Effect of sexual dimorphism in bill length on foraging behavior: an experimental analysis of hummingbirds

We examined whether sexual differences in trophic morphology are associated with sexual differences in foraging behavior through two laboratory experiments on rufous hummingbirds (Selasphorus rufus) designed to compare probing abilities (maximum extraction depths) and handling times of sexes at flowers. Bills of female S. rufus are about 10.5% longer than bills of males, and this difference was associated with sexual differences in foraging abilities. Maximum extraction depths of female S. rufus were significantly greater than those of males, and no overlap between the sexes was observed. Moreover, handling times of females were shorter than handling times of males at flowers having longer corollas (15 mm). Thus, because of their longer bills, female S. rufus have the potential to feed from longer flowers than males, and can do so more quickly. We suggest that no single mechanism is responsible for the evolution of sexual dimorphism in bill lengths of hummingbirds, but rather that the dimorphism probably reflects the combined effects of reproductive role division and intersexual food competition, and possibly, sexual selection.     

The Role of Flower Width in Hummingbird Bill Length‐Flower Length Relationships1

Observations of hummingbirds feeding at flowers longer or shorter than their bills seem to contradict the view that bill lengths of hummingbirds evolved in concert with the lengths of their flowers. Recent experiments, however, indicate that a hummingbird's ability to feed at artificial flowers of different lengths depends on the widths of the flowers. We examined if the broad range of flower lengths visited by many hummingbird species can be explained by the widths of the flowers. We predicted that both short‐ and long‐billed hummingbirds would include long, wide flower species in their diets, but that short‐billed hummingbirds would not include long, narrow flower species because nectar in these species might be beyond the reach of their bills. If so, the slope of the regression for flower width versus flower length should be smaller for flower species visited by longer‐billed hummingbirds relative to those visited by shorter‐billed hummingbirds. Analyses of data sets for some North American and Monteverde hummingbirds and their food plants were consistent with this prediction, and bill lengths were significantly correlated with the slopes of the regressions of flower width versus length for seven hummingbird species. Comparisons of observed flower use by some Monteverde hummingbird species to flower assemblages generated at random suggest that these significant regressions were not simply a result of allometric relationships between flower lengths and widths, but in some cases reflected active choice by the birds. The two hummingbird–flower data sets also differed significandy in the scaling of corolla width relative to corolla length. In particular, the Monteverde data set contained a large number of long, narrow flower species, which we suggest is a consequence of a different floral evolutionary history and association with long‐billed hummingbird species. The evolutionary effects of hummingbirds and their flowers upon one another are more complex than has generally been realized, and a consideration of corolla length jointly with other floral characters may improve our understanding of hummingbird‐flower relationships.     

Nectar extraction by hummingbirds: response to different floral characters

Summary Handling times of hummingbirds (Amazilia rutila and Cynanthus latirostris) visiting artificial flowers were a positive function of corolla length, nectar volume and nectar concentration. Corolla angle had no consistent effects on handling times. A multiple regression model explained 83% of the variation in handling times for these two species. The model also closely fit independent data from another hummingbird, Archilochus colubris, suggesting that it is general enough to apply to other medium-sized, short-billed hummingbird species. When examined across the range of variation normally encountered by hummingbirds in nature, corolla length and nectar volume had the largest effect on nectar extraction rates. At corolla lengths longer than a hummingbird's bill handling time increases markedly. Hummingbirds maximize their net rate of energy intake by selecting flowers with the shortest corolla, the highest nectar concentrations and the highest nectar volume. Since there is a positive relation between bill length and nectar extraction rate, it is surprising that most hummingbirds have relatively short bills.     

