Overview
Brief Summary
Biology
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Comprehensive Description
Description
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Distribution
Range Description
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Geographic Range
Plecotus auritus is found all across Eurasia, from Spain east to Japan, and south into India.
Biogeographic Regions: palearctic (Native )
- Roberts, G., A. Hutson. 2004. "The Bat Conservation Trust" (On-line). Accessed 03/23/04 at http://www.bats.org.uk/batinfo/ble.htm.
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Range
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Physical Description
Morphology
Physical Description
As their common name implies, P. auritus have large ears--almost as long as their bodies. When in flight, the bats hold the ears fully erect and extended forward. At rest, their ears fold and curl sideways in a way that resembles ram horns. During hibernation the bats fold and tuck ears down, so that only the long pointed ear cover is visible.
P. auritus have relatively large eyes without a tapetum lucidum, and slit-shaped nostrils that open laterally. They usually weigh 6-12 grams and females are slightly larger than males. They have long, silky fur that is brownish on the upper side and grayish brown below. The dental formula for the P. auritus is 2/3, 1/1, 2/3, 3/3=36.
(Grzimek, 1975; Howard, 1995; Swift, 1998)
Range mass: 6 to 12 g.
Average mass: 8 g.
Other Physical Features: endothermic ; bilateral symmetry
Average basal metabolic rate: 0.082 W.
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Ecology
Habitat
Habitat and Ecology
Systems
- Terrestrial
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Habitat
In general, P. auritus seem to prefer higher altitudes. In the summer, the long-eared bat can most often be found roosting in hollow trees at the edge of parks or woodlands. They are also commonly found clustering next to a chimney or along the beams of large roof spaces in stables, barns, lofts, and older buildings. From mid October to early April they hibernate in caves, mineshafts, hollow trees, under roofs, and in underground sites. Favorite roost sites of the long-eared bat can often be indicated by stains on the timbers.
Range elevation: 1,400 (high) m.
Habitat Regions: temperate ; terrestrial
Terrestrial Biomes: forest
Other Habitat Features: suburban
- Burton, M. 1962. University Dictionary of Mammals of the World. NY: Thomas Y. Crowell Company.
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Habitat
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Trophic Strategy
Food Habits
P. auritus are insectivorous, feeding mainly on Lepidoptera (moths). They are opportunistic foragers, feeding on the most available insects, including beetles, flies, earwigs, and spiders. Long-eared bats forage in a variety of ways, such as catching insects in free flight, landing on the ground to capture prey, or hovering in mid-air to listen for movements of insects to pick them off the foliage. They forage at night, usually relatively close to their roost.
(Burton, 1962; Roberts and Hutson, 2001)
Animal Foods: insects; terrestrial non-insect arthropods
Primary Diet: carnivore (Insectivore )
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Associations
Ecosystem Roles
P. auritus harbor relatively few parasites comparted to other bats, perhaps due to its small colony size. Several species of fleas in the family Ischnopsyllidae and mites in Spinturnicidae have been recorded on long-eared bats.
The only species of internal parasites that have been noted in P. auritus are bacteria in the genus Grahamella.
Mutualist Species:
- Grahamella (internal parasite)
- Ischnopsyllidae (Bat fleas)
- Spincturnidae (Mites) including:
- Spincturnix plecotina
- Ornithonussus pipistrelli
- Neomyobia plecotia
- Leptotrombidium russicum
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Predation
Long-eared bats avoid most predators by only flying at night; however, they are still sometimes captured by some nocturnal predators such as owls and cats. The domestic cat is the most significant mammalian predator, especially to bats roosting under the roofs of houses. Their habit of flying close to the ground to forage and landing to catch insects makes them especially vulnerable to cats.
Known Predators:
- tawny owls (Strix aluco)
- barn owls (Tyto alba)
- long-eared owls (Asio otus)
- domestic cats (Felis silvestris)
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Known predators
Tyto alba
Asio otus
Felis silvestris
Strix aluco
This list may not be complete but is based on published studies.
- Myers, P., R. Espinosa, C. S. Parr, T. Jones, G. S. Hammond, and T. A. Dewey. 2006. The Animal Diversity Web (online). Accessed February 16, 2011 at http://animaldiversity.org. http://www.animaldiversity.org
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Known prey organisms
Arthropoda
Insecta
This list may not be complete but is based on published studies.
- Myers, P., R. Espinosa, C. S. Parr, T. Jones, G. S. Hammond, and T. A. Dewey. 2006. The Animal Diversity Web (online). Accessed February 16, 2011 at http://animaldiversity.org. http://www.animaldiversity.org
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Associations
Basilia nana ectoparasitises Plecotus auritus
Other: minor host/prey
Animal / parasite / ectoparasite
Nycteribia kolenatii ectoparasitises Plecotus auritus
Other: minor host/prey
In Great Britain and/or Ireland:
Animal / parasite / ectoparasite
Phthiridium biarticulata ectoparasitises Plecotus auritus
Other: minor host/prey
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Life History and Behavior
Life Expectancy
Lifespan/Longevity
Climate is a very important factor for the survival of the young long-eared bat. Poor weather during lactation results in delayed growth, abandonment by mother and high mortality. Although records show that P. auritus are able to live up to thirty years, the average lifespan is seven years for males, sixteen years for females, and fifteen years for the sexes combined. High longevity could be due to the large amounts of time spent in a state of torpor, when the metabolic rate is very low.
