Feeding and maturation by soybean looper (Lepidoptera: Noctuidae) larvae on soybean affected by weed, fungus, and nematode pests.

Feeding and maturation by the soybean looper, Pseudoplusia includens (Walker) (Lepidoptera: Noctuidae), were investigated in a 2-yr study on 'Davis' soybean, Glycine max (L.) Merr., grown alone and combined with the weed hemp sesbania, Sesbania exaltata (Raf.) Rybd. ex. A. W. Hill, the root-knot nematode, Meloidogyne incognita (Kofoid & White) Chitwood, and the charcoal rot fungus, Macrophomina phaseolina (Tassi) Goid. Of the three pests, hemp sesbania had the greatest effects on plant growth and insect feeding and maturation. When fed foliage from soybean stressed by hemp sesbania, soybean looper larvae remained longer in feeding stages, consumed more foliage, and showed altered weight gain compared with larvae fed control foliage. Results suggest that nutrient (s) critical for proper development of larvae may have been limited in weed-stressed soybean foliage. Less dramatic results were observed when larvae fed on foliage from soybean with roots colonized by the charcoal rot fungus. Such larvae consumed more foliage, weighed more, and showed a slight increase in larval feeding period, but only in 1 yr of the study. Colonization of soybean roots by the root-knot nematode had no consistent effects on either the soybean host or insect.

Wax and Cutin Layers in Maize Kernels Associated with Resistance to Aflatoxin Production by Aspergillus flavus.

Thirteen maize hybrids and one maize population, MAS:gk, were screened for susceptibility to aflatoxin production by Aspergillus flavus . Marked differences in aflatoxin B1 production were detected among the maize genotypes tested. Most commercial hybrids consistently supported high levels of aflatoxin accumulation. Aflatoxin levels did not differ between intact and wounded kernels of these genotypes. However, different results were obtained from 4 of the 13 hybrids and the maize population MAS:gk. Levels of aflatoxin accumulation in intact kernels of these genotypes were lower than in the previous susceptible group of genotypes. In addition, aflatoxin levels were higher in wounded than in intact kernels. MAS:gk not only supported the lowest levels of aflatoxin production in intact kernels, but aflatoxin levels in endosperm-wounded kernels also were significantly lower in MAS:gk than in wounded kernels of all tested hybrids. Treatment with KOH to remove cutin from intact kernels prior to inoculation with A. flavus effected substantial increases in aflatoxin accumulation in MAS:gk, but only marginal increases in the susceptible hybrid Pioneer 3154. Removing wax from the surface of MAS:gk kernels greatly increased the susceptibility of this genotype to aflatoxin accumulation. When wax removal was combined with treatment with potassium hydroxide (KOH) or purified cutinase, aflatoxin levels in kernels were equal to those in wounded control kernels in both genotypes. These results indicated that wax and cutin layers of maize kernel pericarps may play a role in resistance to aflatoxin accumulation in MAS:gk and some other genotypes. However, results suggest further that resistance in MAS:gk also may be due to other preformed compounds as well.