Skip to main content
Log in

The reproductive success of the parasitic bat fly Basilia nana (Diptera: Nycteribiidae) is affected by the low roost fidelity of its host, the Bechstein’s bat (Myotis bechsteinii)

  • Original Paper
  • Published:
Parasitology Research Aims and scope Submit manuscript

Abstract

We studied the reproductive ecology of the bat fly Basilia nana on free-ranging colonial female and solitary male Bechstein’s bats (Myotis bechsteinii) during one reproductive season. The reproduction of B. nana took place from April to September, and the production of puparia in bat roosts was high. The metamorphosis of the flies took a minimum of 30 days, and at least 86% of the puparia metamorphosed successfully. However, only about 30% of flies from puparia deposited in female roosts and 57% of flies from puparia deposited in male roosts emerged in the presence of Bechstein’s bats and were thus able to survive. The significantly higher emergence success of bat flies in male roosts was caused by the higher roost fidelity of the solitary males compared with the social females. Our results indicate that bats can control the reproductive success of bat flies by switching and selecting roosts.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Archer MS, Cardinal BR (2001) Seasonal reproduction and host infestation rates for Nycteribiids of the large bentwing bat. Med Vet Entomol 15:452–454

    Article  PubMed  CAS  Google Scholar 

  • Bize P, Roulin A, Tella JL, Bersier JF, Richner H (2004) Additive effects of ectoparasites over reproductive attempts in the long-lived alpine swift. J Anim Ecol 73:1080–1088

    Article  Google Scholar 

  • Blanco G, De la Puente J, Corroto M, Baz T, Colas J (2001) Condition-dependent immune defence in the Magpie: how important is ectoparasitism. Biol J Linn Soc 72:279–286

    Google Scholar 

  • Bowman AS, Coons LB, Needham GR, Sauer JR (1997) Tick saliva: recent advances and implications for vector competence. Med Vet Entomol 11(3):277–285

    PubMed  CAS  Google Scholar 

  • Clayton DH, Moore J (1997) Host–parasite evolution: general principles and Avian models. Oxford University Press, Oxford

    Google Scholar 

  • Durden LA, Polur RN, Nims T, Banks CW, Oliver JH (2004) Ectoparasites and other epifaunistic arthropods of sympatric cotton mice and golden mice: comparisons and implications for vector-borne zoonotic diseases. J Parasitol 90(6):1293–1297

    Article  PubMed  Google Scholar 

  • Fitze PS, Clobert J, Richner H (2004) Long-term life-history consequences of ectoparasite-modulated growth and development. Ecology 85 (7):2018–2026

    Article  Google Scholar 

  • Giorgi MS, Arlettaz R, Christe P, Vogel P (2001) The energetic grooming costs imposed by a parasitic mite (Spinturnix myoti) upon its bat host (Myotis myotis). Proc R Soc Lond B Biol Sci 268:2071–2075

    Article  CAS  Google Scholar 

  • Hase A (1931) Über die Lebensgewohnheiten einer Fledermausfliege in Venezuela; Basilia bellardii RONDANI (Fam Nycteribiidae–Diptera Pupipara). Z Parasitenkd 3:220–257

    Article  Google Scholar 

  • Hùrka K (1964) Distribution, bionomy and ecology of the European bat flies with special regard to the Czechoslovak fauna (Dip, Nycteribiidae). Acta Univ Carol Biol 1964(3):167–234

    Google Scholar 

  • Kerth G (1998) Sozialverhalten und genetische Populationsstruktur bei der Bechsteinfledermaus (Myotis bechsteinii). Wissenschaft und Technik Verlag, Berlin

    Google Scholar 

  • Kerth G, König B (1996) Transponder and an infrared-video camera as methods in a field study on the social behaviour of Bechstein’s bats (Myotis bechsteini). Myotis 34:27–34

    Google Scholar 

  • Kerth G, König B (1999) Fission, fusion and nonrandom associations in female Bechstein’s bats (Myotis bechsteinii). Behaviour 136:1187–1202

    Article  Google Scholar 

  • Kerth G, Morf L (2004) Behavioural and genetic data suggest that Bechstein’s bats predominately mate outside the breeding habitat. Ethology 110(12):987–999

