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Male Mating History in Antheraea mylitta and its Effect on Ejaculation Size and Female Reproductive Fitness

  • Received : 2011.02.11
  • Accepted : 2011.05.16
  • Published : 2011.06.30

Abstract

Reproductive activity in the economically important insect, Antheraea mylitta is very important because the female reproduces only once in her life time and the aging is very rapid and costly. It is a capital breeder and strictly a monoandrous species. To know how strategically the insect behaves and the male allocates its ejaculate resource more prudently during its successive mating with virgin females to maximize its own fitness and the fitness of the female with whom it mated, both being most important to sericulture industry. So, the present study was undertaken and the results revealed fresh and virgin females always prefer to mate with fresh virgin males (84%) and receives high dose of ejaculates leading to higher hatchability than to virgin males of one day old (13.7%) and one day old males with mating experience (2.3%). The ejaculation size (as referred to eupyrene sperm count in the ejaculation) declined significantly over successive mating (r = -0.9931, P < 0.001), so also the male body weight (r = -0.9560, P < 0.001). The quantity of ejaculate passed to female also dramatically declined during aging (r = -0.9982, P < 0.001). It was found that male weight contribute substantially to the quantum of ejaculate (r = -0.9519, P < 0.001), so also higher fecund females receive relatively more ejaculate than the lower group to reach higher reproductive fitness. The life time fecundity was found to be $334{\pm}31$.

