Reduced female mating receptivity and activation of oviposition in two Callosobruchus species due to injection of biogenic amines

Journal of Insect Physiology

Volumn 56, Issue 3, 2010, Pages 271-276

  Yamane, Takashi ^a   Miyatake, Takahisa ^a  

^a OKAYAMA UNIVERSITY   (Japan)

Author keywords

Biogenic amine; Callosobruchus; Oviposition; Receptivity; Tyramine

Indexed keywords

BIOGENIC AMINE;

BEETLE; BEHAVIORAL ECOLOGY; BIOGENIC MATERIAL; DEVELOPMENTAL BIOLOGY; EGG PRODUCTION; MATING BEHAVIOR; MODEL TEST; OVIPOSITION; REPRODUCTIVE COST; SPECIES DIVERSITY; TOXIC MATERIAL;

ANIMAL; ARTICLE; BEETLE; DRUG EFFECT; EGG LAYING; FEMALE; MALE; PHYSIOLOGY; SEXUAL BEHAVIOR;

ANIMALS; BEETLES; BIOGENIC AMINES; FEMALE; MALE; OVIPOSITION; SEXUAL BEHAVIOR, ANIMAL;

BRUCHINAE; CALLOSOBRUCHUS; CALLOSOBRUCHUS CHINENSIS; CALLOSOBRUCHUS MACULATUS; COLEOPTERA; HEXAPODA;

EID: 75749151969     PISSN: 00221910     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jinsphys.2009.10.011     Document Type: Article

References (72)

