Efficient floret inspection by honeybees in capitula of Carduus acanthoides

Abstract. 1. The floret inspection by honeybees Apis mellifera ligustica on inflorescences of Carduus acanthoides was studied in a natural patch. First-day stage capitula were protected with a net hood against insect visits. The next day, the net hood was removed at the time of maximal nectar accumulation, allowing a bee to visit the inflorescence. Walking trajectories on the capitula, the number of florets inspected and the duration of the visit were recorded. After the bee's departure, the inflorescence was cut off and analysed in the laboratory to determine the presence or absence of nectar in each of its florets.
2. Bees made inspection trajectories without a defined systematic pattern.
3. The number of floret inspections performed represented a high percentage of the available florets (57.37 ± 2.81%; mean ± SE; n = 8).
4. The number of depleted florets coincided with the number of floret inspections.
5. The number of times a floret is visited in a bee's trajectory is non-random.
6. Strategies that might account for this high foraging efficiency are discussed.     

The effect of nectar abundance on foraging patterns of bumble bees

Abstract.

• 1 Bumble bees (Bombus spp.) fed more on previously screened, nectar-rich plots of cow vetch (Vicia cracca) and white clover (Trifolium repens), and remained longer on inflorescences there, than on continually-exploited plots of these flowers. No significant differences between previously screened and continually available plots occurred in the number of individuals visiting these two areas, the number of inflorescences per visit, the number of florets visited per inflorescence, and the percentage of inflorescences rejected.
• 2 Individual bees were analysed in greater detail. They visited more inflorescences and spent longer times on cow vetch in the previously-screened plots, whether moving from previously-screened to continually available areas, or vice versa. On white clover the same pattern held for bees moving from previously screened to continually available plots, but not for those moving from continually available to previously-screened areas.

     

Choice of flowers by foraging honey bees (Apis mellifera): possible morphological cues

Abstract.

• 1 Honey bees foraging for nectar on lavender (Lavandula stoechas) chose inflorescences with more of their flowers open. The number of open flowers predicted whether an inflorescence was visited by bees, inspected but rejected, or ignored. Inflorescences chosen arbitrarily by observers had numbers of open flowers intermediate between those of visited and ignored inflorescences.
• 2 Differences in morphological characters between types of inflorescence correlated with nectar volume and sugar weight per flower so that visited inflorescences had a disproportionately greater volume of nectar and weight of sugar per flower and greater variance in nectar volume.
• 3 Although there were significant associations between nectar content and the morphological characters of inflorescences, discriminant function analysis revealed discrimination on the basis of morphology rather than nectar content.
• 4 Visited inflorescences tended to have smaller than average flowers but bees tended to probe the largest flowers on visited inflorescences.
• 5 Choice of flowers within inflorescences is explicable in terms of the relationship between flower size and nectar content.

     

Behavioral responses by bumble bees to variation in pollen availability

Summary Pollen-collecting bumble bees (Bombus spp.) detect differences between individual flowers in pollen availability and alter their behavior to capitalize on rewarding flowers. Specific responses by bees to increased pollen availability included: longer visits to flowers; visits to more flowers within an inflorescence, including an increased frequency of revisits; an increased likelihood of grooming while the bee flow between flowers within the inflorescence; and more protracted inter-flower flights, probably because of longer grooming bouts. The particular suite of responses that a bee adopted depended on the pollen-dispensing mechanism of the plant species involved. Bees buzzed previously-unvisited Dode-catheon flowers longer than empty flowers. In contrast, pollen availability did not significantly affect the duration of visits to Lupinus flowers, which control the amount of pollen that can be removed during a single visit. Simulation results indicate that the observed movement patterns of bumble bees on Lupinus inflorescences would return the most pollen per unit of expended energy. The increased foraging efficiency resulting from facultative responses by bees to variation in pollen availability, especially changes in the frequency and intensity of grooming, could correspondingly decrease pollen dispersal between plants.     

