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Biological Control of Insect Pests: Southeast Asian Prospects - EcoPort

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108 <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 />

Host plants<br />

cages in Papua New Guinea, larvae pupated in strongly spun cocoons<br />

covered with particles <strong>of</strong> chewed wood, suggesting that pupation on bark<br />

may occur in the field. In India, Sengupta and Behura (1955, 1957) record<br />

pupation generally inside the fruit, the moth emerging through an exit hole.<br />

The pupal period lasts from 9 to 14 days, so that the total period from egg to<br />

adult takes from 28 to 41 days. Adult longevity is 8 to 9 days. Adult males<br />

can be distinguished from females by having expanded dark brown, hairy,<br />

mesothoracic tibiae (Leefmans and Van der Vecht 1930; Vožte<br />

1936;<br />

Kalshoven 1981; Fenner 1987, 1997; Golez 1991a).<br />

Adults are generally nocturnal and, during the day, spend most <strong>of</strong> their<br />

time resting under leaves on the tree. They are seldom attracted to light.<br />

Females prefer to oviposit on fruit protected from direct light. Newly<br />

hatched larvae stay together and tunnel into the fruit near where the eggs<br />

were laid. If later instar larvae are crowded, some may leave by suspending<br />

themselves on silken threads, which also facilitate transfer to other fruits. A<br />

shorter developmental period was observed for both males and females<br />

reared on the pulp than on the seed <strong>of</strong> carabao mangoes, although those<br />

reared on the seeds were larger and lived longer, females producing more<br />

eggs. Development differed slightly on different mango varieties (Golez<br />

1991a).<br />

In cages in Papua New Guinea only a small proportion <strong>of</strong> pupae yielded<br />

adults in the several months after pupation, suggesting a pupal diapause<br />

which may synchronise the life cycle with the seasonal fruiting <strong>of</strong> its host<br />

(Fenner 1987, 1997).<br />

The commonest host, wherever D. sublimbalis occurs, is Mangifera indica,<br />

but there are records also from M. odorata in Papua New Guinea and<br />

Indonesia from M. minor in Papua New Guinea (F. Dori pers. comm. 1997).<br />

and from Bouea burmanica in Thailand (Beller and Bhenchitr 1936). All<br />

four belong to the family Anacardiaceae (Sengupta and Behura 1955;<br />

Kalshoven 1981; M. Schaffer pers. comm. 1997). Larvae are unable to<br />

develop on parts <strong>of</strong> the mango tree other than the fruit, or in the fruit <strong>of</strong><br />

avocado, chico, guava, jackfruit, papaya, santol, sineguelas or star apple<br />

(Golez 1991a). However, as the genus Mangifera contains many species it is<br />

quite possible that further wild hosts will be found (Fenner 1997). Indeed the<br />

label data, quoted earlier, on specimens collected well outside the major<br />

fruiting season <strong>of</strong> M. indica suggests that this may well be so. The genus<br />

Mangifera contains about 62 species <strong>of</strong> tall evergreen trees which are native<br />

to the area stretching from India to Papua New Guinea, with the greatest

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