Flies evolved small bodies and cells at high or fluctuating temperatures.

Recent theory predicts that the sizes of cells will evolve according to fluctuations in body temperature. Smaller cells speed metabolism during periods of warming but require more energy to maintain and repair. To evaluate this theory, we studied the evolution of cell size in populations of Drosophila melanogaster held at either a constant temperature (16°C or 25°C) or fluctuating temperatures (16 and 25°C). Populations that evolved at fluctuating temperatures or a constant 25°C developed smaller thoraxes, wings, and cells than did flies exposed to a constant 16°C. The cells of flies from fluctuating environments were intermediate in size to those of flies from constant environments. Most genetic variation in cell size was independent of variation in wing size, suggesting that cell size was a target of selection. These evolutionary patterns accord with patterns of developmental plasticity documented previously. Future studies should focus on the mechanisms that underlie the selective advantage of small cells at high or fluctuating temperatures.

Indirect selection of thermal tolerance during experimental evolution of Drosophila melanogaster.

Natural selection alters the distribution of a trait in a population and indirectly alters the distribution of genetically correlated traits. Long-standing models of thermal adaptation assume that trade-offs exist between fitness at different temperatures; however, experimental evolution often fails to reveal such trade-offs. Here, we show that adaptation to benign temperatures in experimental populations of Drosophila melanogaster resulted in correlated responses at the boundaries of the thermal niche. Specifically, adaptation to fluctuating temperatures (16-25°C) decreased tolerance of extreme heat. Surprisingly, flies adapted to a constant temperature of 25°C had greater cold tolerance than did flies adapted to other thermal conditions, including a constant temperature of 16°C. As our populations were never exposed to extreme temperatures during selection, divergence of thermal tolerance likely reflects indirect selection of standing genetic variation via linkage or pleiotropy. We found no relationship between heat and cold tolerances in these populations. Our results show that the thermal niche evolves by direct and indirect selection, in ways that are more complicated than assumed by theoretical models.

Heat tolerance during embryonic development has not diverged among populations of a widespread species (Sceloporus undulatus).

The frequency and magnitude of heat waves have increased in recent decades, imposing additional stresses on organisms in extreme environments. Most reptilian embryos are regularly exposed to thermal stress because they develop in shallow, warm soils for weeks to months. We studied cardiac performance during warming to infer lethal temperatures for embryonic lizards in the Sceloporus undulatus complex. Embryos from four populations throughout the geographical range (New Jersey, South Carolina, Colorado, and Arizona) were warmed at a rate observed in natural nests. Embryos from all populations exhibited a similar pattern of thermal sensitivity, as follows: heart rate rose between 34 and 41°C, remained stable between 41 and 44°C, and dropped sharply between 44 and 47°C. No embryos recovered from cardiac arrest, indicating that the upper lethal temperature was ≤47°C. Despite the putative selective pressures, the thermal limit to cardiac performance seems to have been conserved during the evolution of this species.