Abstract. Predators are widely assumed to create selection that shapes the evolution of prey escape abilities. However, this assumption is difficult to test directly due to the challenge of recording both predation and its evolutionary consequences in the wild. We examined these events by studying natural and experimental populations of Trinidadian guppies, Poecilia reticulata, which occur in distinct high-predation and low-predation environments within streams. Importantly, in the last two decades several populations of guppies have been experimentally introduced from one type of predatory environment into the other, allowing measurements of the consequences of change. We used this system to test two hypotheses: First, that changes in predatory environments create phenotypic selection favoring changes in escape ability of guppies, and second, that this selection can result in rapid evolution. For the first test we compared escape ability of wild caught guppies from high-versus low-predation environments by measuring survival rates during staged encounters with a major predator, the pike cichlid Crenicichla alta. We used guppies from three streams, comparing two within-stream pairs of natural populations and three within-stream pairs of an introduced population versus its natural source population. In every comparison, guppies from the high-predation population showed higher survival. These multiple, parallel divergences in guppy survival phenotype suggest that predatory environment does create selection of escape ability. We tested our second hypothesis by rearing guppies in common garden conditions in the laboratory, then repeating the earlier experiments using the F 2 generation. As before, each comparison resulted in higher survival of guppies descended from the high-predation populations, demonstrating that population differences in escape ability have a genetic basis. These results also show that escape ability can evolve very rapidly in nature, that is, within 26-36 generations in the introduced populations. Interestingly, we found rapid evolutionary loss of escape ability in populations introduced into low-predation environments, suggesting that steep fitness trade-offs may influence the evolution of escape traits.Key words. Genetic divergence, geographic variation, phenotypic selection, Poecilia reticulata, predator-prey interaction. Many fields of biology assume that predators are the primary factor shaping the evolution of prey escape abilities. However, this causal hypothesis is difficult to test due to the challenge of measuring selection by predators and the evolutionary consequences for prey in a single, natural system. Several studies demonstrate that predators create phenotypic selection favoring enhanced escape ability of prey (e.g., Brodie 1992;Dugatkin 1992;McCollum and Van Buskirk 1996;Watkins 1996), and others show that genetically based differences in escape ability among related prey populations or species are correlated with predatory environment (e.g., Seghers 1974;Sinervo and Losos 199...

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In this study, we use the bacterium Escherichia coli to examine evolutionary responses to environmental acidity fluctuating temporally among pH 5.3, 6.3, 7.0, and 7.8 (5,000-15 nM [H(+)]). Two experimental protocols of temporal variation were used. One group (six replicate lines) of populations evolved for 2,000 generations during exposure to a cycled regime fluctuating daily between pH 5.3 and 7.8. The other group (also in six replicate lines) evolved during exposure for 2,000 generations to a randomly shifting regime fluctuating stochastically each day among pH 5.3, 6.3, 7.0, and 7.8. Adaptation to these fluctuating acidity regimes was measured as a change in fitness relative to the common ancestor by direct competition experiments in both constant and fluctuating pH regimes. For comparisons with constant pH evolution, a group evolved at a constant pH of 5.3 and another group evolved at pH 7.8 were also tested. This study initiated the first long-term laboratory natural selection experiment on adaptation to variable acidity and addressed key questions concerning patterns of adaptation (trade-offs, specialists, generalists, plasticity, transitions, and acclimation) in temporally fluctuating environments.

This study uses the enteric bacterium

Numerous studies have examined sexual dimorphism in the morphology and behavior of vertebrates; very few, however, have explicitly investigated the possibility of gender differences in physiological performance, despite the observations of such differences in humans. In this study, I investigated physiological sexual dimorphism in the lizard genus Cnemidophorus by measuring five whole-animal traits, all of which are likely to influence fitness in these species: burst speed, endurance, maximal exertion capacity, standard metabolic rate, and evaporative water loss rate. Because at least some of these traits are known to be strongly influenced by body size, I tested for dimorphism using both absolute and size-corrected trait values. An examination of six Cnemidophorus species and subspecies revealed a strong trend toward higher absolute trait values in males for all variables except endurance. Most of the dimorphism in standard metabolic rate and evaporative water loss rate could be explained by differences in body mass between males and females; for the locomotor traits, however, body size explained only a small fraction of the overall sexual dimorphism. The portion of trait differences not explained by body size was likely due to gender differences in physiology, such as differences in relative muscularity and fat content.