Models of optimal foraging and resource partitioning: deep corollas for long tongues

We model the optimal foraging strategies for 2 nectarivore species,differing in the length of their proboscis, that exploit thenectar provided by 2 types of flowers, differing in the depthsof their corollas. When like flowers appear in clumps, nectarivoresmust decide whether to forage at a patch of deep or shallowflowers. If nectarivores forage optimally, at least one flowertype will be used by a single nectarivore species. Long-tonguedforagers will normally visit deep flowers and short-tonguedforagers shallow flowers, although extreme asymmetries in metaboliccosts may lead to the opposite arrangement. When deep and shallowflowers are randomly interspersed, nectarivores must decide,on encounter with a flower, whether to collect its nectar orcontinue searching. At low nectarivore densities, the optimalstrategy involves exploiting every encountered flower; however,as nectarivore densities increase and resources become scarce,long-tongued individuals should start concentrating on deepflowers and short-tongued individuals on shallow flowers. Therefore,regardless of the spatial distribution of flowers, corolla depthcan determine which nectarivore species exploit the nectar fromeach flower type in a given community. It follows that corollaelongation can evolve as a means to keep nectar thieves at bayif short-tongued visitors are less efficient pollinators thanlong-tongued visitors.     

Flower reshaping in the transition to hummingbird pollination in Loasaceae subfam. Loasoideae despite absence of corolla tubes or spurs

Many angiosperm lineages present transitions from bee to hummingbird pollination. The flower design in most of these lineages includes either corolla tubes or nectar spurs, structures that commonly experienced an elongation with the acquisition of hummingbird pollination. It is proposed that this increases the fit between the bird head and flower structures, and isolates or partially blocks bees from the interaction. But can this transition occur if the ancestral flower design lacks tubes or spurs? Here we focus on the transition from bee to hummingbird pollination in the Loasaceae subfamily Loasoideae. Loasoideae flowers have radial corollas with separated petals; therefore, they do not display corolla tubes nor nectar spurs. These flowers also present a whorl of nectar scales and staminodes, unique to the subfamily, which is involved in flower–pollinator fit and in nectar harvesting. To explore flower shape adaptation to hummingbird pollination, we tested for correspondence between pollinators and flower shape in Loasoideae. In order to achieve this, we first compared the evolutionary history of flower phenotype and pollination mode, and then used stochastic character mapping and geometric-morphometric variables in a comparison of alternative evolutionary models. The results of our study suggest that the transition from bee to bird pollination was accompanied by changes in the shape of the staminodial complex, along with the evolution of relatively closed corollas. Moreover, while bird pollination seems to be the end point in the evolution of pollination syndromes in many angiosperm lineages, rodent pollinated flowers probably evolved from ancestral bird pollinated flowers in Loasoideae. Our findings suggest that the evolution of bird pollinated flowers from ancestral bee pollinated flowers does not require the presence of corolla tubes or spurs, and can take place as long as the flower design includes structures participating in flower–pollinator fit.     

DOWN THE TUBE: POLLINATORS, PREDATORS, AND THE EVOLUTION OF FLOWER SHAPE IN THE ALPINE SKYPILOT, POLEMONIUM VISCOSUM

Abstract We address how a conflict between pollinator attraction and avoidance of flower predation influences the evolution of flower shape in Polemonium viscosum. Flower shape in P. viscosum is the product of an isometric relationship between genetically correlated (r_A= 0.70) corolla flare and length. Bumblebee pollinators preferentially visit flowers that are more flared and have longer tubes, selecting for a funnel‐shaped corolla. However, flower shape also influences nectar‐foraging ants that sever the style at its point of attachment to the ovary. Surveys of ant damage show that plants having flowers with flared, short corollas are most vulnerable to ant predation. Consistent with this result, the ratio of corolla length to flare is significantly greater in a krummholz (high predation risk) population than in a tundra (low predation risk) population. To explicitly test whether the evolution of a better defended flower would exact a cost in pollination, we created tubular flowers by constricting the corolla during development. Performance of tubular flowers and natural controls was compared for defensive and attractive functions. In choice trials, ants entered control flowers significantly more often than tubular ones, confirming that the evolution of tubular flowers would reduce the risk of predation. However, in a bumblebee‐pollinated population, tubular flowers received significantly less pollen and set fewer seeds than controls. A fitness model incorporating these data predicts that in the absence of the genetic correlation between corolla length and flare, intermittent selection for defense could allow tubular flowers to spread in the krummholz population. However, in the tundra, where bumblebees account for nearly all pollination, the model predicts that tubular flowers should always confer a fitness disadvantage.     