Bills and tongues of nectar-feeding birds: A review of morphology,function and performance,with intercontinental comparisons

The bills and tongues of nectar-feeding birds differ from continent to continent. The major differences are that: (i) the tongues of A Australian honeyeaters are broader any more fimbricated at the tip than the bifurcated tongues of sunbirds and hummingbirds; (ii) the bills of hummingbirds are more uniformly narrow and taper less markedly towards their tips than those of sun-birds and honeyeaters; and (iii) bill curvatures are generally greater for sunbirds and honey-creepers than for hummingbirds. A variety of hummingbirds has straight or even slightly upturned bills, while bills for all sunbirds, honeycreepers and honeyeaters are decurved to some extent. Despite differences in tongue morphology, hummingbirds, sunbirds and honeyeaters extract nectar at a similar range of rates, averaging approximately 40 γL s^?1 from ad libitum feeders, and 1–15 γL^?1 from flowers. All tongues collect nectar by capillarity, with licking rates of 6–17 s^?1. Licking behaviour has been little studied, although speeds of licking respond to changes in sugar concentration and corolla length. The tongues of honeyeaters are broad, and may need to be brush-tipped in order to allow capillary collection of nectar. Brush-tipped tongues can cover large surface areas on each lick, and may allow honeyeaters to exploit nectar and honeydew that is thinly spread over large surface areas. Bill lengths of nectarivorous birds are similar in all regions, though species of hummingbird have the shortest and longest bills. Bill lengths largely determine the range of floral lengths that can be legitimately probed. Maximum floral lengths exceed bill lengths, since hummingbirds, sunbirds and honeyeaters protrude their tongues beyond the tips of their bills. Rates of nectar extraction, however, decline rapidly once the floral length exceeds bill length. Decurved bills may have evolved in honeyeaters and sunbirds to enable perching birds to reach flowers at the ends of branches more easily. Consistent differences in bill length between the sexes suggest that males and females may exploit different floral resources or different proportions of the same resources. For honeyeaters and sunbirds, males have longer bills than females, but the reverse is true for many hummingbirds.     

Dissimilar bill shapes in new world tropical versus temperate forest foliage-gleaning birds

Summary The bill shape of foliage-gleaning birds in temperate and tropical new world forests is dissimilar. Tropical species have longer and narrower bills than their temperate zone counterparts. In addition, their bills are longer for a given body size. These differences cannot be readily explained as phylogenetic artifacts. I suggest that the distinct bill morphology of the two assemblages is determined by the type of insects that comprise the largest size classes of potential prey. These large insects are particularly important since they generally comprise the bulk of the nestling diet for insectivorous birds. In tropical forests Orthoptera are probably the most abundant large soft-bodied arthropods; they form an important resource for foliage-gleaning birds during the breeding (rainy) seasons. Most temperate zone foliage-gleaning birds rely almost entirely upon caterpillars when breeding. Long, narrow bills are thought to close more rapidly than shorter, broader bills. These long, fast bills may be required to efficiently harvest active Orthoptera. Migrant warblers may face morphological constraints from breeding successfully in lowland tropical forests. While the short-billed temperate zone birds can survive the tropical dry season by foraging on small arthropods, they may be inefficient at handling large Orthoptera to feed to nestlings.     

The foraging behaviour of Australian honeyeaters: a review and some comparisons with hummingbirds

The foraging behaviour of Australian honeyeaters is reviewed in terms of diet, foraging selectivity, foraging flight mode, quality and quantity of nectar encountered per flower, flower densities encountered and effect of predation. At the same time comparisons are made between honeyeaters and hummingbirds. These two groups of birds are superficially similar. Both feed on nectar and insects. Both tend to have long curved bills and tongues adapted for removal of nectar from flowers. Both tend to feed at long, red flowers. However, on close inspection, honeyeaters and hummingbirds are quite dissimilar. For example, many honeyeaters include fruit in their diets. Hummingbirds almost never eat fruit. Honeyeaters appear to be considerably less nectarivorous and more insectivorous than hummingbirds. Honeyeaters are, for the most part, larger than hummingbirds and they usually perch while feeding whereas hummingbirds usually hover. Honeyeaters but not hummingbirds often flock while feeding. Predation appears to be considerably more important for honeyeaters than for hummingbirds. Territorial defense of flowers seems common in hummingbirds but uncommon in honeyeaters. These differences are discussed in detail and explanations are offered for them wherever possible.     

