Cabbage beetles, Colaphellus bowringi, undergoing an imaginal summer and winter diapause in the soil, show a great difference in diapause duration (from several months to more than 3 years) under natural conditions. The effects of diapause duration on future reproduction in the beetle are investigated at 25 C with an LD 14 : 10 h photoperiod and under natural conditions. The fecundity of postdiapause adults with a short diapause of 5 months and nondiapause adults is similar, showing that a short diapause has no affect on reproduction, whereas the longevity of postdiapause adults with a short diapause of 5 months is significantly shorter than nondiapause adults, showing that a short diapause has a negative affect on longevity. The mean total egg production per female and longevities of postdiapause adults with long diapause periods of 16, 22, 29 and 34 months are similar to nondiapause adults, but the mean daily egg production per female is significantly higher than nondiapause adults, showing that extended diapause has a positive effect on postdiapause reproduction. The offspring of postdiapause parents require a relatively shorter time for egg development compared with the offspring of nondiapause parents, showing that diapause has a positive effect on their offspring's performance. However, there are no significant differences among offspring performance in terms of survival, adult longevity, mean egg production per female and mean daily egg production per female.
Induction of larval diapause is a photoperiodically controlled event in the life history of the moth Pseudopidorus fasciata. In the present study, the photoperiodic counter of diapause induction has been systematically investigated. The required day number (RDN) for a 50% response was determined by transferring from a short night (LD 16:8) to a long night (LD 12:12) or vice versa at different times after hatching, The RND differed significantly between short- and long-night cycles at different temperatures. The RDN for long-night cycles at 20, 22, 25 and 28 degrees C was 11.5, 9.5, 7.5 and 8.5 days, respectively. The RDN for short-night cycles was 3 days at 22 degrees C and 5 days at 20 degrees C indicating that the effect of one short night was equivalent to the effect of 2-3 long nights effect. Night-interruption experiments of 24h photoperiods by a 1 h light pulse showed that the most crucial event for the photoperiodic time measurement in this moth was whether the length of pre-interruption (D(1)) or the post-interruption (D(2)) scotophases exceeded the critical night length (10.5 h). If D(1) or D(2) exceeded 10.5 h diapause was induced. The diapause-averting effect of a single short-night cycle (LD 16:8) against a background of long nights (LD 12:12) showed that the photoperiodic sensitivity was greatest during the first 7 days of the larval period and the highest sensitivity was on the fourth day. Both non-24 and 24 h light-dark cycle experiments revealed that the photoperiodic counter in P. fasciata is able to accumulate both long and short nights during the photosensitive period, but in different ways. The information from short-night cycles seems to be accumulated one by one in contrast to long-night cycles where six successive cycles were necessary for about 50% diapause induction and eight cycles for about 90% diapause. These results suggest the accumulation of long-night and short-night cycles may be based on different mechanisms.
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