Skip to main content
Log in

The cost of mating with a non-virgin male in a monandrous butterfly: experimental evidence from the speckled wood, Pararge aegeria

  • Original Article
  • Published:
Behavioral Ecology and Sociobiology Aims and scope Submit manuscript

Abstract

Contrary to vertebrates, sperm production in insects may bear considerable costs for males. This is especially true in species that donate spermatophores containing sperm and nutrient-rich accessory gland products like in butterflies. Hence, spermatophores at first and subsequent copulations can differ in a quantitative and qualitative way. Such effects have particularly been shown in polyandrous species providing large spermatophores. Here we experimentally tested the effect of male mating status (virgin male vs recently mated male) on copulation duration, spermatophore size and females’ fitness components in a monandrous butterfly Pararge aegeria that typically donates small spermatophores. Copulations with non-virgin males lasted on average five times longer than that with virgin males and resulted in a spermatophore which was on average three times smaller. Number of eggs laid and female life span were not affected by the mating status treatment, but there was a significant effect on the number of living caterpillars a female produced, as copulations with virgin males resulted in higher numbers of larval offspring. Interestingly, the difference in spermatophore mass at the first and the second copulation increased with male body size. This suggests differential spermatophore allocation decisions among males of different size. Consequences for females and potential mechanisms influencing female fitness components are discussed. Given the small absolute size of spermatophores in P. aegeria, components other than consumable nutrients (perhaps hormones) should cause the observed effects.

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

  • Bissoondath CJ, Wiklund C (1995) Protein content of spermatophores in relation to monandry/polyandry in butterflies. Behav Ecol Sociobiol 37:365–371

    Article  Google Scholar 

  • Bissoondath CJ, Wiklund C (1996a) Effect of male mating history and body size on ejaculate size and quality in two polyandrous butterflies Pieris napi and P. rapae (Lepidoptera: Pieridae). Funct Ecol 10:457–464

    Article  Google Scholar 

  • Bissoondath CJ, Wiklund C (1996b) Male butterfly investment in successive ejaculates in relation to mating system. Behav Ecol Sociobiol 39:285–292

    Article  Google Scholar 

  • Boggs CL (1990) A general model of the role of male-donated nutrients in female insects’ reproduction. Am Nat 136:598–617

    Article  Google Scholar 

  • Boggs CL (1997) Reproductive allocation from reserves and income in butterfly species with differing adult diets. Ecology 78:181–191

    Google Scholar 

  • Boggs CL (2003) Environmental variation, life histories, and allocation. In: Boggs CL, Wat WB, Ehrlich PR (eds) Butterflies: ecology and evolution taking flight. University of Chicago Press, Chicago, pp 185–206

    Google Scholar 

  • Boggs CL, Gilbert LE (1979) Male contribution to egg production in butterflies: evidence for transfer of nutrients at mating. Science 206:83–84

    Article  PubMed  Google Scholar 

  • Dewsbury DA (1982) Ejaculate cost and male choice. Am Nat 119:601–610

    Article  Google Scholar 

  • Gillott C (2003) Male accessory gland secretions: modulators of female reproductive physiology and behavior. Annu Rev Entomol 48:163–184

    Article  PubMed  CAS  Google Scholar 

  • Hack MA (1997) The effects of mass and age on standard metabolic rate in house crickets. Physiol Entomol 22:325–331

    Article  Google Scholar 

  • Hughes L, Chang BSW, Wagner D, Pierce NE (2000) Effects of mating history on ejaculate size, fecundity, longevity, and copulation duration in the ant-tended lycaenid butterfly, Jalmenus evagoras. Behav Ecol Sociobiol 47:119–128

    Article  Google Scholar 

  • Kaitala A, Wiklund C (1994) Polyandrous females forage for matings. Behav Ecol Sociobiol 35:385–388

    Google Scholar 

  • Karlsson B (1987) Variation in egg weight, oviposition rate and reproductive reserves with female age in a natural population of the speckled wood butterfly, Pararge aegeria. Ecol Entomol 12:473–476

    Google Scholar 

  • Karlsson B (1998) Nuptial gifts, resource budgets, and reproductive output in a polyandrous butterfly. Ecology 79:2931–2940

    Article  Google Scholar 

  • Karlsson B, Van Dyck H (2005) Does habitat fragmentation affect temperature-related life-history traits? A laboratory test with a woodland butterfly. Proc R Soc B 272:1257–1263

    Article  PubMed  Google Scholar 

  • Karlsson B, Wickman PO (1990) Increased reproductive effort as explained by body size and resource allocation in the speckled wood butterfly, Pararge aegeria (L.). Funct Ecol 4:609–617

