Female mating receptivity inhibited by injection of male-derived extracts in Callosobruchus chinensis

Journal of Insect Physiology

Volumn 54, Issue 2, 2008, Pages 501-507

  Yamane, Takashi ^a   Kimura, Yoshinobu ^b   Katsuhara, Maki ^a   Miyatake, Takahisa ^a  

^a OKAYAMA UNIVERSITY   (Japan)

^b OKAYAMA UNIVERSITY   (Japan)

Author keywords

Accessory gland; Adzuki bean beetle; Remating inhibition; Seminal fluid; Testis

Indexed keywords

BEETLE; FEMALE; INHIBITION; MATING BEHAVIOR; REPRODUCTIVE BIOLOGY;

ANIMAL; ARTICLE; BEETLE; CHEMISTRY; DRUG EFFECT; FEMALE; MALE; MALE GENITAL SYSTEM; PHYSIOLOGY; SEXUAL BEHAVIOR;

ANIMALS; BEETLES; FEMALE; GENITALIA, MALE; MALE; SEXUAL BEHAVIOR, ANIMAL;

BRUCHINAE; CALLOSOBRUCHUS CHINENSIS; COLEOPTERA; VIGNA ANGULARIS;

EID: 38749124714     PISSN: 00221910     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jinsphys.2007.11.009     Document Type: Article

References (55)