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. Blenau W., and Baumann A. Molecular and pharmacological properties of insect biogenic amine receptors: lessons from Drosophila melanogaster and Apis mellifera. Archives of Insect Biochemistry and Physiology 48 (2001) 13-38
3. Boucher L., and Huingnard J. Transfer of male secretions from the spermatophore to the female insect in Caryedon serratus. Journal of Insect Physiology 33 (1987) 55-63
4. Borovsky D., Carlson D.A., Hancock R.G., Rembold H., and Vanhandel E. De novo biosynthesis of juvenile hormone III and hormone I by the accessory glands of the male mosquito. Insect Biochemistry and Molecular Biology 24 (1994) 437-444
5. Chen P.S. The functional morphology and biochemistry of insect male accessory glands and their secretions. Annual Review of Entomology 29 (1984) 233-255
6. 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
7. Chapman T., Miyatake T., Smith H.K., and Partridge L. Interactions of mating, egg production and death rates in Mediterranean fruit fly, Ceratitis capitata females. Proceedings of the Royal Society of London Series B 265 (1998) 1879-1894
8. Clark J., and Lange A.B. The association of serotonin with the spermatheca of the locust Locusta migratoria. Biogenic Amines 17 (2002) 43-62
9. Clark J., and Lange A.B. Octopamine modulates spermathecal muscle contractions in Locusta migratoria. Journal of Comparative Physiology A 189 (2003) 105-114
10. Cole S.H., Carney G.I., McClung C.A., Willard S.S., Taylor B.J., and Hirsh J. Two functional but non-complementing Drosophila tyrosine decarboxylase genes: distinct roles for neural tyramine and octopamine in female fertility. The Journal of Biological Chemistry 280 (2005) 14948-14955
11. Crudgington H.S., and Siva-Jothy M.T. Genital damage, kicking and early death. Nature 407 (2000) 855-856
12. da Silva R., and Lange A.B. Tyramine as a possible neurotransmitter/neuromodulator at the spermatheca of the African migratory locust, Locusta migratoria. Journal of Insect Physiology 54 (2008) 1306-1313
13. Destephano D.B., and Brady U.N. Prostaglandin and prostaglandin synthetase in the cricket, Acheta demesticus. Journal of Insect Physiology 23 (1977) 905-911
14. Dombroski T.C.D., Simoes Z.J.P., and Bitondi M.M.G. Dietary dopamine causes ovary activation in queenless Apis mellifera workers. Apidologie 34 (2003) 281-289
15. Donini A., and Lange A.B. Evidence for a possible neurotransmitter/neuromodulator role of tyramine on the locust oviducts. Journal of Insect Physiology 50 (2004) 351-361
16. Eady P.E. Why do male Callosobruchus maculatus beetles inseminate so many sperm?. Behavioral Ecology and Sociobiology 36 (1995) 25-32
17. Eady P.E., Wilson N., and Jackson M. Copulating with multiple mates enhances female fecundity but not egg-to-adult survival in the bruchid beetle Callosobruchus maculatus. Evolution 54 (2000) 2161-2165
18. Eady P.E., Roguman-Jones P., and Brown D.V. Prior oviposition, female receptivity and last-male sperm precedence in the cosmopolitan pest Callosobruchus maculatus (Coleoptera: Bruchidae). Animal Behaviour 67 (2004) 559-565
19. Eady P.E., Hamilton L., and Lyons R.E. Copulation, genital damage and early death in Callosobruchus maculatus. Proceedings of the Royal Society of London Series B 274 (2007) 247-252
20. Eberhard W.G. Female Control: Sexual Selection by Cryptic Female Choice (1996), Princeton University Press, Princeton, NJ
21. Edvardsson M., and Tregenza T. Why do male Callosobruchus maculatus harm their mates?. Behavioral Ecology 16 (2005) 788-793
22. Evans P.D. Biogenic amines in the insect nervous system. Advances in Insect Physiology 15 (1980) 317-473
23. Fahrbach S.E., and Mesce K.A. "Neuroethoendocrinology": integration of field and laboratory studies in insect neuroendocrinology. Hormones and Behavior 48 (2005) 352-359
24. Fan Y., Rafaeli A., Moshitzky P., Kubli E., Choffat Y., and Applebaum S.W. Common functional elements of Drosophila melanogaster sex peptide stimulates juvenile hormone biosynthesis and depresses sex pheromone production in Helicoverpa armigera. Insect Biochemistry and Molecular Biology 30 (2000) 805-812
25. Gillott C. Arthropoda-Insecta. In: Adiyodi K.G., and Adiyodi R.G. (Eds). In Reproductive Biology of Invertebrates, Accessory Sex Glands vol. III (1988), Wiley, New York 319-471
26. Gillott C. Male accessory gland secretions: modulators of female reproductive physiology and behavior. Annual Review of Entomology 48 (2003) 163-184
27. Harano T., and Miyatake T. Heritable variation in polyandry in Callosobruchus chinensis. Animal Behaviour 70 (2005) 299-304
28. Harano T., Yasui Y., and Miyatake T. Direct effects of polyandry on female fitness in Callosobruchus chinensis. Animal Behaviour 71 (2006) 539-548
29. Hirashima A. Regulation of bombykol production by tyramine and octopamine in Bombyx mori. Journal of Pesticide Science 33 (2008) 21-23
30. Huignard J. Influence de la copulation sur la fonction reproductrice femalle chez Acanthoscelides obtectus (Coléoptère Bruchidae). I. Copulation et spermatophore. Annales des Sciences Naturelles, Zoologie, Paris 16 (1974) 361-434
31. Huignard J. Influence de la copulation sur la fonction reproductrice femalle chez Acanthoscelides obtectus (Coléoptère Bruchidae). II. Analyse expérimentale. Annales des Sciences Naturelles, Zoologie, Paris 17 (1975) 1-66
32. Huingnard J. Transfer and fate of male secretions deposited in the spermatophore of females of Acanthoscelides obtectus Say (Coleoptere Bruchidae). Journal of Insect Physiology 29 (1983) 55-63
33. Huignard J., Quesneau-Thierry A., and Barbier M. Isoloment, action biologique et evolution des substances paragoniales contenus dans le spermatophore d' Acanthoscelides obtectus (Coléoptère Bruchidae). Journal of Insect Physiology 23 (1977) 351-357
34. Kubli E. Sex peptides: seminal peptides of the Drosophila male. Cellular and Molecular Life Sciences 60 (2003) 1689-1704
35. Libersat F., and Pflüger H.J. Monoamines and the orchestration of behavior. BioScience 54 (2004) 17-25
36. 2 on oviposition in Teleogryllus commodus. Entomologia Experimentalis et Applicata 25 (1979) 107-119