    Article  Google Scholar 

  • Karube F, Kobayashi M (1999) Presence of eupyrene spermatrozoa in vestibulum accelerates oviposition in the silkworm moth, Bombyx mori. J Insect Physiol 45:947–957

    Article  PubMed  CAS  Google Scholar 

  • Krebs JR, Davies NB (1993) Behavioural ecology: an evolutionary approach. Cambridge University Press, Cambridge

    Google Scholar 

  • Kubli E (2003) Sex-peptides: seminal peptides of the Drosophila male. Cell Mol Life Sci 60:1689–1704

    Article  PubMed  CAS  Google Scholar 

  • Lange AB, Loughton BG (1985) An oviposition-stimulating factor in the male accessory reproductive gland of the locust, Locusta migratoria. Gen Comp Endocrinol 57:208–215

    Article  PubMed  CAS  Google Scholar 

  • Littell RC, Milliken GA, Stroup WW, Wolfinger RD (1996) SAS system for mixed models. SAS Institute, Cary, NC

    Google Scholar 

  • Molleman F, Zwaan BJ, Brakefield PM (2004) The effect of male sodium diet and mating history on female reproduction in the puddling squinting bush brown Bicyclus anynana (Lepidoptera). Behav Ecol Sociobiol 56:404–411

    Article  Google Scholar 

  • Nylin S, Wickman PO, Wiklund C (1995) Life-cycle regulation and life history plasticity in the speckled wood butterfly: are reaction norms predictable? Biol J Linn Soc 55:143–157

    Article  Google Scholar 

  • Oberhauser KS (1989) Effects of spermatophores on male and female monarch butterfly mating success. Behav Ecol Sociobiol 25:237–246

    Article  Google Scholar 

  • Pivnick KA, McNeil JN (1987) Puddling in butterflies: sodium affects reproductive success in Thymelicus lineola. Physiol Entomol 12:461–472

    Google Scholar 

  • Royer L, McNeil JN (1993) Male investment in the European corn-borer, Ostrinia nubilalis (Lepidoptera, Pyralidae)—impact on female longevity and reproductive performance. Funct Ecol 7:209–215

    Article  Google Scholar 

  • Rutowski RL, Gilchrist GW (1986) Copulation in Colias eurytheme (Lepidoptera: Pieridae): patterns and frequency. J Zool (Lond) 209:115–124

    Google Scholar 

  • Rutowski RL, Gilchrist GW, Terkanian B (1987) Female butterflies mated with recently mated males show reduced reproductive output. Behav Ecol Sociobiol 20:319–322

    Article  Google Scholar 

  • Shreeve TG (1986) Egg-laying by the speckled wood (Pararge aegeria): the role of female behaviour, host plant abundance and temperature. Ecol Entomol 11:229–236

    Google Scholar 

  • Simmons LW (1993) Some constraints on reproduction for male bush-crickets, Requena verticalis (Orthoptera, Tettigoniidae)—diet, size and parasite load. Behav Ecol Sociobiol 32:135–139

    Article  Google Scholar 

  • Svärd L (1985) Paternal investment in a monandrous butterfly, Pararge aegeria. Oikos 45:66–70

    Article  Google Scholar 

  • Svärd L, Wiklund C (1986) Different ejaculate delivery strategies in first versus subsequent matings in the swallowtail butterfly Papilio machaon L. Behav Ecol Sociobiol 18:325–330

    Article  Google Scholar 

  • Svärd L, Wiklund C (1988) Fecundity, egg weight and longevity in relation to multiple matings in females of the monarch butterfly. Behav Ecol Sociobiol 23:39–43

    Article  Google Scholar 

  • Svärd L, Wiklund C (1989) Mass and production rate of ejaculates in relation to monandry/polyandry in butterflies in butterflies. Behav Ecol Sociobiol 24:395–402

    Article  Google Scholar 

  • Svärd L, Wiklund C (1991) The effect of ejaculate mass on female reproductive output in the European swallowtail butterfly, Papilio machaon (l) (Lepidoptera, Papilionidae). J Insect Behav 4:33–41

    Article  Google Scholar 

  • Tamhankar AJ (1995) Host influence on mating-behavior and spermatophore reception correlated with reproductive output and longevity of female Earias insulana (boisduval) (Lepidoptera, Noctuidae). J Insect Behav 8:499–511

    Article  Google Scholar 

  • Thornhill R, Alcock J (1983) The evolution of insect mating systems. Harvard University Press, Cambridge

    Google Scholar 

  • Tolman T, Lewington R (1997) Butterflies of Britain and Europe. Harper Collins, London

