Tadarida teniotisEuropean free-tailed bat

Ge­o­graphic Range

Eu­ro­pean free-tailed bats (Tadarida teni­o­tis) are a palearc­tic species na­tive to south­ern and Mediter­ranean Eu­rope, north­ern Africa, and Myan­mar.

In south­east­ern Eu­rope, a colony of Eu­ro­pean free-tailed bats were found on Rila Moun­tain in the east­ern Rhodopes Moun­tains. In India, sev­eral colonies have been found in Bihar, west Ben­gal, and Ker­ala. There are also colonies in the Dehradun and Tehri-Gar­whal dis­tricts of Ut­tarak­hand, India. Colonies of Eu­ro­pean free-tailed bats have been re­ported in three of the Do­de­canese is­lands off of Greece. These is­lands in­clude Rhodes, Karpathos, and Kos. There are cur­rently seven re­ported colonies in Bul­garia. Colonies of Eu­ro­pean free-tailed bats have been re­ported in cen­tral Asia, Japan, and Tai­wan. There have also been colonies re­ported in the Madeira and Ca­nary is­lands. (Benda and Uhrin, 2017; Chakravarty, 2017; Nowak, 1999; Pan­dourski, 2014)

Habi­tat

Eu­ro­pean free-tailed bats in­habit ex­tremely trop­i­cal areas, as well as some tem­per­ate zones. They in­habit warmer re­gions of the Do­de­canese is­lands off of Greece, as well as more tem­per­ate areas high in the Alps. Eu­ro­pean free-tailed bats in­habit areas with an el­e­va­tion of 400 to 500 m. These bats avoid colder cli­mates be­cause they lack the phys­i­ol­ogy to sur­vive sea­sonal food short­ages. To ob­tain a min­i­mal rate of me­tab­o­lism in tor­por, Eu­ro­pean free-tailed bats in­habit areas rang­ing from 7.5 to 10°C. In win­ter, Eu­ro­pean free-tailed bats se­lect roosts that os­cil­late around 10°C.

Hintze et al. (2016) found that Eu­ro­pean free-tailed bats ben­e­fit from dam con­struc­tion, un­like many other species. Dams act as drink­ing and for­ag­ing areas and in­crease over­all ac­tiv­ity of Eu­ro­pean free-tailed bats in the area. Eu­ro­pean free-tailed bats for­age above lakes and in scrub­lands, wood­lands, and urban areas. (Ar­let­taz, et al., 2000; Benda and Uhrin, 2017; Chakravarty, 2017; Dal­houmi, et al., 2016; Dal­houmi, et al., 2014; Hintze, et al., 2016; Mata, et al., 2016; Nowak, 1999; Pan­dourski, 2014; Tiago, et al., 2004)

  • Aquatic Biomes
  • lakes and ponds
  • Other Habitat Features
  • urban
  • Range elevation
    3100 to 0 m
    10170.60 to 0.00 ft

Phys­i­cal De­scrip­tion

Eu­ro­pean free-tailed bats have long, broad ears that point to­wards their face. Their ears are rounded at the top and touch at the base in the front. Eu­ro­pean free-tailed bats have black and grey pelage, but some in­di­vid­u­als have a brown tint to them. Their fur is short and silky and has been com­pared to mole pelage. At least one third of their tails ex­tend be­yond their uropatag­ium, the mem­brane be­tween their legs. The ends of their tails have stiff hairs that are used as tac­tile or­gans. Their tails are be­tween 40 to 52 mm in length. Eu­ro­pean free-tailed bats have a long muz­zle and five creases in their upper lips. Their wings are long and nar­row. On av­er­age, Eu­ro­pean free-tailed bats have a wingspan of 450 mm. They range from 122 to 139 mm in body length. Right fore­arm lengths (RFAs) for Eu­ro­pean free-tailed bats av­er­age 54 to 64 mm. They have a nar­row uropatag­ium with short, vel­vety pelage. Eu­ro­pean free-tailed bats weigh, on av­er­age, 20 to 30 g. There are no ob­vi­ous dif­fer­ences be­tween males and fe­males, but fe­males do eat more and are more ag­gres­sive while hunt­ing. This is at­trib­uted to fe­males need­ing more en­ergy dur­ing the ma­ter­nity sea­son. Eu­ro­pean free-tailed bats have a basal meta­bolic rate of 200.4 cm^3 oxy­gen/hour. (Dietz and Hel­versen, 2004; Dietz and Keifer, 2016; Firouz, 2005; Hoath, 2003; Marom, et al., 2006; Mata, et al., 2016; Verts and Car­raway, 1998)