Effect of floral orifice width and shape on hummingbird-flower interactions

Nectar guides are common among insect-pollinated plants, yet are thought to be rare or absent among hummingbird-pollinated plants. We hypothesize that the lower lips and trumpet-shaped orifices of many hummingbird flowers act as nectar guides to direct hummingbirds to the flowers' nectar and orient the birds for pollination. To test this hypothesis we conducted laboratory experiments using flowers of Monarda didyma (bee balm) and M. fistulosa (wild bergamot), which have orifice widths of about 4 mm and 2 mm, respectively, and latex flowers with orifice widths of 4 mm and 2 mm and three orifice shapes (trumpet, lipped, and lipless). Rubythroated hummingbirds (Archilochus colubris) made fewer errors during bill insertion and spent a smaller proportion of their feeding visit in error at M. didyma flowers than at M. fistulosa flowers, and at unaltered flowers of both species than at flowers with lower lips removed. Handling times were longer at both lipped and lipless flowers of M. didyma than at those of M. fistulosa, and at lipped than at lipless flowers of M. didyma. The average duration of contact between a hummingbird and a flower's anthers and stigma was longer at M. didyma than at M. fistulosa for both lipped and lipless flowers, and at lipped than at lipless M. didyma flowers. Hummingbirds missed the openings of latex flowers with their bills more frequently and spent a greater percentage of their total feeding visit in error at (i) 2-mm than at 4-mm flowers of all three shapes, (ii) lipless flowers than at trumpet or lipped flowers, and (iii) lipped flowers than at trumpet flowers of both widths. The duration of hummingbird/anther contact was longer at (i) 2-mm than at 4-mm flowers of all shapes, (ii) lipped than at trumpet or lipless flowers, and (iii) lipless than at trumpet flowers for both widths. No significant differences in handling times of hummingbirds were observed among any of the latex flower shapes or widths. Our results demonstrate that orifice shapes can act as guides by reducing the frequency of feeding errors by visiting hummingbirds, and that effects of orifice shape on pollination must be considered in conjunction with flower widths and locations of anthers and stigmas.     

The flowerpiercers' hook: an experimental test of an evolutionary trade-off

The evolution of features that enhance an organism's performance in one activity can adversely affect its performance in another. We used an experimental approach to document a trade-off associated with the evolution of the long hook at the tip of the bill of birds belonging to the genus Diglossa (flowerpiercers). In Diglossa, the more derived flower-robbing nectarivorous species have maxillae (upper jaws) that terminate in enlarged curved hooks. The ancestral frugivorous species have maxillae with relatively small hooks. We mimicked bill evolution by clipping the terminal bill hook of nectarivorous Cinnamon-bellied Flowerpiercers (Diglossa baritula) to resemble the frugivorous condition. We found that birds with experimentally shortened bills ingested fruit more efficiently, but had a reduced ability to rob flowers. Birds with intact bills, by contrast, were good flower robbers but poor frugivores. The evolution of a hooked bill endowed flowerpiercers with the ability to efficiently pierce flowers and extract nectar, but hindered their efficiency to feed on fruit.     