Floral ecology of Oreocharis pumila (Gesneriaceae): a novel case of sigmoid corolla

Attraction of pollinators and successful pollen transfer represent the primary targets of selection during flower evolution, leading to repeated evolutionary shifts between pollinators and consequently to the diversification of floral forms. However, most studies in floral evolution focus on the characteristics of flowers with straight corolla tube. Here, we report on an unusual form of sigmoid corolla combined with protandry and herkogamy in a Chinese species of Gesneriaceae, Oreocharis pumila (formerly Opithandra pumila). Contrary to species with sigmoid corollas studied previously, the base of the corolla tube of this species is inclined at an oblique angle downwards before the tube bends forward, and the stigma and anthers are included in the upper part of the corolla tube. The plants were found to be self‐compatible but incapable of autonomous selfing. Successful pollination was found to depend fully on the presence of insect pollinators (Nomia sp.) and pollen grains are the greatest reward for the visitors. Different from the other sigmoid flowers, the sigmoid corolla of O. pumila was not found to favor insect pollinators with long flexible proboscises. A mechanical fit between floral morphology and pollinator was found, in which only small insect visitors with specialized visiting behavior are legitimate pollinators. The protandry combined with herkogamy in the sigmoid corolla tube strongly ensures pollination efficiencies. Oreocharis pumila is the only species with sigmoid corolla in the genus Oreocharis. We hypothesize that such a corolla has arisen through selection due to inadequate pollination in early spring in the mountainous habitat that O. pumila occupies.     

Nectarless flowers with deep corolla tubes in Pedicularis: does long pistil length provide an arena for male competition?

Pollinator‐mediated selection does not seem to have a direct influence on the evolution of a long corolla tube in a nectarless flower. We hypothesized that the long pistil length of the nectarless flower with a deep corolla tube provided an opportunity for male competition. Pedicularis siphonantha, a nectarless and partially self‐incompatible lousewort with substantial variation in corolla tube length, was used to test the hypothesis. We tested whether and how corolla tube length affected seed production per capsule and seed germination rate with different pollination treatments. Flowers were hand‐pollinated with pollen from one self donor and one outcross donor and mixed pollen grains consisting of equal amounts from the two donor types, respectively. Additionally, seeds from open‐pollinated flowers with different corolla tube lengths were collected separately for measurement of germination rate. Pollination treatment and corolla tube length significantly affected number of seeds per capsule. Moreover, a significant positive relationship between seeds per capsule and corolla tube length was found when mixed hand pollination was conducted. Seeds of self hand‐pollinated flowers had a lower germination rate than those from outcross‐pollinated flowers. Under open pollination, seeds from flowers with longer corolla tubes tended to have higher germination rate. In P. siphonantha, outcross pollen may have a higher probability of contributing to the next generation when transferred to flowers with longer corolla tubes. The pistil length, therefore, should be seen as a female choice mechanism, which provides an arena for male‐to‐male competition. © 2015 The Linnean Society of London, Botanical Journal of the Linnean Society, 2015, 179 , 526–532.     

