Evaluation of sampling effort required to assess pollen species richness on pollinators using rarefaction.

PREMISE: Understanding the flower visitation history of individual pollinators is key in the study of pollination networks, but direct tracking is labor intensive and, more important, does not capture information about the previous interactions of an individual. Therefore, a protocol to detect most of the pollen species on the body surfaces of an individual pollinator could elucidate its flower visitation history. METHODS AND RESULTS: Under a microscope, we observed 6.0-µL droplets from a sample solution (1.0 or 3.0 mL) containing pollen grains collected from individuals of six major pollinator functional groups. To clarify how many droplets need to be observed to detect all pollen species within the solution, we examined up to 10 droplets collected from each individual insect. Sample-based rarefaction curve analyses of the data showed that we could detect ~90% of the pollen species and the plant-pollinator links in the networks by observing six droplets. CONCLUSIONS: The rarefaction curve analysis for pollen-on-pollinator studies is a useful preliminary step for minimizing the time and labor required while maximizing the data on the flower visitation history of each individual pollinator and revealing any hidden flower-pollinator interactions.

The choosing of sleeping position in the overnight aggregation by the solitary bees Amegilla florea urens in Iriomote Island of Japan.

In addition to the process of joining the sleeping aggregation, the choice of sleeping position is an important night-time behaviour of small diurnal insects because of the increased risk for predator attacks as well as bad weather. The aggregation behaviour of the solitary bee Amegilla florea urens was investigated to elucidate the choice of sleeping position on substrates. Male and female constructed single-sex aggregations on hanging leaves during May and June, respectively. Most individuals tended to form aggregations with other individuals while few individuals slept alone. During the aggregation forming, both the number of individuals that tried to join the aggregation and the completion time of aggregation increased with the number of sleeping individuals, whereas the success rate of joining was unaffected. The sleeping positions of subsequent arrivals on the substrates were higher than those of the first arrivals in female aggregations. Therefore, the first female to arrive tended to be located near the bottom of a hanging substrate. Dissecting sleeping females showed that they contained mature oocytes, indicating that sexually mature individuals formed aggregations. In male aggregations, however, we could not find a clear relationship between the position on substrates and the arrival sequence. We suggest that the purpose for sleeping in aggregations might be a dilution effect for nocturnal predation and that the females that finished both nesting and foraging quickly could choose the optimal positions in the aggregation when they arrived on the sleeping substrates.

Low flower-size variation in bilaterally symmetrical flowers: Support for the pollination precision hypothesis.

PREMISE OF THE STUDY: The evolutionary shift from radial to bilateral symmetry in flowers is generally associated with the evolution of low flower-size variation. This phenomenon supports the hypothesis that the lower size variation in bilateral flowers can be attributed to low pollinator diversity. In this study, we propose two other hypotheses to explain low flower-size variation in bilateral symmetrical flowers. To test the three hypotheses, we examined the relative importance of pollinator diversity, composition, and bilateral symmetry itself as selective forces on low flower-size variation. METHODS: We examined pollinator diversity and composition and flower-size variation for 36 species in a seminatural ecosystem with high bee richness and frequent lepidopteran visitation. KEY RESULTS: Bilateral flowers were more frequently visited than radial flowers by larger bees, but functional-group diversity of the pollinators did not differ between symmetry types. Although bilateral flowers had significantly lower flower-size variation than radial flowers, flower-size variation did not vary with pollinator diversity and composition but was instead related to bilateral symmetry. CONCLUSIONS: Our results suggest that the lower size variation in bilateral flowers might have evolved under selection favoring the control of pollinator behavior on flowers to enhance the accurate placement of pollen on the body of the pollinator, independent of pollinator type. Because of the limited research on this issue, future work should be conducted in various types of plant-pollinator communities worldwide to further clarify the issue.