Positive effects of flower abundance and synchronous flowering on pollination success,and pollinia dispersal in rewardless Changnienia amoena (Orchidaceae)

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. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 99 , 477–488.     

Floral resources,pollinators and fruiting in a threatened tropical deciduous tree

Aims Nothapodytes nimmoniana (Family Icacinaceae) is a deciduous tree species distributed in Asia facing severe population decline. Wood chips from the tree are a source of camptothecin, a globally sought-after alkaloid with cancer-treating properties, and are harvested unsustainably in natural forests. We studied the pollination ecology of the species and asked if there are constraints in pollination and fruiting success in its natural populations. We also discuss the potential effects of wood extraction on pollinators and reproductive success in the population.Methods The study was carried out during the flowering season in two populations with varying exploitation levels, both located in the Protected Area Network in the Western Ghats of Karnataka State. We assessed floral resource availability and measured pollinator diversity and activity in the canopy from the perspective of the biology of the species. We quantified pollinator abundance and percent fruit set as a function of population density.Important findings Flowers belong to the fly pollination syndrome and are open to visits by generalists such as Apis dorsata and Trigona iridipennis. Fruiting success did not vary between exploited and unexploited sites, but there was a significant difference in pollinator assemblage. In a lean male flowering year, fruit set was low, suggesting pollen limitation in the population. No fruiting was recorded in the second year at the site where trees were felled soon after the flowering period. We argue that when male floral resources are altered in exploited populations, pollinators of generalist nature may show a shift in foraging pattern. Also, generalist plants may be as susceptible to pollination loss as are specialist plants. The need for outcrossing in the species would probably exacerbate this vulnerability.     

Pollination of the European food-deceptive Traunsteinera globosa (Orchidaceae): the importance of nectar-producing neighbouring plants

European food-deceptive orchids generally flower early in spring and rely on naïve pollinators for their reproduction. Some species however, flower later in the summer, when many other rewarding plants species are also in bloom. In dense flowering communities, deceptive orchids may suffer from competition for pollinator resources, or might alternatively benefit from higher community attractiveness. We investigated the pollination strategy of the deceptive species Traunsteinera globosa, and more specifically whether it benefited from the presence of coflowering rewarding species. We carried out a population survey to quantify the density and reproductive success of the orchid as well as the density of all coflowering species. Our results suggest that the deceptive orchid not only benefited from the presence of coflowering species, but that interestingly the density of the species Trifolium pratense was significantly positively correlated with the orchid's reproductive success. This species might simply act as a magnet species attracting pollinators near T. globosa, or could influence the orchid reproductive fitness through a more species-specific interaction. We propose that morphological or colour similarities between the two species should be investigated in more detail to decipher this pollination facilitation effect.     

Effects of multiple competitors for pollination on bumblebee foraging patterns and Mimulus ringens reproductive success

When co‐occurring plant species overlap in flowering phenology they may compete for the service of shared pollinators. Competition for pollination may lower plant reproductive success by reducing the number of pollinator probes or by decreasing the quality of pollen transport to or from a focal species. Pair‐wise interactions between plants sharing pollinators have been well documented. However, relatively few studies have examined interactions for pollination among three or more plant species, and little is known about how the outcomes and mechanisms of competition for pollination may vary with competitor species composition. To better understand how the dynamics of competition for pollination may be influenced by changes in the number of competitors, we manipulated the presence of two competitors, Lythrum salicaria and Lobelia siphilitica, and quantified reproductive success for a third species, Mimulus ringens. Patterns of pollinator preference and interspecific transitions in mixed‐species arrays were significantly influenced by the species composition of competitor plants present. Both pair‐wise and three‐species competition treatments led to a similar ～ 40% reduction in Mimulus ringens seed set. However, the patterns of pollinator foraging we observed suggest that the relative importance of different mechanisms of competition for pollination may vary with the identity and number of competitors present. This variation in mechanisms of competition for pollination may be especially important in diverse plant communities where many species interact through shared pollinators.     

