Floral morphology mediates temporal variation in the mating system of a self-compatible plant.

The mating system of self-compatible plants may fluctuate between years in response to ecological factors that cause variation in the deposition of self pollen vs. outcross pollen on stigmas. Such temporal variation may have significant ecological and evolutionary consequences, but it has rarely been studied, and the mechanisms that mediate temporal variation have almost never been investigated. We tested for variation in the proportion of seeds self-fertilized (s) between two years within 19 populations of the short-lived herb Aquilegia canadensis. Selfing varied widely among populations (range in s = 0.17-1.00, mean s = 0.82) but was inconsistent across years, indicating significant temporal variation. Three populations exhibited especially wide swings in the mating system between years. Mean s did not decrease with increasing population size (N), nor was the fluctuation in s associated with mean N or the change in N. As expected, s declined with increasing separation between anthers and stigmas within flowers (herkogamy), and s fluctuated to a greater extent in populations with more herkogamous flowers. Self-compatible plants can experience wide temporal variation in self-fertilization, and floral traits such as herkogamy may mediate temporal variation by forestalling self-pollination and thus allowing outcrossing during periods when pollinators are frequent.

Insect predators affect plant resistance via density- and trait-mediated indirect interactions.

Predators can affect herbivores both through direct consumption (density-mediated interactions) and by changing behavioural, physiological or morphological attributes of the prey (trait-mediated interactions). These effects on the herbivore can in turn affect the plant through density- and trait-mediated indirect interactions (DMIIs and TMIIs). While the effects of DMIIs and TMIIs imposed by predators has been shown to influence plant density and plant communities, we know little about the effects on plant quality. In addition, the DMII and TMII components of the predator may influence each other so that the total effect of the predator on the plant is not simply the sum of the DMII and TMII. We examined DMIIs and TMIIs between a stinkbug predator and a caterpillar, and show how these interactions affect plant quality, as measured by damage, resistance to herbivores, and a defence chemical, peroxidase. We used novel methods to estimate the independent and non-additive contribution of DMIIs and TMIIs to the plant phenotype. Both predator-induced DMIIs and TMIIs caused decreases in the amount of caterpillar herbivory on plants; a strong non-additive effect between the two resulted from redundancy in their effects. TMIIs initiated by the predator were primarily responsible for a decrease in induced plant resistance. However, DMIIs predominated for reducing the production of peroxidase. These data demonstrate how DMIIs and TMIIs initiated by predators cascade through tri-trophic interactions to affect plant damage and induced resistance.

Experimental analysis of biparental inbreeding in a self-fertilizing plant.

Localized dispersal and mating may genetically structure plant populations, resulting in matings among related individuals. This biparental inbreeding has significant consequences for the evolution of mating systems, yet is difficult to estimate in natural populations. We estimated biparental inbreeding in two populations of the largely self-fertilizing plant Aquilegia canadensis using standard inference as well as a novel experiment comparing apparent selfing between plants that were randomly relocated within populations to experimental control plants. Using two allozyme markers, biparental inbreeding (b) inferred from the difference between single-locus and multilocus estimates of selfing (b = s(s) - s(m)) was low. Less than 3% of matings involved close relatives (mean b = 0.029). In contrast, randomly relocating plants greatly reduced apparent selfing (mean s(s) = 0.674) compared to control plants that had been dug up and replanted in their original locations (s(s) = 0.953, P = 0.002). Based on this difference in s(s), we estimated that approximately 30% of all matings involved close relatives (mean b = 0.279, 95% CL = 0.072-0.428). Inference from s(s) - s(m) underestimated b in these populations by more than an order of magnitude. Biparental inbreeding is thought to influence the evolution of self-fertilization primarily through reducing the genetic cost of outcrossing. This is unlikely to be of much significance in A. canadensis because inbreeding depression (a major cost of selfing) is much stronger than the cost of outcrossing. However, biparental inbreeding combined with strong inbreeding depression may influence selection on dispersal.