Horizontal transfer of indoxacarb in the German cockroach, Blattella germanica (L.), was examined under laboratory conditions. Results show that a single bait-fed adult cockroach (i.e., the donor) transferred indoxacarb to numerous primary recipients (secondary mortality),which then became secondary donors. These recipients subsequently became donors to other cockroaches and caused significant mortality in other members of the aggregation, resulting in tertiary kill. Indoxacarb was effectively transferred among adult cockroaches and resulted in significant secondary mortality. When adult males served as donors and vectored the insecticide to adult males, the donor:recipient ratio affected the mortality of the recipients and the rate of secondary mortality increased with increasing the ratio of donors to recipients. Furthermore, secondary mortality in the untreated cockroaches was significantly affected by the freshness of excretions from the donors, the presence of alternative food, and the duration of contact between the donors and the recipients. Ingested indoxacarb was most effectively translocated when the recipients interacted with freshly symptomatic donors in the absence of alternative food. The transfer of indoxacarb continued beyond secondary mortality and resulted in significant tertiary mortality. Excretions from a single bait-fed adult killed 38/50 (76%) nymphs within 72 h. The dead nymphs then vectored indoxacarb to 20 adult males and killed 16/20 (81%) recipients within 72 h. Behavioral mechanisms involved in the horizontal transfer of indoxacarb may include: contact with excretions, necrophagy, emetophagy, and ingestion of other excretions that originate from the donors.

Using both topical application and substrate (sand) treatments the toxicities of seven new generation soil termiticides were evaluated to determine the LD50 and LC50 against two economically important subterranean termite species, eastern subterranean termite, Reticulitermes flavipes (Kollar), and Formosan subterranean termite, Coptotermes formosanus Shiraki. The lethal dose toxicity (LD50) rankings for R. flavipes from highest to lowest were: fipronil > bifenthrin > chlorantraniliprole > cyantraniliprole > imidacloprid > chlorfenapyr > indoxacarb; the rankings for C. formosanus were fipronil > imidacloprid > chlorantraniliprole > cyanthraniliprole> bifenthrin > chlorfenapyr > indoxacarb. The respective lethal concentration toxicity (LC50) rankings were fipronil > bifenthrin > chlorfenapyr > indoxacarb > cyantraniliprole > chlorantraniliprole > imidacloprid for R. flavipes; and fipronil > chlorfenapyr > bifenthrin >imidacloprid > cyantraniliprole > chlorantraniliprole > indoxacarb for C. formosanus. The study provides an opportunity to directly compare toxicity, action speed, and bioavailability among this group of newer generation soil termiticides.

Horizontal transfer of indoxacarb among workers of the Formosan subterranean termite, Coptotermes formosanus Shiraki, was examined under laboratory conditions. The effects of dose (0, 10, 20, 50, 100 or 200 ng AI per donor), donor:recipient ratio (1:1, 1:4 or 1:9) and post-exposure time (2, 4, 8, 16, 20 and 24 days) on lethal transfer of indoxacarb were investigated using a donor/recipient model in groups of 100 workers. Transfer of lethal doses from donors to recipients was evidenced by significant recipient mortality in 13 out of 15 treatments within 24 days post-exposure. Dosage significantly affected indoxacarb transfer. Higher doses resulted in greater recipient mortality than lower doses. The highest dose tested resulted in 100% death of recipients and donors within 20 days. A dose of 100 ng resulted in recipient mortalities ranging from 68 to 100%, whereas doses < or =50 ng killed <60% of recipients within 24 days. Donor:recipient ratio also had considerable effect on indoxacarb transfer. At 24 days post-exposure, greater recipient mortalities were observed at ratios > or =1:4 at doses > or =20 ng, but only at a ratio 1:1 at dose 10 ng. Recipient mortality increased significantly as post-exposure time increased. The higher the doses applied on donors, the shorter were the times required for the onset of recipient mortality to occur and for recipients to reach maximum mortality. Significantly greater recipient mortalities were not observed at doses 20 and 50 ng until more than 20 days post-exposure, indicating a delayed activity of indoxacarb. Possible transfer mechanisms are discussed.