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.
Cold-season beetles, Catops nigricans Spence, Choleva agilis Illiger and Choleva elongata Payk., i.e. beetles which start to lay eggs in autumn, which are active during the winter in the adult stage and develop from the egg stage to the adult stage mainly during the winter months, were collected from various locations in north-western Europe and reared in the laboratory at varying temperatures and photoperiods.
Reproduction of all species started in autumn and continued during the winter months. Highest reproductive and survival rates occurred at low temperatures and within a small thermal window ranging from 5° to 10°C: The fitness of individuals decreased at higher and lower temperatures. The lower thermal threshold for all developmental stages was in the range from -5°C to +2°C. The metabolisms of the species were independent of temperature in both dormant and non-dormant stages and were elevated in the low temperature range in comparison to other species which show a temperature-dependent reaction pattern.
Optimal dates for reproduction were determined by the duration of an obligatory adult summer diapause. In C. nigricans, which favours the litter layer of deciduous forests, this duration was fine-tuned by exogenic factors, such as photoperiod and temperature. In contrast, the soil-inhabiting species Ch. elongata showed a homeostatic response pattern, independent of temperature and photoperiod. Heritability (h2) of the duration of diapause was approximately 0.26 in C. nigricans, less pronounced in Ch. agilis (ca. 0.12) and not evident in the subterranean species Ch. elongata.
All three species compensated for the vagaries of climate through bet-hedging tactics. Bet-hedging is so pervasive that a recent substantial increase in temperature seems to have a negligible effect on the distribution pattern of all three species. Based on life-history data it is conceivable that both soil-inhabiting Choleva species, which require a relatively low thermal sum for their development, were already present in western Europe during the sub-arctic conditions when ice shields reached their maximum extension during glacial periods by shifting their activity from the cold to the warm season. The Atlantic fringe north of the Pyrenees, where the climate was not cold enough for permafrost during glacial stages, was probably the only refuge where Ch. elongata might have survived. In contrast, the Mediterranean region should have been the northernmost refuge for C. nigricans during glacial periods. This species has relatively high day-degree requirements (= 1150 d°) for individual development when compared to both Choleva species (= 700 d°).
In searching both for food to produce eggs and for suitable oviposition sites, females of aphidophagous ladybirds must be adapted to exploit prey that vary greatly in their occurrence and abundance over both space and time. A simple model of ladybird searching and oviposition behaviour emerged in the 1950s: adult ladybirds are highly mobile in traversing the landscape, but become less active and produce more eggs as their rate of aphid consumption increases. The net result is that most eggs tend to be laid at sites of high aphid density. Laboratory and field experiments and observations over the past several decades have generally supported this basic model, although the linkage between ladybird dispersal activity and local aphid density often appears to be relatively weak. Not all ladybird eggs are laid in patches of high aphid density. Females use resources from limited prey consumption to produce eggs in modest numbers. They may thus be prepared to lay some eggs quickly when they succeed in finding aphids in high numbers, but otherwise they may have little choice but to lay these eggs in suboptimal sites. Upon locating patches of high prey density, females are faced with the decision of how long to remain. The basic model raises the possibility that these females become passively trapped at such patches until local aphid density collapses. Recent studies, however, suggest that detection of oviposition-deterring pheromones may promote earlier departure from prey patches. Females may also have an innate tendency to disperse throughout their lives regardless of local conditions, as a bet-hedging strategy to spread their eggs widely over space. Additional studies are needed to evaluate further the degree to which females actively determine and vary the rhythms of dispersal and reproduction in response to the unpredictable and short-lived nature of populations of their aphid prey