Reproductive trait variation in the functionally dioecious and morphologically heterostylous island endemic Chassalia corallioides (Rubiaceae)

Documenting the floral biology and breeding system of species throughout the Rubiaceae family provides data on the number of times heterostyly and dioecy may have evolved in this large family. The objectives of this paper are to quantify (a) whether Chassalia corallioides , a small tree endemic to La Reunion Island in the Indian Ocean, is another example of the evolution of dioecy from distyly and (b) whether reproductive traits linked to male and female function vary over the ecological distribution of this species. Quantification of pollen production and fruit set following controlled and natural pollinations demonstrate that this species is dioecious. Male flowers have longer corolla tubes than female flowers. Female flowers have long styles with stigmas placed above the anthers whereas males have short styles with stigmas placed below the anthers. Stigmas and anthers are reciprocally placed in each morph, illustrating that the species is morphologically heterostylous. Both fecundity and flower size are negatively correlated with altitude. In male plants, corollas are shorter and wider and anthers are placed closer to the mouth of the corolla tube with increasing altitude. Male plants flowered more often than female plants, the likely cause of the male biased sex ratio in each of the two years studied. The evolution of dioecy in relation to the island biogeography of the region and the diversification of the genus Chassalia is discussed.     

Are Nectar Sugar Composition and Corolla Tube Length Related to the Diversity of Insects that Visit Asteraceae Flowers?

Abstract: In this work, we analysed interspecific variation in nectar sugar composition, corolla tube length, and the diversity of floral visitors of 35 Asteraceae species. The potential correlations between these variables could arise either as a result of selection to improve pollinator attractiveness or simply as a consequence of phylogenetic constraints. Samples of nectar and flowers, and data on floral visitors, were obtained from living plants in natural populations from Argentina. Asteraceae species showed a large variability in corolla tube length. Nectar of most species presented a larger proportion of hexoses than sucrose. All species were visited by numerous insects belonging to 2 different orders. Results showed that floral traits are not significantly correlated with the diversity of floral visitors. These characters seem to be linked to the phylogeny of the species. Early branching species (species phylogenetically close to the root of the Asteraceae tree) tend to have longer corollas, higher sucrose proportions and lesser diversity of floral visitors than late branching species. Considering that longer corolla tubes and higher nectar sucrose percentages may indicate some specialization in the pollination system, we suggest that there is an evolutionary tendency toward generalist pollination systems within the family.     

Persistent bill and corolla matching despite shifting temporal resources in tropical hummingbird‐plant interactions

By specialising on specific resources, species evolve advantageous morphologies to increase the efficiency of nutrient acquisition. However, many specialists face variation in resource availability and composition. Whether specialists respond to these changes depends on the composition of the resource pulses, the cost of foraging on poorly matched resources, and the strength of interspecific competition. We studied hummingbird bill and plant corolla matching during seasonal variation in flower availability and morphology. Using a hierarchical Bayesian model, we accounted for the detectability and spatial overlap of hummingbird‐plant interactions. We found that despite seasonal pulses of flowers with short‐corollas, hummingbirds consistently foraged on well‐matched flowers, leading to low niche overlap. This behaviour suggests that the costs of searching for rare and more specialised resources are lower than the benefit of switching to super‐abundant resources. Our results highlight the trade‐off between foraging efficiency and interspecific competition, and underline niche partitioning in maintaining tropical diversity.     

The relative strength of different floral visitors driving floral evolution within a <Emphasis Type="Italic">Primula secundiflora</Emphasis> population

Floral visitor assemblages within plant populations are usually composed of different visitors, and the relative abundance of these visitors also varies. Therefore, identifying the relative strength of these floral visitors driving floral evolution within the population is an important step in predicting the evolutionary trajectory of floral traits. Using supplemental hand pollination and nectar-robbing exclusion treatments, we experimentally identified the relative strengths of legitimate pollinators (that visit flowers through the corolla tube entrance) and nectar robbers (that visit flowers by biting a hole in the corolla tube or using an existing hole) driving floral evolution within the Primula secundiflora population. We also estimated legitimate pollinator- and nectar robber-mediated selection separately for pin and thrum flowers. Both legitimate pollinators and nectar robbers mediated selection on pollination efficiency traits in P. secundiflora population. Legitimate pollinators mediated selection for wider corolla tubes, whereas nectar robbers mediated selection for longer corolla tubes. In addition, nectar robber-mediated selection on corolla tube length marginally varied between the pin and thrum flowers. Nectar robber mediated selection for longer corolla tube length in the pin flowers not in the thrum flowers. These results indicate that legitimate pollinators and nectar robbers within a population can drive differential evolutionary trajectories of floral traits.     