Mobility of Impatiens capensis flowers: effect on pollen deposition and hummingbird foraging

Flexible pedicels are characteristic of birdpollinated plants, yet have received little attention in studies of hummingbird-flower interactions. A major implication of flexible pedicels is that flowers may move during pollination. We examined whether such motion affected interactions between ruby-throated hummingbirds (Archilochus colubris) and jewelweed (Impatiens capensis) by increasing pollen deposition and by altering the effectiveness of nectar removal. For I. capensis, flower mobility enhanced pollen deposition: birds had significantly longer contact with anthers and more pollen deposited on their bills and crowns when foraging at mobile flowers than at flowers that had been experimentally immobilized. In contrast, flower mobility imposed a cost on hummingbirds by significantly increasing their handling times and reducing their extraction rates relative to their interactions with immobile flowers. Field observations indicated that the motion observed during hummingbird visits did not occur when bees (Bombus spp., Apis mellifera) visited I. capensis flowers, which suggests that the mobility of I. capensis flowers is an adaptation for hummingbird pollination.     

Ornithophilous canopy species in the Atlantic rain forest of southeastern Brazil

ABSTRACT.   In tropical ecosystems, birds play a relevant role in plant reproduction. Although hummingbirds are regarded as the most important vertebrate pollinators in the Neotropics, the possible role of perching birds as pollinators has been neglected. From 2003 to 2005, we observed 68 species of plants visited by birds in an Atlantic rainforest in southeastern Brazil, including three canopy species: Spirotheca rivieri (Malvaceae, Bombacoidea), Schwartzia brasiliensis (Marcgraviaceae), and Psittacanthus dichrous (Loranthaceae). Flowers of these three species were visited by 15 different species of perching birds and by hummingbirds. The flowers of these three plants are colorful, ranging from deep red or purple to orange. Spirotheca rivieri blooms during the austral winter and Schwartzia brasiliensis during the summer. The flowers of these two species produce copious amounts of dilute nectar in easily accessible structures and both species appear to depend primarily on perching birds as pollinators, with hummingbirds being secondary or minor pollen vectors. The tubular, narrow flowers of P. dichrous are produced during the austral summer and are visited primarily by hummingbirds. Perching birds also visit the flowers, but destroy them. Our results suggest that previous estimates of the number of perching birds that feed on nectar may be too low and that flowers pollinated by perching birds may be more common in the canopy of Neotropical forests than previously thought.     

The distributions of morphologically specialized hummingbirds coincide with floral trait matching across an Andean elevational gradient

Morphological trait matching between species affects resource partitioning in mutualistic systems. Yet, the determinants of spatial variation in trait matching remain largely unaddressed. Here, we generate a hypothesis that is based on the geographical distributions of species morphologies. To illustrate our hypothesis, as a study system we use hummingbirds in the tropical Andes. Hummingbirds with specialized morphologies (i.e., long or curved bills) may forage on flowers that are inaccessible to hummingbirds with generalized bill morphologies (i.e., small‐to‐medium‐sized bills with no curvature), yet the vast majority of hummingbirds have generalized bill morphologies. Thus, we propose that trait matching across space is determined by the distribution of morphological specialists. In the Andes, we observe the richness of specialized hummingbird morphotypes to peak at high and low elevations. Therefore, we hypothesize that trait matching should be most influential in predicting pairwise interactions at high and low elevations. We illustrate our hypothesis by field observations along an elevational gradient in Podocarpus National Park (Ecuador). Using Bayesian hierarchical modeling of interaction frequencies in combination with network analyzes, we found that hummingbirds at high and low elevations contributed to resource partitioning by foraging on morphologically close‐matching flowers. Moreover, at high and low elevations, hummingbirds with specialized morphologies showed a stronger tendency to visit close‐matching flowers than morphological non‐specialists did. In contrast, at mid‐elevations, hummingbirds were not attracted to morphologically close‐matching flowers. These results suggest that the spatial distribution of specialized morphotypes determines trait matching and the partitioning of interactions within hummingbird–plant communities. Abstract in Spanish is available with online material.     

