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Biological Control of Insect Pests: Southeast Asian Prospects - EcoPort

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48 <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 />

Natural enemies<br />

Two groups <strong>of</strong> hymenopterous parasitoids attack (but are restricted to)<br />

aphids, a larger one consisting <strong>of</strong> species belonging to the family Aphidiidae<br />

and a smaller group belonging to the family Aphelinidae. Both groups occur<br />

worldwide as solitary endoparasitoids. Although many <strong>of</strong> the species are<br />

recorded as having an extensive host range, there is almost always a<br />

significant degree <strong>of</strong> host restriction. Hosts are frequently some (but not all)<br />

<strong>of</strong> the species in a particular aphid genus or several closely related genera.<br />

There is good evidence that there are biotypes within some parasitoid<br />

species, since populations from some hosts or some areas parasitise a<br />

narrower range <strong>of</strong> hosts than the species as a whole. There may also be<br />

differences between biotypes in their preference for the host aphid when<br />

feeding on a particular host plant or in a particular habitat. When a parasitoid<br />

is abundant on a preferred host it may occasionally attack a nearby nonpreferred<br />

host, as with Diaeretiella rapae,<br />

a major parasitoid <strong>of</strong> the cabbage<br />

aphid Brevicoryne brassicae,<br />

which has occasionally been recorded from<br />

both A. craccivora and A. gossypii,<br />

but for which it exhibits a low preference<br />

(Dhiman et al. 1983). There are some species (or biotypes <strong>of</strong> species) that<br />

have been found capable <strong>of</strong> generally causing high levels <strong>of</strong> parasitisation <strong>of</strong><br />

A. craccivora.<br />

Those selected by Starù (1967a, b) are shown in bold italics in<br />

table 4.4.1 and might be considered first as potential species for biological<br />

control introductions to areas where they do not already occur. Valuable<br />

reviews <strong>of</strong> the effectiveness <strong>of</strong> aphid parasitoids are provided by Carver<br />

(1989), Hagen and van den Bosch (1968) and Hughes (1989).<br />

Although many coccinellids, syrphids, chrysopids, hemerobiids and a<br />

few predator species from other insect families attack aphids, their impact in<br />

regulating populations is generally regarded as disappointing, although they<br />

must certainly at times limit economic damage. The efficiency <strong>of</strong> a predator<br />

depends upon its searching ability and effectiveness in capturing prey. The<br />

numbers <strong>of</strong> predators seem to be greatest when aphid numbers are already<br />

declining after a peak in abundance and, thus, their apparently great impact<br />

at that time may actually have little significance in population regulation.<br />

Predators can increase rapidly in numbers only after their prey has become<br />

sufficiently abundant, so there is an important time lag between prey and<br />

predator numbers (Hemptinne and Dixon 1991).<br />

Coccinellids have been used successfully for the biological control <strong>of</strong><br />

several, relatively sessile, coccid pests, whereas results have generally been<br />

poor against aphids. One <strong>of</strong> the reasons is that adult coccinellids and their<br />

larvae are poor at capturing other than first instar aphids (Dixon 1989).<br />

Indeed, the survival <strong>of</strong> newly-hatched beetle larvae is very dependent upon

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