Long corollas as nectar barriers in <Emphasis Type="Italic">Lonicera implexa</Emphasis>: interactions between corolla tube length and nectar volume

Long corollas are a classical example of nectar barriers, because they prevent undesired visitors from consuming the reward intended for more effective pollinators. As the investment in nectar barriers increases, flower attractiveness and nectar rewards may also increase to maintain loyal visitation of most effective pollinators; and flowers may become more prone to nectar robbing. We evaluated the effect of nectar barriers (corolla tube length), two related traits (nectar volume and upper lip size) and the associated risk of nectar robbing, on the fecundity of Lonicera implexa plants from three populations differing in the abundance of its most efficient pollinator, the hummingbird hawkmoth Macroglossum stellatarum. Corolla tube length varied most among individuals within populations (45–46 % of total variance) and inflorescences within individuals (23–32 %), and showed little variation among populations (0.2–11 %). Longer corolla tubes were always associated with larger nectar volumes and larger upper lips, although the strength of the relationships varied across populations and years. Robbing frequency increased with corolla tube length, decreased with nectar volume and upper lip size, and its weak effects on fecundity were predominantly positive. Plant fecundity peaked at two different optima: long corollas with little nectar and short corollas with abundant nectar. However, the exact shape of the interaction between corolla length and nectar volume, as well as the combination of traits showing the highest fecundity, differed between populations and years. This variation could be explained by among-population differences in pollinator assemblages, and inter-annual changes in resources dedicated to reproduction. Our study shows that large nectar volumes can modulate the effect of corolla length as a nectar barrier, and that the combination of these two traits that maximises fecundity may be related to the identity of pollinators within each population.     

Resource competition triggers the co-evolution of long tongues and deep corolla tubes

Background

It is normally thought that deep corolla tubes evolve when a plant''s successful reproduction is contingent on having a corolla tube longer than the tongue of the flower''s pollinators, and that pollinators evolve ever-longer tongues because individuals with longer tongues can obtain more nectar from flowers. A recent model shows that, in the presence of pollinators with long and short tongues that experience resource competition, coexisting plant species can diverge in corolla-tube depth, because this increases the proportion of pollen grains that lands on co-specific flowers.

Methodology/Principal Findings

We have extended the model to study whether resource competition can trigger the co-evolution of tongue length and corolla-tube depth. Starting with two plant and two pollinator species, all of them having the same distribution of tongue length or corolla-tube depth, we show that variability in corolla-tube depth leads to divergence in tongue length, provided that increasing tongue length is not equally costly for both species. Once the two pollinator species differ in tongue length, divergence in corolla-tube depth between the two plant species ensues.

Conclusions/Significance

Co-evolution between tongue length and corolla-tube depth is a robust outcome of the model, obtained for a wide range of parameter values, but it requires that tongue elongation is substantially easier for one pollinator species than for the other, that pollinators follow a near-optimal foraging strategy, that pollinators experience competition for resources and that plants experience pollination limitation.     