    Google Scholar 

  • Trivers RL (1972) Paternal investment and sexual selection. In: Campbell B (ed) Sexual selection and the descent of man. Aldine, Chicago, pp 136–179

    Google Scholar 

  • Torres-Vila LM, Jennions MD (2005) Male mating history and female fecundity in the Lepidoptera: do male virgins make better partners? Behav Ecol Sociobiol 57:318–326

    Article  Google Scholar 

  • Torres-Vila LM, Rodriguez-Molina MC (2002) Egg size variation and its relationship with larval performance in the Lepidoptera: the case of the European grapevine moth Lobesia botrana. Oikos 99:272–283

    Article  Google Scholar 

  • Torres-Vila LM, Rodriguez-Molina MC, Jennions MD (2004) Polyandry and fecundity in the Lepidoptera: can methodological and conceptual approaches bias outcomes? Behav Ecol Sociobiol 55:315–324

    Article  Google Scholar 

  • Van Dyck H (2003) Mate location, a matter of design? Adaptive morphological variation in the speckled wood butterfly. In: Boggs CL, Watt WB, Ehrlich PR (eds) Butterflies: evolution and ecology taking flight. University of Chicago Press, Chicago, pp 353–366

    Google Scholar 

  • Ward KE, Landolt PJ (1995) Influence of multiple matings on fecundity and longevity of female cabbage-looper moths (Lepidoptera, Noctuidae). Ann Entomol Soc Am 88:768–772

    Google Scholar 

  • Watanabe M, Wiklund C, Bon’no M (1998) The effect of repeated matings on sperm numbers in successive ejaculates of the cabbage white butterfly Pieris rapae. J Insect Behav 11:559–570

    Article  Google Scholar 

  • Wedell N (1993) Mating effort or paternal investment—incorporation rate and cost of male donations in the wartbiter. Behav Ecol Sociobiol 32:239–246

    Article  Google Scholar 

  • Wedell N (1996) Mate quality affects reproductive effort in a paternally investing species. Am Nat 48:1075–1088

    Article  Google Scholar 

  • Wedell N, Karlsson B (2003) Paternal investment directly affects female reproductive effort in an insect. Proc R Soc Lond B 270:2065–2071

    Article  CAS  Google Scholar 

  • Wickman PO, Karlsson B (1987) Changes in egg color, egg weight and oviposition rate with the number of eggs laid by wild females of the small heath butterfly, Coenonympha pamphilus. Ecol Entomol 12:109–114

    Google Scholar 

  • Wiklund C (2003) Sexual selection and the evolution of butterfly mating systems. In: Boggs CL, Watt WB, Ehrlich PR (eds) Butterflies: ecology and evolution taking flight. University of Chicago Press, Chicago, pp 67–90

    Google Scholar 

  • Wiklund C, Karlsson B (1984) Egg size variation in satyrid butterflies: adaptive vs. historical “Bauplan”, and mechanistic explanations. Oikos 43:391–400

    Article  Google Scholar 

  • Wiklund C, Persson A (1983) Fecundity, egg weight variation and its relation to offspring fitness in the speckled wood butterfly, Pararge aegeria, or why don’t butterfly females lay more eggs? Oikos 40:53–63

    Article  Google Scholar 

  • Wiklund C, Persson A, Wickman PO (1983) Larval aestivation and direct development as alternative strategies in the speckled wood butterfly, Pararge aegeria, in Sweden. Ecol Entomol 8:233–238

    Google Scholar 

  • Wiklund C, Kaitala A, Lindström V, Abenius J (1993) Polyandry and its effect on female reproduction in the green-veined white butterfly, Pieris napi. Behav Ecol Sociobiol 33:25–34

    Article  Google Scholar 

  • Wiklund C, Kaitala A, Wedell N (1998) Decoupling of reproductive rates and parental expenditure in a polyandrous butterfly. Behav Ecol 9:20–25

    Article  Google Scholar 

  • Wiklund C, Karlsson B, Leimar O (2001) Sexual conflict and cooperation in butterfly reproduction: a comparative study of polyandry and female fitness. Proc R Soc Lond B 268:1661–1667

    Article  CAS  Google Scholar 

Download references

Acknowledgements

Two anonymous referees provided valuable comments on the manuscript. This study was supported by a grant of the University of Antwerp (GOA 15R/3942).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hans Van Dyck.

Additional information

Communicated by N. Wedell

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lauwers, K., Van Dyck, H. The cost of mating with a non-virgin male in a monandrous butterfly: experimental evidence from the speckled wood, Pararge aegeria . Behav Ecol Sociobiol 60, 69–76 (2006). https://doi.org/10.1007/s00265-005-0142-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00265-005-0142-4

Keywords

Navigation