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Pollination in gymnosperms is usually accomplished by means of wind, but some groups are insect-pollinated. We show that wind and insect pollination occur in the morphologically uniform genus Ephed ...

Plant-pollinator interactions are thought to have shaped much of floral evolution. Yet the relative importance of pollinator shifts and coevolutionary interactions for among-population variation in floral traits in animal-pollinated species is poorly known. This study examined the adaptive significance of spur length in the moth-pollinated orchid Platanthera bifolia.Geographical variation in the length of the floral spur of P. bifolia was documented in relation to variation in the pollinator fauna across Scandinavia, and a reciprocal translocation experiment was conducted in south-east Sweden between a long-spurred woodland population and a short-spurred grassland population.Spur length and pollinator fauna varied among regions and habitats, and spur length was positively correlated with the proboscis length of local pollinators. In the reciprocal translocation experiment, long-spurred woodland plants had higher pollination success than short-spurred grassland plants at the woodland site, while no significant difference was observed at the grassland site.The results are consistent with the hypothesis that optimal floral phenotype varies with the morphology of the local pollinators, and that the evolution of spur length in P. bifolia has been largely driven by pollinator shifts.

Pollination success and pollen dispersal in natural populations depend on the spatial-temporal variation of flower abundance. For plants that lack rewards for pollinators, pollination success is predicted to be negatively related to flower density and flowering synchrony. We investigated the relationships between pollination success and flower abundance and flowering synchrony, and estimated pollinia dispersal distance in a rewardless species, Changnienia amoena (Orchidaceae). The results obtained in the present study revealed that male pollination success was negatively influenced by population size but was positively affected by population density, whereas female pollination success was independent of both population size and density. Phenotypic analysis suggested that highly synchronous flowering was advantageous through total pollination success, which is in contrast to previous studies. These results indicate that pollination facilitation rather than competition for pollinator visits occurs in this rewardless plant. The median distance of pollinia dispersal was 11.5 m (mean distance = 17.5 m), which is comparable to that of other rewardless plants but longer than for rewarding plants. However, pollen transfer occured mainly within populations; pollen import was a rare event. Restricted gene flow by pollinia and seeds probably explains the previous population genetic reporting a high degree of genetic differentiation between populations.

Pollinator-mediated selection has been suggested as a key driver of speciation in plants. We examined the potential role of hawkmoth pollinators in driving allopatric divergence and maintaining sympatric coexistence of morphotypes in the African iris Gladiolus longicollis. Floral tube length in this species varies from 35 mm to 130 mm across its geographic range and reflects the prevailing tongue lengths of local hawkmoth assemblages. The distribution of floral tube lengths is bimodal with two relatively discrete categories—long (about 90 mm) or short (about 50 mm)—that match the bimodal distribution of hawkmoth tongue lengths in eastern South Africa. At a contact site between these two floral morphs, we found few individuals of intermediate length, suggesting limited gene flow between morphs despite their interfertility. A difference in flowering phenology appears to be the main isolating barrier between morphs at this site. Long- and short-tubed morphs differed markedly in the chemical composition of their floral fragrance, a trait that could be used as a cue for morph-specific foraging by hawkmoths. Positive directional selection on tube length was found to occur in both morphs.

We have recently found that the morphologically determined subspecies Gymnadenia conopsea ssp conopsea in Sweden includes early and late flowering individuals. We were interested in the interactions between the flowering time groups; if there were gene flow between them and if so this was detrimental or advantageous. A spatially mixed population of early and late flowering individuals was studied using three microsatellite loci. We measured patterns in genetic differentiation and inferred occurrence of hybridisation and introgression. Variation in flowering time, fertility and relative and absolute fruit set was measured. The pattern of introgression between flowering-time groups differed between loci. In two of the three investigated loci, allele separation was distinct between early and late flowering plants and one genetically obvious hybrid was infertile. In the third locus, several alleles were shared between the two flowering time variants. The degree of introgression was associated to fruit set failure, which was higher in the late flowering plants and lower in early flowering plants. A small group of early flowering individuals with somewhat delayed flowering compared to the main group was genetically distinct and had lower relative and absolute fruit set. This group was not genetically intermediate, but rather constituting an independent group, with lower fruit set possibly caused by absence of pollinators. There seem to be a strong barrier against introgression into the late flowering group which is kept genetically distinct and less diverse. The early flowering group is diverse, includes two subgroups and seems to benefit from gene flow.