POLLINATION IN FLORAL SCENT MORPHS OF POLEMONIUM VISCOSUM: A MECHANISM FOR DISRUPTIVE SELECTION ON FLOWER SIZE

Plants of Polemonium viscosum have flowers that are either sweet or skunky in scent. The two morphs are preferentially pollinated by insects of strongly contrasting body size: bumblebee queens specialize on sweet flowers, flies on skunky ones. In this study 13 characters were examined in plant specimens from five populations to identify major components of intraspecific variation in flower and inflorescence morphology and test their correlation with floral scent. Factor analysis identified four major axes of morphological variation. The first explained 22% of the variance among specimens and correlated strongly with four flower size characters: sepal length, corolla tube length, corolla lobe width, and corolla lobe length. Floral scent morphs differed significantly in the multivariate representation of flower size defined by these characters. Sweet flowers had wider corolla lobes, longer corolla tubes, and longer sepals than skunky ones. Corolla lobe width accounted for the greatest amount of intermorph divergence. Divergence in flower size between morphs was maintained in mixed populations at four locations in alpine Colorado, with corollas of sweet flowers significantly broader or more flared than those of skunky flowers. Patterns of pollen receipt suggest that this difference is adaptive. In the sweet morph, pollination intensity and purity increased significantly with corolla flare. Conversely, in the skunky morph, corolla flare had little influence on pollination intensity and had a strong negative effect on purity. These findings suggest that selection for effective pollination should favor intraspecific divergence in flower size in Polemonium viscosum.     

Convergence of anti-bee pollination mechanisms in the Neotropical plant genus <Emphasis Type="Italic">Drymonia</Emphasis> (Gesneriaceae)

The neotropical plant genus Drymonia displays a remarkable variety of floral shapes and colors. One feature that is particularly important to coevolution with pollinators involves the variable shapes and widths of corolla tubes. To evaluate the evolutionary context for changes in corolla shape, we constructed a phylogeny of 50 of the 75 species of Drymonia using molecular markers from plastid (trnK-matK) and nuclear regions (ITS and ETS). Mapping tube shapes on the phylogeny supports open, bell-shaped (campanulate) corolla shape as the ancestral character state for Drymonia, with multiple independent origins of constriction in the corolla tube. Corollas with constrictions take one of three tube shapes: a constricted flower opening and throat with a large, expanded pouch on the lower surface (hypocyrtoid); a constricted flower opening and throat lacking an expanded pouch on the lower surface (urceolate); or a constricted opening and throat where the sides of the corolla appear laterally compressed. Fieldwork demonstrates euglossine bees (mostly Euglossa spp. and Epicharis spp.) visit campanulate corollas while hummingbirds visit corollas that are constricted. Results support eight independent origins of constricted corolla tubes from ancestors with campanulate corolla tubes: 3 hypocyrtoid clades, 3 laterally compressed clades, and 3 urceolate clades (one of which represents a shift from a hypocyrtoid ancestor). Constricted corollas are associated with shifts from the ancestral condition of poricidal anther dehiscence, which presents pollen to pollinators in multiple small doses, to the derived condition of longitudinal anther dehiscence, which presents all pollen to pollinators simultaneously. The association of hummingbird pollination with constricted corolla tubes suggests that narrowing evolved as a barrier mechanism that prohibits the visitation of flowers by bees.     

Morphological variation in relation to flower use in bumblebees

To understand resource partitioning in a bumblebee community, we analyzed various morphological characters. A total of 1269 individuals of six bumblebee species, Bombus ardens, B. hypocrita, B. diversus, B. ignitus, B. honshuensis and B. beaticola, were examined and principal component analysis showed that the bumblebee species were clearly differentiated. Glossa, prementa and head lengths were positively correlated with the second component, and a longer proboscis was associated with a narrower body, which may help bees to intrude into and access deep‐lying nectar sources. Bombus diversus, with a long proboscis and narrow body, preferred flowers with a long corolla tube, whereas B. hypocrita and B. ignitus, which have short proboscises and wide bodies, visited flowers with short corollas or dish‐shaped flowers. Two pairs of consubgeneric species that have similar morphological characteristics, B. ardens and B. beaticola, and B. hypocrita and B. ignitus, divided flower resources by habitat selection and seasonal partitioning. For resource partitioning among bumblebee species, not only morphology but also other factors, such as habitat and seasonal preference, flower use, foraging behavior, and interspecific interactions, are responsible.     

