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

Coleomagilla maculata (DeGeer), O. insidiosus, and C. carnea (except those of C. maculata) did<br />

not complete development on pollen diet, although pollen was provided to larvae for a<br />

limited period of time (Pilcher et al., 1997). However, pollen contains relatively low amounts<br />

of Bt toxin, and the larvae generally do not feed on pollen under natural conditions.<br />

The concentration of Cry1Ab in pollen is very low (2.57 to 2.94 μg per gram dry weight) as<br />

compared with that of the leaves (Koziel et al., 1993; Fearing et al., 1997). Only the adults<br />

feed on pollen to supplement their diet for ovary maturation.<br />

Diversity of the arthropod community in transgenic cotton has been found to be similar<br />

to that in conventional cotton without spraying, but the Shannon’s index for total arthropod<br />

community and neutral insect subcommunity in Bt cotton fi elds was signifi cantly<br />

higher than in sprayed plots at the mid- and late-growing stages of cotton (Li et al., 2003;<br />

Men, Ge, and Liu, 2003). Bt cotton may increase the numbers and stability of arthropods<br />

in a cotton ecosystem and improve the management of insect pests. The diversity of the<br />

arthropod community in Bt cotton fi elds is greater than that in conventional cotton, suggesting<br />

that Bt cotton is highly favorable for integrated management of cotton pests (Wu,<br />

Peng, and Jia, 2003). However, Cui and Xia (2000a, 2000b) observed that Bt transgenic cottons<br />

resulted in a decrease in species abundance and numbers of individual species. In the<br />

absence of cotton bollworm, H. armigera on transgenic cotton (the dominant pest in cotton),<br />

the red spider mite and thrips become the dominant pests. Bt cotton was effective in<br />

controlling H. armigera, but the populations of Aphis gossypii Glover, Thrips tabaci Lind., and<br />

Lygus lucorum (Mayer-Dur) increased in Bt cotton fi elds under natural or chemical control<br />

compared to that in the normal cotton fi elds (Sun et al., 2002). The population of Chrysopa<br />

formosa Brauer increased in transgenic cotton fi elds, but that of predators such as Orius<br />

minutus (L.), Deraeocoris punctulatus (Fallen), and several parasitoids decreased in transgenic<br />

cotton fi elds. Seed treatment of transgenic cotton with imidacloprid resulted in an<br />

increase in numbers of coccinellid beetles, C. septempunctata and Cheilomenes sexmaculatus<br />

(Fab.); green lace wing, C. carnea; Lynx spider, Oxyopes javanus Thorell; orb spider, Argiope<br />

minuta (Karsh); wolf spider, Lycosa pseudoannulata (Boes. and Str.); long-jawed spider,<br />

Tetragnatha javana (Thorell); Neoscona theisi (Walch.); and Peucetia viridana (Stal) (Kannan,<br />

Uthamasamy, and Mohan, 2004). The populations of nontarget insect pests were signifi -<br />

cantly greater in transgenic cotton than those in normal cotton plots. Species diversity and<br />

numbers varied between bivalent (cry1Ac CpTi) and univalent (cry1Ac) transgenic plots<br />

(Sun et al., 2003). The population of A. gossypii, A. biguttula biguttula, and Bemisia tabaci<br />

(Genn.) was lower by 33.0%, 50.6%, and 22.7%, in bivalent cotton than in univalent cotton,<br />

respectively. However, the population of T. tabaci and L. lucorum was higher by 208.9 and<br />

18.4%, respectively. The numbers of leafhoppers, A. biguttula biguttula; grey weevil,<br />

Myllocerus sp.; red cotton bug, Dysdercus keonigii F.; and aphids, A. gossypii have been<br />

found to be similar between the Bt transgenic and nontransgenic cotton (Sharma and<br />

Pampapathy, 2006). However, damage by the bollworms, H. armigera and Earias vittella (F.)<br />

was signifi cantly lower in transgenic cotton compared to nontransgenic cotton. There were<br />

no apparent effects of transgenic cotton on the relative abundance of predatory spiders,<br />

Clubiona sp. and Neoscona sp., coccinellid, C. sexmaculatus and the chrysopid, C. carnea<br />

(Figure 11.2). However, the abundance of spiders, coccinellids, and chrysopids was very<br />

low in insecticide-protected plots toward the end of the cropping season (Sharma,<br />

Pampapathy, and Arora, 2007).<br />

There were no differences in trap captures of major ground-dwelling coleopteran predators<br />

such as carabids and staphylinids between Bt-and non-Bt potato fi elds treated with<br />

weekly sprays of a microbial Bt-based formulation containing Cry3Aa, biweekly applications<br />

of permethrin, early and mid-season in-furrow applications of systemic insecticides

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