Two invasive acacia species secure generalist pollinators in invaded communities

Exotic entomophilous plants need to establish effective pollinator interactions in order to succeed after being introduced into a new community, particularly if they are obligatory outbreeders. By establishing these novel interactions in the new non-native range, invasive plants are hypothesised to drive changes in the composition and functioning of the native pollinator community, with potential impacts on the pollination biology of native co-flowering plants. We used two different sites in Portugal, each invaded by a different acacia species, to assess whether two native Australian trees, Acacia dealbata and Acacia longifolia, were able to recruit pollinators in Portugal, and whether the pollinator community visiting acacia trees differed from the pollinator communities interacting with native co-flowering plants. Our results indicate that in the invaded range of Portugal both acacia species were able to establish novel mutualistic interactions, predominantly with generalist pollinators. For each of the two studied sites, only two other co-occurring native plant species presented partially overlapping phenologies. We observed significant differences in pollinator richness and visitation rates among native and non-native plant species, although the study of β diversity indicated that only the native plant Lithodora fruticosa presented a differentiated set of pollinator species. Acacias experienced a large number of visits by numerous pollinator species, but massive acacia flowering resulted in flower visitation rates frequently lower than those of the native co-flowering species. We conclude that the establishment of mutualisms in Portugal likely contributes to the effective and profuse production of acacia seeds in Portugal. Despite the massive flowering of A. dealbata and A. longifolia, native plant species attained similar or higher visitation rates than acacias.     

Linné's floral clock is slow without pollinators--flower closure and plant-pollinator interaction webs

Temporal patterns of flower opening and closure within a day are known as Linné's floral clock. Time of flower closure has been explained mainly by light in the traditional botanical literature. We show with a set of experiments that Asteraceae flower heads can close within three hours after pollination, whereas un-pollinated flower heads stay open until the late afternoon. This suggests that closing time strongly depends on pollinators. Using plant-pollinator interaction webs we further demonstrate that the daily pattern of flower opening and the rapid response to pollination can impose strong temporal dynamics on interspecific interactions within a single day. We observed pollinator species turnover and changes in facilitation vs. competition among plants. Our results show for the first time that pollination induces rapid flower closure on the community level. This causes imprecision in Linné's floral clock with far-reaching consequences for plant-pollinator interactions.     

Pollination outcomes reveal negative density‐dependence coupled with interspecific facilitation among plants

Pollination is thought to be under positive density‐dependence, destabilising plant coexistence by conferring fitness disadvantages to rare species. Such disadvantage is exacerbated by interspecific competition but can be mitigated by facilitation and intraspecific competition. However, pollinator scarcity should enhance intraspecific plant competition and impose disadvantage on common over rare species (negative density‐dependence, NDD). We assessed pollination proxies (visitation rate, pollen receipt, pollen tubes) in a generalised plant community and related them to conspecific and heterospecific density, expecting NDD and interspecific facilitation due to the natural pollinator scarcity. Contrary to usual expectations, all proxies indicated strong intraspecific competition for common plants. Moreover interspecific facilitation prevailed and was stronger for rare than for common plants. Both NDD and interspecific facilitation were modulated by specialisation, floral display and pollinator group. The combination of intraspecific competition and interspecific facilitation fosters plant coexistence, suggesting that pollination can be a niche axis maintaining plant diversity.     

Co-flowering plants support diverse pollinator populations and facilitate pollinator visitation to sweet cherry crops

Many food crops depend on animal pollination to set fruit. In light of pollinator declines there is growing recognition of the need for agro-ecosystems that can sustain wild pollinator populations, ensuring fruit production and pollinator conservation into the future. One method of supporting resident wild pollinator populations within agricultural landscapes is to encourage and maintain floral diversity. However, pollinator visitation to crop plants can be affected either positively (facilitation) or negatively (competition) by the presence of co-flowering plants. The strength and direction of the facilitative/competitive relationship is driven by multiple factors, including floral abundance and the degree of overlap in pollinator visitation networks. We sought to determine how plant-pollinator networks, within and surrounding sweet cherry (Prunus avium) orchards, change across key time points during the cherry flowering season, in three growing regions in Australia. We found significant overlap in the suite of flower visitors, with seven taxa (including native bees, flies, hoverflies and introduced honey bees, Apis mellifera) observed visiting cherry and other co-flowering species within the orchard and/or the wider surrounding matrix. We found evidence of pollinator facilitation with significantly more total cherry flower visits with increasing percent cover of co-flowering plants within the wider landscape matrix and increased visitation to cherry by honey bees with increasing co-flowering plant richness within the orchard. During the cherry flowering period there was a significant positive relationship between pollinator richness on cherry and pollinator richness on co-flowering plants within the orchard and the area of native vegetation surrounding orchards. Outside of the crop flowering season, co-flowering plants within the orchard and wider landscape matrix supported the same pollinator taxa that were recorded visiting cherry when the crop was flowering. This shows wild plants help support the pollinators important to crop pollination, outside of the crop flowering season, highlighting the role of co-flowering plants within pollinator-dependent cropping systems.     