  • Sexual Dimorphism
  • sexes alike
  • Range mass
    20 to 30 g
    0.70 to 1.06 oz
  • Range length
    122 to 139 mm
    4.80 to 5.47 in
  • Average wingspan
    450 mm
    17.72 in
  • Average basal metabolic rate
    200.4 cm3.O2/g/hr

Re­pro­duc­tion

When Eu­ro­pean free-tailed bats mate, fe­males will form groups of up to nine fe­males. These harems are then ac­tively pro­tected by a sin­gle male, ac­cord­ing to An­cil­lotto and Russo (2014). Dur­ing the mat­ing process, males are more ag­gres­sive than fe­males. Eu­ro­pean free-tailed bats will bite, punch, chase, and call ag­gres­sively to en­tice mates. Other tac­tics used to en­tice mates in­clude smelling one an­other, touch­ing, and oc­ca­sion­ally jump­ing on the legs of an­other bat briefly. Once a male has found a fe­male, he will mount by push­ing the fe­male to the ground and hold­ing her still while mat­ing. While there are no records of promis­cu­ity for Eu­ro­pean free-tailed bats, other mem­bers of the genus, such as Brazil­ian free-tailed bats (Tadarida brasilien­sis), are known to be promis­cu­ous, mat­ing mul­ti­ple times with mul­ti­ple bats. (An­cil­lotto and Russo, 2014; Kee­ley and Kee­ley, 2004)

The breed­ing sea­son for Eu­ro­pean free-tailed bats lasts from May to Oc­to­ber. Mat­ing oc­curs in spring, and birth oc­curs in fall. They only give birth to one pup per preg­nancy. There are no known records for the ges­ta­tion pe­riod of Eu­ro­pean free-tailed bats, but an­other mem­ber of the fam­ily, Brazil­ian free-tailed bats (Tadarida brasilien­sis), have a ges­ta­tion pe­riod of 77 to 100 days.

Newly-born brazil­ian free-tailed bats are about two-thirds the body length of adults and, on av­er­age, weigh about 12 g at birth. Young are weaned at 6 weeks. Fe­males reach sex­ual ma­tu­rity at a year old, and males reach sex­ual ma­tu­rity at two years of age. In Mex­i­can free-tailed bats (Tadarida brasilien­sis mex­i­cana), young are in­de­pen­dent at around 7 weeks of age. They breed only once, due to fer­til­iza­tion hap­pen­ing im­me­di­ately after in­sem­i­na­tion. Mem­bers of the genus Tadarida do not store sperm.

Eu­ro­pean free-tailed bats are iteroparous, mean­ing they breed mul­ti­ple times in their lives. They are also vi­vip­a­rous, mean­ing they give birth to live young. (Amorim, et al., 2015; Arm­strong, 2008; Bar­clay, 1994; Krutzsch, et al., 2002; Marom, et al., 2006; Pa­padimi­tiou, et al., 2009)

  • Breeding interval
    European free-tailed bats breed once a year
  • Breeding season
    May to October
  • Range number of offspring
    1 (high)

