Macropterous individuals of wing polymorphic semiaquatic bugs (Heteroptera: Gerromorpha) usually occur at a high frequency if there is a need to leave an unfavorable habitat or in a generation migrating to/from an overwintering site. Velia caprai (Veliidae) is usually found in unpredictable habitats, but the macropterous morph is rare. Laboratory, mesocosm and field experiments were used to test the hypothesis that individuals of this species migrate by walking rather than by flight. Laboratory experiments that focused on the development of macropterous morph under conditions that usually stimulate the development of this morph in water striders were unsuccessful. A high temperature shortened the duration of nymphal development, but no winged specimens of Velia caprai developed in the laboratory when reared under either high or low temperatures, long or short photoperiods or on the surface of water or wet filter paper. Mesocosm experiments with apterous adults revealed they are able to walk on land. Both the males and females dispersed by walking in semi-natural conditions. Long-term field experiments using mark and recapture confirmed that this species can disperse by walking. Apterous individuals can compensate for downstream drift by upstream terrestrial migration and colonize newly established pools and ditches even several tens of meters from source sites. The development of a macropterous morph in response to environmental factors is replaced by terrestrial dispersal in V. caprai.
The influence of photoperiod on the thermal requirements for development was discovered for the first time in insects during experiments on the linden-bug, Pyrrhocoris apterus. The effect of photoperiod on the duration of linden-bug development at five constant temperatures (20, 22, 24, 26 and 28°C) was measured and the thermal requirements for development at three photoperiods (14, 17 and 20 h light per day) were calculated. Bugs from four geographic populations were used in these experiments: Pyatigorsk (44°02´N, 43°04´E), Borisovka (50°36´N, 36°01´E), Mikhailov (54°15´N, 39°0´E) and Ryazan (54°36´N, 39°42´E). From the values of individual development times at different temperatures the coefficient of linear regression of development rate (the inverse of the duration) on temperature and the thermal threshold for development were calculated. Both these parameters were found to decrease significantly with decrease in day-length for all four populations studied. It means that at shorter day-lengths nymphal development is less dependent on temperature compared to the development at longer day-lengths. These effects seem to be adaptive. The development times of nymphs at relatively high temperatures (above 24-25°C) are shorter under long-days than under short days which should be advantageous at the height of summer when the days are long and the weather is warm. In the contrast, at relatively low temperatures (below 24-25°C) the nymphs develop significantly faster under short-days than under long days, which is advantageous at the end of summer as it allows the nymphs to reach the adult stage, the only stage capable of overwintering. The influence of photoperiod on the thermal reaction norm appeared to be more or less gradual, i.e. the shorter the day-length the shallower the slope of the regression line of development rate on temperature and the lower the thermal threshold for development. An analysis of the literature shows that this effect of photoperiod on the thermal requirements for development is widespread among insects but has been overlooked by previous authors. The authors conclude that the variation in the development time observed in insects at different seasons, photoperiods or food regimes, or from different populations, etc., are generally due to some modification of the thermal reaction norms and more specifically to differences in the thermal requirements for development.
Colonies of M. rubra, M. ruginodis and M. scabrinodis were collected in four geographic regions: Kiev, Ukraine (50.5°N, 30.5°E - first two species), Vladimir, Russia (56.2°N, 40.4°E - only last species), St. Petersburg, Russia (59.3°N, 30.3°E - all three species) and Chupa, Murmansk prov., Russia (66.3°N, 33.7°E - last two species). After artificial overwintering experimental cultures consisting of 150 workers and one queen were established and kept at 16, 18, 20, 22, 24 and 26°C under long (22 h) day lengths. The workers reared eggs laid by queens into rapid (non-diapause) brood pupae and diapause larvae, which were removed and counted. The results showed the distinct latitudinal variation in the temperature effects on rapid brood rearing and in the thermal requirements for development. First, the period during which new rapid brood pupae appeared was found to be longer and the total number of pupae produced to be greater in ants from more southern populations. The number of diapause larvae reared by ant cultures was also usually greater, in ants from southern sites. Second, low temperatures reduced the period of rapid brood production and the number of pupae reared to a greater degree in ants from northern populations. It means that northern Myrmica colonies rear rapid brood under lower temperatures evidently worse in comparison with ants from southern regions. Third, eggs and larvae from more northern sites appeared to develop faster than southern brood at temperatures above 16-18°C. This was because brood development in northern populations was more temperature dependent, i.e. characterised by higher slopes of regression lines of development rate on temperature. The sum of effective temperatures decreased with the advance to North. The higher slopes were always associated with higher thermal thresholds for development. We conclude that the reaction norm of Myrmica colonies, in response to temperature, changes according to the local climate in such a way that brood rearing, growth and development of individuals become more temperature dependent in more severe environments with colder and shorter summers. This lead to the increase of the physiological and developmental responses at higher temperatures at the expense of a decrease within lower temperature range. In fact Myrmica colonies from northern populations need on average higher temperatures in their nests for successful production of new adults as compared to southern ants.
Typically, the relationship between insect development and temperature is described by two characteristics: the minimum temperature needed for development to occur (Tmin) and the number of day degrees required (DDR) for the completion of development. We investigated these characteristics in three English populations of Thrips major and T. tabaci [Cawood, Yorkshire (N53°49', W1°7'); Boxworth, Cambridgeshire (N52°15', W0°1'); Silwood Park, Berkshire (N51°24', W0°38')], and two populations of Frankliniella occidentalis (Cawood; Silwood Park). While there were no significant differences among populations in either Tmin (mean for T. major = 7.0°C; T. tabaci = 5.9°C; F. occidentalis = 6.7°C) or DDR (mean for T. major = 229.9; T. tabaci = 260.8; F. occidentalis = 233.4), there were significant differences in the relationship between temperature and body size, suggesting the presence of geographic variation in this trait. Using published data, in addition to those newly collected, we found a negative relationship between Tmin and DDR for F. occidentalis and T. tabaci, supporting the hypothesis that a trade-off between Tmin and DDR may constrain adaptation to local climatic conditions.