Integrated Management of Tomato Spotted Wilt on Field-Grown Tomatoes.

Epidemics of spotted wilt caused by Tomato spotted wilt virus (TSWV) vectored by Frankliniella occidentalis and possibly other thrips species occur regularly in tomato in the southeastern United States. Field experiments were conducted to determine the effects of UV-reflective mulch, acibenzolar-S-methyl (plant activator), and insecticides on progress of tomato spotted wilt incidence and population dynamics of flower thrips (including F. occidentalis, F. tritici, and F. bispinosa). Whole plots of tomatoes grown on UV-reflective and black polyethylene mulch were divided into subplots of acibenzolar-S-methyl and no acibenzolar-S-methyl, and sub-subplots of insecticide and no insecticide for thrips control. The UV-reflective mulch was more effective than black polyethylene mulch each year in reducing colonization of thrips in May and the consequent primary infections of tomato spotted wilt. Application of acibenzolar-S-methyl further reduced tomato spotted wilt incidence in 2000 and 2002, when disease pressure was great. Reproduction of thrips on tomato was poor in these experiments, but their control in the insecticide-treated sub-subplots prevented secondary spread in both years. The combination of UV-reflective mulch, acibenzolar-S-methyl, and insecticides was very effective in reducing tomato spotted wilt incidence in tomato.

Methods for detection of Anticarsia gemmatalis nucleopolyhedrovirus DNA in soil.

Two methods, phenol-ether and magnetic capture-hybridization (MCH), were developed and compared with regard to their sensitivities and abilities to extract the DNA of the insect baculovirus Anticarsia gemmatalis nucleopolyhedrovirus (AgMNPV) from soil and to produce DNA amplifiable by PCR. Laboratory experiments were performed with 0. 25 g of autoclaved soil inoculated with different viral concentrations to optimize both methods of baculovirus DNA extraction and to determine their sensitivities. Both procedures produced amplifiable DNA; however, the MCH method was 100-fold more sensitive than the phenol-ether procedure. The removal of PCR inhibitors from the soil appeared to be complete when MCH was used as the viral DNA isolation method, because undiluted aliquots of the DNA preparations could be amplified by PCR. The phenol-ether procedure probably did not completely remove PCR inhibitors from the soil, since PCR products were observed only when the AgMNPV DNA preparations were diluted 10- or 100-fold. AgMNPV DNA was detected in field-collected soil samples from 15 to 180 days after virus application when the MCH procedure to isolate DNA was coupled with PCR amplification of the polyhedrin region.

Thripenema fuscum n. sp. (Tylenchida: Allantonematidae), a Parasite of the Tobacco Thrips, Frankliniella fusca (Thysanoptera).

Thripenema fuscum n. sp., a parasite of the tobacco thrips, Frankliniella fusca, is described and illustrated from material collected from peanut (Arachis hypogaea) in Marianna, Florida. Thripenema fuscura can be distinguished from all other previously described Thripenema spp. by the dorsal curvature of the male and the presence of a stylet in the male. Highest parasitism rates of F. fusca by T. fuscum in peanuts were 51% in 1995 and 68% in 1996.