Fe­male Eu­ro­pean free-tailed bats usu­ally con­tinue to care for their young after wean­ing, and ju­ve­niles stay in the same roost for some time be­fore leav­ing on their own. There is lit­tle in­for­ma­tion on record for Eu­ro­pean free-tailed bats, but Brazil­ian free-tailed bats (Tadarida brasilien­sis) are very sim­i­lar. Fe­male Brazil­ian free-tailed bats form nurs­ery colonies in which to leave their pups while they for­age. Fe­males in the colonies are the pri­mary care­givers, but males will take on a more ac­tive role such as cre­at­ing roost spots and de­fend­ing the roost, fe­male, and young. Fe­males and their pups will also com­mu­ni­cate with each other acousti­cally, con­tin­u­ing from birth and fol­low­ing par­tu­ri­tion. (An­cil­lotto and Russo, 2014; Kunz and Hood, 2000)

  • Parental Investment
  • altricial
  • female parental care
  • pre-fertilization
    • provisioning
  • pre-hatching/birth
    • provisioning
      • female
  • pre-weaning/fledging
    • provisioning
      • female

Lifes­pan/Longevity

The longest known lifes­pan of Eu­ro­pean free-tailed bats in the wild is 13 years, based on a sin­gle male that was tracked while alive. He was at least 13 the last time he was cap­tured. This is also the longest recorded lifes­pan for any species of the fam­ily Tadarida. Eu­ro­pean free-tailed bats are not kept in cap­tiv­ity. (Ibanez and Jorda-Perez, 2006)

  • Range lifespan
    Status: wild
    13 (high) years

Be­hav­ior

Eu­ro­pean free-tailed bats live in colonies, but do not in­ter­act with other species very often. They com­mu­ni­cate using echolo­ca­tion calls. There use many unique fre­quen­cies that sig­nal preda­tors, de­tect veg­e­ta­tion when fly­ing, or are used when near other Eu­ro­pean free-tailed bats. Around 47 unique calls have been recorded. They also use touch and sight to sense the world around them. They are non-mi­gra­tory by na­ture, and are mostly seden­tary. Eu­ro­pean free-tailed bats are noc­tur­nal and can fly. They in­vest a great deal of en­ergy in rear­ing young, and even con­tinue to care for ju­ve­niles after they are ready to leave the roost. Eu­ro­pean free-tailed bats live in large colonies, and are in­sec­tiv­o­rous. (Ibanez and Jorda-Perez, 2006; An­cil­lotto and Russo, 2014; Bayef­sky-Anand, et al., 2008; Ibanez and Jorda-Perez, 2006; Ry­dell and Ar­let­taz, 1994; Ry­dell, et al., 1995; Tiago, et al., 2004)

Home Range

A home range for Eu­ro­pean free-tailed bats has not been re­ported, but they are sim­i­lar to Brazil­ian free-tailed bats (Tadarida brasilien­sis) in many other ways. Brazil­ian free-tailed bats have an av­er­age home range of 0.75 km^2. They de­fend their roost­ing spots in­stead of try­ing to de­fend this very large home range. Exact ter­ri­tory sizes are un­known for both Eu­ro­pean free-tailed bats and Brazil­ian free-tailed bats. (En­gesser, et al., 2017)

Com­mu­ni­ca­tion and Per­cep­tion

Eu­ro­pean free-tailed bats com­mu­ni­cate using low fre­quency (11 to 12 kHz) echolo­ca­tion calls. There have been 47 unique call fre­quen­cies recorded both in the wild and in en­clo­sures. The echolo­ca­tion calls of these bats change from re­gion to re­gion, as well as year to year. Eu­ro­pean free-tailed bat echolo­ca­tion calls con­tained buzzes when they were around food sources, or other Eu­ro­pean free-tailed bats. This buzzing was not con­sis­tent enough to dif­fer­en­ti­ate be­tween so­cial and food buzzes based on sound alone. By using longer echolo­ca­tion calls, Eu­ro­pean free-tailed bats are able to de­tect and avoid veg­e­ta­tion while fly­ing. Their ad­vanced hear­ing also helps them lo­cate and stay away from preda­tors, or de­tect prey. Eu­ro­pean free-tailed bats also use sight to track food and find places to roost. They also use tac­tile senses in order to make sure they have enough head­space when roost­ing, as well as to sense the en­vi­ron­ment around them. (Bayef­sky-Anand, et al., 2008; Ry­dell and Ar­let­taz, 1994; Ry­dell, et al., 1995)

Food Habits

Using low fre­quency echolo­ca­tion, Eu­ro­pean free-tailed bats feed on large, tym­pa­nate in­sects. Two in­sect or­ders, Lep­i­doptera (moths and but­ter­flies) and Neu­roptera (green lacewings and antlion), com­prise 90% of the diets of Eu­ro­pean free-tailed bats in more tem­per­ate is­land cli­mates.

