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Biological Control of Insect Pests: Southeast Asian Prospects - EcoPort

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80 <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 />

Comments<br />

Larvae <strong>of</strong> Aphidoletes reportedly feed exclusively as predators on aphids<br />

and are hence more host-specific than many <strong>of</strong> the other predators:<br />

A. aphidimyza is the best known <strong>of</strong> the cecidomyiid predators. Adults<br />

emerge during the day from pupae in the soil. They generally fly between<br />

sunset and sunrise. Orange-coloured eggs are laid singly or in clusters <strong>of</strong> up<br />

to 40, usually on plants near aphid colonies. Females live up to 14 days in the<br />

laboratory and lay about 100 eggs. These hatch after 3Ð4 days and first instar<br />

larvae immediately seek out and attack aphids. They usually attack by<br />

piercing a leg joint or some other joint. A toxin is perhaps injected, since the<br />

aphid is rapidly immobilised before its body fluids are extracted. The<br />

shrivelled bodies <strong>of</strong> some aphids remain attached to the plant by the stylet.<br />

Larval development involves 3 instars and takes 7 to 14 days (Harris 1973).<br />

On the other hand, Herpai (1991) reports 21 days from egg to adult (egg 3<br />

days, larva 8 days, pupa 10 days).<br />

Roberti (1946) gave a figure <strong>of</strong> 60 to 80 Aphis gossypii attacked per day.<br />

Predator larvae usually drop to the soil to pupate. They construct small silk<br />

cocoons in the top few millimetres <strong>of</strong> soil, but occasionally cocoons may be<br />

spun on plants. Larvae pupate within a few days <strong>of</strong> cocoon construction and<br />

adults emerge after 1Ð3 weeks depending upon temperatures. The life cycle<br />

can be completed in about 3 weeks at temperatures above 21¡C (Harris 1973;<br />

Herpai 1991).<br />

Harris (1973) does not record it from A. craccivora. Two<br />

hyperparasitoids <strong>of</strong> A. aphidimyza are known in Africa, the platygasterid<br />

Synopeas rhanis and an unidentified braconid (Harris 1973).<br />

There are many reports in the literature that natural enemies play an<br />

important role in reducing (and probably regulating) the abundance <strong>of</strong> pest<br />

aphids. More than 100 biological control programs have been mounted<br />

against at least 26 aphid species and 48% <strong>of</strong> them have reported success<br />

(HŒgvar and H<strong>of</strong>svang 1991). Twenty three species <strong>of</strong> aphidiid parasitoids<br />

have been used in classical biological control <strong>of</strong> aphids and the parasitoids<br />

became established in 32 out <strong>of</strong> 55 attempts (Greathead 1989). Most pest<br />

aphids are attacked in their native range by many parasitoids and predators<br />

and by a few pathogenic fungi. However, many <strong>of</strong> the natural enemies have<br />

not accompanied their aphid hosts when these have spread into new regions.<br />

Indeed, they may not even be present throughout the presumed native range<br />

<strong>of</strong> their host. Since both the direct and indirect damage caused by aphids<br />

seem to be proportional to their numbers, any reduction is potentially<br />

beneficial. Even in the case <strong>of</strong> virus transmission, where the feeding (or

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