Community studies have shown that plant species are often pollinated by multiple pollinators; however, networks of heterospecific pollen transfer (HPT) in natural communities remain largely unexplored. We analyzed pollen deposition on stigmas of 57 flowering species to build a picture of plant-plant interactions via HPT in a biodiverse alpine meadow in southwest China. Plant species were categorized as pollen donors or recipients by their link numbers and link qualities. We identified 3609 heterospecific pollen grains, representing 410 links among 69 pollen species. Each plant species received on average 7.2 pollen species and donated its pollen to 5.5 species; only a few species donated or received large amounts of pollen or pollen from a large number of species. Compared to specialized plants, generalized plants tended to receive more heterospecific pollen but exported no more pollen to other species. Plant position in the network was related to both floral traits (stigma position) and pollinator generalization level. When different species share the same pollinator, bidirectional HPT may occur, but this was rarely observed in the species-rich community, indicating that interspecific pollen interference was largely unidirectional. Our study highlights the importance of understanding how sympatric flowering plants reduce deleterious effects of HPT, for example via stigma position. This study is the first to present a pollen transfer network for an entire community and to unravel its properties using directed network analysis.

A pervasive hypothesis at the interface of ecology and evolution is that biotic interactions contribute to regional biodiversity by accelerating adaptation and speciation. We investigated this question in the context of closely related, bumble bee‐pollinated plants (Pedicularis spp.) in the Hengduan Mountains of south‐central China, where they exhibit spectacular levels of richness, endemism, and floral diversity. Because these species co‐occur frequently, flower synchronously, and share pollinators during the brief reproductive season, we predict that pollinator‐mediated interactions may influence their community assembly and evolutionary diversification. If disparity in floral traits reduces competitive interactions between species, as would happen if floral isolation mitigates reproductive interference caused by heterospecific pollen flow, then species with dissimilar flowers should co‐occur more often, yielding greater floral diversity at local scales than expected by chance. Moreover, if such interactions have repeatedly driven character displacement, then floral traits should exhibit homoplasy, the phylogenetic signature of labile evolution. We present evidence supporting these predictions, and find that local species richness is best explained by a model including both floral diversity and phylogenetic distance. Our results suggest that a dynamic mosaic of pollinator‐mediated interactions among Pedicularis in the Hengduan region promotes ecological sorting through recurrent selection against reproductive interference, causing rapid species turnover at local scales, and accelerating the rate of floral divergence among species. Together these processes may have contributed to the remarkable accumulation of florally diverse species of Pedicularis endemic to the Hengduan Mountains biodiversity hotspot.

Flower stalks of Pulsatilla cernua, an early spring herb in north temperate Asia, changed position from erect to pendulous and back to erect during 6-10 d anthesis. We tested three possible explanations for this movement. Our results showed that (1) this movement is unlikely to be a mechanism to attract pollinators or enhance pollen output, because no pollinator preference was observed between erect and pendulous flowers and we found no buzz-pollination in this species; (2) hand self-pollination yielded higher seed set than open pollination in the field, but spontaneous selfing rarely occurred. Among open-pollinated flowers, seed set was depressed by emasculation, indicating that in the presence of insects, self-pollen provided reproductive assurance in this protogynous and self-compatible species. However, the change in flower orientation cannot be explained as reproductive assurance in that even self-pollination largely depended on pollinator visits rather than gravity. (3) A pollen germination experiment indicated that pollen damage by water is serious in this species. We deduced that the bending of the flower stalk during anthesis was to avoid rain damage to pollen grains in this species. During the 3-6 d period of pollen presentation, the petals elongated and were covered with unwettable hairs. Together with flower stalk movement, this was enough to protect the organs inside the flower from rain. This movement of the flower stalk seems to be important to maintain pollen viability in a rainy habitat with a scarcity of pollinators.