Displacement of flowering phenologies among plant species by competition for generalist pollinators

We model the evolution of allochronic isolation between sympatric animal‐pollinated plant species via displacement of their flowering times. The plant species share generalist pollinators and either produce inviable hybrid seeds or do not hybridize at all. Displacement of flowering times between reproductively isolated species reduces competition for pollinators and the formation of inviable hybrid seeds. Under strong pollen limitation, competition for pollinators causes rapid evolution of allochronic isolation both for hybridizing and nonhybridizing species. Under weak pollen limitation, allochronic isolation evolves rapidly for hybridizing species but more slowly for nonhybridizing species. Positive density‐dependent pollinator visitation rate at low flower densities facilitates allochronic isolation under weak pollen limitation. Allochronic isolation among sympatric species sharing generalist pollinators could be common under any intensity of pollen limitation if the flowering season is sufficiently long.     

Factors related to the inter‐annual variation in plants' pollination generalization levels within a community

The number of pollinators of a plant species is considered a measure of its ecological generalization and may have important evolutionary and ecological implications. Many pollination studies report inter‐annual fluctuations in the composition of pollinators to particular species. However, the factors causing such variation are still poorly understood. Here we investigate how flowering duration and plant and pollinator assemblages influenced the inter‐annual changes in the functional generalization level of the 20 most common plant species of a semi‐natural meadow in southern Norway. We also studied the extent to which changes in generalization levels were controlled by flower‐shape and flowering time. Large inter‐annual changes in generalization levels were common and there was no relationship between the generalization level one year and the following. Generalization level of particular plant species increased with flowering duration, sampling effort, and the abundance of managed honeybees in the community. Generalization level decreased with the flowering synchrony between the focal plant species and the rest of the plant community and with the focal species’ own abundance, which we attribute to inter‐specific competition for pollinator attraction and foraging decisions made by pollinators. Plants with different flower‐shapes and flowering times did not differ in the extent of inter‐annual variation in generalization levels. Most studies do not consider the effect of the plant community on the generalization level of particular plant species. We show here that both pollinator and plant assemblages can affect the inter‐annual variation in generalization levels of plant species. Studies like ours will help to understand how pollination interactions are structured at the community level, and the ecological and evolutionary consequences that these inter‐annual changes in generalization levels may have.     

Does community‐level floral abundance affect the pollination success of a rewardless orchid,Calanthe reflexa Maxim.?

Decreases in pollinator abundance may particularly constrain plants that lack floral rewards, since they are poor competitors for pollinators in the plant community. Here, we documented the pollination ecology of a rewardless orchid, Calanthe reflexa Maxim., and examined effects of forest understory degradation by deer browsing on pollination success of the species in the light of a change in the abundance of neighboring flowering plants in 2010 and 2011. Bombus species were the only pollinators at each site and the flowering phenology of C. reflexa did not overlap with that of other rewarding plants. Pollinator visit rates (assessed by time‐lapse photography), and pollinia removal rate were higher in the undegraded understory site than the degraded site in both years, while the fruit set ratio did not differ between the sites in 2011. Coverage by neighboring flowering plants was extremely low in the degraded site. Our results suggest that, although its flowering phenology and consequently lower interspecific competition of C. reflexa with rewarding plants for attracting bumblebees, neighboring flowering plants may play an important role for maintaining the visitation frequency of bumblebees of C. reflexa and contribute to its pollination success.     

