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Biological Control of Insect Pests: Southeast Asian Prospects - EcoPort

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70 <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 />

VIETNAM<br />

A. gossypii was one <strong>of</strong> four aphids surveyed for parasitoids by Starù and<br />

Zelenù (1983), but the number <strong>of</strong> aphidiid species found (2) was surprisingly<br />

low. Lipolexis scutellaris was commoner than Lysiphlebia mirzai. The<br />

former parasitises a number <strong>of</strong> other Aphis species, including Aphis<br />

spiraecola (= A. citricola), A. craccivora and A. nerii. Some unidentified<br />

aphelinid parasitoids were also present.<br />

Starù and Zelenù (1983) suggest that Lipolexis scutellaris may be a<br />

valuable species for transfer elsewhere and also that Vietnam would benefit<br />

from the introduction <strong>of</strong> additional parasitoid species.<br />

The major parasitoid species<br />

General features <strong>of</strong> the Aphidiidae<br />

Different populations <strong>of</strong> many Aphidiidae have differing biological<br />

properties and are <strong>of</strong>ten known as biotypes, i.e. contrasting groups, each<br />

consisting <strong>of</strong> individuals <strong>of</strong> the same species. Biotypes are recognised by<br />

biological function rather than morphology and consist <strong>of</strong> those individuals<br />

that behave similarly as far as our immediate interests are concerned<br />

(Mackauer and Way 1976).<br />

The members <strong>of</strong> this family attack aphids exclusively and are probably<br />

the most commonly observed cause <strong>of</strong> aphid mortality in the field. In<br />

Europe, many, if not all, aphid colonies come to include some mummified<br />

individuals (i.e. dead aphids containing a fully-grown parasitoid larva or<br />

pupa) (Starù 1970). Aphidiidae may hibernate as prepupae within host<br />

mummies. All are solitary endoparasitoids. All aphid stages are attacked<br />

except the eggs, but alatae are least <strong>of</strong>ten attacked. The parasitoid egg is<br />

usually inserted anywhere in the aphid abdomen. The preferred aphid larval<br />

instar varies with the parasitoid species, but younger instars are usually<br />

chosen. If adult aphids are parasitised the parasitoid larva may not complete<br />

its development before the insect dies, so that the parasitoid perishes also.<br />

Oviposition into an aphid does not ensure the successful development <strong>of</strong> a<br />

parasitoid, since the host may be unsuitable or it may already be parasitised:<br />

defence and immune responses are common. However parasitised hosts are<br />

usually distinguished by the parasitoid and receive no further eggs.<br />

If an aphid is parasitised during the last larval instar, a mummy is formed<br />

after it moults to the adult. The first and second instars <strong>of</strong> aphidiid<br />

parasitoids generally feed on haemolymph, but the last instar attacks the<br />

alimentary canal and other organs, ultimately killing its host. The parasitoid<br />

larva then spins a cocoon and pupates inside the empty aphid skin. The adult<br />

emerges through a small circular hole usually cut dorsally or apically near

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