SummaryTo minimize interspecific pollination, it has been suggested that pollen is placed on different parts of a pollinator's body corresponding to the conspecific location of pollen pickup by the stigma.Although Pedicularis is regarded as a classic example of pollinator-mediated floral isolation, such reciprocal pollen placement has not been demonstrated experimentally. This leads us to question previous observations of pollen release in Pedicularis species.Here, we show that pollen grains are released from the tip, rather than the basal opening, of the galea (the hoodlike upper lip of the corolla) in eight nectarless Pedicularis species, mimicking pollen release from poricidal anthers. We used safranin-stained pollen within anthers to track pollen placement in three Pedicularis species, and showed that pollen was deposited on numerous parts of the bumblebee's body. However, fluorescent powder placed on the stigmas to detect the contact location on the bumblebee's body was deposited mainly on the major position of pollen placement in each of the three species.Such segregation of pollen placement and pickup between species sharing the same pollinator probably helps to reduce reproductive interference, but the positions of pollen placement and stigma contact on the bumblebee's body were not as precise as previously thought.

Although there has been much experimental work on floral traits that are under selection from mutualists and antagonists, selection by abiotic environmental factors on flowers has been largely ignored. Here we test whether pollen susceptibility to rain damage could have played a role in the evolution of the reproductive architecture of Davidia involucrata, an endemic in the mountains of western China. Flowers in this tree species lack a perianth and are arranged in capitula surrounded by large (up to 10 cm x 5 cm) bracts that at anthesis turn from green to white, losing their photosynthetic capability. Flowers are nectarless, and pollen grains are presented on the recurved anther walls for 5-7 days. Flower visitors, and likely pollinators, were mainly pollen-collecting bees from the genera Apis, Xylocopa, Halictus, and Lasioglossum. Capitula with natural or white paper bracts attracted significantly more bees per hour than capitula that had their bracts removed or replaced by green paper. Experimental immersion of pollen grains in water resulted in rapid loss of viability, and capitula with bracts lost less pollen to rain than did capitula that had their bracts removed, suggesting that the bracts protect the pollen from rain damage as well as attracting pollinators.

To inspire new ideas in research on pollination ecology, we list the most important unanswered questions in the field. This list was drawn up by contacting 170 scientists from different areas of pollination ecology and asking them to contribute their opinion on the greatest knowledge gaps that need to be addressed. Almost 40% of them took part in our email poll and we received more than 650 questions and comments, which we classified into different categories representing various aspects of pollination research. The original questions were merged and synthesised, and a final vote and ranking led to the resultant list. The categories cover plant sexual reproduction, pollen and stigma biology, abiotic pollination, evolution of animal-mediated pollination, interactions of pollinators and floral antagonists, pollinator behaviour, taxonomy, plant-pollinator assemblages, geographical trends in diversity, drivers of pollinator loss, ecosystem services, management of pollination, and conservation issues such as the implementation of pollinator conservation. We focused on questions that were of a broad scope rather than case-specific; thus, addressing some questions may not be feasible within single research projects but constitute a general guide for future directions. With this compilation we hope to raise awareness of pollination-related topics not only among researchers but also among non-specialists including policy makers, funding agencies and the public at large. download Appendix

Sonication behaviour of B. friseanus differs among Pedicularis species, not only because worker bees assort themselves among plant species by body size, but also because bees of a given size adjust the buzz frequency to achieve a vibration velocity corresponding to the floral traits of each plant species. These findings, and the floral traits that characterize these and other buzz-pollinated species, are compatible with the hypothesis of vibration-induced triboelectric charging of pollen grains.

Pollinator-mediated stabilizing selection (PMSS) has been proposed as the driver of the evolutionary shift from radial to bilateral symmetry of flowers. Studies have shown that variation in flower size is lower in bilateral than in radial species, but whether bilateral flowers experience more stabilizing selection pressures by employing fewer, more specialized pollinators than radial flowers remains unclear. To test the PMSS hypothesis, we investigate plant-pollinator interactions from a whole community in an alpine meadow in Hengduan Mountains, China, to examine: (i) variance in flower size and level of ecological generalization (pollinator diversity calculated using functional groups) in 14 bilateral and 13 radial species and (ii) the role pollinator diversity played in explaining the difference of variance in flower size between bilateral and radial species. Our data showed that bilateral species had less variance in flower size and were visited by fewer pollinator groups. Pollinator diversity accounted for up to 40 per cent of the difference in variance in flower size between bilateral and radial species. The mediator effect of pollinator diversity on the relationship between floral symmetry and variance in flower size in the community is consistent with the PMSS hypothesis.