Evolutionary change in the construction of the nursery environment when parents are prevented from caring for their young directly.

Parental care can be partitioned into traits that involve direct engagement with offspring and traits that are expressed as an extended phenotype and influence the developmental environment, such as constructing a nursery. Here, we use experimental evolution to test whether parents can evolve modifications in nursery construction when they are experimentally prevented from supplying care directly to offspring. We exposed replicate experimental populations of burying beetles (Nicrophorus vespilloides) to different regimes of posthatching care by allowing larvae to develop in the presence (Full Care) or absence of parents (No Care). After only 13 generations of experimental evolution, we found an adaptive evolutionary increase in the pace at which parents in the No Care populations converted a dead body into a carrion nest for larvae. Cross-fostering experiments further revealed that No Care larvae performed better on a carrion nest prepared by No Care parents than did Full Care larvae. We conclude that parents construct the nursery environment in relation to their effectiveness at supplying care directly, after offspring are born. When direct care is prevented entirely, they evolve to make compensatory adjustments to the nursery in which their young will develop. The rapid evolutionary change observed in our experiments suggests there is considerable standing genetic variation for parental care traits in natural burying beetle populations-for reasons that remain unclear.

Pollination success following loss of a frequent pollinator: the role of compensatory visitation by other effective pollinators.

Pollinator abundance is declining worldwide and may lower the quantity and quality of pollination services to flowering plant populations. Loss of an important pollinator is often assumed to reduce the amount of pollen received by stigmas of a focal species (pollination success), yet this assumption has rarely been tested experimentally. The magnitude of the effect, if any, may depend on the relative efficiency of the remaining pollinators, and on whether the loss of one pollinator leads to changes in visitation patterns by other pollinators. To explore how a change in pollinator composition influences pollination of Asclepias verticillata, we excluded bumble bees from plots in large and small populations of this milkweed species. We then quantified pollinator visitation rates, pollen export and pollen receipt for control plots and for plots where bumble bees were experimentally excluded. We found that exclusion of bumble bees did not reduce pollen receipt by A. verticillata flowers. Visitation by Polistes wasps increased markedly following bumble bee exclusion, both in small populations (186 % increase) and in large populations (400 % increase). Because Polistes wasps were as efficient as bumble bees at pollen transfer, increased wasp visitation offset lost bumble bee pollination services. Thus, loss of a frequent pollinator will not necessarily lead to a decline in pollination success. When pollinator loss is followed by a shift in the composition and abundance of remaining pollinators, pollination success will depend on the net change in the quantity and quality of pollination services.

Variation in signal-preference genetic correlations in Enchenopa treehoppers (Hemiptera: Membracidae).

Fisherian selection is a within-population process that promotes signal-preference coevolution and speciation due to signal-preference genetic correlations. The importance of the contribution of Fisherian selection to speciation depends in part on the answer to two outstanding questions: What explains differences in the strength of signal-preference genetic correlations? And, how does the magnitude of within-species signal-preference covariation compare to species differences in signals and preferences? To address these questions, we tested for signal-preference genetic correlations in two members of the Enchenopa binotata complex, a clade of plant-feeding insects wherein speciation involves the colonization of novel host plants and signal-preference divergence. We used a full-sibling, split-family rearing experiment to estimate genetic correlations and to analyze the underlying patterns of variation in signals and preferences. Genetic correlations were weak or zero, but exploration of the underlying patterns of variation in signals and preferences revealed some full-sib families that varied by as much as 50% of the distance between similar species in the E. binotata complex. This result was stronger in the species that showed greater amounts of genetic variation in signals and preferences. We argue that some forms of weak signal-preference genetic correlation may have important evolutionary consequences.