Abstract
Methods of measurement have been a major obstacle to the detection of Z. mays L. genotypes resistant to infection by A. flavus and aflatoxin production. Mature grain of field-inoculated hybrids was evaluated for preharvest aflatoxin contamination in 1977, 1978 and 1980, and laboratory-inoculated mature kernel samples were evaluated for aflatoxin production in 1981. In each year, ground grain of 8 commercial hybrids sampled 25, 40 and 56 days after anthesis was infused in antibiotic-amended agar which was placed in petri plates and inoculated with the fungus. After incubation for 7 days at 30.degree. C, evaluations were made for colony diameter, sporulation amount, and sporulation distribution. Colony diameter was a better criterion than sporulation characteristics for detecting differences among hybrids. Grain harvested 25 days after anthesis supported greater fungal growth than that harvested at 40 and 56 days. Various kernel genotypes having endosperm classifed as amylose extender, brittle, dull, floury, normal, shrunken, soft starch, sugary or waxy in B37 .times. Oh43 (dent) and/or Ia453 .times. Ia5125 (sweet) backgrounds were similarly tested. Colony diameters and amounts of sporulation were significantly different among endosperm genotypes within these backgrounds. Differences among hybrids and endosperm variants were more consistent for aflatoxin contamination than for colony characteristics. Mycelial growth was clearly enhanced by the presence of sugary endosperm. The more restricted growth on starchy types was consistent with that found for mature kernels of the commercial hybrids. Sugar content of the kernels was an overriding favor contributing to differences among genotypes for aflatoxin contamination of kernel samples in this study.

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