Community Organization Among Neotropical Nectar-Feeding Birds

Assemblages of neotropical hummingbirds are organized accordingto parameters of available resources and morphological-behavioralattributes of particular hummingbird species. We distinguishfive types of flowers relative to hummingbird foraging, andwe define six community roles for hummingbirds in exploitationof various flower types. These roles are: high-reward trapliners,which visit but do not defend nectar-rich flowers with longcorollas; territorialists, which defend dense clumps of somewhatshorter flowers; lowreward trapliners, which forage among avariety of dispersed or nectar-poor flowers; territory-parasitesof two types (large marauders and small filchers); and generalists,which follow shifting foraging patterns among various resources.Simple communities on islands usually contain one species oflow-reward trapliner or generalist and one territorial species,and sometimes support one high-reward trapliner; often thesespecies are sexuallydimorphic. More complex mainland communitiessupport varying numbers of species in different roles, dependingon the relative importance and constancy of different flowertypes. High-reward trapliners are particularly important inforest under-stories, while forest canopies and open habitatssupport large numbers of shorter-billed, mobile birds fillingthe other five roles. We conclude by pointing out the many parallelsthat exist with other consumer groups.     

Bee- to bird-pollination shifts in <Emphasis Type="Italic">Penstemon</Emphasis>: effects of floral-lip removal and corolla constriction on the preferences of free-foraging bumble bees

Plants might be under selection for both attracting efficient pollinators and deterring wasteful visitors. Particular floral traits can act as exploitation barriers by discouraging the unwelcome visitors. In the genus Penstemon, evolutionary shifts from insect pollination to more efficient hummingbird pollination have occurred repeatedly, resulting in the convergent evolution of floral traits commonly present in hummingbird-pollinated flowers. Two of these traits, a reduced or reflexed lower petal lip and a narrow corolla, were found in a previous flight-cage study to affect floral handling time by bumble bees, therefore potentially acting as “anti-bee” traits affecting preference. To test whether these traits do reduce bumble bee visitation in natural populations, we manipulated these two traits in flowers of bee-pollinated Penstemon strictus to resemble hummingbird-adapted close relatives and measured the preferences of free-foraging bees. Constricted corollas strongly deterred bee visitation in general, and particularly reduced visits by small bumble bees, resulting in immediate specialization to larger, longer-tongued bumble bees. Bees were also deterred—albeit less strongly—by lipless flowers. However, we found no evidence that lip removal and corolla constriction interact to further affect bee preference. We conclude that narrow corolla tubes and reduced lips in hummingbird-pollinated penstemons function as exploitation barriers that reduce bee access to nectaries or increase handling time.     

Reproductive ecology of distylous Palicourea Padifolia (Rubiaceae) in a tropical montane cloud forest. I. Hummingbirds' effectiveness as pollen vectors

The adaptiveness of distyly has been typically investigated in terms of its female function, specifically pollen receipt. However, pollen loads on stigmas can only provide moderate support for Darwin's hypothesis of the promotion of legitimate crosses. To determine the effectiveness of hummingbirds as pollen vectors between floral morphs and the consequences in terms of male (pollen transfer) and female function (pollen receipt) in Palicourea padifolia (Rubiaceae), floral visitors, their foraging modes, and temporal patterns of floral visitation were observed and documented. Differences in pollen and stigma morphology, pollen flow, rates of pollen deposition, and/or stigmatic pollen loads were then evaluated for their contribution toward differences in reproductive output between floral morphs. A pollination experiment with stuffed hummingbirds that varied in bill size was done to evaluate the contribution of bill variation toward differences between floral morphs in pollen receipt and pollen transfer and female reproductive output. Anthers of long-styled flowers contained significantly more and smaller pollen grains than those of short-styled flowers, independently of corolla and anther lengths. The shape and orientation of the stigma lobes differed between morphs and were significantly longer among short-styled flowers. Hummingbird visitation rates did not differ significantly between floral morphs, and foraging movements from focal plants towards neighboring plants were independent of floral morph. Stigmatic pollen loads under field conditions and those after controlled hummingbird visitation, along with rates of pollen accumulation through the day indicated that stigmas of short-styled flowers receive proportionately more legitimate (intermorph) pollen grains than did those of long-styled flowers. However, the species of hummingbird was marginally significant in explaining variation in pollen deposition on stigmas. Lastly, intermorph pollinations of P. padifolia resulted in significant differences in fruit production between floral morphs, independent of pollination treatment and pollinator species; short-styled flowers proportionately developed almost twice the number of fruits developed by long-styled flowers.     

