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Further Evidence for the Role of Cantharidin in the Mating Behaviour of Blister Beetles (Coleoptera: Meloidae) 원문보기

Integrative biosciences, v.11 no.2, 2007년, pp.141 - 146  

Nikbakhtzadeh, Mahmood Reza (Department of Medical Parasitology & Entomology, Tarbiat Modares University) ,  Hemp, Claudia (Department of Animal Ecology II, University of Bayreuth) ,  Ebrahimi, Babak (Department of Entomology, The Ohio State University)

Abstract AI-Helper 아이콘AI-Helper

Cantharidin is produced by blister beetles (Coleoptera: Meloidae) and smaller oedemerid beetles (Coleopetra: Oedemeridae) and is found in hemolymph and various tissues. The function of cantharidin in the courtship behaviour of meloids had never been fully established. Our studies show a correlation ...

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대상 데이터

  • 5 KV and AC: 40 mA. Ten random areas of the gold coated samples were examined under a Cambridge electron microscope (Cambridge Instruments®) and photograhps were taken with a Nikon Coolpix 995 digital camera. To determine pore density within any frame of a sample, cuticular pores were counted over an area of 24.
  • They were collected manually while sitting on different shrubs of the families Astraceae, Compositeae and Leguminoseae. The insects were transported to the Medical Entomology Department at Tarbiat Modares University, where they were maintained in the laboratory.

데이터처리

  • 9% confidence level. Cuticular pore density in experiments with more than two groups was analysed by a one-way ANOVA as a parametric test, and significant means were separated with Tukey HSD posthoc test at the P < 0.01 and P< 0.001 levels. Whenever cuticular pore density was compared within two groups, student /-test was used to indicate the significance atP = 0.
  • A: Median (± minimum and maximum data, n = 5) titre of cantharidin (ng/mg dry weight) in the male antennal segments of Epicauta nyassensis. Kruskal-Wallis ANOVA test, P< 0.05. B: Mean number (±SD, n = 5) of cuticular pores on the male antennal segments of Epicauta nyassensis per 24.
  • A: Median (± minimum and maximum data, n = 5) titre of cantharidin (ng/mg dry weight) in the male antennal segments of Epicauta nyassensis. Kruskal-Wallis ANOVA test, P< 0.05. B: Mean number (±SD, n = 5) of cuticular pores on the male antennal segments of Epicauta nyassensis per 24.
  • 3. Mean number (±SD, n = 5) of cuticular pores on the scape (A) and pedicel (B) segments of male and female antennae per 24.5 (um2 of SEM visible field, Epicauta nyassensis ***: statistically significant difference using Mann-Whitney U-test, at P< 0.001 level of confidence.
  • 5 um2 of SEM visile field. Rectangles with different letter on top indicate statistically significant differences from each other using ANOVA, Tukey HSD-test at P< 0.001 level of confidence.
  • 5 pm2 of SEM visible field. Rectangles with the same letter on top are not statistically different from each other using ANOVA, Tukey HSD-test at P< 0.05 level of confidence.
  • The data of the internal distribution of cantharidin were analysed by Kruskal-Wallis ANOVA test. If the test showed any significant difference within an experiment, the statistically significant group(s) was determined by a Tukey Kramer test.
  • 001 levels. Whenever cuticular pore density was compared within two groups, student /-test was used to indicate the significance atP = 0.001 level, unless variable P was more than 1 and therefore analysed by Mann- Whitney t7-test. Apart from the Tukey-Kramer test, the statistical analyses were carried out using Statistica Package (Kernel version 5.

이론/모형

  • 001 level, unless variable P was more than 1 and therefore analysed by Mann- Whitney t7-test. Apart from the Tukey-Kramer test, the statistical analyses were carried out using Statistica Package (Kernel version 5.5 A, StatSoft Inc., 1999, USA).
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참고문헌 (24)

  1. Adam H and Czihak G (1964) Arbeitsmethoden, der makroskopischen und mikroskopischen Anatomie. Gustav Fischer Verlag, Stuttgart, 583 pp 

  2. Bin F, Isidoro N and Romani R (1999) Antennal structures of Hymenoptera: Sensilla or glands? Atti dell Accademia Nazionale Italiana di Entomologia Rendiconti XLVII: 251-263 

  3. Carrel JE, Doom JP and McCormick JP (1986) Identification of cantharidin in false blister beetles (Coleoptera. Meloidae) From Florida. J Chem Ecol 12: 741-747 

  4. Carrel JE, McCairel MH, Slagle AJ, Doom JP, Brill J and McCormick JP (1993) Cantharidin production in a blister beetle. Experientia 49: 171-174 

