Who can open the flower? Assessment of the flower opening force of mammal‐pollinated Mucuna macrocarpa

Effective pollinators in Fabaceae species with papillionaceous flowers should have sufficient force to open the petals and expose the stamens and pistils from the keel petals. Here, we assessed the force that is required (operative force) to open the petals of the mammal‐pollinated Mucuna macrocarpa, in parallel with estimating the force of bee species. The operative force of M. macrocarpa was quantified by a digital force gauge and the force of three bee species that frequent these flowers was estimated from body mass. The operative force was 1.635 ± 0.146 (mean ± SD) newton (N). This force was far larger than that estimated for the largest bee in the study area. In addition, the operative force of M. macrocarpa was 16–409 times greater than that of bee‐pollinated plants. Our results demonstrate that the operative force of M. macrocarpa flowers is adapted to mammalian openers, preventing potential nectar robbers.     

Apios americana,a fly-pollinated papilionaceous flower?

In the flowers ofApios americana the vexillum remains ± in its bud position. In this way, a dark cavity is formed displaying a bright window at its base. Insect visitors are attracted to the hidden inflorescences by scent. In their attempt to reach the window they trigger an explosive release of stigma and pollen. Stigmatic fluid glues pollen to the visitor. All characters of the flower fit well into the myiophilous syndrome and thus flies are expected to be the proper pollinators.Apios americana seems to be the only myiophilous exception within the predominantly melittophilousFabaceae.     

Does flower phenology mirror the slowdown of global warming?

Although recent global warming trends in air temperature are not as pronounced as those observed only one decade ago, global mean temperature is still at a very high level. Does plant phenology – which is believed to be a suitable indicator of climate change – respond in a similar way, that is, does it still mirror recent temperature variations? We explored in detail long-term flowering onset dates of snowdrop, cherry, and lime tree and relevant spring temperatures at three sites in Germany (1901–2012) using the Bayesian multiple change-point approach. We investigated whether mean spring temperature changes were amplified or slowed down in the past decade and how plant phenology responded to the most recent temperature changes. Incorporating records with different end points (i.e., 2002 and 2012), we compared differences in trends and inferred possible differences caused by extrapolating phenological and meteorological data. The new multiple-change point approach is characterized by an enhanced structure and greater flexibility compared to the one change point model. However, the highest model probabilities for phenological (meteorological) records were still obtained for the one change point (linear) model. Marked warming trends in the recent decade were only revealed for mean temperatures of March to May, here better described with one or two change point models. In the majority of cases analyzed, changes in temperatures were well mirrored by phenological changes. However, temperatures in March to May were linked to less strongly advancing onset dates for lime tree flowering during the period 1901-2012, pointing to the likely influence of photoperiodic constraints or unfulfilled chilling requirements. Due to the slowdown of temperature increase, analyses conducted on records ending in 2002 demonstrated distinct differences when compared with records ending in 2012. Extrapolation of trends could therefore (along with the choice of the statistical method) lead to distinctly different results and most recent data should be integrated in order not to over- or underestimate future phenological changes.     

Do pollinators influence the assembly of flower colours within plant communities?

The co-occurrence of plant species within a community is influenced by local deterministic or neutral processes as well as historical regional processes. Floral trait distributions of co-flowering species that share pollinators may reflect the impact of pollinator preference and constancy on their assembly within local communities. While pollinator sharing may lead to increased visitation rates for species with similar flowers, the receipt of foreign pollen via interspecific pollinator movements can decrease seed set. We investigated the pattern of community flower colour assembly as perceived by native honeybee pollinators within 24 local assemblages of co-flowering Oxalis species within the Greater Cape Floristic Region, South Africa. To explore the influence of pollinators on trait assembly, we assessed the impact of colour similarity on pollinator choices and the cost of heterospecific pollen receipt. We show that flower colour is significantly clustered within Oxalis communities and that this is not due to historical constraint, as flower colour is evolutionarily labile within Oxalis and communities are randomly structured with respect to phylogeny. Pollinator observations reveal that the likelihood of pollinators switching between co-flowering species is low and increases with flower colour similarity. Interspecific hand pollination significantly reduced seed set in the four Oxalis species we investigated, and all were dependant on pollinators for reproduction. Together these results imply that flower colour similarity carries a potential fitness cost. However, pollinators were highly flower constant, and remained so despite the extreme similarity of flower colour as perceived by honeybees. This suggests that other floral traits facilitate discrimination between similarly coloured species, thereby likely resulting in a low incidence of interspecific pollen transfer (IPT). If colour similarity promotes pollinator attraction at the community level, the observed clustering of flower colour within communities might result from indirect facilitative interactions.     

