chlorantranilipole and novaluron

chlorantranilipole has been researched along with novaluron* in 2 studies

Other Studies

2 other study(ies) available for chlorantranilipole and novaluron

ArticleYear
Survival and Locomotory Behavior of Earwigs After Exposure to Reduced-Risk Insecticides.
    Journal of economic entomology, 2017, 08-01, Volume: 110, Issue:4

    The conservation of natural enemies is an important tactic to promote biological control of arthropod pests. The earwig Doru luteipes (Sccuder) is the most important predator of the fall armyworm Spodoptera frugiperda (J.E. Smith) in corn fields. One way of conserving these predators in the field is by using only selective insecticides when the pest population reaches the economic threshold. Some recent insecticides such as azadirachtin, chlorantraniliprole, and novaluron have been claimed to pose reduced risk for natural enemies. Nevertheless, there is a dearth of information regarding the selectivity of these insecticides upon earwigs in specific. In this study, we carried out a series of laboratory assays to examine the survivorship and locomotory behavior of D. luteipes after exposure to fresh dry residue of azadirachtin, chlorantraniliprole, and novaluron. Our results show a significant survival reduction for D. luteipes nymphs exposed to fresh residues of chlorantraniliprole and novaluron. In the behavioral studies, adults of D. luteipes stopped more often, spent more time resting (inactive), and moved more slowly immediately after exposure to chlorantraniliprole residue. These results suggest that chlorantraniliprole may mediate an impaired movement and a behavior arrestment of earwigs after contact with this insecticide fresh residue. This could translate into reduced foraging efficiency, and increase exposure and insecticide uptake. Although chlorantraniliprole and novaluron showed a potential to undermine the biological control provided by earwigs, it is yet essential to conduct field trials in order to confirm our laboratory results.

    Topics: Animals; Female; Insecta; Insecticides; Limonins; Locomotion; Longevity; Male; Nymph; ortho-Aminobenzoates; Pesticide Residues; Phenylurea Compounds; Predatory Behavior

2017
A laboratory assessment of the toxic attributes of six 'reduced risk insecticides' on Galendromus occidentalis (Acari: Phytoseiidae).
    Chemosphere, 2011, Volume: 84, Issue:1

    The modified excised leaf disc method was used to measure the effects of six insecticides on eggs, larvae, adults, and female fecundity of Galendromus occidentalis (Nesbitt) in a 'worst case laboratory exposure'. This study identified insecticides that would be recommended for tier II field evaluations for an integrated pest management program. Commercially formulated insecticides were applied with a thin-layer chromatography sprayer adjusted to 10.34 kPa (1.5 psi), at the recommended label concentrations in Canada. LC(50) values were estimated from aliquots above and below that concentration. Spinetoram and spirotetramat were toxic at label concentrations. The label concentration for spinetoram was 34.3-fold the LC(50) estimate (0.006 gL(-1)) and for spirotetramat the label concentration was 7.7-fold the LC(50) estimate (0.03 gL(-1)). Clothianidin was considerably less toxic and the label concentration was 0.15-fold the LC(50) estimate (2.29 gL(-1)). Estimates of LC(50) for novaluron and chlorantraniliprole could not be established. Both materials showed slight toxicity to at least one growth stage of the predator. Novaluron, clothianidin and chlorantraniliprole should be evaluated in the field for compatibility in IPM programs. Flubendiamide was harmless to all growth stages and it is recommended for inclusion in IPM programs without additional tier II field evaluations. Field evaluations with spinetoram and spirotetramat should be pursued only if alternatives are unavailable.

    Topics: Acari; Animals; Benzamides; Female; Fertility; Guanidines; Insecticides; Laboratories; Larva; Macrolides; Male; Neonicotinoids; ortho-Aminobenzoates; Phenylurea Compounds; Risk Assessment; Sulfones; Thiazoles

2011