(Miller et al. 1983b). This paper reports on the subsequent appearance of the fungus, ergosterol and mycotoxins in the husk, axial stem and stalk.
MATERIALS AND METHODS
Inoculation and Sampling of CornFull details of the methods used are given by Miller et al. (1983b). In summary, ears of corn were inoculated by a toothpick method with Fusarium graminearum isolate M69 and plants were taken at random at weekly intervals from 2 to 9 wk thereafter. The ears were husked, the plant stalks were cut into 10-cm sections to 50 cm above and below the point of attachment of the ear, and ca. l-mm tansverse slices were removed from the stalk and ear attachment stem (axial stalk) for analysis for fungi. All husks, axial stem and stalk samples were stored frozen ( -l8"C)
Moisture and Ash DeterminationsMoisture and ash were determined in duplicate by heating samples (2 g) in a vacuum oven overnight at 60oC and, after measurement of the weight loss, in a muffle furnace (600'C) for 2h.
RESULTS HuskThe moisture content of the husk remained constant at ca. 7 6Vo for weeks 2-4 and then decreased to 47Vo by week 9, while the ash content increased considerably (from2.7 to 4.0Vo, on a dry weight basis). Ergosterol levels increased steadily until reaching a maximum (at 370 ppm) at week 6 and then declined by 25Vo over the next 3 wk (Fig. lA). Deoxynivalenol levels reached a maximum (370 ppm) after 6 wk and then plateaued, while 15-acetyldeoxynivalenol levels peaked (59 ppm) at week 3 and then quickly dropped to about l2-15 ppm until harvest (Fig. 1A). Zearalenote remained low (< 0.3 pm) and only began to make a significant appearance in the last few weeks, reaching a maximum (5.2 ppm) at harvest.