The genetics of phenotypic plasticity. IX. Genetic architecture, temperature, and sex differences in Drosophila melanogaster.

We examined the genetic architecture of plasticity of thorax and wing length in response to temperature in Drosophila melanogaster. Reaction norms as a function of growth temperature were analyzed in 20 isofemale lines in a natural population collected from Grande Ferrade near Bordeaux (southern France) in two different years. We found evidence for a complex genetic architecture underlying the reaction norms and differences between males and females. Reaction norms were negative quadratics. Genetic correlations were moderately high between traits within environments. Among characteristic values, the magnitudes of genetic correlations varied among traits and sexes. We hypothesized that genetic correlations among environments would decrease as temperatures became more different. This expectation was upheld for only one trait, female thorax length. For males for both traits, the correlations were large for both very similar and very different temperatures. These correlations may constrain the evolution of the shape of the reaction norms. Whether the extent of independence implies specific regulatory genes or only a specific allelic regulation of trait genes can not be decided from our results.

Adaptive phenotypic plasticity: consensus and controversy.

Phenotypic plasticity is an environmentally based change in the phenotype. Understanding the evolution of adaptive phenotypic plasticity has been hampered by dissenting opinions on the merits of different methods of description, on the underlying genetic mechanisms, and on the way that plasticity is affected by natural selection in a heterogeneous environment. During much of this debate, the authors of this article have held opposing views. Here, we attempt to lay out current issues and summarize the areas of consensus and controversy surrounding the evolution of plasticity and the reaction norm (the set of phenotypes produced by a genotype over a range of environments).

Size and fecundity hierarchies in an herbaceous perennial.

Inequalities in size in populations have potentially important effects on fitness but have rarely been examined in natural populations. I measured size (number of culms) and fecundity (number of spikelets) in five populations of the grass Danthonia spicata from 1981 to 1985. The populations were in sites in a Pinus-Quercus-Populus forest in northern lower Michigan, USA comprising a secondary succession sequence. The sites had been burned in 1980, 1954, 1948, 1936, and 1911, respectively. Mean sizes and fecundities and the amount of hierarchy in size and fecundity, measured by the Gini coefficient, were compared between the YOUNG population, 1980 burn site, and the OLD populations, 1954, 1948, 1936, and 1911 burn sites. I found large differences in mean size and fecundity between the YOUNG and OLD populations with much larger individuals in the YOUNG population. No differences in size hierarchies were found in either the first year of measurement or after five years. The fecundity hierarchies showed no significant difference among the populations in the first year but after five years the YOUNG population showed a significant decrease in amount of inequality. The longterm patterns of size and fecundity hierarchies differed because fecundity was a cumulative trait while size was not. Size inequalities may not always be a good measure of fecundity inequalities. Short-term measures of inequality in perennials may not be a good indicator of long-term values. In contrast to greenhouse studies, habitat light levels did not affect size hierarchies although they did affect fecundity hierarchies.