Biological control provides an environmentally harmonious and potentially stable management tactic to combat noxious pests such as Bemisia tabaci, notorious for its resistance to synthetic pesticides. Bioassays conducted under control chamber conditions integrating applications of the parasitoid Encarsia formosa, reared for 20 years on Trialeurodes vaporariorum, and the fungus Verticillium lecanii on the third-fourth instar nymphs of B. tabaci on tomato, showed a comparable effect between the parasitoid-fungus combined treatment and the fungus treatment alone (70.7% vs. 70.4%). Analysis of our results indicates antagonism between the two biocontrol agents related to the parasitoidsÕ ability to discriminate between infected and healthy B. tabaci nymphs. The parasitoid treatment alone produced 36.3% mortality, with no mortality in the distilled water controls. The behavioural performance of the parasitoid could have either genetic or environmental causes. Bioassays studying the feeding habit of the imported mirid predator Macrolophus caliginosus (adults) and the indigenous mirid Camptotylus reuteri (nymphs and adults) on eggs, or early second instar nymphs of B. tabaci, and choice preference tests indicated a significant difference in feeding between M. caliginosus and C. reuteri. There was no significant difference in percentage feeding of M. caliginosus on eggs (2.2%) or second instar nymphs (8.0%). There was a significant difference in feeding of M. caliginosus adults (18.6%) when offered eggs and second instars in the same arena compared with eggs or second instars offered separately. These results could be attributed to the biological behaviour of the predator having a type III functional response. Studies with the local C. reuteri species showed no significant difference in adult and nymphal consumption on second instars of B. tabaci compared with nymphs on eggs. However, C. reuteri adults fed less on eggs compared with nymphs. This local predatory species appears to be more efficient than M. caliginosus in feeding on particular stages of B. tabaci without depending on prey density. This is further supported by the low consumption of both adults and nymphs in the choice test (4% and 2.3%, respectively) compared with M. caliginosus adults (18.6%).

In aphidophagous systems, trophic interactions between parasitoids and predators, termed intraguild predation, are frequently asymmetric. To mitigate predation risk for themselves and their offspring, intraguild prey may exploit associative learning to gain accurate information about patch quality. Therefore, costs of unnecessary escape behavior are avoided. We used sweet pepper patches (Capsicum annuum L., cv. ‘Mazurka’) (Solanaceae), sustaining Macrosiphum euphorbiae (Thomas) or Myzus persicae (Sulzer) (Homoptera: Aphididae) aphids, as a model system to quantify the foraging behaviors of the parasitoid Aphelinus abdominalis (Dalman) (Hymenoptera: Aphelinidae), when confronted with predatory second instar Chrysopa carnea (Stephens) (Neuroptera: Chrysopidae). The behavior of predator‐naive or predator‐experienced A. abdominalis foraging in a patch with or without C. carnea was recorded and analyzed using a multiple video observation system. We investigated (i) whether A. abdominalis could learn to detect the presence of a predator in a patch, (ii) the impact of the predator presence on the learning and motor learning of the parasitoid, and (iii) the effects of the aphid species on the guild interactions. Results showed that the presence of, or experience with the predator does not affect A. abdominalis learning or motor learning. We discuss the behavioral and ecological implications of our finding. Overall, predator‐induced aphid mobility increased the frequency and allocation time of Aphelinus oviposition activities, especially when Ma. euphorbiae was the host. The predator imposed indirect fitness costs on the parasitoid. Aphelinus abdominalis searched more often and longer, resulting in a tendency towards reduced Ma. euphorbiae parasitism rate in patches harboring C. carnea.