  5. Dettner K. (1997) Inter and intraspecific transfer of toxic insect compound cantharidin. In: Dettner K, Bauer G, and Volkl W (eds), Vertical Food Web Interactions, Springer Verlag, Berlin, pp 115-145 

  6. Dixon AFG, Martin-Smith M and Smith SJ (1963) Isolation of cantharidin from Meloe proscarabeus. Can Pharmacol J 29: 501-503 

  7. Eisner T, Smedley SR, Young DK, Eisner M, Roach B and Meinwald J (1996a) Chemical basis of courtship in a beetle (Neopyrochroa flabellate): Cantharidin as precopulatory enticing agent. Proc Natl Acad Sci 93: 6494-6498 

  8. Eisner T, Smedley SR, Young DK, Eisner M, Roach B and Meinwald J (1996b) Chemical basis of courtship in a beetle (Neopyrochroa flabellate): Cantharidin as nuptial gift. Proc Natl Acad Sci 93: 6499-6503 

  9. Frenzel M, Dettner K, Wirth D, Waibel J and Boland W (1992) Cantharidin analogues and their attractancy for ceratopogonid flies (Diptera: Ceratopogonidae). Experientia 48: 106-111 

  10. Frenzel M and Dettner K (1994) Quantification of cantharidin in canthariphilous Ceratopogonidae (Diptera), Anthomyiidae (Diptera) and cantharidin producing Oedemeridae (Coleoptera). J Chem Ecol 20: 1795-1812 

  11. Gerber GH, Curch NS and Rempel JG (1971) The structure, formation, histochemistry, fate, and formations of the spermatophore of Lytta nuttalli Say (Coleoptera: Meloidae). Can J Zool 49: 1595-1610 

  12. Hemp C, Hemp A and Dettner K (1999) Attraction of the colour beetle species Pallenothriocera rufimembris by cantharidin (Cleridae: Coleoptera). Entomol Gener 24: 115-123 

  13. Holz C, Streil G, Dettner K, Diitemeyer J and Boland W (1994) Intersexual transfer of a toxic terpenoid during copulation and its parental allocation to developmental stages: Quantification of cantharidin in cantharidin-producing oedemerids (Coleoptera: Oedemeridae) and canthariphilous pyrochroids (Coleoptera: Pyrochroidae). Z Naturforsch 49c: 856-864 

  14. Isidoro N, Romani R, Velasquez D, Renthal R, Bin F and Vinson SB (2000) Antennal glands in queen and worker of the fire ant, Solenopsis invicta Buren: first report in female social Aculeata (Hymenoptera: Formicidae). Insectes Soc 47: 236-240 

  15. McCormick JP and Carrel J.E. (1987) Cantharidin biosynthesis and function in meloid beetles. In: Prestwitch GD and Blomquist GJ (eds), Pheromone Biochemistry, Academic Press, Orlando, pp 307-350 

  16. Nikbakhtzadeh MR (2004) Transfer and distribution of cantharidin within selected members of blister beetles (Coleoptera: Meloidae) and its probable importance in sexual behaviour. Dissertation zur Erlangung des Doktorgrades der Naturwissenschaften an der Fakultat fur Biologie, Chemie und Geowissenschaften der Universitat Bayreuth. Bayreuth. 105 pp 

  17. Pinto JD (1974) Courtship behaviour in Linsleya compressicornis and its taxonomic significance. Pan Pac Entomol 50: 1-8 

  18. Pinto JD (1975) Intra and interspecific courtship bahaviour in blister beetles of the Genus Tegrodera (Meloidae). Ann Etomol Soc Am 68: 275-284 

  19. Sch ${'\{u}}$ tz C and Dettner K. (1992) Cantharridin secretions by elytral notches of male Anthicid species (Coleoptera: Anthicidae). Z Naturforsch 47C: 290-299 

  20. Selander RB (1986) Rearing blister beetles. Insecta Mundi 1: 209-220 

  21. Sierra Jr, Woggon WD and Schmidt H. (1976) Transfer of cantharidin during copulation from the adult male to the female Lytta vesicatoria (Spanish flies). Experientia 32: 142-144 

  22. Singh P and Moore RF (1985) Handbook ofInsect Rearing. Vol 1. Elsevier Publications, Amsterdam, 488 pp 

  23. Snead JS and Alcock J (1985) Aggregation formation and assortative mating in two meloid beetles. Evolution 39: 1123-1131 

  24. Wcislo WT (1998) Sexual dimorphism of wasp antenna1 structure in relation to parasitic and non-parasitic behaviour (Hymenoptera: Sphecidae). J Hym Res 7: 178-181 

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