Biochemical activity of centipedegrass against fall armyworm larvae.

Centipedegrass,Eremochloa ophiuroides (Munro) Hack, severely inhibits growth of the fall armyworm larva,Spodoptera frugiperda (J.E. Smith).

Kairomones and their use for management of entomophagous insects. XV. : Identification of several acids in scales ofHeliothis zea moths and comments on their possible role as kairomones forTrichogramma pretiosum.

Acids found in moth scales of laboratory-rearedHeliothis zea (Boddie) moths are hexanoic, heptanoic, octanoic, nonanoic, 2- (or 3-) furan carboxylic, phenylacetic, benzoic, sorbic, and 4-hydroxybenzoic acid. The last two of these acids are preservatives added to the artifical diet as sorbic acid and methyl-p-hydroxybenzoate. FemaleTrichogramma pretiosum Riley exhibited increased rates of parasitization ofH.

Kairomones and their use for management of entomophagous insects : XIV. Response ofTelenomus remus to abdominal tips ofSpodoptera frugiperda, (Z)-9-tetradecene-1-ol acetate and (Z)-9-dodecene-1-ol acetate.

Telenomus remits Nixon is a parasitoid that attacks egg masses ofSpodoptera frugiperda (J.E. Smith).

Kairomones and their use for management of entomophagous insects : XIII. Kairomonal activity forTrichogramma spp. of abdominal tips, excretion, and a synthetic sex pheromone blend ofHeliothis zea (Boddie) moths.

Volatile chemicals emanating from an excretion (apparently meconium) and abdominal tips of femaleHeliothis zea (Boddie) moths mediated increased rates of parasitization ofH. zea eggs byTrichogramma pretiosum Riley. A blend of synthetic chemicals, consisting of hexadecanal, (Z)-7-hexadecenal, (Z)-9-hexadecenal, and (Z)-11-hexadecenal, which has been identified as the sex pheromone of and from the abdominal tip of femaleH.

Extraction, cleanup, and quantitative determination of aflatoxins in corn.

A method is proposed for extraction and cleanup of corn samples for the quantitation of 4 aflatoxins by high pressure liquid chromatography (HPLC). After aqueous methanol extraction, ammonium sulfate treatment, and partition of aflatoxins into chloroform, sample extracts are partially purified on Sep-Pak cartridges or small columns packed with HPLC grade silica; cleanup requires only 13 mL solvent/sample. Aflatoxins B1, B2, G1, and G2 in the purified extract are resolved in ca 10 min by normal phase HPLC on a microparticulate (5 mum) silica gel column with a 50% water-saturated chloroform-cyclohexane-acetonitrile-ethanol solvent, and are measured by ultraviolet fluorescence in a silica gel-packed flowcell.