Range lifespan
Status: wild: over 30 (high) years.
Average lifespan
Status: wild: 15 years.
Average lifespan
Status: wild: 12.0 years.
- Howard, R. 1995. York, England: William Sessions Limited.
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Lifespan, longevity, and ageing
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Reproduction
Reproduction
Mating System: polygynandrous (promiscuous)
These bats and mate in autumn. For males, sperm production reaches its peak in late August and September, when the testes are descended. The testes regress and sperm production ceases in November. Females delay fertilization until spring (late April or May).
Females only bear one offspring per breeding season (every year); twins are very rare.
Breeding interval: once per year
Breeding season: Autumn
Range number of offspring: 1 to 3.
Average number of offspring: 1.
Range gestation period: 60 to 70 days.
Range weaning age: 40 to 45 days.
Average weaning age: 42 days.
Range age at sexual or reproductive maturity (female): 12 to 15 months.
Range age at sexual or reproductive maturity (male): 12 to 15 months.
Key Reproductive Features: seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); viviparous ; delayed implantation
Average number of offspring: 1.33.
The gestation period of Long-eared bats is relatively long, but the specifics are unknown. The young are altricial at birth, born pink and hairless with disproportionately large feet, used to grasp their mothers' fur once they are born. They feed on their mothers' milk until they are three weeks old, and then are left in the roost while the mother leaves to forage for food. At six weeks old they are weaned and able to forage for themselves. Females are often ready to breed at one year old and males are sexually mature at fifteen months.
(Roberts and Hutson, 2001; Swift, 1998)
Parental Investment: altricial ; female parental care
- Roberts, G., A. Hutson. 2004. "The Bat Conservation Trust" (On-line). Accessed 03/23/04 at http://www.bats.org.uk/batinfo/ble.htm.
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Molecular Biology and Genetics
Molecular Biology
Statistics of barcoding coverage: Plecotus auritus
Public Records: 0
Species: 11
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/least concern
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Conservation Status
US Migratory Bird Act: no special status
US Federal List: no special status
CITES: no special status
IUCN Red List of Threatened Species: least concern
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Status
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Trends
Population
Population Trend
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Threats
Threats
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Threats
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Management
Conservation Actions
Maintenance of natural habitat, especially forests with mature trees is required.
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Conservation
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Relevance to Humans and Ecosystems
Benefits
Economic Importance for Humans: Positive
They consume large numbers of insect pests.
Positive Impacts: controls pest population
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Wikipedia
Brown long-eared bat
The brown long-eared bat or common long-eared bat (Plecotus auritus) is a fairly large European bat. It has distinctive ears, long and with a distinctive fold. It is extremely similar to the much rarer grey long-eared bat which was only validated as a distinct species in the 1960s.
An adult brown long-eared bat has a body length of 4.5-4.8 cm, a tail of 4.1-4.6 cm, and a wing length of 4-4.2 cm. The ears are 3.3-3.9 cm in length, and readily distinguish this from most other bat species.
They are relatively slow flyers compared to other bat species.
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Habitat
It is found in Europe. The UK distribution can be found on the National Biodiversity Network website and can be seen here.
This species appears to prefer caves as roosting sites, but roosts in trees holes, buildings and bat boxes as well. The roosts in trees may be close to the ground.
It hunts above woodland, often by day, and mostly for moths, gleaning insects from leaves and bark. This is one of the bats for which eyesight is more important than echolocation in finding prey (Stevens 2005).
Echolocation
Echolocation is used to find prey. The frequencies used by this bat species for echolocation lie between 27-56 kHz, have most energy at 45 kHz and have an average duration of 2.5 ms. [1][2]
Gallery
References
| Wikimedia Commons has media related to: Plecotus auritus |
- Woodland Management For Bats Guide
- Chiroptera Specialist Group (1996). Plecotus auritus. 2006. IUCN Red List of Threatened Species. IUCN 2006. www.iucnredlist.org. Retrieved on 12 May 2006.
- Stevens, Martin (2005): The role of eyespots as anti-predator mechanisms, principally demonstrated in the Lepidoptera. Biol. Rev. 80(4): 573–588. doi:10.1017/S1464793105006810 (HTML abstract)
- ^ Parsons, S. and Jones, G. (2000) 'Acoustic identification of twelve species of echolocating bat by discriminant function analysis and artificial neural networks.' J Exp Biol., 203: 2641-2656.
- ^ Obrist, M.K., Boesch, R. and Flückiger, P.F. (2004) 'Variability in echolocation call design of 26 Swiss bat species: Consequences, limits and options for automated field identification with a synergic pattern recognition approach.' Mammalia., 68 (4): 307-32.
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