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100 Biotechnological Approaches for Pest Management and Ecological Sustainability<br />

produce distinct volatile blends in response to damage by H. virescens and H. zea (de Moraes<br />

et al., 1998). The parasitic wasp, Cardiochiles nigriceps (Vier.) exploits these differences to<br />

distinguish the plant infestation by H. virescens from that by H. zea, and selectively prefers<br />

the plants damaged by H. virescens. Therefore, the nature of insect-host plant interactions<br />

is critical in determining the extent of parasitization by the natural enemies. This type of<br />

strategy is compatible with biological control (Williams, Elzen, and Vinson, 1988). In contrast,<br />

plant secondary compounds such as tomatine in the insect host’s diet may affect the<br />

parasitization. In other cases, changes in host suitability due to the insect host’s diet can<br />

infl uence the developmental rate, size, survival, parasitization success, sex ratio, fecundity,<br />

and life span of the parasitoids (Vinson and Barbosa, 1987).<br />

Compatibility of Plant Resistance and Biological Control<br />

A synergism between plant resistance and biological control is a valuable phenomenon in<br />

the development of practical insect pest management. The trichogrammatid egg parasitoids<br />

of H. armigera are highly active on sorghum, but nearly absent on chickpea and pigeonpea,<br />

whereas the larval parasitoid, C. chlorideae is active in sorghum, pearl millet, and chickpea,<br />

but inactive in pigeonpea (Figure 4.9) (Pawar, Bhatnagar, and Jadhav, 1986). Pigeonpea genotypes<br />

with resistance to the pod borer, H. armigera have no adverse affects on larval parasitization<br />

and mortality under fi eld conditions (Sharma, Pampapathy, and Wani, 2006).<br />

Pearl millet genotypes also have no adverse effects on the parasitization of the larvae of<br />

Oriental armyworm, M. separata (Sharma et al., 2004). Insects feeding on a resistant plant<br />

generally have a slower growth and extended developmental period, and poorly developed<br />

insects are more vulnerable to natural enemies for a longer period, and this increases<br />

the probability of mortality due to biotic and abiotic factors. Insects developing slowly on<br />

resistant varieties are more effectively regulated by the predators than those feeding on<br />

the susceptible varieties (Price et al., 1980). In certain cases, the plant secondary compounds<br />

imparting resistance to insects are compatible with the performance of natural enemies,<br />

for example, Cotesia congregata (Say) [monophagous parasitoid of Manduca sexta (L.)] shows<br />

no detrimental effects on exposure to nicotine in tobacco (Barbosa et al., 1986). Gossypol in<br />

the pigment glands of cotton ingested by H. virescens has no adverse effect on C. sonorensis.<br />

Larger adults of C. sonorensis are produced on insect larvae fed on low concentrations of<br />

Parasitism (%)<br />

45<br />

40<br />

35<br />

30<br />

25<br />

20<br />

15<br />

10<br />

5<br />

0<br />

Trichogramma<br />

chilonis<br />

Campoletis<br />

chlorideae<br />

Carcelia illota<br />

Sorghum Pearl millet Groundnut Pigeonpea Chickpea<br />

FIGURE 4.9 Parasitism of Helicoverpa armigera by Trichogramma chilonis (eggs), Campoletis chlorideae (larvae),<br />

and Carcelia illota (larvae).

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