Differential effects of flower feeding in an insect host–parasitoid system

In many insect host–parasitoid systems, both the host and its parasitoids forage on shared floral resources. As a result of insect behaviour, morphology and physiology, flower species may act selectively at different levels of such systems, e.g., between the trophic levels of hosts and parasitoids, between species within a guild, between sexes or individuals within a species or between life history traits within an individual. We asked if effects of selectivity are consistent across levels in the horse chestnut leafminer, Cameraria ohridella, and its parasitoid complex. Insects were exposed singly in no-choice feeding trials to twelve common flower species and their survival and reproduction were recorded. Only one of twelve flower species (Ranunculus acris) tended to selectively favour the longevity of leafminers, but not of parasitoids. No flower species were found to favour parasitoids only. Both trophic levels profited from feeding on Anthriscus sylvestris, however, parasitoids benefited up to eight times more than their hosts. No differences were found among the species of the parasitoid guild, but females lived significantly longer than males, and single individuals within species were able to exploit generally unfavourable flower species. Out of the seven flower species that increased the longevity of leafminer females, only Chaerophyllum hirsutum significantly enhanced the number of eggs laid. Fecundity was generally positively correlated with longevity of leafminer females, but two flower species (C. hirsutum, Taraxacum officinale) had an additional positive effect on fecundity. In conclusion, we demonstrated that flowers act differently on life history traits in a host–parasitoid system at a multitude of biological levels and that these effects are not always consistent across levels. Selective plant-derived resources can therefore modify herbivore–natural enemy interactions in ways that are more complex than currently appreciated.     

Can semiochemicals attract both western flower thrips and their anthocorid predators?

Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae) (western flower thrips, WFT) is a key pest in a range of crops worldwide. Anthocorid species (Hemiptera) are important natural enemies of thrips. Several experiments were undertaken to determine whether a thrips lure, methyl isonicotinate (MI), affected the behaviour of WFT and anthocorids found in outdoor crops. Currently, this volatile compound is used in conjunction with sticky traps for monitoring thrips predominantly in greenhouses in Northern Europe. In the present study, in a nectarine [Prunus persica (L.) (Rosaceae)] orchard and an outdoor capsicum [Capsicum annuum L. (Solanaceae)] crop in Spain, blue sticky and white water traps with MI caught significantly more WFT than traps without MI. The volatile compound also significantly increased both blue sticky and white water trap capture of anthocorids – predominantly Orius laevigatus (Fieber) (Hemiptera: Anthocoridae) – in the capsicum crop. These results indicate that the behaviour of both WFT and O. laevigatus were altered by the presence of the compound and suggest there is potential to develop novel tools based on MI in conjunction with biological control strategies for thrips management.     

β-Glucan synthetase II activity upon callose formation in the flower ofArabidopsis thaliana

Callose formation was observed in the pollens during flower development and pollen tube grown in the pistil ofA. thaliana. The accumulation of callose occurred in the tetrad in the flower bud and pollen tube. Therefore, the activity of β-glucan synthetase II (GS II), which is responsible for synthesizing the callose, was measured in the flowers on the same developmental stages. The enzyme activity was increased by about 10% while the level of callose contents was increased by about 70% in tetrads. Then, callose accumulation was increased during pollen tube growth by about 30% higher than the other stages and enzyme activity was detected, 30% more too. These results suggest that callose plays an important role in the growth of pollen and pollen tube by increasing GS II activity.     

How does plant richness affect pollinator richness and temporal stability of flower visits?

