Using a tethered-insect technique, we investigated within-and between-population variation in the postalighting host-plant preference and specificity of female Helicoverpa armigera from four populations. No significant difference occurred among populations in host-plant preference. Differences in host-plant preference existed among female moths within a population, and these differences are under genetic control and heritable. Most females ranked maize, sorghum and tobacco highest, followed by cotton varieties DP90 and HG660. The least-preferred plants were cowpea and lucerne. A few females (20%) differed from this general pattern and among each other, and reversed the rank order of host plants. Within a population, individual female moths differed in their host-plant specificity, with some individuals being more generalist than others. Similarly, significant differences occurred in host-plant specificity among populations. The relevance of these findings are discussed in relation to polyphagy in H. armigera.Larvae were reared on a standard artificial diet for Helicoverpa spp. (Teakle 1991) in order to minimise the influence of host-plant experience on oviposition preference (Jenny et al. 1968;Firempong and Zalucki 1991). First-and second-instar larvae were reared collectively in plastic containers at 25"C, a relative humidity of 75% and a photoperiod of 12: 12 h. To prevent cannibalism (Twine 1971), third-instar larvae were held individually in plastic containers (28 mL). Larvae collected from the field were identified to species from physical characteristics (Cantrell 1981;Cahill et al. 1984), and larvae of H. punctigera were discarded. Pupae were removed from the plastic containers, sterilised in 0.2% sodium hypochlorite solution and their sex determined. Eclosed adult females were permanently marked on their wings with a pen, and transferred to a mating cage (40 x 25 x 25 cm) in a 1 : 1 ratio of females to males, and supplied with 5% sucrose solution. Adults were held for three days after eclosion to allow mating and egg maturation. To ensure that females of only H. armigera were used in assays, adult moths were rechecked with Common's (1953) key for adults. Voucher specimens of H. armigera tested were deposited in the Insect Collection of the Department of Entomology, The University of Queensland.