Variation in floral morphology within a population of Aster hispidus var. tubulosus (Asteraceae,Astereae)

The family Asteraceae has a particular inflorescence, the capitulum, consisting of ray florets and disc florets. The ray florets function as petals that attract pollinators. Marked variation in the ray floret morphology is known in a natural population of Aster hispidus var. tubulosus (Asteraceae). We analyzed the variation and found two distinct types in the ray florets, the long tubular ray floret and the ligulate ray floret. In this species, therefore, the variation in floral morphology among capitula, each of which is the basic pollination unit, is caused by the variation in the composition of the two ray floret types among capitula. We evaluated the sources of the observed variation in the floral morphology among capitula within a population using a hierarchical analysis that separated within‐individual (i.e. among capitula within each individual) and between‐individual components of the variation. We found that the main source of the variation lay at the between‐individual level, not at the between‐capitulum level nested within individuals. This finding will provide the basic knowledge that enables future study exploring whether the between‐individual variation in floral morphology caused by the compositional variation of the ray floret types leads to differential pollination success of individual plants in species of Asteraceae.     

Evidence for mutualism between a flower-piercing carpenter bee and ocotillo: use of pollen and nectar by nesting bees

Abstract.

• 1 Carpenter bees (Xylocopa californica arizonensis) in west Texas, U.S.A., gather pollen and ‘rob’ nectar from flowers of ocotillo (Fouquieria splendens). When common, carpenter bees are an effective pollen vector for ocotillo. We examined ocotillo's importance as a food source for carpenter bees.
• 2 The visitation rate of carpenter bees to ocotillo flowers in 1988 averaged 0.51 visits/flower/h and was 4 times greater than that of queen bumble bees (Bombus pennsylvanicus sonorus), the next most common visitor. Nectar was harvested thoroughly and pollen was removed from the majority of flowers. Hummingbird visits were rare.
• 3 Pollen grains from larval food provisions were identified from sixteen carpenter bee nests. On average, 53% of pollen grains sampled were ocotillo, 39% were mesquite (Prosopis glandulosa), and 8% were Zygophyllaceae (Larrea tridentata or Guaiacum angustifolium). Carpenter bee brood size averaged 5.8 per nest.
• 4 We measured the number of flowers, and production of pollen and nectar per flower by mature ocotillo plants, as well as the quantity of pollen and sugar in larval provisions. An average plant produced enough pollen and nectar sugar to support the growth of eight to thirteen bee larvae. Ocotillo thus has the potential to contribute significantly to population growth of one of its key pollinators.
• 5 Although this carpenter bee species, like others, is a nectar parasite of many plant species, it appears to be engaged in a strong mutualism with a plant that serves as both a pollen and as a nectar source during carpenter bee breeding periods.

     

Anthecology ofSchrankia nuttallii (Mimosaceae) on the tallgrass prairie

Schrankia nuttalii flowers through late spring on the tallgrass prairie. Although each stem produces an average of 26 capitate inflorescences only 12% of those inflorescences will open each day to disperse and receive polyads. Each inflorescence may live up to 48 hours but anthers abscise by late afternoon on the first day and the filaments change color and lose their scent. The 78–93 florets comprising each inflorescence open synchronously before dawn or during early morning hours. First day inflorescences ofS. nuttallii are herkogamous and fragrant. They are nectarless. Bombyliid flies and male bees are infrequent floral foragers so the major pollinators include female bees representing five families;Anthophoridae, Apidae, Colletidae, Halictidae, andMegachilidae. All foraging insects ignore second day inflorescences although stigmas are still receptive. Although 97% of all bees collected onS. nuttallii carrySchrankia polyads in their scopae or corbiculae 59% also carry the pollen/pollinaria of one or more coblooming angiosperms. At least 98% of all bees carrying mixed pollen loads incorporate the pollen/pollinaria of one or more nectariferous taxa (e.g.Asclepias spp.,Asteraceae, Convolvulaceae, Delphinium spec., etc.). Species of halictid bees are more likely to carry pure loads ofS. nuttallii polyads (70%) than bees of the four remaining families. Due to the nectarless florets and high degree of polylectic foraging bee-pollination inS. nuttallii converges more closely with the pollination systems of some AustralianAcacia spp. than with most other xeric/tropical genera of mimosoids studied in the western hemisphere.     