Effects of patch size and density on flower visitation and seed set of wild plants: a pan-European approach

1.  Habitat fragmentation can affect pollinator and plant population structure in terms of species composition, abundance, area covered and density of flowering plants. This, in turn, may affect pollinator visitation frequency, pollen deposition, seed set and plant fitness.
2.  A reduction in the quantity of flower visits can be coupled with a reduction in the quality of pollination service and hence the plants' overall reproductive success and long-term survival. Understanding the relationship between plant population size and/or isolation and pollination limitation is of fundamental importance for plant conservation.
3.  We examined flower visitation and seed set of 10 different plant species from five European countries to investigate the general effects of plant populations size and density, both within (patch level) and between populations (population level), on seed set and pollination limitation.
4.  We found evidence that the effects of area and density of flowering plant assemblages were generally more pronounced at the patch level than at the population level. We also found that patch and population level together influenced flower visitation and seed set, and the latter increased with increasing patch area and density, but this effect was only apparent in small populations.
5.   Synthesis. By using an extensive pan-European data set on flower visitation and seed set we have identified a general pattern in the interplay between the attractiveness of flowering plant patches for pollinators and density dependence of flower visitation, and also a strong plant species-specific response to habitat fragmentation effects. This can guide efforts to conserve plant–pollinator interactions, ecosystem functioning and plant fitness in fragmented habitats.     

Temporal variations in the linkages between plants and flower visitors and the pollination success of Primula modesta along the snowmelt gradient

Although pollination networks between plants and flower visitors are diverse and flexible, seed production of many plant species is restricted by pollen limitation. Obligate outcrossers often suffer from low pollinator activity or severe interspecific competition for pollinator acquisition among co-flowering species. This study focused on seasonal changes in plant–flower visitor linkages in an alpine ecosystem and examined whether and how this seasonality affected the seed-set of Primula modesta, a self-incompatible distylous herb having long-tubed flowers. First, we recorded the linkages between plants and flower visitors along the snowmelt gradient. Then, pollination experiment was conducted to estimate the degree of pollen limitation over the course of flowering season of P. modesta. Flower visitors were classified by their tongue length based on the morphological matching with P. modesta flowers. As the season progressed, plant–visitor linkages became more diverse and generalized, and the visitation frequency to P. modesta flowers increased. In the later part of the season, however, the seed set of P. modesta was significantly reduced due to severe pollen limitation, presumably because of increased competition for long-tongued pollinators among co-flowering species. The present study revealed that pollinator availability for specialist species may be restricted even when plant–visitor linkages are diverse and generalized as a whole. In the case of P. modesta, morphological matching and competition for pollinators might be the main factors explaining this discrepancy.     

Functional Significance of Interspecific Variation in Burmeistera Flower Morphology: Evidence from Nectar Bat Captures in Ecuador

What causes flowers to diverge? While a plant's primary pollinator should strongly influence floral phenotype, selective pressures may also be exerted by other flower visitors or competition with other plants for pollination. Species of the primarily bat‐pollinated genus Burmeistera (Campanulaceae) frequently cooccur, with up to four species in a given site, and broadly overlap in flowering phenology, typically flowering throughout the year. The genus displays extensive interspecific variation in floral morphology in the degree that the reproductive parts (anthers and stigma) are exserted outside of the corolla, and species can be roughly classified as either long or short‐exserted. I tested two hypotheses regarding the functional significance of such variation: (1) exsertion lengths correspond to pollination by bat species of different sizes; and (2) variation serves to partition pollinator's bodies spatially and thus reduces interspecific pollen transfer. I captured bats in Ecuador to evaluate the identity and location of the Burmeistera pollen they were carrying. Results show that exsertion does not correspond to specialization on different pollinators; different bat species carried pollen of both flower types just as frequently. In support of the second hypothesis, pollen from flowers of different exsertion lengths was found to occur on different regions of bats' heads. This may serve to reduce competition for pollination among coexisting Burmeistera.     