Unidirectionality of floral colour changes

Many angiosperms have arranged their flowers in inflorescences forming a distinct signalling unit to flower visitors. In some species, the flowers of inflorescences undergo a temporal colour change corresponding exactly to a change in the reward status. Based on information obtained from the spectral reflection curves of pre-change and postchage colours of flower corollas and/or floral guides, it was possible to demonstrate that the colour phase associated with reward closely corresponds to the visual stimuli which trigger behavioural responses of inexperienced flower visitors, and that the colour phase associated with less reward corresponds to visual stimuli less attractive to naïve flower visitors. Reciprocal colour changes were not observed. It is to be assumed that the unidirectionality of floral colour changes is an adaptation of angiosperms aimed at the guidance of first-time flower visitors. Signalling reward to inexperienced flower visitors is an additional function of floral colour changes. The main function of floral colour changes, however, is to provide cues with which the flower visitors can learn to associate one colour phase with reward.     

MECHANISM OF SELECTION FAVORING A WIDE TUBULAR COROLLA IN CAMPANULA PUNCTATA

A previous study of Campanula punctata pollinated by Bombus diversus showed greater male reproductive success in plants with wider corollas when male reproductive success was measured by paternity analysis. Pollen removal alone was not a good measure of male reproductive success. The aim of the current study is to elucidate the mechanism underlying the selection on corolla width in C. punctata. Multiple regression analysis of male reproductive success in experimental populations revealed that the advantage of a wide corolla to the male is independent of the corolla width of pollen recipients, indicating that the position of pollen deposited on Bombus may not be an important factor for selection. However, the number of pollen grains that fell on the petal or off the flower and were lost at the first visit of Bombus (pollen fall) decreased with increasing corolla width, so that most pollen grains removed from a wide flower were deposited onto the pollinator. In a narrow flower, a greater proportion of the pollen removed was wasted through pollen fall. Pollen removal does not reflect male reproductive success, at least in part because of the loss of pollen in some flowers through pollen fall. The positive relationship between wider corollas and reduced loss of pollen through pollen fall is likely to lead to greater male reproductive success of wider flowers under repeated visits of pollinators. Decreased pollen fall, probably due to more gentle contact between pollen and bees in flowers with wider corollas, may be one of the mechanisms underlying the selection on corolla width of C. punctata.     

The importance of bees as pollinators in the short corolla bromeliad Aechmea caudata in southern Brazil

The majority of bromeliad species are pollinated by vertebrates, mainly hummingbirds and bats. However, bees are among the most frequent visitors in some short-corolla species with ornithophilous features, but only few studies identified insects as pollinators of these bromeliads. The importance of visitors for pollination success in Aechmea caudata (Bromeliaceae) was determined through the frequency and pollination effectiveness (measured as seed set/single visit) of its visitors in a secondary Atlantic forest area in southern Brazil. Aechmea caudata is self-incompatible and therefore pollinator-dependent. A total of 16 species were recorded visiting their flowers. Bees were the most rich and frequent taxon (91% of 647 visits). Bombus morio was the most frequent species (41%). Although the floral features of A. caudata, such as scentless, tubular corollas, yellow and red flowers, and nectar secretion during the whole diurnal anthesis, are related to ornithophily, the single hummingbird species Thalurania glaucopis failed to pollinate the flowers. Its low frequency (2.5%) apparently did not promote the pollen flux between conspecific bromeliads. Pollination tests showed that no seeds developed after hummingbird visits. Seeds were formed only at flowers visited by B. morio. We discuss our findings by contrasting them with the results on the similar and sympatric A. lindenii and by emphasizing the importance of bees for pollination of bromeliads with short corolla. Our results show that pollination effectiveness together with frequency data are necessary to analyze the complex interactions between plants and their flower visitors.     