Eu­ro­pean free-tailed bats show sex-re­lated vari­a­tion in eat­ing habits. On av­er­age, fe­male Eu­ro­pean free-tailed bats con­sumed larger moths than males. Ry­dell and Ar­let­taz (1994) at­tribute this to fe­male Eu­ro­pean free-tailed bats need­ing more en­ergy while they are preg­nant or lac­tat­ing. Whit­taker et al. (1994) found dif­fer­ent diet com­po­si­tions in Is­rael. Eu­ro­pean free-tailed bat diets in these areas were dom­i­nated by bee­tles (Coleoptera) and moths. Al­though Eu­ro­pean free-tailed bats are con­sid­ered an aer­ial-hawk­ing bat, their echolo­ca­tion sets them apart from most aer­ial-hawk­ing bats; most other aer­ial-hawk­ing bats do not eat tym­pa­nate in­sects. (Mata, et al., 2016; Mata, et al., 2018; Ry­dell and Ar­let­taz, 1994; Whit­taker, et al., 1994)

  • Animal Foods
  • insects

Pre­da­tion

Do­mes­tic cats (Felis catus) are a preda­tor to many species of bats in penin­su­lar Italy; this in­cludes Eu­ro­pean free-tailed bats. An­cil­lotto et al. (2013) stud­ied these bats in penin­su­lar Italy be­tween 2009 and 2011. They found that that 2 in every 14 adult Eu­ro­pean free-tailed bats are caught by cats. In Is­rael, Eu­ro­pean free-tailed bats are preyed upon by Lan­ner fal­cons (Falco biarmi­cus). Yosef (1991) found that Lan­ner fal­cons are suc­cess­ful in catch­ing Eu­ro­pean free-tailed bats 29% of the time. (An­cil­lotto, et al., 2013; Yosef, 1991)

Ecosys­tem Roles

Eu­ro­pean free-tailed bats are known to be hosts to a rare species of flea known as Araeop­sylla ge­stroi. This species of flea is al­most ex­clu­sive to the Tadarida genus. These fleas feed on Eu­ro­pean free-tailed bats, and can cause skin ir­ri­ta­tion. (Lewis, 1976; Medvedev and Boris, 2013; Serra-Cobo, et al., 2002; Szen­ti­vanyi, et al., 2016)

Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Be­cause Eu­ro­pean free-tailed bats eat many lep­i­dopteran species, such as moths that feed on eco­nom­i­cally im­por­tant crops, they have the po­ten­tial to con­trol pest species. How­ever, no re­ports have shown di­rect ev­i­dence of pest con­trol. (Ric­cucci and Lanza, 2014)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Schatz et al. (2013) re­port that an­ti­bod­ies for lyssaviruses have been found in Eu­ro­pean free-tailed bats in Spain; this is the genus of viruses that in­cludes ra­bies. How­ever, al­though these bats may carry ra­bies, there are no known re­ports in all of Eu­rope of a rabid Eu­ro­pean free-tailed bat in­fect­ing a human. (Schatz, et al., 2013)

  • Negative Impacts
  • injures humans
    • carries human disease

Con­ser­va­tion Sta­tus

Ac­cord­ing to the IUCN Red List, Eu­ro­pean free-tailed bats are a species of "Least Con­cern." Eu­ro­pean free-tailed bats are not listed on the US Fed­eral List, the CITES list, or the State of Michi­gan List.

