Effect of horizontal transfer of barrier insecticides to control Argentine ants (Hymenoptera: Formicidae).

Horizontal transfer of three contact insecticides, bifenthrin, beta-cyfluthrin, and fipronil, was tested in laboratory colonies. Donor ants were exposed for 1 min to insecticide-treated sand substrates and placed with unexposed ant colonies at two different temperatures. Mortality was monitored to compare the ability of donors to transfer lethal doses of these insecticides to untreated individuals. Treated donor insects, live or dead, were added into colonies to determine the importance of donor behavior on lethal transfer. Fipronil was readily transferable between individuals, resulting in high mortality rates. Bifenthrin and beta-cyfluthrin were less transferable, exhibiting moderate-to-low mortality rates similar to the controls. Greater mortality occurred at 27-29 degrees C than at 21-23 degrees C for bifenthrin, but not the other treatments or controls. Colony mortality did not significantly increase when adding live donors, suggesting that necrophoresis was probably an important donor behavior in addition to grooming and trophallaxis on horizontal transfer.

Effect of delayed toxicity of chemical barriers to control Argentine ants (Hymenoptera: Formicidae).

Brief exposures of Argentine ants to four different insecticide treatments, bifenthrin, beta-cyfluthrin, bifenthrin + beta-cyfluthrin, and fipronil, were conducted to determine Kaplan-Meier product limit survivorship percentiles (SPs) at 21-23 and 27-29 degrees C. Bifenthrin, beta-cyfluthrin, and bifenthrin + beta-cyfluthrin provided rapid kill at 21-23 degrees C with SP10 values ranging from 11.2 to 33.7 min. Fipronil provided delayed toxicity at 21-23 degrees C with SP10 values ranging from 270 to 960 min. At 27-29 degrees C, all of the SP10 values significantly decreased. Field tests in which Argentine ants were induced to forage across insecticide-treated surfaces were used to determine the effect that speed of action has on foraging and recruitment ability, and whether these insecticides are repellent. The slower-acting fipronil allowed a greater amount of foraging and consequently a greater fraction of the colony to be exposed, whereas fast-acting bifenthrin, beta-cyfluthrin, and bifenthrin + beta-cyfluthrin inhibited recruitment, resulting in fewer ants being exposed and killed. Implications for controlling ants by using perimeter barrier treatments are discussed.