The pollination biology of Changnienia amoena , an endangered terrestrial orchid, was investigated at two sites in the Shennongjia Mountains, Hubei, central China. The results show that the orchid is exclusively pollinated by bumblebees. In Longmenhe, Bombus ( Diversobombus ) trifasciatus is the primary effective pollinator, whereas B. ( Tricornibombus ) imitator is the only pollinator in Guanmenshan. These two bumblebees can be treated as a functional group because they carry pollinaria on the same position on their bodies and have similar pollinating behaviours. The morphological traits of the flower adapt precisely to the pollinators. Visitation by bumblebees is mainly in the first half of the flowering period of C. amoena . Pollinarium removal and pollinia deposition take place when bumblebees withdraw from the flower. Crossing experiments show that C. amoena is a self-compatible and outcrossing species. Fruit set in this species is low and may result from limited pollinators because 87.5% of individuals set fruits under hand-pollination, but only 6‐12% of individuals set fruits under natural conditions. These results imply that it is important to conserve the pollinator community together with the plants when conservation management for this endangered species is undertaken. Artificial pollination would also be a useful measure to facilitate restoration of the small populations. © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 150 , 165‐175. ADDITIONAL KEYWORDS: adaptation ‐ bumblebee ‐ flowering phenology ‐ fruit set ‐ pollinarium removal ‐ pollinia deposition.

We estimated selection on three morphological characters in the hermaphroditic, hawkmoth-pollinated orchid Platanthera bifolia and explored selection surfaces through male and female function. The work was carried out in northern Sweden during two flowering seasons (1994 and 1995) in one natural population and one season (1995) in another natural population. Fitness was estimated as number of pollinia removed (male function) and number of fruits produced (female function). We detected directional selection towards larger inflorescence size (flower number) through both sex functions in both populations in 1995. In 1994, with an unusually dry growing season, 78% of the individuals failed to set any fruit, and there was selection for larger inflorescences only through male function. In this year, there was selection towards longer flower spurs, which could be a direct or indirect effect of spurs being shortened by drought. The results demonstrate that selection patterns may vary temporally and spatially, and that the 'male function hypothesis' may be applicable as female function is more resource dependent than male function.

Mimicry, as an adaptive explanation for the resemblance between organisms, is not always readily distinguishable from, inter alia, coincidence, shared ancestry, or convergent evolution. We tested the hypothesis that two rare South African orchid taxa Brownleea galpinii ssp. major (nectar-producing) and Disa cephalotes ssp. cephalotes (non-rewarding) are mimics of the nectar-producing flowers of a relatively common species, Scabiosa columbaria (Dipsacaceae), with which they always occur sympatrically. Flowers of the orchids were apparently unscented and had similar dimensions and almost identical spectral reflectance to the flowers of Scabiosa. The orchids were pollinated exclusively by long-proboscid flies (Tabanidae and Nemestrinidae) that feed mainly on nectar in Scabiosa flowers. Choice experiments showed that these flies did not discriminate between the orchids and Scabiosa when alighting on their flat-topped inflorescences. However, flies were not attracted to related orchids dissimilar to Scabiosa, or to inflorescences of B. galpinii that had been artificially reconstructed in the shape of a spike, rather than a flat-topped capitulum. A phylogenetic analysis showed traits that give the orchids a resemblance to Scabiosa, such as a flat-topped inflorescence and cream floral colouration with dark spots and short spurs, to be mostly apomorphic features, and therefore likely to be relatively recent adaptations for mimicry. We caution that the term mimic should not be applied to species whose resemblance to another species is due entirely to plesiomorphic traits that, in all likelihood, evolved prior to the ecological association. © 2003 The Linnean Society of London, Biological Journal of the Linnean Society, 2003, 80, 289–304.

Darwin's mechanistic model whereby selection favours plants with flower tubes that exceed the tongue length of the primary pollinator, was tested using unmanipulated plants of the hawkmoth-pollinated South African iris, Gladiolus longicollis. The study population was characterized by exceptionally large phenotypic variation in flower-tube length (range 56-129 mm). Directional selection on tube length was revealed by a significant positive relationship between this trait and both fruit and seed set. Selection was attributed to the effect of tube length on pollen receipt, as supplemental hand pollinations showed fruit and seed set in the population to be pollen limited. Indirect selection on tube length may also occur through the correlation of this trait with inflorescence height, although direct selection on the latter trait was significant only for seed set. The main pollinators at the study site were individuals of the large hawkmoth Agrius convolvuli that had tongue lengths of 85-135 mm. Other hawkmoths had tongues that were much too short to reach the nectar in G. longicollis flowers and seldom carried pollen of G. longicollis. Flowers with tubes shorter than the tongues of A. convolvuli are apparently not effectively pollinated because stigmas do not contact the moth's head effectively. This study demonstrates that selection may occur among plants with natural phenotypic variation in flower-tube length, and supports Darwin's model of pollinator-mediated selection.