地下结实植物白番红花的繁育系统与传粉生物学

地下结实是植物用来防御不利环境的一种策略, 研究地下结实植物的繁殖特性, 可以揭示它们的繁殖对策多样性, 对于探讨环境选择压力对其繁育系统及后代适合度的影响具有重要意义。白番红花(Crocus alatavicus)是一种分布在天山西部亚高山带、具地下芽和地下结实特性的早春短命植物。我们采用野外观测和统计分析方法, 对该物种的繁育系统与传粉生物学及其对亚高山环境的适应进行了研究。研究结果表明: 白番红花具有先花后叶的特性, 于4月上中旬始花, 呈爆发式开花式样; 花白色, 无花蜜无气味; 开花时, 下位子房位于地下, 花蕾在地上开放并随光照变化而开闭; 单花花期为6–9 d, 花萎蔫时花粉活性仍保持在75.39±5.69%, 柱头可授期为8 d。人工授粉实验结果显示, 该物种属于兼性异交繁育系统, 且具有自主自花授粉能力。白番红花属于泛化传粉系统, 鲁熊蜂 (Bombus lucorum)、老条蜂 (Anthophora senilis)和黄腹地花蜂 (Andrena capillosa)是有效传粉昆虫, 通过采食花粉进行传粉, 访花频率分别为0.50±0.27次•花–1•h–1、0.18±0.08次•花–1•h–1和0.13±0.05次•花–1•h–1。在天山西部亚高山早春环境中, 白番红花不仅利用其开花式样、泛化传粉系统及早春空白生态位来提高传粉效率, 而且通过自交亲和及主动自花授粉等繁育系统特征来弥补传粉昆虫少及访花频率低的不足, 从而保障繁殖成功。     

Variation in floral characters,particularly floral scent,in sapromyophilous Stemona species

Flowers or inflorescences often deploy various signals, including visual, olfactory, and gustatory cues, that can be detected by their pollinators. In many plants, these cues and their functions are poorly understood. Deciphering the interactions between floral cues and pollinators is crucial for analyzing the reproductive success of flowering plants. In this study, we examined the composition of the fetid floral scents produced by several Stemona species, including nine S. tuberosa populations from across China, using dynamic headspace adsorption, gas chromatography, and mass spectrometry techniques. We compared variations in floral phenotype, including floral longevity, nectar rewards, pollinator behavior, and flower length and color among the Stemona species. Of the 54 scent compounds identified, the major compounds include fetid dimethyl disulfide, dimethyl trisulfide, 1‐pyrroline, butyric acid, p‐cresol, isoamyl alcohol, and indole. We detected striking differentiation in floral scent at both the species and population level, and even within a population of plants with different colored flowers. Floral characteristics related to sapromyophily and deceptive pollination, including flower color mimicking livor mortis and a lack of nectar, were found in five Stemona species, indicating that Stemona is a typical sapromyophilous taxon. Species of this monocot genus might employ evolutionary tactics to exploit saprophilous flies for pollination.     

Disentangling multiple drivers of pollination in a landscape-scale experiment

Animal pollination is essential for the reproductive success of many wild and crop plants. Loss and isolation of (semi-)natural habitats in agricultural landscapes can cause declines of plants and pollinators and endanger pollination services. We investigated the independent effects of these drivers on pollination of young cherry trees in a landscape-scale experiment. We included (i) isolation of study trees from other cherry trees (up to 350 m), (ii) the amount of cherry trees in the landscape, (iii) the isolation from other woody habitats (up to 200 m) and (iv) the amount of woody habitats providing nesting and floral resources for pollinators. At the local scale, we considered effects of (v) cherry flower density and (vi) heterospecific flower density. Pollinators visited flowers more often in landscapes with high amount of woody habitat and at sites with lower isolation from the next cherry tree. Fruit set was reduced by isolation from the next cherry tree and by a high local density of heterospecific flowers but did not directly depend on pollinator visitation. These results reveal the importance of considering the plant''s need for conspecific pollen and its pollen competition with co-flowering species rather than focusing only on pollinators’ habitat requirements and flower visitation. It proved to be important to disentangle habitat isolation from habitat loss, local from landscape-scale effects, and direct effects of pollen availability on fruit set from indirect effects via pollinator visitation to understand the delivery of an agriculturally important ecosystem service.     

