.1°C).[3] Bats enter torpor-arousal cycles approximately every 10–20 days, with torpor bouts averaging 215 hours, during which metabolic rate remains low.[3] Physiological adaptations include autumn fat accumulation reaching up to 30% of body mass to fuel the extended dormancy, alongside resistance to cold-induced arousal that minimizes energy loss.[47] Hibernation roosts are selected for stable temperatures of 4–8°C, primarily underground sites such as caves, mines, and tunnels, where bats cluster in groups to enhance thermoregulation through shared body heat.[48] In northern regions, natural sites are scarce, leading to increased use of anthropogenic structures like cellars and buildings for overwintering.[49] Climate variability poses challenges, as warming trends may alter hibernation timing and disrupt access to preferred cold roosts, potentially increasing arousal frequency and energy demands.[50]Conservation
Status and threats
The Northern bat (Eptesicus nilssonii) is assessed as Least Concern on the IUCN Red List, based on a 2016 global evaluation that noted its widespread distribution and lack of detected population declines at the time. However, regional assessments reveal variations, with the species classified as Vulnerable in Norway due to documented declines since 2007 and in Switzerland where it faces high national priority threats.[51][25] Population trends are stable in core Eurasian ranges but show declines in northern Europe, particularly in Sweden where acoustic monitoring along road transects indicated a 59% reduction in activity over 30 years (1988–2017), equating to an annual decline of 3.0% in unlit areas.[4] In hibernacula across its range, the species exhibits uneven distribution, with small clusters averaging around 20 individuals per site in maternity and winter roosts.[5] Agricultural intensification in northern regions has contributed to these declines by reducing insect availability through pesticide use and habitat alteration.[4] Major threats include habitat loss from deforestation and roost disturbance during building renovations, which disrupt maternity colonies and hibernation sites.[25] Climate change exacerbates pressures by altering insect prey abundance and hibernation patterns, potentially shifting distributions northward while intensifying challenges at high latitudes.[4] The fungal pathogen causing white-nose syndrome (Pseudogymnoascus destructans) has been detected on E. nilssonii in Europe, leading to skin lesions, but it has not yet caused widespread mortality as in North America.[52] Monitoring efforts, such as passive acoustic surveys in Latvia from 2020–2022, reveal patchy occurrence with higher activity in the northwest and southwest compared to the southeast, highlighting uneven regional presence.[53] A high-quality reference genome assembled in 2024 supports genetic studies to better understand threats and adaptations.[2] In southern isolates, such as fragmented populations in Romania, the species is vulnerable due to limited connectivity and habitat isolation.[54]Conservation measures
The Northern bat (Eptesicus nilssonii) is protected under Annex IV of the EU Habitats Directive, which requires strict protection of its habitats and prohibits deliberate capture, killing, or disturbance across member states.[55] In national legislation, the species receives full protection in countries like Sweden, where it is classified as near threatened and safeguarded under the Swedish Environmental Code, and Latvia, where it falls under the country's Nature Protection Law prohibiting harm to bats.[56][20] The Convention on International Trade in Endangered Species (CITES) does not apply, as the species is not listed due to its Least Concern global status.[55] Management efforts emphasize roost protection, with guidelines under the EU Habitats Directive mandating the preservation of maternity and hibernation sites, including buffers around trees and buildings used by the bats. In northern forests, artificial bat boxes have been deployed as supplementary roosting options, particularly in boreal regions of Scandinavia and Eastern Europe, to compensate for habitat loss from forestry activities. Habitat restoration initiatives in boreal zones, such as rewetting wetlands, have shown promise in enhancing bat activity by improving foraging areas near roosts.[57] Research initiatives include the 2024 reference genome assembly of E. nilssonii, which supports studies on genetic adaptations to northern climates and informs conservation breeding programs.[2] Acoustic monitoring programs, such as the multi-year passive surveys in Latvia, track distribution and population trends to guide site-specific protections.[58] International efforts involve organizations like Bat Conservation International, which promotes awareness and habitat enhancement for polar bat species including E. nilssonii, and cross-border monitoring under the EUROBATS agreement in regions such as the Alps and Carpathians to assess high-altitude populations.[59][60][61] In protected areas, these measures have contributed to population stabilization for E. nilssonii, particularly where roost safeguards and habitat connectivity are prioritized, though challenges persist in developing climate-resilient strategies to address warming-induced shifts in hibernation and foraging patterns.[55][3]References
- https://www.[researchgate](/page/ResearchGate).net/publication/352209943_Use_of_habitat_and_foraging_time_by_females_of_Eptesicus_nilssonii_Chiroptera_Vespertilionidae