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The native hyperparasitoid complex of the invasive aphid parasitoid Lysiphlebus testaceipes (Hymenoptera: Braconidae: Aphidiinae) in Benin, West Africa

Published online by Cambridge University Press:  04 February 2014

T. Hofsvang*
Affiliation:
Plant Health and Plant Protection Division, Norwegian Institute for Agricultural and Environmental Research (Bioforsk), Høgskoleveien 7, N-1432Ås, Norway
I. Godonou
Affiliation:
International Institute of Tropical Agriculture (IITA), IITA-Benin, 08 BP 0932, Tri Postal, Cotonou, Benin
G.T. Tepa-Yotto
Affiliation:
Plant Health and Plant Protection Division, Norwegian Institute for Agricultural and Environmental Research (Bioforsk), Høgskoleveien 7, N-1432Ås, Norway International Institute of Tropical Agriculture (IITA), IITA-Benin, 08 BP 0932, Tri Postal, Cotonou, Benin
M.-G. Sæthre
Affiliation:
Plant Health and Plant Protection Division, Norwegian Institute for Agricultural and Environmental Research (Bioforsk), Høgskoleveien 7, N-1432Ås, Norway
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Abstract

A 2-year study in a vegetable-growing area (Tori, Hla Avamé) in Benin has shown that the invasive aphid parasitoid Lysiphlebus testaceipes (Cresson) was attacked by three species of native hyperparasitoids. On several occasions, hyperparasitoids emerged from more than 90% of the mummies collected. The dominating hyperparasitoid was Syrphophagus africanus (Gahan). Two species in the genera Pachyneuron (Pteromalidae) and Aphanogmus (Ceraphronidae), respectively, were also recorded as hyperparasitoids. Charipinae hyperparasitoids were lacking. The only aphid host present at Hla Avamé was Aphis gossypii Glover, a dominating species in vegetable agroecosystems in Benin.

Type
Research Papers
Copyright
Copyright © ICIPE 2014 

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References

Brodeur, J. (2000) Host specificity and trophic relationships of hyperparasitoids, pp. 163183. In Parasitoid Population Biology (edited by Hochberg, M. E. and Ives, A. R.). Princeton University Press, Princeton, New Jersey.CrossRefGoogle Scholar
Brodeur, J. and Rosenheim, J. A. (2000) Intraguild interactions in aphid parasitoids. Entomologia Experimentalis et Applicata 97, 93108.CrossRefGoogle Scholar
Farrell, J. A. and Stufkens, M. J. (1990) The impact of Aphidius rhopalosiphum (Hymenoptera: Aphidiidae) on populations of the rose grain aphid (Metopolophium dirhodum) (Hemiptera: Aphididae) on cereals in Canterbury, New Zealand. Bulletin of Entomological Research 80, 377383.CrossRefGoogle Scholar
Ganyo, K. K., Tounou, A. K., Agboton, C., Dannon, E. A., Pittendrigh, B. R. and Tamò, M. (2012) Interactions between the aphid parasitoid Lysiphlebus testaceipes (Hymenoptera: Aphidiidae) and its hyperparasitoid Syrphophagus africanus (Hymenoptera: Encyrtidae). International Journal of Tropical Insect Science 32, 4555.CrossRefGoogle Scholar
Hougardy, E. and Mills, N. J. (2009) Factors influencing the abundance of Trioxys pallidus, a successful introduced biological control agent of walnut aphid in California. Biological Control 48, 2229.CrossRefGoogle Scholar
Kanuck, M. J. and Sullivan, D. J. (1992) Ovipositional behavior and larval development of Aphidencyrtus aphidivorus (Hymenoptera: Encyrtidae), an aphid hyperparasitoid. Journal of the New York Entomological Society 100, 527532.Google Scholar
Noyes, J. S. (2011) Universal Chalcidoidea Database. World Wide Web electronic publication. Available at:www.nhm.ac.uk/entomology/chalcidoids (accessed accessed 11 January 2012).Google Scholar
Ragsdale, D. W., Landis, D. A., Brodeur, J., Heimpel, G. E. and Desneux, N. (2011) Ecology and management of the soybean aphid in North America. Annual Review of Entomology 56, 375399.CrossRefGoogle ScholarPubMed
Sanders, D. and van Veen, F. J. F. (2010) The impact of an ant–aphid mutualism on the functional composition of the secondary parasitoid community. Ecological Entomology 35, 704710.CrossRefGoogle Scholar
Sæthre, M.-G., Godonou, I., Hofsvang, T., Tepa-Yotto, G. T. and James, B. (2011) Aphids and their natural enemies in vegetable agroecosystems in Benin. International Journal of Tropical Insect Science 31, 103117.CrossRefGoogle Scholar
Schellhorn, N. A., Kuhman, T. R., Olson, A. C. and Ives, A. R. (2002) Competition between native and introduced parasitoids of aphids: nontarget effects and biological control. Ecology 83, 27452757.CrossRefGoogle Scholar
Schooler, S. S., De Barro, P. and Ives, A. R. (2011) The potential for hyperparasitism to compromise biological control: why don't hyperparasitoids drive their primary parasitoid hosts extinct? Biological Control 58, 167173.CrossRefGoogle Scholar
Starý, P. (1988) Aphelinidae, pp. 185188. In Aphids: Their Biology, Natural Enemies and Control Volume B (edited by Minks, A. K. and Harrewijn, P.). Elsevier, Amsterdam.Google Scholar
Starý, P., Lumbierres, B. and Pons, X. (2004) Opportunistic changes in the host range of Lysiphlebus testaceipes (Cr.), an exotic aphid parasitoid expanding in the Iberian Peninsula. Journal of Pest Science 77, 139144.CrossRefGoogle Scholar
Sullivan, D. J. and Völkl, W. (1999) Hyperparasitism: multitrophic ecology and behaviour. Annual Review of Entomology 44, 291315.CrossRefGoogle Scholar
Tepa-Yotto, T. G. (2013) Lysiphlebus testaceipes (Cresson) (Hymenoptera: Braconidae, Aphidiinae) in Benin: its potential as a biological control agent for integrated aphid management in vegetable systems. Thesis number 2013: 41. Norwegian University of Life Sciences (UMB), Ås, Norway.Google Scholar