Eu­ro­pean free-tailed bats are most threat­ened by de­for­esta­tion, habi­tat loss caused by ur­ban­iza­tion, and the use of pes­ti­cides. There is some ev­i­dence to sup­port them being neg­a­tively af­fected by de­for­esta­tion. Eu­ro­pean free-tailed bats are also, po­ten­tially, af­fected by wind farms. These are not con­sid­ered major threats to the species at this time.

Eu­ro­pean free-tailed bats are pro­tected by na­tional leg­is­la­tion in many in­di­vid­ual places, such as the states of India, and they are in­ter­na­tion­ally pro­tected through the Bonn Con­ven­tion and the Bern Con­ven­tion. The Bonn Con­ven­tion, in Ap­pen­dix II, states that any state in the range of a mi­gra­tory species has to take ac­tion to con­serve roost­ing areas. The Bern Con­ven­tion states the in­tent to con­serve plant life and the nat­ural habi­tats of wildlife. (Benda and Pirac­cini, 2016)

Con­trib­u­tors

Stephanie Crouch (au­thor), Rad­ford Uni­ver­sity, Lau­ren Bur­roughs (ed­i­tor), Rad­ford Uni­ver­sity, Layne DiBuono (ed­i­tor), Rad­ford Uni­ver­sity, Lind­sey Lee (ed­i­tor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity.

Glossary

Palearctic

living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.

World Map

acoustic

uses sound to communicate

altricial

young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

colonial

used loosely to describe any group of organisms living together or in close proximity to each other - for example nesting shorebirds that live in large colonies. More specifically refers to a group of organisms in which members act as specialized subunits (a continuous, modular society) - as in clonal organisms.

echolocation

The process by which an animal locates itself with respect to other animals and objects by emitting sound waves and sensing the pattern of the reflected sound waves.

endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

female parental care

parental care is carried out by females

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

insectivore

An animal that eats mainly insects or spiders.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

motile

having the capacity to move from one place to another.

mountains

This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.

native range

the area in which the animal is naturally found, the region in which it is endemic.

nocturnal

active during the night

polygynandrous

the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.

scrub forest

scrub forests develop in areas that experience dry seasons.

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

social

associates with others of its species; forms social groups.

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

urban

living in cities and large towns, landscapes dominated by human structures and activity.

visual

uses sight to communicate

viviparous

reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.

Ref­er­ences

Al­fonso, B. 2018. Ad­vances on the group com­po­si­tion, mat­ing sys­tem, roost­ing and flight be­hav­iour of the Eu­ro­pean free-tailed bat (Tadarida teni­o­tis). Mam­malia, 82/5: 460-468.

Amorim, F., V. Mata, P. Beja, H. Re­belo. 2015. Ef­fects of a drought episode on the re­pro­duc­tive suc­cess of Eu­ro­pean free-tailed bat (Tadarida teni­o­tis). Mam­malian Bi­ol­ogy, 80/3: 228-236.

An­cil­lotto, L., D. Russo. 2014. Se­lec­tive ag­gres­sive­ness in Eu­ro­pean free-tailed bats (Tadarida teni­o­tis): In­flu­ence of fa­mil­iar­ity, age and sex. Die Natur­wis­senschaften, 101/3: 221-228.

An­cil­lotto, L., M. Serangeli, D. Russo. 2013. Cu­riosty killed the bat: Do­mes­tic cats as bat preda­tors. Mam­malian Bi­ol­ogy, 78/5: 369-372.

Ar­let­taz, R., C. Ruchet, J. Aeschi­mann, E. Brun, M. Genoud, P. Vogel. 2000. Phys­i­o­log­i­cal traits af­fect­ing the dis­tri­b­u­tion and win­ter­ing strat­egy of the bat Tadarida teni­o­tis. Ecol­ogy, 81/4: 1004-1014.

Arm­strong, K. 2008. Brazil­ian free-tailed bat. Mam­malian Species, 4: 1-6.

Bar­clay, R. 1994. Con­straints on re­pro­duc­tion by fly­ing ver­te­brates: En­ergy and cal­cium. Amer­i­can Nat­u­ral­ist, 144/6: 1021-1031.

