Sexual crosses were used to determine the genetic basis of resistance to the sterol 14 ␣-demethylase inhibitor fungicide prochloraz in the cereal eyespot pathogen Tapesia yallundae. an even number of sensitive and resistant progeny. This indicated the segregation of a single major gene for resistance in each cross, which was confirmed by the use of backcrosses, crosses between F 1 progeny, and control crosses between sensitive parents. However, there was also evidence of additional quantitative genetic components responsible for the increased IG 50 s of the more resistant isolates. A further cross was made between isolate PR11 and an F 1 progeny arising from isolate 11-3-18, and this also yielded progeny which were entirely prochloraz resistant. This suggested that resistance genes were allelic in these two isolates, with resistance conferred by a gene at the same locus (or closely linked loci), despite the fact that the isolates (PR11 and 11-3-18) originated from different continents.A major reason for the continued success of agricultural production in the developed world has been the availability of chemicals to control pests and diseases in crops. Of these, the sterol 14 ␣-demethylase inhibitor (DMI) fungicides represent the largest and most important group of modern antifungal compounds, possessing excellent protectant, curative, and eradicant properties against a wide range of fungal species (35). Most DMI fungicides are derivatives of imidazoles or triazoles and have remained highly effective in most field applications despite many years of intense agricultural use and their singlesite mode of action. However, decreased sensitivity and field resistance to certain DMIs has been reported in at least 13 species of plant pathogen (10).The imidazole prochloraz (1-{N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]carbamoyl}-imidazole; trade name, Sportak) was launched in 1977 and has since been registered for use on more than 30 different crops in 50 countries worldwide (37; Prochloraz-technical information,