Mass flowering of dipterocarp forests in the aseasonal tropics

At irregular intervals of 2 to 10 years the aseasonal tropical rain forests in west Malesia come into heavy mass flowering, followed by mast fruiting. During a heavy flowering almost half the mature individuals and over 80% of the canopy and emergent tree Species in a forest may flower. This involves over 200 tree species in a forest flowering over a short period of 3–4 months. The pollination needs during a mass flowering appears to be overcome in several ways. A rapid increase in the number of pollinators seems to occur in the forest. This is partly caused by the migration of pollinators from the fringes of the forest to forage on the superabundance of flowers. At the same time, some groups of plants which share common pollinators appear to reduce pollinator competition by flowering in interspecific sequence. Many members of the family Dipterocarpaceae have evolved sequential flowering too. They also share unique pollinators, common flower thrips which appear to build up rapidly in numbers by feeding and breeding on the millions of dipterocarp flower buds which are present several weeks before the flowering. The environmental cue for this irregular, but widespread mass flowering can be traced to a small dip of about 2° C below mean night-time temperature for 4 or 5 nights. The conditions for such temperature drops occur during El Nino events.     

COMPETITION FOR HUMMINGBIRD POLLINATION SHAPES FLOWER COLOR VARIATION IN ANDEAN SOLANACEAE

One classic explanation for the remarkable diversity of flower colors across angiosperms involves evolutionary shifts among different types of pollinators with different color preferences. However, the pollinator shift model fails to account for the many examples of color variation within clades that share the same pollination system. An alternate explanation is the competition model, which suggests that color divergence evolves in response to interspecific competition for pollinators, as a means to decrease interspecific pollinator movements. This model predicts color overdispersion within communities relative to null assemblages. Here, we combine morphometric analyses, field surveys, and models of pollinator vision with a species‐level phylogeny to test the competition model in the primarily hummingbird‐pollinated clade Iochrominae (Solanaceae). Results show that flower color as perceived by pollinators is significantly overdispersed within sites. This pattern is not simply due to phylogenetic history: phylogenetic community structure does not deviate from random expectations, and flower color lacks phylogenetic signal. Moreover, taxa that occur in sympatry occupy a significantly larger volume of color space than those in allopatry, supporting the hypothesis that competition in sympatry drove the evolution of novel colors. We suggest that competition among close relatives may commonly underlie floral divergence, especially in species‐rich habitats where congeners frequently co‐occur.     

New insights into plants co‐existence in species‐rich communities: The pollination interaction perspective

Questions

In animal‐mediated pollination, pollinators can be regarded as a limiting resource for which entomophilous plant species might interact to assure pollination, an event pivotal for their reproduction and population maintenance. At community level, spatially aggregated co‐flowering species can thus be expected to exhibit suitable suites of traits to avoid competition and ensure pollination. We explored the problem by answering the following questions: (1) are co‐flowering species specialized on different guilds of pollinators; (2) do co‐flowering pollinator‐sharing species segregate spatially; and (3) do co‐flowering pollinator‐sharing species that diverge in anther position spatially aggregate more than those that converge in anther position?

Study Site

Euganean Hills, NE Italy.

Methods

Plant composition, flowering phenology and interactions between each entomophilous plant species and pollinating insects were monitored every 15 days in 40 permanent plots placed in an area of 16 ha. We quantified the degree of flowering synchrony, pollinator‐sharing and spatial aggregation between each pair of entomophilous species. We then tested the relationship between the degree of co‐flowering, pollinator‐sharing and spatial aggregation, and between spatial aggregation and anther position.

Results

Entomophilous species converged, at least partially in flowering time, and the phenological synchronization of flowering was significantly associated with the sharing of pollinator guilds. Co‐flowering pollinator‐sharing species segregated spatially. Furthermore, co‐flowering pollinator‐sharing species that diverged in anther position aggregated more than those that converged in anther position.

Conclusions

Reproductive traits that facilitate the co‐existence of co‐flowering species include specialization on different pollinator guilds and a phenological displacement of the flowering time. Furthermore, in circumstances of increased competition due to phenological synchronization, pollinator‐sharing and spatial aggregation, the chance of effective pollination might depend on differences in anther position, resulting in a divergent pollen placement on pollinator bodies. One of the most interesting results we obtained is that the presence of one mechanism does not preclude the operation of others, and each plant species can simultaneously exhibit different strategies. Although more studies are needed, our results can provide additional information about plant–plant interactions and provide new insights into mechanisms allowing the co‐existence of a high number of plant species in local communities.