Keywords

References

  1. Arnqvist G, Daniclsson I (1999) Postmating sexual selection: the effects of male body size and recovery period on paternity and egg production rate in a water strider. Behav Ecol 10, 358-365. https://doi.org/10.1093/beheco/10.4.358
  2. Bissoondath CJ, Wiklund C (1996) Effect of male mating history and body size on ejaculate mass and quality in two polyandrous butterflies Pieris napi and Pieris rapae (Lepidoptera: Pieridae). Funct Ecol 10, 457-464. https://doi.org/10.2307/2389938
  3. Boggs CL (1990) A general model of the role of male - donated nutrients in female insects reproduction. Am Nat 136, 598-617. https://doi.org/10.1086/285118
  4. Cook PA, Wedell N (1996) Ejculate dynamics in butterflies: a strategy for maximizing fertilization success. Proc R Soc Lond B 263, 1047-1051. https://doi.org/10.1098/rspb.1996.0154
  5. Damiens D, Boivin G (2006) Why do sperm-depleted parasitoid males continue to mate. Behav Ecol 17, 138-143.
  6. Eady PE (1995) Why do male Callosobruchus maculatus beetles inseminate so many sperm. Behav Ecol Sociobiol 36, 25-32. https://doi.org/10.1007/BF00175725
  7. Engqvist L, Sauer KP (2003) Determinants of sperm transfer in the scorpionfly Panorpa cognate: male variation, female condition and copulation duration. J Evo Biol 16, 1196- 1204. https://doi.org/10.1046/j.1420-9101.2003.00613.x
  8. Fischer K, Zimmer K, Wedell N (2009) Correlated responses to selection on female egg size and male reproductive traits in a butterfly. Evol Eco 23, 389-402. https://doi.org/10.1007/s10682-007-9233-1
  9. Flint HM, Kressin EL (1969) Transfer of sperms by irradiated Heliothis virescens (Lepidoptera: Noctuidae) and relationship to fecundity. Can Ento 101, 500-507. https://doi.org/10.4039/Ent101500-5
  10. Fox CW, Mclennan LA, Mousseau TA (1995a) Male body size affects female lifetime reproductive success in a seed beetle. Anim Behav 50, 281-284. https://doi.org/10.1006/anbe.1995.0242
  11. Fox CW, Hichman DL, Raleigh EL, Mousseau TA (1995b) Paternal investment in a seed beetle (Coleoptera: Bruchidae): influence of male size, age, and mating history. Ann Entomol Soc Am 88, 101-103.
  12. Gage MJG (1998) Influence of sex, size and symmetry on ejaculate expenditure in a moth. Behav Ecol 9, 592-597. https://doi.org/10.1093/beheco/9.6.592
  13. Gage AR, Barnard CJ (1996) Male crickets increase sperm number in relation to competition and female size. Behav Ecol Sociobiol 38, 349-353. https://doi.org/10.1007/s002650050251
  14. Gillott C (2003) Male accessory gland secretions: modulators of female reproductive physiology and behavior. Annu Rev Entomol 48, 163-184. https://doi.org/10.1146/annurev.ento.48.091801.112657
  15. Gwynne DT (1984) Sexual selection and sexual differences in Mormon crickets (Orthoptera, Teggigoniidae, Anabrus simplex). Evolution 38, 1011-1022. https://doi.org/10.2307/2408435
  16. Karlsson B (1998) Nuptial gifts, resource budgets, and reproductive output in a polyandrous butterfly. Ecology 79, 2931- 2940. https://doi.org/10.1890/0012-9658(1998)079[2931:NGRBAR]2.0.CO;2
  17. Lauer MJ (1996) Effect of sperm depletion and starvation on female mating behavior in the water strider, Aquarius remigis. Behav Ecol Sociobiol 38, 89-96. https://doi.org/10.1007/s002650050221
  18. Lewis SM (2004) Multiple mating and repeated copulations: effects on male reproductive success in red flour beetles. Anim Behav 67, 799-804. https://doi.org/10.1016/j.anbehav.2003.05.013
  19. Lewis Z, Wedell N (2007) Effects of adult feeding on male mating behavior in the butterfly, Bicyclus anynana (Lepidoptera: Nymphalidae). J Insect Behav 20, 201-213. https://doi.org/10.1007/s10905-007-9075-2
  20. Mallard ST, Barnard CJ (2003) Competition, fluctuating asymmetry and sperm transfer in male gryllid crickets (Gryllus bimaculatus and Gryllodes sigillatus). Behav Ecol Sociobiol 53, 190-197.
  21. Moore PJ, Harris EW, Montrose TW, Levin D, Moore AJ (2004) Constraints on evolution and postcopulatory sexual selection: trade-offs among ejaculate characteristics. Evolution 58, 1773-1780. https://doi.org/10.1111/j.0014-3820.2004.tb00460.x
  22. Ofuya TI (1995) Multiple mating and its consequences in male of Callosobruchus maculatus (F.) (Coleoptera: Bruchidae). J Stored Prod Res 31, 71-75. https://doi.org/10.1016/0022-474X(94)00031-N
  23. Rath SS (2000) Survival probability and fertility in male moths of Antheraea mylitta D. (Lepidoptera: Saturniidae) during aging. Int J Wild Silkmoth & Silk 5, 39-42.
  24. Rath SS, Prasad BC, Thangavelu K (2002) Age related mating schedule in Antheraea mylitta- A strategic approach to increase seed production; in Advances in Indian sericulture research. Dandin SB, Gupta VP (eds.), pp. 412-417, Central Sericultural Research and Training Institute, Mysore, India.
  25. Rath SS, Sinha BRRP, Sinha SS (1997) Age specific changes in reproductive potential and longevity in female moths of Antheraea mylitta D. (Lepidoptera: Saturniidae). Indian J Seric 36, 39-42.
  26. Rath SS, Narian R, Singh MK, Suryanaryana N (2007) Effect of mating delay and mating duration on reproductive performance of Antheraea mylitta. Int J Indust Entomol 14, 113- 119.
  27. Reinhold K, Kurtz J, Engqvist L (2002) Cryptic male choice: sperm allocation strategies when female quality varies. J Evol Biol 15, 201-209. https://doi.org/10.1046/j.1420-9101.2002.00390.x
  28. Ronn JL, Katvala M, Arnqvist G (2008) Interspecific variation in ejaculate variation and associated effects on female fitness in seed beetles. J Evol Biol 21, 461-470. https://doi.org/10.1111/j.1420-9101.2007.01493.x
  29. Savalli UM, Fox CW (1998) Genetic variation in paternal investment in a seed beetle. Anim Behav 56, 953-961. https://doi.org/10.1006/anbe.1998.0853
  30. Savalli UM, Fox CW (1999a) The effect of male mating history on paternal investment, fecundity and female remating in seed beetle Callosobruchus maculatus. Funct Ecol 13, 169-177. https://doi.org/10.1046/j.1365-2435.1999.00287.x
  31. Savalli UM, Fox CW (1999b) The effect of male size, age, and mating behavior on sexual selection in seed beetle Callosobruchus maculatus. Ethol Ecol Evol 11, 49-60. https://doi.org/10.1080/08927014.1999.9522841
  32. Simmons LW, Craig M, Llorens T, Schinzig M, Hoskens D (1993) Bushcricket spermatophore vary in accord with sperm competition and parental investment theory. Proc R Soc Lond B 251, 183-186. https://doi.org/10.1098/rspb.1993.0027
  33. Sokal RR, Rohlf FJ (1995) Biometry. Freeman, New York.
  34. 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. https://doi.org/10.1007/s00265-004-0857-7
  35. Vahed K (1998) The function of nuptial feeding in insectsreview of empirical studies. Biol Rev 73, 43-78. https://doi.org/10.1017/S0006323197005112
  36. Vahed K (2006) Larger ejaculate volumes are associated with a lower degree of polyandry across bushcricket texa. Proc R Soc B 273, 2387-2394. https://doi.org/10.1098/rspb.2006.3593
  37. Wedell N (1992) Protandry and mate assessment in the wart biter Decticus verrucivorus (Orthoptera: Tettigoniidae). Behav Ecol Sociobiol 31, 301-308.
  38. Wedell N, Cook PA (1999) Strategic sperm allocation in the small white butterfly Pieris rapae (Lepidopteraa: Pieridae). Funct Ecol 13, 85-93. https://doi.org/10.1046/j.1365-2435.1999.00286.x
  39. Wedell N, Gage MJG, Parker GA (2002) Sperm competition, male prudence and sperm-limited females. Trends Ecol Evol 17, 313-320. https://doi.org/10.1016/S0169-5347(02)02533-8
  40. Wightman JA (1978) The ecology of Callosobruchus analis (Coleoptera: Bruchine): energetics and energy reserves of the adults. J Anim Ecol 47, 132-142.
  41. Wiklund C, Kaitala A (1995) Sexual selection for large male in a polyandrous butterfly: the effect of body size on male versus female reproductive success in Pieris napi. Behav Ecol 6, 6-13. https://doi.org/10.1093/beheco/6.1.6