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Biological Control of Insect Pests: Southeast Asian Prospects - EcoPort

Biological Control of Insect Pests: Southeast Asian Prospects - EcoPort

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220 <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 />

Clarke and Walter (1992) postulate that, because N. viridula oviposits<br />

only rarely during summer in southeast Queensland, T. basalis is largely<br />

without its preferred host for 60Ð90 days during which daily temperatures<br />

average more than 25¡C. This exceeds the average survival time <strong>of</strong> adult<br />

females at this temperature. Adult survival <strong>of</strong> T. basalis in summer is thus<br />

held to be the most likely factor limiting its populations. This postulate<br />

assumes that the egg masses <strong>of</strong> native pentatomid hosts <strong>of</strong> T. basalis are also<br />

in short supply over summer. It also appears not to apply to the far hotter but<br />

moister climate <strong>of</strong> the Ord Irrigation Area in far northern Western Australia,<br />

where N. viridula continues to be under generally excellent control.<br />

AFRICA<br />

N. viridula does not appear to be regarded as an important pest in northern<br />

Africa where its eggs are attacked by a number <strong>of</strong> Scelionidae, including<br />

Trissolcus aloysiisabaudiae, T. basalis, T. lepelleyi, T. maro, T. sipius and<br />

Telenomus seychellensis. Trissolcus basalis occurs mainly in coastal areas<br />

and the others are reported primarily from the eastern and central half <strong>of</strong> the<br />

continent. T. basalis was introduced to South Africa from Australia, New<br />

Zealand and USA, although there is some evidence that it may have already<br />

occurred there prior to these introductions (Giliomee 1958; Greathead<br />

1971). In Malawi eggs laid on macadamia were reported to experience an<br />

average <strong>of</strong> 74% parasitisation by Trissolcus maro and Telenomus<br />

seychellensis (Croix and Thindwa 1986). In Somalia Trissolcus<br />

alloysiisabaudiae is very abundant and may cause 100% parasitisation <strong>of</strong><br />

N. viridula eggs on cotton (Paoli 1933). T. lepelleyi and T. sipius attack<br />

N. viridula eggs in East Africa, the latter being known only from Kenya.<br />

Psix striaticeps, which occurs in tropical Africa and India, has been bred<br />

from N. viridula eggs (Jones 1988).<br />

ARGENTINA<br />

N. viridula was first recorded in 1919. Since the native tachinid parasitoid<br />

Trichopoda giacomellii was unable to maintain populations at sufficiently<br />

low levels, three parasitoid wasps were introduced, <strong>of</strong> which the most<br />

effective is Trissolcus basalis (Crouzel and Saini 1983; Porta and Crouzel<br />

1984).<br />

In Buenos Aires Province, mortality <strong>of</strong> N. viridula eggs was found to be<br />

due mainly to parasitisation by T. basalis, that <strong>of</strong> 1st to 3rd instar nymphs to<br />

predation and that <strong>of</strong> adults (together with reduction in egg production) to<br />

parasitisation by Trichopoda giacomellii. Adult mortality and reduction in<br />

egg production was found to be density dependent. Three egg parasitoids<br />

were present, Trissolcus basalis (95% <strong>of</strong> total parasitisation), Telenomus<br />

mormideae and Telenomus sp.. Nymphal mortality was principally due to<br />

spiders and predatory bugs (Podisus sp.), although there was also some

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