    Article  Google Scholar 

  • Kerth G, Reckardt R (2003) Information transfer about roosts in female Bechstein’s bats: an experimental field study. Proc R Soc Lond B Biol Sci 270:511–515

    Article  Google Scholar 

  • Kerth G, Mayer F, König B (2000) Mitochondrial DNA (mtDNA) reveals that female Bechstein’s bats live in closed societies. Mol Ecol 9:793–800

    Article  PubMed  CAS  Google Scholar 

  • Kerth G, Safi K, König B (2002) Mean colony relatedness is a poor predictor of colony structure and female philopatry in the communally breeding Bechstein’s bat (Myotis bechsteinii). Behav Ecol Sociobiol 52:203–210

    Article  Google Scholar 

  • Leong MC, Marshall AG (1968) The breeding biology of the bat–fly Eucampsipoda sundaicum THEODOR, 1955 (Diptera: Nycteribiidae). Malay Nat J 21:171–180

    Google Scholar 

  • Lewis SE (1995) Roost fidelity of bats—a review. J Mammal 76(2):481–496

    Article  Google Scholar 

  • Lewis SE (1996) Low roost-site fidelity in pallid bats: associated factors and effect on group stability. Behav Ecol Sociobiol 39:335–344

    Article  Google Scholar 

  • Lively CM (1996) Host–parasite coevolution and sex—do interactions between biological enemies maintain genetic variation and cross-fertilization? Bioscience 46(2):107–114

    Article  Google Scholar 

  • Löhrl H (1953) Fledermaus-Fliegen. Nat Volk 83:182–185

    Google Scholar 

  • Marshall A (1970) The life cycle of Basilia hispida THEODOR 1967 (Diptera: Nycteribiidae) in Malaysia. Parasitology 61:1–18

    Article  Google Scholar 

  • Marshall AG (1971) The ecology of Basilia hispida (Diptera: Nycteribiidae) in Malaysia. J Anim Ecol 40:141–154

    Article  Google Scholar 

  • Marshall AG (1981) The ecology of ectorparasitic insects. Academic, London

    Google Scholar 

  • Møller AP (1993) Ectoparasites increase the cost of reproduction in their hosts. J Anim Ecol 62:309–322

    Article  Google Scholar 

  • Ryberg O (1947) Studies on bats and bat parasites. Bokförlaget Svensk Natur, Stockholm, Sweden

    Google Scholar 

  • Schulz H (1938) Über Fortpflanzung und Vorkommen von Fledermausfliegen (Fam. Nycteribiidae—Diptera, Pupipara). Z Parasitenkd 10:297–328

    Article  Google Scholar 

  • Theodor O (1954) Nycteribiidae. In: Lindner E (ed.) Die Fliegen der paläarktischen Region, vol 12. Stuttgart, Germany, pp 1–43

    Google Scholar 

  • Theodor O (1967) An illustrated catalogue of the Rothschild collection of Nycteribiidae (Diptera) in the British Museum (Natural History). Britisch Museum (Natural History), London, United Kingdom, pp viii, 1–506

  • Van Valen L (1973) A new evolutionary law. Evol Theory 1:1–30

    Google Scholar 

  • Waage JK (1979) The evolution of insect/vertebrate association. Biol J Linn Soc 12:187–224

    Article  Google Scholar 

Download references

Acknowledgements

We thank D. Dechmann, A. Ross-Gillespie, B. König and D. Turner for helpful comments on the manuscript. We are grateful to N. Bansac and S. Rauchfuss for their assistance in the field, to G. Lexa for leasing her apartment and to B. König for her constant support. The handling, marking and observation of Bechstein’s bats were done under license from the nature conservancy department of the government of Lower Frankonia. We gratefully acknowledge its support and that of the local department of forestry. This work was supported by the Swiss National Science Foundation (SNF; 31-59556.99).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Karsten Reckardt.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Reckardt, K., Kerth, G. The reproductive success of the parasitic bat fly Basilia nana (Diptera: Nycteribiidae) is affected by the low roost fidelity of its host, the Bechstein’s bat (Myotis bechsteinii). Parasitol Res 98, 237–243 (2006). https://doi.org/10.1007/s00436-005-0051-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00436-005-0051-5

Keywords

Navigation