Differences in pollinator effectiveness of birds and insects visiting Banksia menziesii (Proteaceae)

Summary The effectiveness of nectarivorous birds, introduced honey bees and staphylined beetles as pollinators of Banksia menziesii was assessed. Staphylinids removed substantial amounts of pollen but did not deposit any onto stigmata. Abundance of beetles on inflorescences was related to the mean number of florets opening per day. Honey bees collecting pollen were more likely to effect pollination than those collecting nectar which only contacted stigmata when arriving or leaving an inflorescence. Nectar-foraging birds probed between florets 10.2±0.8 (±SE) times, contacting 8–16 stigmata during each probe. Bees visited inflorescences ten times more frequently than birds although they deposited only 25% of the pollen that birds did on stigmata. Fruit set was ten times greater on inflorescences visited by birds than on inflorescences visited by bees. Bees were capable of removing as much pollen as birds but, because of direct pollen transfer to birds when florets opened during foraging, actual removal was probably much less. Selection for floret opening during nectar foraging by birds may have resulted from pollen removal by non-pollinating animals, such as staphylinids.     

Caste-specific patterns of flower visitation in bumble bees (Bombus kirbyellus) collecting nectar from Polemonium viscosum

ABSTRACT.

• 1 Foraging routes of worker and queen bumble bees (Bombus kirbyellus Curtis) collecting nectar from flowers of the alpine sky pilot, Polemonium viscosum Nutt., were followed and the corolla tube length, corolla diameter, floral scent, and number of flowers on plants visited or bypassed by bees were monitored. Additionally, the number and proportion of flowers visited per inflorescence and distance flown from each to the next were recorded. Queens and workers differed significantly in choice of flowers. However, intra-inflorescence visitation rates and departure distances were similar between castes. Castes differed in the extent to which visitation reflected patch quality versus individual floral traits.
• 2 Both queens and workers failed to visit skunky-flowered plants more often than they failed to visit sweet-flowered ones, and preferred large over small inflorescences. However, queens visited large-flowered plants more often than small-flowered ones, while workers preferred flowers with shorter corolla tubes, regardless of their diameter. Although a number of studies have documented caste specialization on alternate species of host plants, ours is one of the first to show that morphological preferences promote comparable foraging differences between castes on monospecific plant resources.
• 3 Queens, once on a plant, responded to floral traits by probing more flowers on large inflorescences, as well as on those with broader floral form. Workers did not alter intra-inflorescence visitation rate in response to floral traits.
• 4 For workers, no significant relationship was demonstrated between the likelihood of passing by a plant and the number of flowers probed on the previous inflorescence visited. Thus, workers appeared to accept or reject each plant of P. viscosum independently. However, queens passed by fewer plants when leaving rich inflorescences than poor ones. These results suggest that workers use only individual plant acceptability in choosing which plants to visit, whereas queens base plant choice on patch and individual attributes. Such differences between castes in foraging rules when exploiting the same floral resource have received little attention, and provide insights into the heterogeneity of harvestable reward distributions from the perspective of the forager population.

     

Influence of resource topography on pollinator flight directionality of two species of bees

Analyses of the search patterns of ApisMellifera workers foraging on artificial inflorescences and Bombus Pennsylvanicusqueens foraging on inflorescences of red clover are used to identify a general rule specifying intrapatch search patterns. Bees land, move about the inflorescences in search of nectar, and come to a last-faced position from which takeoff occurs. Last-faced directions are generated by a forward-moving tendency while probing artificial inflorescences or real florets. This tendency is modulated by restricted bee locomotion, caused by the size and shape of the visited inflorescence and the spatial distribution of florets within such inflorescences. The result is that bees tend to circle inflorescences. The process is terminated with an undefined stopping rule, whereupon bees usually depart in the direction they last face. The last-faced direction is a by-product of intrafloral search and becomes less associated with arrival directions as intrafloral search continues. Pollinator flight directionality is usually represented as a frequency distribution of angular changes in direction which typically has a mean near 0° and a variance that increases with increases in energy gain. We show that these characteristics are artifacts of pooling mirror-image movement data sets;a mean of 0° is the result of canceling the means of the left- and right-hand turns. The putative increased variance associated with energy gain is the result of adding the variances associated with left- and right-handed turns. These computational artifacts may be avoided by changing the sign of the left-handed turns prior to pooling with the right-handed turns (or vice versa). Pooling bee visits based only on the number of florets probed can destroy information relevant to studies examining behavioral mechanisms of flight directionality. Analytical problems encountered when turns exceed 360° are also addressed.     