37. Loher W., Ganjian I., Kudo I., Stanley-Samuelson D.W., and Tobe S.S. Prostaglandins: their role in egg-laying in the cricket Teleogryllus commodus. Proceedings of the National Academy of Sciences USA 78 (1981) 7835-7838
38. 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
39. 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
40. Monastirioti M. Distinct octopamine cell population residing in the CNS abdominal ganglion controls ovulation in Drosophila melanogaster. Developmental Biology 264 (2003) 38-49
41. Monastrioti M., Linn C.E., and White K. Characterization of Drosophila tyramine β-hydroxylase gene and isolation of mutant flies lacking octopamine. Journal of Neuroscience 16 (1996) 3900-3911
42. Moshitzky P., Fleischmann I., Chaimov N., Saudan P., Klauser S., and Kubli E. SP activates juvenile hormone biosynthesis in the Drosophila melanogaster corpus allatum. Archives of Insect Biochemistry and Physiology 32 (1996) 363-374
43. Neckameyer W.S., and Weinstein J.S. Stress affects dopaminergic signaling pathways in Drosophila melanogaster. Stress-The International Journal of the Biology of the Stress 8 (2005) 117-131
44. Park Y.I., Shy S., Ramaswamy S.B., and Srinivasan A. Mating in Heliothis virescens: transfer of juvenile hormone during copulation by male to female and stimulation of biosynthesis of endogenous juvenile hormone. Archives of Insect Biochemistry and Physiology 38 (1998) 100-107
45. Quinn G., and Keough M.J. Experimental Design and Data Analysis for Biologist (2002), Cambridge University Press, Cambridge 537 pp
46. Rice W.R. Analyzing tables of statistical tests. Evolution 43 (1989) 223-225
47. Roeder T. Tyramine and octopamine: ruling behavior and metabolism. Annual Review of Entomology 50 (2005) 447-477
48. Rönn J., Katvala M., and Arnqvist G. The costs of mating and egg production in Callosobruchus seed beetles. Animal Behaviour 72 (2006) 335-342
49. Sakurai G., and Kasuya E. 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 26 (2008) 93-98
50. SAS Institute. StatView 5.0J (1998), SAS Institute Inc., Cary, NC
51. SAS Institute. JMP 6.0.3. (2005), SAS Institute Inc., Cary, NC
52. Sasaki K., and Harano K. Potential effects of tyramine on the transition to reproductive workers in honeybees (Apis mellifera L.). Physiological Entomology 32 (2007) 194-198
53. Sasaki K., Yamasaki K., Tsuchida K., and Nagao T. Gonadotropic effects of dopamine in isolated workers of the primitively eusocial wasp, Polistes chinensis. Naturwissenschaften 96 (2009) 625-629
54. Savalli U.M., and Fox C.W. Genetic variation in paternal investment in a seed beetle. Animal Behaviour 56 (1998) 953-961
55. Savalli U.M., and Fox C.W. The effect of male mating history on paternal investment, fecundity and female remating in the seed beetle Callosobruchus maculatus. Functional Ecology 13 (1999) 169-177
56. Sherwood D.R., and Levine E. Copulation and its duration affects female weight, oviposition, hatching patterns, and ovarian development in the western corn rootworm (Coleoptera: Chrysomelidae). Journal of Economic Entomology 86 (1993) 1664-1671
57. Simmons L.W. Sperm Competition and its Evolutionary Consequences in the Insects (2001), Princeton University Press, Princeton
58. Stanley-Samuelson D.W., and Loher W. Arachidonic and other long-chain polyunsaturated fatty acids in spermatophores and spermathecae of Teleogryllus commodus: significance in prostaglandin-mediated reproductive behavior. Journal of Insect Physiology 29 (1983) 41-45
59. Stanley-Samuelson D.W., Peloquin J.J., and Loher W. Egg-laying in response to prostaglandin injection in Teleogryllus commodus. Physiological Entmology 11 (1986) 213-219
60. Thompson G.J., Yockey H., Lim J., and Oldroyd B.P. Experimental manipulation of ovary activation and gene expression in honey bee (Apis mellifera) queens and workers: testing hypotheses of reproductive regulation. Journal of Experimental Zoology 307A (2007) 600-610
61. Tseng H.F., Yang R.L., Lin C., and Horng S.B. The function of multiple mating in oviposition and egg maturation in the seed beetle Callosobruchus maculatus. Physiological Entomology 32 (2007) 150-156
62. Utida S. Studies on Experimental Population of the Azuki Bean Weevil Callosobruchus chinensis (L.). I. The Effect of Population Density on the Progeny Population vol. 48 (1941), Memoris College Agriculture, Kyoto Imperial University 1-31 pp.
63. Utida S. Studies on Experimental Population of the Azuki Bean Weevil Callosobruchus chinensis (L.). IV. Analysis of Density Effect with Respect to Fecundity and Fertility of Eggs vol. 51 (1941), Memoris College Agriculture, Kyoto Imperial University 1-26 pp.
64. Wang M., and Horng S. Egg dumping and life history strategy of Callosobruchus maculatus. Physiological Entomology 29 (2004) 26-31
65. Webster R.P., and Cardé R.T. The effects of mating, exogenous juvenile hormone and juvenile hormone analogue titre, calling and oviposition in the omnivorous leafroller moth (Platynota stultana). Journal of Insect Physiology 30 (1984) 113-118
66. Wedell N. Female receptivity in butterflies and moths. The Journal of Experimental Biology 208 (2005) 3433-3440
67. Wilson N., Tufton T.J., and Eady P.E. The effect of single, double, and triple mating on the lifetime fecundity of Callosobruchus analis and Callosobruchus maculatus (Coleoptera: Bruchidae). Journal of Insect Behavior 12 (1999) 295-306
68. Wolfner M.F. Tokens of love: Functions and regulation of Drosophila male accessory gland products. Insect Biochemistry and Molecular Biology 27 (1997) 179-192
69. Yamaja Setty B.N., and Ramaiah T.R. Effect of prostaglandins and inhibitors of prostaglandin biosynthesis on oviposition in the silkmoth Bombyx mori. Indian Journal of Experimental Biology 13 (1980) 539-541
70. Yamane T., Kimura Y., Katsuhara M., and Miyatake T. Female mating receptivity inhibited by injection of male-derived extracts in Callosobruchus chinensis. Journal of Insect Physiology 54 (2008) 501-507
71. Yamane T., Kimura Y., and Miyatake T. Female mating receptivity after injection of male-derived extracts in Callosobruchus maculatus. Journal of Insect Physiology 54 (2008) 1522-1527
72. Yanagi S., and Miyatake T. Costs of mating and egg production in female Callosobruchus chinensis. Journal of Insect Physiology 49 (2003) 823-827