Variability effects by consumers exceed their average effects across an environmental gradient of mussel recruitment.

The implicit assumption that properties of natural systems deduced from the average statistics from random samples suffice for understanding them focuses the attention of ecologists on the average effects of processes and responses, and often, to view their variability as noise. Yet, both kinds of effects can drive dynamics of ecological systems and their covariation may confound interpretation. Predation by crabs and snails on competitively dominant mussels has long been recognized as an important process structuring communities on rocky shores of the Northwest Atlantic Ocean. We experimentally manipulated the average intensity of predation in plots across a gradient of mussel recruitment to separately estimate the average and variability of responses of mussel recruitment and community composition. Predation did not affect the average number of mussels recruited to plots, nor the average multivariate composition of the community. Plots from which predators were excluded showed a ~ 30% increase in spatial variability of mussel recruitment. After 1 year, the spatial variability in community composition was greater than that observed among plots that predators could access. An important, but less recognized, aspect of predation is its dampening effect on variability of community structure. As accelerating rates of environmental change disrupt species interactions, variability effects of ecological processes and corresponding responses are likely to be increasingly important determinants of community dynamics.

Sex-specific repression of dachshund is required for Drosophila sex comb development.

The origin of new morphological structures requires the establishment of new genetic regulatory circuits to control their development, from initial specification to terminal differentiation. The upstream regulatory genes are usually the first to be identified, while the mechanisms that translate novel regulatory information into phenotypic diversity often remain obscure. In particular, elaborate sex-specific structures that have evolved in many animal lineages are inevitably controlled by sex-determining genes, but the genetic basis of sexually dimorphic cell differentiation is rarely understood. In this report, we examine the role of dachshund (dac), a gene with a deeply conserved function in sensory organ and appendage development, in the sex comb, a recently evolved male-specific structure found in some Drosophila species. We show that dac acts during metamorphosis to restrict sex comb development to the appropriate leg region. Localized repression of dac by the sex determination pathway is necessary for male-specific morphogenesis of sex comb bristles. This pupal function of dac is separate from its earlier role in leg patterning, and Dac at this stage is not dependent on the pupal expression of Distalless (Dll), the main regulator of dac during the larval period. Dll acts in the epithelial cells surrounding the sex comb during pupal development to promote sex comb rotation, a complex cellular process driven by coordinated cell rearrangement. Our results show that genes with well-conserved developmental functions can be re-used at later stages in development to regulate more recently evolved traits. This mode of gene co-option may be an important driver of evolutionary innovations.