Selective advantage of ray florets in Scalesia affinis and S. pedunculata (Asteraceae), two endemic species from the Galápagos

The presence of neuter ray florets in species within Asteraceae is generally believed to increase pollinator attraction. In the endemic Galápagos genus Scalesia (Asteraceae) a natural variation in the presence/absence of neuter ray florets is found. To evaluate whether the presence of ray florets plays a selective role on female reproductive success we chose two species of Scalesia, Scalesia affinis that carries ray florets and S. pedunculata that is rayless. On Santa Cruz Island capitula of S. pedunculata were equipped with fake ray florets while others were untouched. On Isabela Island ray florets were removed on half of the capitula of S. affinis. In S. affinis rayed capitula received more pollinators and more pollen, which resulted in a significantly higher embryo production. In S. pedunculata no effect on embryo production was found. The disagreement between the two species may correspond to a difference in visitation frequency, S. pedunculata receiving many more visit than S. affinis. Thus, ray floret development proved beneficial in pollinator-restricted localities.     

Foraging behavior of honeybees on white clover

Summary Measurements of several aspects of foraging behavior of honeybees on white clover and of factors that might influence it were made at one-to-two-week intervals during the season. Other measurements were made on intervening days. Individual blossoms yielded a mean of from 0.02 to 0.08 l of nectar containing 42 to 65% sugar during the season. On one day when the nectar averaged 65% sugar, bees with pollen on their corbiculae carried a mean of 5.2 mg of pollen and 37.3 mg of nectar; bees without pollen carried a mean of 37.9 mg of nectar. On 10 occasions each of 50 bees were timed while foraging a single blossom; the mean foraging speed differed significantly on the 10 occasions, and varied from 1.5 to 3.0 seconds per blossom. Each of 18 bees was timed during visits to 25 blossoms, and the total time required for the same bees to forage from the blossoms on 25 racemes was also measured. The mean foraging speed of these bees varied from 1.1 to 4.5 seconds per blossom; the differences were highly significant. These bees foraged 7.0 to 26.0 blossoms per minute, and there was a strong negative correlation between the mean seconds required for bees to forage blossoms and the mean number of blossoms foraged per minute. Fifty one bees observed for a total of 314.5 minutes foraged an average of 18.4 blossoms per minute and 3.4 blossoms per inflorescence. Sixty one per cent of the flights of foraging bees were made to inflorescences estimated to be less than 5 inches from the starting point.Published as Technical Contribution N^o 4244 from theTexas Agricultural Experiment Station.     

THE MORPHOLOGY OF THE INFLORESCENCE OF RAGWEEDS (AMBROSIA-FRANSERIA : COMPOSITAE)

Payne, Willard W. (U. Michigan, Ann Arbor.) The morphology of the inflorescence of ragweeds (Ambrosia-Franseria: Compositae). Amer. Jour. Bot. 50(9): 872–880. Illus. 1963.—The ragweeds possess an inflorescence which is highly modified in relation to anemophily. Several trends from primitive to specialized character expressions may be seen in the morphology of the unisexual capitula and florets. An evolutionary scheme is presented whereby the catkinlike, acropetally maturing, staminate spike and the sessile, centrifugally developing, fruiting involucre cluster are derived from basic inflorescence types within the Compositae. Morphological evidence suggests that: (1) the taxa Ambrosia and Franseria should be combined under the older generic name Ambrosia; (2) the ragweeds and their relatives as a group appear to occupy a position intermediate between the Heliantheae and Anthemideae, as currently delimited within the Compositae.     

