Hostname: page-component-586b7cd67f-dlnhk Total loading time: 0 Render date: 2024-11-28T15:13:36.742Z Has data issue: false hasContentIssue false

Age-related responsiveness of male Bactrocera latifrons (Diptera: Tephritidae) to α-ionol+cade oil relative to age of sexual maturity

Published online by Cambridge University Press:  01 March 2008

Grant T. McQuate*
Affiliation:
USDA-ARS-PBARC, US Pacific Basin Agricultural Research Center, PO Box 4459, Hilo, HI 96720, USA
Aimé H. Bokonon-Ganta
Affiliation:
Department of Plant and Environmental Protection Sciences, College of Tropical Agriculture and Human Resources, University of Hawaii, Honolulu, HI 96822, USA
Eric B. Jang
Affiliation:
USDA-ARS-PBARC, US Pacific Basin Agricultural Research Center, PO Box 4459, Hilo, HI 96720, USA
Russell H. Messing
Affiliation:
Department of Plant and Environmental Protection Sciences, College of Tropical Agriculture and Human Resources, University of Hawaii, Honolulu, HI 96822, USA
*
Get access

Abstract

Bactrocera latifrons (Hendel) is a tephritid fruit fly of primarily Asian distribution that became established in Hawaii in 1983 and recently invaded Africa, being detected in Tanzania in 2006 and in Kenya in 2007. Although males of the majority of dacine fruit flies respond to either methyl eugenol or cuelure, B. latifrons shows little to no response to these lures. Instead, B. latifrons males respond to α-ionol+cade oil. Male age-related responsiveness to α-ionol+cade oil (using wind tunnel bioassays) relative to the age of sexual maturity (assessed through spermathecal dissections) was documented using wild B. latifrons adults. Relative to the peak response observed at day 28, males exceeded 50, 75 and 90% of the peak response at days 7, 14 and 21, respectively. No females younger than 16 days old were mated. Based on a sigmoidal regression of the percentage of inseminated females versus age, 50% of females were inseminated when 18.8 days old, with the percentage increasing to 75 and 90% at 19.8 and 20.9 days of age, respectively. At 24 days and older, 100% of females were mated. The observation that no female B. latifrons were mated by day 14, while 14-day-old male flies achieved over 75% of the peak response to α-ionol+cade oil, suggests that α-ionol+cade oil mass trapping has some potential to remove males from the field before they can contribute to increasing field populations through matings, as previously found with the oriental fruit fly, B. dorsalis (Hendel), and its respective male lure, methyl eugenol. The effectiveness of the removal of males before they mate, though, would be expected to be less for B. latifrons than the male annihilation achieved in the use of methyl eugenol with B. dorsalis because the male lure for B. latifrons is weaker overall.

Type
Research Paper
Copyright
Copyright © ICIPE 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

This article reports the results of research only. Mention of a proprietary product does not constitute an endorsement or a recommendation by the USDA for its use.