Island–mainland difference in <Emphasis Type="Italic">Nicotiana glauca</Emphasis> (Solanaceae) corolla length: a product of pollinator-mediated selection?

A match between floral and pollinator traits, such as that between unique island plants and pollinators, is often thought to be the product of pollinator-mediated selection. I examined whether the floral morphology of an introduced hummingbird-pollinated plant, Nicotiana glauca (tree tobacco, Solanaceae), is under selection by pollinators on the California Channel Islands where it is a recent colonist. I first determined differences in floral morphology and pollinator composition between island and mainland populations of N. glauca. I found that island plants have detectably longer corollas (on average 1 mm) and are visited by hummingbird species with on average 1–2 mm longer bills than common mainland visitors. Corolla length differences were not found to be associated with site abiotic differences. Flower size does not vary consistently with season and corolla width is very consistent across sites. I tested whether island–mainland corolla length differences are the product of pollinator-mediated selection by measuring phenotypic selection and per visit effectiveness. Contrary to expectations, a longer corolla was not consistently associated with higher pollen transfer or seed count on the islands. Per visit effectiveness of longer and shorter-billed hummingbirds did differ; however, effectiveness did not depend on corolla length. Although I failed to detect expected patterns of selection for longer corollas on islands, I cannot rule out weak or past pollinator-mediated selection. It is also possible that despite the apparent match between pollinator and floral traits, island–mainland differences in corolla length are instead due to other environmental effects, selection unrelated to pollinators, or stochastic processes such as drift.     

An Assemblage of Hummingbird-pollinated Flowers in a Montane Forest in Southeastern Brazil

Relationships between ornithophilous flowers and hummingbirds have been little studied in southern South America, where hummingbird species richness is low. We studied an ornithophilous flower assemblage and the hummingbird pollinators in a montane forest in southeastern Brazil. Twenty-three native hummingbird-pollinated plant species in 21 genera and 14 families were observed. Bromeliaceae, Fabaceae, Gesneriaceae, and Lobeliaceae are represented by more than one species within the assemblage. Flower shapes vary from narrow tube to bowl-shape, but tubular flowers prevail. The variety of flower shapes and sizes results in diverse pollen placement on the body parts of hummingbird visitors, although pollen is deposited mostly on the bill. Sugar concentration in nectar averages 22.1%, and nectar volume per flower averages 16.9 μl. The plant populations bloom for one month to year-round, and their flowering approaches the steady-state pattern. Four flower subsets may be defined within the assemblage, each subset related to the bill size and foraging habits of the most frequent bird visitor. Of the six species of hummingbirds recorded at the study site, four are common and largely resident. The four hummingbirds differ in bill size, body mass, and favoured foraging sites, attributes which reflect their favoured flower subsets. One hermit and one trochiline hummingbird share most of the flower species they use, these two birds being the major pollinators within the flower assemblage. This montane forest community may be viewed as medium-rich in ornithophilous flower species and poor in hummingbird species.     

Adaptive trade-off in floral morphology mediates specialization for flowers pollinated by bats and hummingbirds

Evolution toward increased specificity in pollination systems is thought to have played a central role in the diversification of angiosperms. Theory predicts that the presence of trade-offs in adapting to different pollinator types will favor specialization, yet few studies have attempted to characterize such interactions in nature. I conducted flight cage experiments with bats, hummingbirds, and artificial flowers to examine effects of corolla width on pollination. I videotaped visits to analyze pollinator behavior and counted pollen grains transferred to stigmas. Results demonstrated that flower-pollinator fit is critical to effective pollination; wide corollas guided bat snouts better, and narrow corollas guided hummingbird bills better. Poor fit resulted in variable entry angles and decreased pollen transfer. A model using these results predicts that wide corollas will be selected for when bats make more than 44% of the visits and narrow corollas when they make fewer. Intermediate corollas are never favored (i.e., generalization is always suboptimal). This is the first study to clearly document a pollinator-mediated fitness trade-off in floral morphology.     