Visitation rate of pollinators and nectar robbers to the flowers and inflorescences of Tabebuia aurea (Bignoniaceae): effects of floral display size and habitat fragmentation

Large floral displays favour pollinator attraction and the import and export of pollen. However, large floral displays also have negative effects, such as increased geitonogamy, pollen discounting and nectar/pollen robber attraction. The size of the floral display can be measured at different scales (e.g. the flower, inflorescence or entire plant) and variations in one of these scales may affect the behaviour of flower visitors in different ways. Moreover, the fragmentation of natural forests may affect flower visitation rates and flower visitor behaviour. In the present study, video recordings of the inflorescences of a tree species (Tabebuia aurea) from the tropical savannah of central Brazil were used to examine the effect of floral display size at the inflorescence and tree scales on the visitation rate of pollinators and nectar robbers to the inflorescence, the number of flowers approached per visit, the number of visits per flower of potential pollinators and nectar robbers, and the interaction of these variables with the degree of landscape disturbance. Nectar production was quantified with respect to flower age. Although large bees are responsible for most of the pollination, a great diversity of flower insects visit the inflorescences of T. aurea. Other bee and hummingbird species are highly active nectar robbers. Increases in inflorescence size increase the visitation rate of pollinators to inflorescences, whereas increases in the number of inflorescences on the tree decrease visitation rates to inflorescences and flowers. This effect has been strongly correlated with urban environments in which trees with the largest floral displays are observed. Pollinating bees (and nectar robbers) visit few flowers per inflorescence and concentrate visits to a fraction of available flowers, generating an overdispersed distribution of the number of visits per inflorescence and per flower. This behaviour reflects preferential visits to young flowers (including flower buds) with a greater nectar supply.     

Conyza sumatrensis (Retz.) E. H. Walker: A new record from Pakistan

Conyza sumatrensis (Retz.) E. H. Walker (Astereae: Asteraceae) has been recorded in Pakistan for the first time. The species is closely associated with C. bonariensis and C. canadensis. It differs from C. bonariensis in its smaller capitula with a small series of marginal and disc florets that lack a purplish-pink apex, but resembles it in disciform capitula. C. sumatrensis differs from C. canadensis in having five-lobed disc florets and lacking well-developed ray florets. The species is widely distributed in the Potohar region, particularly in Rawalpindi and Islamabad.     

Nectarivore foraging ecology: rewards differing in sugar types

Abstract.

• 1 Honey bees, visiting artificial flower patches, were used as a model system to study the effects of sugar type (sucrose, glucose, fructose, and mixed monosaccharide), caloric reward, and floral colour on nectarivore foraging behaviour. Observed behaviour was compared to the predictions of various (sometimes contradictory) foraging models.
• 2 Bees drank indiscriminately from flowers in patches with a blue-white flower dimorphism when caloric values of rewards were equal (e.g. 1M sucrose in both colours; 1 M sucrose versus 2 M monosaccharide of either type), but when nectar caloric rewards were unequal, they switched to the flower colour with the calorically greater reward.
• 3 In yellow-blue dimorphic flower patches, on the other hand, bees did not maximize caloric reward. Rather, bees were individually constant, some to blue, others to yellow, regardless of the sugar types or energy content of the rewards provided in the two flower morphs.
• 4 The results suggest that optimal foraging theory (maximization of net caloric gain per unit time) is a robust predictor of behaviour with regard to the sugar types common to nectars; such optimal foraging is, however, limited by a superstructure of individual constancy.

     

Nodding Capitula in Superpáramo Asteraceae: An Adaptation to Unpredictable Environment1

Nodding capitula are a striking feature in several Asteraceae species of the Andean superpáramo. In this study, the thermal environment of the nodding inflorescence in Culcitium canescens Humb. & Bonpl. was surveyed by a short-term microclimatic measurement. Temperatures of the nodding inflorescences were higher than temperatures of the surrounding air during the day, while the respective temperatures were comparable during the night. Also, compared to other parts of the plant, the nodding inflorescence provided favorable temperature conditions. An experiment showed that the radiation reflected from the substratum explained most of the variability in the inflorescence temperature. It is suggested that the nodding capitula have evolved to protect the flowers from snow and rain while at the same time ensuring sufficient temperatures for floral development.     