Pollinators play a key role in the reproduction of most plant species, and pollinator and plant diversity are often related. We studied an experimental gradient of plant species richness for a better understanding of plant–pollinator community interactions and their temporal variability, because in non‐experimental field surveys plant richness is often confounded with gradients in management, soil fertility, and community composition. We observed pollinator species richness and frequency of visits six times in 73 plots over two years, and used advanced statistical analysis to account for the high number of zeroes that often occur in count data of rare species. The frequency of pollinator visits increased linearly with both the blossom cover and the number of flowering plant species, which was closely related to the total number of plant species, whereas the number of pollinator species followed a saturation curve. The presence of particularly attractive plant species was only important for the frequency of flower visits, but not to the richness of pollinators. Plant species richness, blossom cover, and the presence of attractive plant species enhanced the temporal stability in the frequency of pollinator visits. In conclusion, grasslands with high plant diversity enhance and stabilize frequent and diverse flower visitations, which should sustain effective pollination and plant reproduction.     

Are pollinators the agents of selection on flower colour and size in irises?

Plant–pollinator interactions are believed to play a major role in the evolution of floral traits. Flower colour and flower size are important for attracting pollinators, directly influencing reproduction, and thus expected to be under pollinator‐mediated selection. Pollinator‐mediated selection is also proposed to play a role in maintaining flower colour polymorphism within populations. However, pigment concentrations, and thus flower colour, are also under selective pressures independent of pollinators. We quantified phenotypic pollinator‐mediated selection on flower colour and size in two colour polymorphic Iris species. Using female fitness, we estimated phenotypic selection on flower colour and size, and tested for pollinator‐mediated selection by comparing selection gradients between flowers open to natural pollination and supplementary pollinated flowers. In both species, we found evidence for pollen limitation, which set the base for pollinator‐mediated selection. In the colour dimorphic Iris lutescens, while pigment concentration and flower size were found to be under selection, this was independent of pollinators. For the polymorphic Iris pumila, pigment concentration is under selective pressure by pollinators, but only for one colour morph. Our results suggest that pollinators are not the main agents of selection on floral traits in these irises, as opposed to the accepted paradigm on floral evolution. This study provides an opposing example to the largely‐accepted theory that pollinators are the major agent of selection on floral traits.     

Why does the flower stalk of Pulsatilla cernua (Ranunculaceae) bend during anthesis?

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.     

On ‘various contrivances’: pollination,phylogeny and flower form in the Solanaceae

Members of the euasterid angiosperm family Solanaceae have been characterized as remarkably diverse in terms of flower morphology and pollinator type. In order to test the relative contribution of phylogeny to the pattern of distribution of floral characters related to pollination, flower form and pollinators have been mapped onto a molecular phylogeny of the family. Bilateral flower symmetry (zygomorphy) is prevalent in the basal grades of the family, and more derived clades have flowers that are largely radially symmetric, with some parallel evolution of floral bilateralism. Pollinator types (‘syndromes’) are extremely homoplastic in the family, but members of subfamily Solanoideae are exceptional in being largely bee pollinated. Pollinator relationships in those genera where they have been investigated more fully are not as specific as flower morphology and the classical pollinator syndrome models might suggest, and more detailed studies in some particularly variable genera, such as Iochroma and Nicotiana, are key to understanding the role of pollinators in floral evolution and adaptive radiation in the family. More studies of pollinators in the field are a priority.     

Molecular cloning of ABNORMAL FLORAL ORGANS: a gene required for flower development in Arabidopsis

 We report the cloning and characterization of the gene ABNORMAL FLORAL ORGANS (AFO), which is required for normal flower development in Arabidopsis. afo mutant flowers show defects in all four floral whorls. The number of organs in each whorl varies. Most flowers consist of reduced numbers of petals and stamens, even though supernumerary sepals and carpels may be observed. Abnormal organ structure is evident from an early stage. Mosaic first whorl organs are common, with some sepals taking on petaloid or staminoid characteristics. Stamens are often deformed, having thin filaments and reduced anthers, yet occasionally producing viable pollen. Partial fertility is indicated by some seed setting. The afo-1 mutation is caused by insertion of a gene trap Ds transposable element. The AFO gene was cloned and is predicted to encode a novel protein of 229 amino acids. The expression of AFO mRNA by northern blot analysis in combination with mutant phenotype suggests that the AFO gene product plays an important role in Arabidopsis flower development. We also report that antherless, a previously described male-sterile mutation, is allelic to afo-1. Received: 3 September 1998 / Revision accepted: 15 December 1998