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Abstract.  1. Variability in life‐history traits of the common pond skater Gerris lacustris (L.) (Heteroptera: Gerridae) was investigated on a small geographical scale in Bavaria, Germany (≈ 49 °N). In an area of approximately 3.5 × 3.0 km, voltinism and wing length data of G. lacustris were recorded from 65 ponds located either in an open field or surrounded by forest.2. Life history differed significantly between populations in the two habitat types. Gerris lacustris showed a bivoltine life‐cycle in most of the field ponds with a high proportion of long‐winged individuals in the diapause generation and a large increase of the short‐winged morph in the midsummer generation. In contrast, almost all populations inhabiting forest ponds were univoltine. Only a few forest populations produced any second generation larvae. The long‐winged morph dominated during the whole season in forest ponds.3. The appearance of first‐instar larvae was delayed by 3–4 weeks in forest ponds compared with field ponds. Presumably, low temperatures led to this reduction in the developmental rate of eggs and larvae. Consequently, ‘field larvae’ of the first generation developed under increasing daylight conditions (triggering direct reproduction and brachyptery) but ‘forest larvae’ developed under a shortening photoperiod (triggering diapause and macroptery).4. Offspring raised from ‘forest parents’ in the laboratory showed the same variability in life history when reared in a cool (16.9 ± 2.4 °C) or warm (23.1 ± 1.8 °C) temperature regime.5. Given the small spatial scale of the study, it is concluded that the variability in the life history of G. lacustris has a strong phenotypic component.

Abst ract . 1. Life-history theory predicts that organisms should speed up development in response to time constraints. However, acceleration of development carries energetic costs that have to be compensated, e.g. by an increase in foraging rate. For the wing dimorphic water strider Gerris lacustris (L.), the hypothesis was tested that the adjustment of development to time constraints is limited by the availability of food resources.2. Six cohorts of larvae hatched increasingly late in the season were reared under two feeding regimes. For each cohort and experimental group the physiological time (in degree-days) of larval development was estimated.3. In both high-and low-food groups there was a significant reduction of physiological time for development towards the end of the season. Furthermore, within cohorts, physiological development time was always lower in the high-food group than in the low-food group. However, there was no significant interaction effect between food treatment and cohort.4. The results demonstrate that G. lacustris has the flexibility to adjust development to time constraints. In addition, 20% of the 'low-food individuals' developed into the short-winged morph while all of the 'high-food individuals' became long-winged. The limitation of food may thus lead to a reduced allocation of energy into the development of the flight apparatus. This may explain the strong increase in short-wingedness at the end of the season in natural populations, which are highly food limited.

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The wing dimorphic water strider Gerris lacustris L. (Heteroptera: Gerridae) switches to a bivoltine life cycle under favorable climatic conditions. The switch in voltinism is accompanied by a reduction of wing development in the directly reproducing midsummer generation, while the diapausing generation has a high fraction of long‐winged individuals. We investigated whether the thermal energy (degree‐days) available in natural habitats constrains the combination of developmental pathway and wing morph. Offspring of G. lacustris were reared under quasi‐natural conditions at two temperature regimes to determine the thermal constant k required to complete adult development in either wing morph. The thermal constant for egg‐to‐adult development of the short‐winged morph was about 20% lower than of the long‐winged morph. Based on the results from the outdoor laboratory experiment, we calculated the total degree‐days necessary to complete the possible combinations of wing morph pattern and voltinism. Comparison of these estimates with the thermal energy actually available during the reproductive season of 2004 for various natural habitats (sun‐exposed field ponds and shaded forest ponds) suggests that voltinism as well as wing morph pattern is strongly limited by the number of degree‐days available in these habitats. On forest ponds, only univoltine life cycles were possible, whereas on field ponds temperature allowed bivoltine life cycles. However, only the eggs laid at the very beginning of the season had the potential to accumulate enough degree‐days to complete a bivoltine life cycle with both generations long‐winged. We conclude that thermal energy is the main environmental constraint limiting voltinism of populations in the two habitat types. Furthermore, the available thermal energy also seems to influence the determination of the seasonal wing pattern in G. lacustris.