1. Aigaki T., Fleischmann I., Chen P.S., and Kubli E. Ectopic expression of sex peptide alters reproductive behavior of female D. melanogaster. Neuron 7 (1991) 557-563
2. Arnqvist G., and Nilsson T. The evolution of polyandry: multiple mating and female fitness in insects. Animal Behaviour 60 (2000) 145-164
3. Arnqvist G., and Rowe L.M. Sexual Conflict (2005), Princeton University Press, Princeton, NJ
4. Bergh J.C., Harris M.O., and Rose S. Factors inducing mated behavior in female Hessian flies (Diptera, Cecidomyiidae). Annals of the Entomological Society of America 85 (1992) 224-233
5. Chapman T., and Davies S.J. Functions and analysis of the seminal fluid proteins of male Drosophila melanogaster fruit flies. Peptides 25 (2004) 1477-1490
6. Chapman T., Liddle L.F., Kalb J.M., Wolfner M.F., and Partridge L. Cost of mating in Drosophila melanogaster females is mediated by male accessory gland products. Nature 373 (1995) 241-244
7. Chapman T., Miyatake T., Smith H., and Partridge L. Interactions of mating, egg production and death rates in Mediterranean fruitfly, Ceratitis capitata females. Proceedings of the Royal Society of London Series B 265 (1998) 1879-1894
8. Chapman T., Bangham J., Vinti G., Seifried B., Lung O., Wolfner M.F., Smith H.K., and Partridge L. The sex peptide of Drosophila melanogaster: female post-mating responses analyzed by using RNA interference. Proceedings of the National Academy of Sciences of the United States of America 100 (2003) 9923-9928
9. Chen P.S. The functional morphology and biochemistry of insect male accessory glands and their secretions. Annual Review of Entomology 29 (1984) 233-255
10. Chen P.S., Stumm-Zollinger E., Aigaki T., Balmer J., Bienz M., and Bohlen P. A male accessory gland peptide that regulates reproductive behaviour of female D. melanogaster. Cell 54 (1988) 291-298
11. Crudgington H.S., and Siva-Jothy M.T. Genital damage, kicking and early death. Nature 407 (2000) 855-856
12. Eady P.E. Why do male Callosobruchus maculatus beetles inseminate so many sperm?. Behavioral Ecology and Sociobiology 36 (1995) 25-32
13. Eberhard W.G. Female Control: Sexual Selection by Cryptic Female Choice (1996), Princeton University Press, Princeton, NJ
14. Gillott C. Arthropoda-insecta. In: Adiyodi K.G., and Adiyodi R.G. (Eds). Reproductive Biology of Invertebrates. Vol. III. Accessory Sex Glands (1988), Wiley, New York 319-471
15. Gillott C. Male accessory gland secretions: modulators of female reproductive physiology and behavior. Annual Review of Entomology 48 (2003) 163-184
16. Gillott C., and Friedel T. Fecundity-enhancing and receptivity-inhibiting substances produced by male insects: a review. In: Adiyodi K.G., and Adiyodi R.G. (Eds). Advances in Invertebrate Reproduction vol. 1 (1977), Peralam-Kenoth, Karivellur 199-218
17. Gromko M.H., Newport M.E.A., and Kortier M.G. Sperm dependence of female receptivity in Drosophila melanogaster. Evolution 38 (1984) 1273-1282
18. Harano T., and Miyatake T. Heritable variation in polyandry in Callosobruchus chinensis. Animal Behaviour 70 (2005) 299-304
19. Harano T., and Miyatake T. Interpopulation variation in female remating is attributable to female and male effects in Callosobruchus chinensis. Journal of Ethology 25 (2007) 49-55
20. Harano T., Yasui Y., and Miyatake T. Direct effects of polyandry on female fitness in Callosobruchus chinensis. Animal Behaviour 71 (2006) 539-548
21. Harmer A.M.T., Radhakrishnana P., and Taylor P.W. Remating inhibition in female Queensland fruit flies: effects and correlates of sperm storage. Journal of Insect Physiology 52 (2006) 179-186
22. Hihara F. Effects of the male accessory gland secretion on oviposition and remating in females of Drosophila melanogaster. Zoological Magazine 90 (1981) 307-316
23. Hozumi N., and Miyatake T. Body-size dependent difference in death-feigning behavior of adult Callosobruchus chinensis. Journal of Insect Behavior 18 (2005) 557-566
24. Huignard J. Influence de la copulation sur la fonction reproductrice femelle chez Acanthoscelides obtectus. I: copulation et spermatophore. Annales des Sciences Naturelles 16 (1974) 361-434
25. Huignard J. Influence de la copulation sur la fonction reproductrice femelle chez Acanthoscelides obtectus. II: analyse expérimentale. Annales des Sciences Naturelles 17 (1975) 1-66
26. Huignard J., Quesneau-Thierry A., and Barbier M. Isolement, action biologique et evolution des substances paragoniales contenues dans le spermatophore d' Acanthoscelides obtectus Say. Journal of Insect Physiology 23 (1977) 351-357
27. Kalb J.M., DiBenedetto A.J., and Wolfner M.F. Probing the function of Drosophila melanogaster accessory glands by directed cell ablation. Proceedings of the National Academy of Sciences of the United States of America 90 (1993) 8093-8099
28. Kuba H., and Itô Y. Remating inhibition in the melon fly, Bactrocera (=Dacus) cucurbitae (Diptera: Tephritidae): copulation with spermless males inhibits female remating. Journal of Ethology 11 (1993) 23-28
29. Kubli E. Sex peptides: seminal peptides of the Drosophila male. Cellular and Molecular Life Sciences 60 (2003) 1689-1704
30. Letsinger J.T., and Gromko M.H. The role of sperm numbers in sperm competition and female remating in Drosophila melanogaster. Genetica 66 (1985) 195-202
31. Liu H., and Kubli E. Sex-peptide is the molecular basis of the sperm effect in Drosophila melanogaster. Proceedings of the National Academy of Sciences of the United States of America 100 (2003) 9929-9933
32. Manning A. A sperm factor affecting the receptivity of Drosophila melanogaster females. Nature 194 (1962) 252-253
33. Manning A. The control of sexual receptivity in female Drosophila. Animal Behaviour 15 (1967) 239-250
34. Miyatake T., and Matsumura F. Intra-specific variation in female remating in Callosobruchus chinensis and C. maculatus. Journal of Insect Physiology 50 (2004) 403-408
35. Miyatake T., Chapman T., and Partridge L. Mating-induced inhibition of remating in female Mediterranean fruit flies Ceratitis capitata. Journal of Insect Physiology 45 (1999) 1021-1028
36. Mossinson S., and Yuval B. Regulation of sexual receptivity of female Mediterranean fruit flies: old hypotheses revisited and a new synthesis proposed. Journal of Insect Physiology 49 (2003) 561-567
37. Peng J., Chen S., Büsser S., Liu H., Honegger T., and Kubli E. Gradual release of sperm bound sex-peptide controls female postmating behavior in Drosophila. Current Biology 15 (2005) 207-213
38. Radharkrishnan P., and Taylor P.W. Seminal fluids mediate sexual inhibition and short copula duration in mated female Queensland fruit flies. Journal of Insect Physiology 53 (2007) 741-745
39. Rice W.R. Analyzing tables of statistical tests. Evolution 43 (1989) 223-225
40. Ridley M. Mating frequency and fecundity in insects. Biological Reviews 63 (1988) 509-549
41. Rönn J., Katvala M., and Arnqvist G. The costs of mating and egg production in Callosobruchus seed beetles. Animal Behaviour 72 (2006) 335-342
42. Rönn J., Katvala M., and Arnqvist G. Coevolution between harmful male genitalia and female resistance in seed beetles. Proceedings of the National Academy of Sciences of the United States of America 104 (2007) 10921-10925
43. Sakurai, G., Kasuya, E., in press. Different female mating rates in different populations do not reflect the benefits the females gain from polyandry in the adzuki bean beetle. Journal of Ethology.
44. SAS Institute. StatView 5.0J (1998), SAS Institute Inc., Cary, NC
45. Savalli U.M., and Fox C.W. Genetic variation in paternal investment in a seed beetle. Animal Behaviour 56 (1998) 953-961
46. Scott D. The timing of the sperm effect on female Drosophila melanogaster receptivity. Animal Behaviour 35 (1987) 142-149
47. Simmons L.W. Sperm Competition and its Evolutionary Consequences in the Insects (2001), Princeton University Press, Princeton, NJ
48. Thornhill R., and Alcock J. The Evolution of Insect Mating Systems (1983), Harvard University Press, Cambridge, MA
49. Utida, S., 1941. Studies on experimental population of the azuki bean weevil Callosobruchus chinensis (L.). I. The effect of population density on the progeny population. Memoirs College Agriculture, Kyoto Imperial University 48, 1-31.
50. Wang M., and Horng S. Egg dumping and life history strategy of Callosobruchus maculatus. Physiological Entomology 29 (2004) 26-31
51. Wedell N. Female receptivity in butterflies and moths. The Journal of Experimental Biology 208 (2005) 3433-3440
52. Wigby S., and Chapman T. Sex peptide causes mating costs in female Drosophila melanogaster. Current Biology 15 (2005) 316-321
53. Wolfner M.F. Tokens of love: functions and regulation of Drosophila male accessory gland products. Insect Biochemistry and Molecular Biology 27 (1997) 179-192
54. Yamane, T., Miyatake, T., in press. Strategic ejaculation and level of polyandry in Callosobruchus chinensis (Coleoptera: Bruchidae). Journal of Ethology.
55. Yanagi S., and Miyatake T. Costs of mating and egg production in female Callosobruchus chinensis. Journal of Insect Physiology 49 (2003) 823-827