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Biological Control of Insect Pests: Southeast Asian Prospects - EcoPort

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76 <strong>Biological</strong> <strong>Control</strong> <strong>of</strong> <strong>Insect</strong> <strong>Pests</strong>: <strong>Southeast</strong> <strong>Asian</strong> <strong>Prospects</strong><br />

temperature and humidity on the development <strong>of</strong> L. fabarum in A. gossypii<br />

and A. craccivora has been reported by Davletshina and Gomolitskia (1975)<br />

and methods for its mass production by Tregubenko and Popushoi (1987).<br />

Lysiphlebus testaceipes Hym.: Aphidiidae<br />

This parasitoid has a natural range extending from North America through<br />

Central America to the northern parts <strong>of</strong> South America. It is now known<br />

also from Hawaii, Australia, Europe and East Africa. It is the commonest<br />

native parasitoid <strong>of</strong> aphids in Mexico (Starù and Remaudi re 1982). It has a<br />

very wide host range, having been reported from at least 79 aphid species (32<br />

in the genus Aphis) in 32 genera (Carver 1984).<br />

Oviposition generally occurs in the abdomen <strong>of</strong> half grown and<br />

unparasitised hosts and, when hosts are scarce, more than one egg may be<br />

deposited (Sekhar 1957). Up to 254 eggs may be laid. It is heavily attacked<br />

by hyperparasitoids in its natural range (eg. 6 species when attacking Aphis<br />

gossypii (Schlinger and Hall 1960) or 7 species (Oatman et al. 1983b)).<br />

L. testaceipes was present in Australia (New South Wales and South<br />

Australia) prior to its introduction as a biological control agent and attacked<br />

an indigenous aphid Aphis acaenovinae (Starù and Carver 1979).<br />

There are many examples to demonstrate that L. testaceipes consists <strong>of</strong><br />

biotypes. Thus, Californian L. testaceipes is unable to complete its<br />

development on Aphis spiraecola, whereas a Cuban strain does so<br />

successfully. The Californian strain did not attack Aphis nerii after<br />

introduction to Hawaii, although a Mexican strain subsequently introduced<br />

did so (Starù 1970). Then again, the biotype from A. craccivora on Robinia<br />

pseudacacia does not parasitise this same aphid on Phaseolus vulgaris;<br />

another biotype prefers A. gossypii on squash to this same aphid on hibiscus<br />

(Sekhar 1960; Tremblay and Barbagallo 1982). The effectiveness <strong>of</strong><br />

Lysiphlebus testaceipes as a parasitoid on A. gossypii is thus significantly<br />

affected by the host plant on which the aphid is feeding (Steinberg et al.<br />

1993).<br />

L. testaceipes is reported to attack A. gossypii in Cuba (Starù 1981),<br />

Mexico (Starù and Remaudi re 1982) and, after introduction to Europe, in<br />

Spain, France and Italy. In Europe it now attacks more than 26 aphid species<br />

including A. craccivora and A. gossypii, <strong>of</strong>ten with high levels <strong>of</strong><br />

parasitisation (Starù et al. 1988a,b,c).<br />

Lysiphlebus testaceipes was successfully introduced in 1923 from<br />

California to Hawaii for the biological control <strong>of</strong> aphids, including Aphis<br />

craccivora and A. gossypii. It soon spread widely throughout the islands,<br />

attacking these and other aphid species. In 1965, a further introduction from<br />

Mexico was made to control the oleander aphid Aphis nerii which had<br />

previously escaped attack. By 1927 several hyperparasitoids were recorded

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