It has been proposed that in non-rewarding animal-pollinated plants the pollination intensity should decrease with increasing population size and should increase with increasing local abundance of reward-producing plants. To test these hypotheses, we examined how population size, local abundance of Salix caprea, and tree cover were related to pollen removal and fruit production in 16 populations of the deceptive, early-flowering and bumblebee-pollinated orchid Calypso bulbosa in northern Sweden in 3 consecutive years. To determine whether fruit production was limited by pollinator visitation, supplemental hand-pollinations were performed in three populations in 3 years. Finally, to examine whether increased fruit production was associated with a reduction in future flower production, vegetative growth or survival, supplemental hand-pollination was repeated for 5 years in one population. The levels of pollen export, pollen deposition, and fruit set of C. bulbosa varied considerably among years and among populations. The proportion of plants exporting pollen was negatively related to population size, and positively related to density of S. caprea and to tree cover in 1 of the 3 years. In the other 2 years, no significant relationship was detected between proportion of plants exporting pollen and the latter three variables. In no year was there a significant relationship between fruit set and population size, density of S. caprea and tree cover. There was substantial among-year variation in the extent to which fruit production was limited by insufficient pollen deposition and in the amount of weather-induced damage to flowers and developing fruits. Fruit set was consistently higher in hand-pollinated than in open-pollinated plants, but this difference was statistically significant in only one of 3 years. Supplemental hand-pollination in 5 consecutive years increased cumulative fruit production 1.8 times, but did not affect flower production, plant size, or survival. Tree cover was negatively correlated with the incidence of frost damage in 1 year. The results indicate that life-time seed production may be pollen limited in C. bulbosa, and that variation in population size and local abundance of the early-flowering, nectar-producing S. caprea can only partly explain the extensive variation in pollinator visitation among populations of this species.

Pollinator-mediated selection has been suggested as a key driver of speciation in plants. We examined the potential role of hawkmoth pollinators in driving allopatric divergence and maintaining sympatric coexistence of morphotypes in the African iris Gladiolus longicollis. Floral tube length in this species varies from 35 mm to 130 mm across its geographic range and reflects the prevailing tongue lengths of local hawkmoth assemblages. The distribution of floral tube lengths is bimodal with two relatively discrete categories--long (about 90 mm) or short (about 50 mm)--that match the bimodal distribution of hawkmoth tongue lengths in eastern South Africa. At a contact site between these two floral morphs, we found few individuals of intermediate length, suggesting limited gene flow between morphs despite their interfertility. A difference in flowering phenology appears to be the main isolating barrier between morphs at this site. Long- and short-tubed morphs differed markedly in the chemical composition of their floral fragrance, a trait that could be used as a cue for morph-specific foraging by hawkmoths. Positive directional selection on tube length was found to occur in both morphs.

We have recently found that the morphologically determined subspecies Gymnadenia conopsea ssp conopsea in Sweden includes early and late flowering individuals. We were interested in the interactions between the flowering time groups; if there were gene flow between them and if so this was detrimental or advantageous. A spatially mixed population of early and late flowering individuals was studied using three microsatellite loci. We measured patterns in genetic differentiation and inferred occurrence of hybridisation and introgression. Variation in flowering time, fertility and relative and absolute fruit set was measured. The pattern of introgression between flowering-time groups differed between loci. In two of the three investigated loci, allele separation was distinct between early and late flowering plants and one genetically obvious hybrid was infertile. In the third locus, several alleles were shared between the two flowering time variants. The degree of introgression was associated to fruit set failure, which was higher in the late flowering plants and lower in early flowering plants. A small group of early flowering individuals with somewhat delayed flowering compared to the main group was genetically distinct and had lower relative and absolute fruit set. This group was not genetically intermediate, but rather constituting an independent group, with lower fruit set possibly caused by absence of pollinators. There seem to be a strong barrier against introgression into the late flowering group which is kept genetically distinct and less diverse. The early flowering group is diverse, includes two subgroups and seems to benefit from gene flow.

Among- and within-population variation at neutral loci is governed by an interaction between stochastic processes and gene flow. A previous study of pollen dispersal in which the transfer of individually marked pollinia was monitored, indicated not only that populations of the nonrewarding, bumblebee-pollinated orchid Calypso bulbosa are connected by substantial levels of gene flow, but also that seed production may be the result of self-fertilization to a considerable extent. We examined the genetic structure of 21 C. bulbosa populations in northern Sweden by F-statistics analyses of variation at three polymorphic allozyme loci. Four populations each consisted of two or three distinct patches, which also allowed us to evaluate among-patch differentiation. The inbreeding coefficient over all loci within populations was high (FIS=0.283). F-statistics indicated that the level of genetic differentiation among patches within populations varied among populations. FST among patches within populations ranged between -0.021 and 0.119 and was significantly different from zero in two of the populations. There was low to moderate genetic differentiation among populations (FST=0. 072). A Mantel test indicated a positive correlation between geographical and genetic distances among populations, but this correlation was dependent on the difference in allele frequencies between the southernmost population sampled and all other populations. Self-fertilization and substructuring within sampling units (within patches and populations) may have contributed to the high inbreeding coefficients observed in many C. bulbosa populations. Long-distance seed and pollen dispersal may account for the low to moderate genetic differentiation among populations.