Bayef­sky-Anand, S., M. Skowron­ski, M. Fen­ton, C. Ko­rine, M. Holderied. 2008. Vari­a­tions in the echolo­ca­tion calls of the Eu­ro­pean free-tailed bat. Jour­nal of Zo­ol­ogy, 275/2: 115-123.

Benda, P., R. Pirac­cini. 2016. "Tadarida teni­o­tis" (On-line). The IUCN Red List of Threat­ened Species e.T21311A2211499. Ac­cessed March 03, 2019 at http://​dx.​doi.​org/​10.​2305/​IUCN.​UK.​2016-2.​RLTS.​T21311A22114995.​en.​.

Benda, P., M. Uhrin. 2017. First records of bats from four Do­de­canese is­lands, Greece (Chi­roptera). Lynx, Se­ries Nova, 48: 15-38.

Chakravarty, R. 2017. A new dis­tri­b­u­tion record of the Eu­ro­pean free-tailed bat Tadarida teni­o­tis (Chi­roptera:Molos­si­dae) from the west­ern Hi­malaya, India. Jour­nal of Threat­ened Taxa, 9/7: 10463-10467.

Corsetti, L. 1990. The Eu­ro­pean free-tailed bat, Tadarida teni­o­tis, in a sub­ur­ban area of Latina, Latium (Cen­tral Italy). As­so­ci­azione Teri­o­log­ica Ital­iana, 2/1: 1825-5272.

Dal­houmi, R., P. Aissa, S. Aulagnier. 2016. Bat species rich­ness and ac­tiv­ity in Bou Hedma Na­tional Park (cen­tral Tunisia). Turk­ish Jour­nal of Zo­ol­ogy, 4/6: 864-875.

Dal­houmi, R., A. Hedfi, P. Aissa, S. Aulagnier. 2014. Bats of Jebel Mghilla Na­tional Park (Cen­tral Tunisia): First sur­vey and habi­tat-re­lated ac­tiv­ity. Trop­i­cal Zo­ol­ogy, 27/2: 53-62.

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En­gesser, S., A. Ri­d­ley, S. Townsend. 2017. El­e­ment rep­e­ti­tion rates en­code func­tion­ally dis­tinct in­for­ma­tion in pied bab­bler clucks and purrs. An­i­mal Cog­ni­tion, 20/5: 953-960.

Firouz, E. 2005. The Com­plete Fauna of Iran. Lon­don, United King­dom: I.B. Tau­ris & Co. Ltd..

Hintze, F., V. Duro, J. Car­valho, C. Eira, P. Ro­drigues, J. Vin­gada. 2016. In­flu­ence of reser­voirs cre­ated by small dams on the ac­tiv­ity of bats. Acta Chi­roptero­log­ica, 18/2: 395-408.

Hoath, R. 2003. A Field Guide to the Mam­mals of Egypt. Cairo, Egypt: The Amer­i­can Uni­ver­sity in Cairo Press.

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Kee­ley, A., B. Kee­ley. 2004. The mat­ing sys­tem of Tadarida brasilien­sis (Chi­roptera:Molos­si­dae) in large high­way bridge colony. Jour­nal of Mam­mal­ogy, 85/1: 113-119.

Krutzsch, P., T. Flem­ing, E. Crich­ton. 2002. Re­pro­duc­tive bi­ol­ogy of male Mex­i­can free-tailed bats (Tadarida brasilin­sis mex­i­cana). Jour­nal of Mam­mal­ogy, 83/2: 489-500.

Kunz, T., W. Hood. 2000. Re­pro­duc­tive Bi­ol­ogy of Bats. San Diego, Cal­i­for­nia: Aca­d­e­mic Press.

Lewis, R. 1976. The fleas (Siphonaptera) of Egypt: An il­lus­trated and an­no­tated key. The Jour­nal of Par­a­sitol­ogy, 53/4: 863-885.

Mar­cel, U., G. Suren, B. Petr. 2009. Does Tadarida teni­o­tis re­ally occur in Crimea? (Chi­roptera: Molos­si­dae). Lynx, Se­ries Nova, 40/1: 115-126.

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