Evolution of sexual dimorphism in bill size and shape of hermit hummingbirds (Phaethornithinae): a role for ecological causation

Unambiguous examples of ecological causation of sexual dimorphism are rare, and the best evidence involves sexual differences in trophic morphology. We show that moderate female-biased sexual dimorphism in bill curvature is the ancestral condition in hermit hummingbirds (Phaethornithinae), and that it is greatly amplified in species such as Glaucis hirsutus and Phaethornis guy, where bills of females are 60 per cent more curved than bills of males. In contrast, bill curvature dimorphism is lost or reduced in a lineage of short-billed hermit species and in specialist Eutoxeres sicklebill hermits. In the hermits, males tend to be larger than females in the majority of species, although size dimorphism is typically small. Consistent with earlier studies of hummingbird feeding performance, both raw regressions of traits and phylogenetic independent contrasts supported the prediction that dimorphism in bill curvature of hermits is associated with longer bills. Some evidence indicates that differences between sexes of hermit hummingbirds are associated with differences in the use of food plants. We suggest that some hermit hummingbirds provide model organisms for studies of ecological causation of sexual dimorphism because their sexual dimorphism in bill curvature provides a diagnostic clue for the food plants that need to be monitored for studies of sexual differences in resource use.     

The effect of nectar guides on pollinator preference: experimental studies with a montane herb

Summary Rare albino morphs of the montane larkspur Delphinium nelsonii differ from common blue-flowered morphs in overall flower color, and in the strength of a contrasting color pattern at the center of the flower that presumably guides pollinators to concealed nectar. Previous studies showed that bumblebees and hummingbirds discriminate against albinos when presented with mixtures of the 2 morphs, and that it takes these pollinators longer to fly between successive flowers on albino than on blue-flowered inflorescences. To explore the link between these observations, we measured pollinator preferences and flower-to-flower flight times (handling times) before and after painting flowers in 2 alternative ways that enhanced albino nectar guides. In all of 16 experimental replicates discrimination against albinos was reduced or eliminated after painting, and albino handling times declined toward values for blue-flowered inflorescences. This consistent result indicates that an inferior nectar guide increases the energetic cost of foraging at albinos. Increased cost in turn explains discrimination, under the reasonable assumption that hummingbirds and bumblebees are sensitive to foraging economics.     

Geographical variation in floral traits of the tree tobacco in relation to its hummingbird pollinator fauna

Nicotiana glauca , a hummingbird pollinated plant, exhibits geographical variation in several floral traits. We examined whether geographical differentiation occurred for different flower characters and if this differentiation could be explained, at least in part, by the existence or abundance of different hummingbird species in the respective pollinator assemblages. The comparison between five populations showed significant variation in six floral traits and two female fitness measures. The traits that better discriminated between populations were corolla length and corolla width. There were metric correlations between corolla length and style length in all populations studied and, in four of the five populations, both corolla length and width were also correlated. Among plants in each population, seed weight was correlated positively and significantly with style exertion, suggesting that fruit quality is dependent on the degree of cross pollination. Assemblages of hummingbirds differed between populations in species composition, visitation frequencies, and bill length. Linear regression involving bill length of the more frequent hummingbird pollinators and corolla length yielded positive and significant relationships. Thus, there appears to be an adjustment between pollinators and flowers traits that have high incidence in the among population variation.  © 2007 The Linnean Society of London, Biological Journal of the Linnean Society , 2007, 90 , 657–667.