Under seasonal conditions, Polydesmus angustus individuals born in the first part of the breeding season have a 1-year life cycle and those born later have a 2-year life cycle (cohort-splitting). In this study, 249 juveniles from four early broods (born in mid-July) and four late broods (born in September) were reared under similar laboratory conditions, to test for possible maternal influences on life-cycle duration. Development times of early- and late-born individuals were compared under four combinations of day length and temperature (16 h - 18°C, 16 h - 16°C, 12 h - 18°C and 12 h - 16°C). The results showed that development time varied significantly in response to day length, temperature and sex, but that of individuals in the early and late broods did not differ significantly (mean development times ± SE: 180 ± 6 and 183 ± 8 days, respectively). There were no significant interactions between birth period and other factors, indicating that the effects of day length, temperature and sex on development time were similar in early- and late-born individuals. This indicates that the extended life cycle of millipedes born late in the season is not maternally determined and that cohort-splitting is controlled entirely by the environmental conditions experienced by the offspring during their development. This conclusion is supported by the absence of significant variation in offspring live weight at birth measured at different times in the breeding season. The results are discussed in relation to the bet-hedging theory, which is often put forward to account for cohort-splitting in arthropods. In P. angustus, the results are consistent with either bet-hedging or adaptive plasticity, but further studies are required to decide which interpretation is correct. and Jean-François David, Jean-Jacques Geoffroy.
First-stadium juveniles of Polydesmus angustus born each month from May to September were reared throughout their life cycle under controlled seasonal conditions. At maturity, the reproductive patterns of 62 females were studied individually. It was confirmed that females born from May to August have a 1-year life cycle and those born from late August onwards a 2-year life cycle (cohort-splitting). A third type of life cycle - interseasonal iteroparity - was observed in a few females born late in the season. On average, annual females started to reproduce when 11.4 months old and produced 3.6 broods per female over 1.8 months; the later they were born from May to August, the later they reproduced the following year. Biennial females started to reproduce when 19.9 months old and produced 3.8 broods per female over 2.2 months; all reproduced early in the breeding season. These results indicate that only annual females can produce an appreciable proportion of biennial offspring from late August onwards, which rules out direct genetic determination of life-cycle duration. The reproductive characteristics of P. angustus suggest a non-genetic mechanism that can drive cohort-splitting. Because individual females reproduce for about 2 months on average, this automatically results in cyclic variation in life-cycle duration (annual/biennial/annual) in the long-term progeny of any female.
Supercooling point (SCP), survival at low temperatures, rate of water loss in dry air at 20°C and survival under desiccating conditions of eggs of Polydesmus angustus (Diplopoda) were determined. The results were compared with those obtained previously for the eight post-embryonic stadia, to obtain an overview of the changes in resistance to cold and desiccation throughout the species' development. The SCP temperatures of egg batches ranged from -14.8 to -30.6°C and were significantly lower than those of the active stadia. Eggs were not affected by prolonged exposure to low temperature above 0°C and survived much better than active stadia when cooled to -6 and -10°C. This indicates that the cold hardiness of P. angustus is highest in the egg stage and decreases during development. On the other hand, the rate of water loss was significantly higher from eggs than from active stadia. When eggs were taken out of their protective nest, they lost water at the high rate of 7% min-1 in dry air. They also survived for a shorter time than active stadia at 76% RH and 20°C. The resistance to desiccation of P. angustus is lowest at the egg stage and increases during development. The results suggest that the life cycle of P. angustus may have responded to selection pressures other than cold and drought, and do not support the hypothesis that cold hardiness and resistance to desiccation are overlapping adaptations in terrestrial arthropods.
First stadium juveniles of P. angustus were reared under controlled seasonal conditions to maturity, reproduction and death. Individuals born in any one breeding season either had a 1-year or a 2-year life cycle (cohort-splitting). The life cycle was annual for individuals born in the first part of the breeding season (May-August), but became biennial for those born later (August-October). Two phenomena were involved: (1) Only individuals reaching the penultimate stadium (stadium VII) before a critical period at the end of spring could become adult in the breeding season following that of their birth. After this time, stadium VII individuals entered into aestivation and only became adult in the second autumn after their birth. (2) Females becoming adult in autumn entered reproductive dormancy and only laid eggs in the following spring. Overall, individuals born at the start of the breeding season easily reached stadium VII before the critical period and were able to breed at I year, whereas individuals born at the end of the breeding season reached stadium VII after the critical period, then had two consecutive periods of dormancy and only bred at 2 years age. Individuals from the same nest born in the middle of the breeding season (August) could have either annual or biennial life cycles, depending on whether they reached stadium VII before or during aestivation. The environmental factors capable of triggering aestivation in subadults and reproductive dormancy in autumn-maturing females are discussed., Jean-Francois David, Marie-Louise Celerier, Jean-Jacques Geoffroy, and Lit