In this paper, the observations of the ecology of a Limantrid moth, the Far Eastern urticating moth, Euproctis flava Bremer, made throughout the life cycle in laboratory and in field are reported. Overwintering in larval stage, this species has a generation in a year (Table 1). The mean duration of each life stage is shown in Table 2. Pupa, adult and egg are found during summer season, as these stages are rather short, the larvae can be seen almost throughout the year. The female moth usually deposits her eggs in a single mass, preferably on the under surface of a leaf. An egg-mass is covered with the hairs of her anal tuft. Each mass contains 200-1, 000 eggs. A female moth can oviposits 1-3 times during her life, therefore 300-1, 500 eggs are produced by a single female. As shown in Table 3, the hatching ratio are favoured in a higher humidity. After hatching, the young larvae gather to a tight colony, until as late as the late autumn, but after hibernation, they tend to scatter to all parts of the trees and the surroundings, entering into a solitary life. The number of larval moultings varies between eleven to seventeen. The number of instars may be influenced by various environmental factors such as : local distributional factor (probably due to the temperature), seasonal disparity of the oviposition time, suitability of the food plant, and the larval population density; further by the difference of sex and the presence of parasitic natural enemies. The period of each instar duration is shown in Table 4. The larvae on an stage of between 9-13 instars hibernate within a winternest, which is spun on the ground or among dead leaves. The records of the entering to and the awakening from hibernation are shown in Tables 5, 6, and 7 and Figs.2 and 3. A mature larva leaves the food plant to seek the pupating site, where they spin a rather loose cocoon and pupate therein. The moth usually emerges out from pupal skin between the hours of 13 : 00 to 16 : 00 in the afternoon, male moths emerge 5-6 days earlier than the females do. The adult insects take no food. The mating takes place in the night-times immediately after emergence, and about 3 days after the mating, the female begins to deposit eggs. The list of food plants, including previous author's records, is shown in Table 8. But, younger instar larvae show tendency of preference to several plants, for example, Quercus spp., Rhododendron spp., Rosa spp., Polygonum spp. and etc. When breeding parallel crowded cultures on different food-plant, marked differences were observed in the rates of larval development and the larval body colour. The result obtained with four different food plants : Quercus serrata, Rhododendron linearifolium, Prunus yedoensis var. macrosepalum and Celtis sinensis var. japonica, for 100 larvae crowded cultures, are given in Fig.7 and Table 9. The results clearly showed that the food-plant can affect the development and colour composition of larva. Larvae reached maturity on Prunus fewer one instar than Quercus and Rhododendron. Larvae bred on Celtis died all until 10th instar. In order to analyse the variability of larval colour pattern, four colour groups were divided, based on the extent of the dorsal black markings on the third to the seventh abdominal segments (Fig. 6). The result shows that the colour composition and the mean colour are affected by the foodplant; Quercus resulting in the darkest with a group mean of 1.78, whilst Prunus produced the lightest with a mean of 2.38. Some effects of population number in association were determined by the comparing of different cultures under solitary to crowded conditions. Larvae of cultures bred less than 10 larvae in association, died all before 8th instar, the culture of 20 larvae reached maturity in 15th instar, whilst that of 50 and 100 larvae in 16th instar. As regards to the variation of colour pattern, the culture of 100 larvae became the dar
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