“…We used a rubber septum containing synthetic pheromone (Shin-Etsu Chemical Co., Ltd., Japan) that was placed at the center of a sticky plate (240 mmϫ250 mm, Takeda Chemical Industries Co., Ltd., Japan) as a pheromone trap. Konno and Tanaka (1996b) and Samudra et al (2002) reported that the mating time differed between the two feeders under laboratory conditions, and if this was the case in our study populations, the sizes and gene frequencies could be differentiated between the trap periods corresponding to different mating activities between the two feeders. Therefore, we collected trapped moths at both midnight and early morning: the traps were set before sunset, the trapped moths (hereafter, first trap samples) were gently collected alive at 1:00 am, a new sticky plate with the pheromone was left until the next morning, and the moths trapped on the new plate (hereafter, second trap samples) were collected in the early morning.…”