盗蜜行为在植物繁殖生态学中的意义

在动植物的相互关系中,盗蜜行为被认为是一种不同于普通传粉者的非正常访花行为。动物之所以要采取这种特殊的觅食策略,有假说认为是由访花者的口器和植物的花部形态不匹配造成的,也有认为是盗蜜行为提高了觅食效率从而使盗蜜者受益。在盗蜜现象中,盗蜜者和宿主植物之间的关系是复杂的。盗蜜对宿主植物的影响尤其是对其繁殖适合度的影响归纳起来有正面、负面以及中性3类。与此同时,盗蜜者的种类, 性别及其掠食行为差异不仅与生境因素密切相关,而且会对宿主植物的繁殖成功产生直接或间接的影响。另外,盗蜜者的存在无疑对其它正常传粉者的访花行为也产生一定的影响,从而间接地影响宿主植物的繁殖成功, 而植物在花部形态上也出现了对盗蜜现象的适应性进化。作者认为, 盗蜜是短嘴蜂对长管型花最有效的一种掠食策略, 它不仅增加了盗蜜者对资源的利用能力, 而且由于盗蜜对宿主植物繁殖成功的不同的影响使其具有调节盗蜜者和宿主之间种群动态的作用, 两者的彼此适应是一种协同进化的结果。     

Interaction between oil-collecting bees and seven species of Plantaginaceae

Oil-bee/oil-flower mutualism evolved through multiple gains and losses of the ability to produce floral oil in plants and to collect it in bees. Around 2000 plant species are known to produce floral oils that are collected by roughly 450 bee species, which use them for the construction of nests and for the larval food. The Plantaginaceae contain several Neotropical species that produce floral oils, the main reward offered by these plants. In the genera Angelonia, Basistemon, Monopera and Monttea, mainly associated with Centris bees, the floral oil is produced in trichomes that are located in the inner corolla. The pollinators of a few species in this neotropical clade of Plantaginaceae are known, and the role of flower morphology as well as the requirements from pollinators and the role of other groups of bees in the pollination of these flowers remains unclear. In this paper we provide a list of the flower visitors of seven Plantaginaceae species (six Angelonia species and Basistemon silvaticus) analyzing their behavior to highlight the legitimate pollinators and illustrating little known aspects of flower morphology and oil-collecting apparatuses of the bees. Two general morphological patterns were observed in the Angelonia flowers: deep corolla tube with short lobes, and short corolla tube with long lobes. Corolla tubes of different length result in pollen adherence to different parts of the insect body. The six Angelonia species and B. silvaticus flowers were visited by 25 oil-collecting bee species (10 Centris, 11 Tapinotaspidini and 4 Tetrapedia species), the majority acting as legitimate visitors. The flowers were also visited by illegitimate bee pollinators, which collected pollen but do not transfer it to the female organ. Specialized collectors of Plantaginaceae floral oils present modifications on the first pair of legs, mainly in the basitarsi but also extended to the tarsomeres. The new records of Tapinotaspidini and Centridini species acting as specialized pollinators of Plantaginaceae suggest that there is a geographic variation in the pollinators of the same plant species, and that the evolutionary scenario of the historical relationships between oil-collecting bees and floral oil producing plants is more complex than previously considered.     

Passive partner choice through exploitation barriers

Floral features that affect the efficiency with which pollinators can harvest their resources, or the profitability they obtain from them, affect the foraging decisions of pollinators. Foraging choices of pollinators, in turn, affect pollen flow: increases in flower constancy lead to more efficient pollen transport. It follows that exploitation barriers—flower traits that differentially affect net intake rates of potential visitors—will promote resource partitioning and enhance pollen export. In this paper we first generalise foraging models to show that exploitation barriers can lead to partial resource partitioning even when flowers are randomly distributed in space. Then we develop a model to study how the foraging rules of pollinators, pollen removal and pollen deposition, affect pollen flow. The model shows that resource partitioning, even incomplete, can substantially increase the efficiency of pollen flow. Finally, we use computer simulations to demonstrate that exploitation barriers promoting partial resource partitioning can evolve. Many of the flower traits associated with pollination syndromes have small but consistent effects on the efficiency with which different taxonomic groups exploit flowers, and can be considered exploitation barriers. Even if these barriers are not strong enough to promote strict specialisation, and may have little effect on the female component of fitness when pollinators are not a limiting resource, they are likely to be selected because they enhance the male component of fitness.