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Biological Control of Insect Pests: Southeast Asian Prospects - EcoPort

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4.4 Aphis gossypii 71<br />

the posterior <strong>of</strong> the mummy. Aphidiid mummies are round and usually<br />

straw-coloured to brown and in some genera (e.g. Ephedrus) always black<br />

and parchment-like. Aphelinid larvae do not spin cocoons, and their<br />

mummies are usually slender and black (Takada 1992).<br />

The chain <strong>of</strong> events that determines host specificity includes, in<br />

sequence, host habitat finding, host finding, host acceptance by the<br />

parasitoid and host suitability.<br />

The last larval instar <strong>of</strong> some parasitoids provokes their aphid hosts to<br />

move away from the plant on which they were feeding. With Lysiphlebus<br />

fabarum, Ephedrus plagiator and Trioxys angelicae this migration <strong>of</strong> premummies<br />

is connected with diapause (under conditions <strong>of</strong> a short day) or<br />

with aestivation (under conditions <strong>of</strong> a long day). Parasitoids usually emerge<br />

without delay from aphids which become mummies where they have been<br />

feeding (Behrendt 1968).<br />

Starù (1970) provides additional details <strong>of</strong> many <strong>of</strong> the species <strong>of</strong><br />

Aphidiidae that follow below and HŒgvar and H<strong>of</strong>svang (1991) a<br />

comprehensive review <strong>of</strong> their biology, host selection and use in biological<br />

control.<br />

Aphelinus abdominalis (= A. flavipes) Hym.: Aphelinidae<br />

This species is widespread in Europe and is recorded also from USSR, India,<br />

Australia and Israel. It is extensively distributed in India as one <strong>of</strong> the<br />

important parasitoids <strong>of</strong> Myzus persicae and A. gossypii. It becomes active<br />

in late May and is abundant during June and July. The incubation time for<br />

eggs is 2 days and adults emerge after 13 days in September (Ramaseshiah<br />

and Dharmadhikari 1969).<br />

When an Indian strain was liberated in a U.K. glasshouse at 23¡C, one<br />

week after artificially infesting plants with A. gossypii, it was unable to<br />

overtake the pest population because the rate <strong>of</strong> increase <strong>of</strong> the pest was<br />

scarcely affected by the parasitoid. Only when aphid overcrowding occurred<br />

and rate <strong>of</strong> increase was self-limited, did the parasiteÕs rate <strong>of</strong> increase (6 ´ per<br />

week) exceed that <strong>of</strong> the aphid. Reducing the glasshouse temperature to 19¡C<br />

slowed the rate <strong>of</strong> aphid increase and permitted the parasitoids to contain the<br />

pest before severe leaf-distortion occurred. On the other hand, when<br />

parasitoids were present at the time that A. gossypii was introduced, aphid<br />

reproduction was suppressed and effective control resulted (Hussey and<br />

Bravenboer 1971).<br />

Aphelinus gossypii Hym.: Aphelinidae<br />

This species was described from Hawaii and is recorded from Australia,<br />

New Zealand, India, Japan and also from Tonga, where it was reared in<br />

abundance from Aphis gossypii on taro (Colocasia esculenta). It is probably

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