References

Carroll, L. E., White, I. M., Friedberg, A., Norrbom, A. L., Dallwitz, M. J. and Thompsan, F. C. (2002) Pest fruit flies of the world. Version: 15th July 2005. http://delta-intkey.com/ffa/www/bac_lati.htm 2002 onwards.Google Scholar
Christenson, L. D. (1963) The male-annihilation technique in the control of fruit flies. Advances in Chemistry Series 41, 431435.Google Scholar
Cunningham, R. T. (1989) Parapheromones, pp. 221230. In World Crop Pests, Vol 3A, Fruit Flies, Their Biology, Natural Enemies and Control (Edited by Robinson, A. S. and Hooper, G.). Elsevier Science Publishers, Amsterdam, The Netherlands.Google Scholar
De Meyer, M., Mohamed, S. and White, I. M. (2007) Invasive fruit fly pests in Africa. http://www.africamuseum.be/fruitfly/AfroAsia.htm.Google Scholar
Drew, R. A. I. (1974) The responses of fruit fly species (Diptera: Tephritidae) in the South Pacific area to male attractants. Journal of the Australian Entomological Society 13, 267270.CrossRefGoogle Scholar
Drew, R. A. I. and Hooper, G. H. S. (1981) The responses of fruit fly species (Diptera: Tephritidae) in Australia to various attractants. Journal of the Australian Entomological Society 20, 201205.CrossRefGoogle Scholar
Fitt, G. P. (1981) The influence of age, nutrition, and time of day on the responsiveness of male Dacus opiliae to the synthetic lure, methyl eugenol. Entomologia Experimentalis et Applicata 30, 8390.CrossRefGoogle Scholar
Flath, R. A., Cunningham, R. T., Liquido, N. J. and McGovern, T. P. (1994) Alpha-ionol as attractant for trapping Bactrocera latifrons (Diptera: Tephritidae). Journal of Economic Entomology 87, 14701476.CrossRefGoogle Scholar
Hanks, J. H. and Wallace, R. E. (1949) Relation of oxygen and temperature in the preservation of tissues by refrigeration. Proceedings of the Society for Experimental Biology and Medicine 71, 196200.CrossRefGoogle ScholarPubMed
Jang, E. B. and Light, D. M. (1991) Behavioral responses of female oriental fruit flies to the odor of papayas at three ripeness stages in a laboratory flight tunnel (Diptera: Tephritidae). Journal of Insect Behavior 4, 751762.CrossRefGoogle Scholar
Jang, E. B., Light, D. M., Binder, R. G., Flath, R. A. and Carvalho, L. A. (1994) Attraction of female Mediterranean fruit flies to the five major components of male-produced pheromone in a laboratory flight tunnel. Journal of Chemical Ecology 20, 920.CrossRefGoogle Scholar
Kendra, P. E., Montgomery, W. S., Epsky, N. D. and Heath, R. R. (2006) Assessment of female reproductive status in Anastrepha suspensa (Diptera: Tephritidae). Florida Entomologist 89, 144151.CrossRefGoogle Scholar
Liquido, N. J., Cunningham, R. T., McQuate, G. T. and Flath, R. A. (2000) Attractants for Bactrocera latifrons (Hendel). U.S. Patent 6,019,964.Google Scholar
Liquido, N. J., Harris, E. J. and Dekker, L. A. (1994) Ecology of Bactrocera latifrons (Diptera: Tephritidae) populations: host plants, natural enemies, distribution, and abundance. Annals of the Entomological Society of America 87, 7184.CrossRefGoogle Scholar
McQuate, G. T. and Peck, S. L. (2001) Enhancement of attraction of α-ionol to male Bactrocera latifrons (Diptera: Tephritidae) by addition of a synergist, cade oil. Journal of Economic Entomology 94, 3946.CrossRefGoogle ScholarPubMed
McQuate, G. T., Keum, Y. -S., Sylva, C. D., Li, Q. X. and Jang, E. B. (2004) Active ingredients in cade oil which synergize the attractiveness of alpha-ionol to male Bactrocera latifrons (Diptera: Tephritidae). Journal of Economic Entomology 97, 862870.CrossRefGoogle Scholar
Metcalf, R. L. (1990) Chemical ecology of Dacinae fruit flies (Diptera: Tephritidae). Journal of Chemical Ecology 83, 10171030.Google Scholar
Mwatawala, M., De Meyer, M., White, I. M., Maerere, A. and Makundi, R. H. (2007) Detection of the solanum fruit fly, Bactrocera latifrons (Hendel) in Tanzania (Dipt., Tephritidae). Journal of Applied Entomology 131, 501503.CrossRefGoogle Scholar
Nakagawa, S., Farias, G. J. and Steiner, L. F. (1970) The response of female Mediterranean fruit flies to male lures in the relative absence of males. Journal of Economic Entomology 63, 227229.CrossRefGoogle Scholar
Nakagawa, S., Steiner, L. F. and Farias, G. J. (1981) Responses of female Mediterranean fruit flies to mature normal males, sterile males, and trimedlure in plastic traps. Journal of Economic Entomology 74, 566567.CrossRefGoogle Scholar
Pereira, R., Teal, P. E. A., Sivinski, J. and Dueben, B. D. (2006) Influence of male presence on sexual maturation in female Caribbean fruit fly, Anastrepha suspensa (Diptera: Tephritidae). Journal of Insect Behavior 19, 3143.CrossRefGoogle Scholar
Pritchard, G. (1970) The ecology of a natural population of Queensland fruit fly, Dacus tryoni. III. The maturation of female flies in relation to temperature. Australian Journal of Zoology 18, 7789.CrossRefGoogle Scholar
SAS Institute Inc. (2002) JMP Statistics and Graphics Guide Version 5. SAS Institute Inc., Cary, North Carolina.Google Scholar
Sokal, R. R. and Rohlf, F. J. (1981) Biometry: The Principles and Practice of Statistics in Biological Research. 2nd edn.W. H. Freeman and Co, San Francisco, California.Google Scholar
SPSS Inc. (2002) SigmaPlot 8.0 User's Guide. SPSS, Inc., Chicago, Illinois.Google Scholar
Steiner, L. F., Mitchell, W. C., Harris, E. J., Kozuma, T. T. and Fujimoto, M. S. (1965) Oriental fruit fly eradication by male annihilation. Journal of Economic Entomology 58, 961964.CrossRefGoogle Scholar
Umeya, K., Sekiguchi, Y. and Ushio, S. I. (1973) The reproductive ability of the oriental fruit fly, Dacus dorsalis Hendel and the response of adults to methyl eugenol. Japanese Journal of Applied Entomology and Zoology 17, 6370.CrossRefGoogle Scholar
Vargas, R. I. and Nishida, T. (1985) Survey for Dacus latifrons (Diptera: Tephritidae). Journal of Economic Entomology 78, 13111314.CrossRefGoogle Scholar
Wee, S.-L. and Tan, K.-H. (2000) Sexual maturity and intraspecific mating success of two sibling species of the Bactrocera dorsalis complex. Entomologia Experimentalis et Applicata 94, 133139.CrossRefGoogle Scholar
Wong, T. T. Y., McInnis, D. O. and Nishimoto, J. I. (1986) Melon fly (Diptera: Tephritidae): sexual maturation rates and mating responses of laboratory-reared and wild flies. Annals of the Entomological Society of America 79, 605609.CrossRefGoogle Scholar
Wong, T. T. Y., McInnis, D. O. and Nishimoto, J. I. (1989) Relationship of sexual maturation rate to response of oriental fruit fly strains (Diptera: Tephritidae) to methyl eugenol. Journal of Chemical Ecology 15, 13991405.CrossRefGoogle ScholarPubMed
Wong, T. T. Y., McInnis, D. O., Ramadan, M. M. and Nishimoto, J. I. (1991) Age-related response of male melon flies Dacus cucurbitae (Diptera: Tephritidae) to cue-lure. Journal of Chemical Ecology 17, 24812487.CrossRefGoogle ScholarPubMed