EFFECTS OF DISPLAY SIZE,FLOWERING PHENOLOGY,AND NECTAR AVAILABILITY ON EFFECTIVE VISITATION FREQUENCY IN COMPARETTIA FALCATA (ORCHIDACEAE)

Comparettia falcata is an epiphytic, neotropical orchid that produces nectar as a pollinator reward. In Puerto Rico, C. falcata is allogamous and pollinated by the endemic hummingbird Chlorostilbon maugaeus. Autogamous pollinations are possible, but may result in reduced fruit set. For the 1989 and 1990 flowering seasons, the probability of pollinarium removals and natural pollinations increased with individual inflorescence display size. However, the frequency of effective pollinator visits was independent of flowering phenology in both years. A positive correlation between inflorescence size and reproductive success occurred in 1990 but not in 1989. In 1990 plants produced longer spurs, a higher standing crop of nectar, and a more concentrated nectar than in 1989. There was no relation between nectar availability (= standing crop of nectar) and sugar concentration in either year. Nectar availability and sugar concentration did not vary among the first four flowers of an inflorescence in either season. Nectar availability was not a good predictor of effective visitation. Comparettia falcata has a higher natural fruit set than tropical deceptive orchids, suggesting that pollinator visitation may be enhanced by nectar reward. The small, dilute nectar volumes secreted by C. falcata may benefit the plant by increasing interplant pollinator movement and pollen dispersal.     

Bees provide pollination service to Campsis radicans (Bignoniaceae), a primarily ornithophilous trumpet flowering vine

1. Pollination syndromes refer to stereotyped floral characteristics (flower colour, shape, etc.) that are associated with a functional group of pollinators (bee, bird, etc.).
2. The trumpet creeper Campsis radicans, endemic to the southeast and mid‐west United States, has been assigned to the hummingbird‐pollination syndrome, due mainly to its red, trumpet‐shaped flowers.
3. Previous studies demonstrated that the ruby‐throated hummingbird Archilochus colubris is C. radicans' primary pollinator, but anecdotal data suggest various bee species may provide pollination service when hummingbirds are absent.
4. This study characterised C. radicans nectar volume and concentration by time of day. Nectar volume was suitable for hummingbirds, but concentration was higher than typical hummingbird‐pollinated plants (～20% w/w); at ～30% w/w, it approached the concentration expected in bee‐pollinated plants (～50% w/w). We also found substantial amounts of nectar at night.
5. Two C. radicans populations received virtually no hummingbird visits, but the number of bees were markedly higher than in the populations previously described. Interestingly, there were no night‐time visitors despite the large quantity of nocturnal nectar.
6. Based on previously published pollen delivery per visit by various species, this study estimated that cumulative deposition by bees routinely reached pollen deposition thresholds for setting fruit in C. radicans. They are, unequivocally, the predominant pollinators in these populations, thus providing pollination service in the absence of hummingbirds.
7. These results highlight C. radicans as a food source for native bees and add to the understanding of how floral phenotypes can facilitate pollination by disparate functional groups.

     

The effect of inflorescence display size and flower position on pollination success in two deceptive and one rewarding orchid

• Inflorescence display size and flower position on the inflorescence play important roles in plant reproduction, in the formation of fruits and are primarily linked to pollinator behaviour. We used three orchids to determine how visitation rates and choice of pollinator depend on number and position of the flowers along the inflorescence.
• We measured reproductive success in (1) natural conditions, (2) hand-pollination experiments and (3) an experimental design, by modifying composition of inflorescences in populations of two deceptive orchids, Orchis anthropophora and O. italica, and one rewarding orchid, Anacamptis coriophora subsp. fragrans.
• There were no differences in natural fruit production in relation to flower position on the inflorescence (i.e. upper versus lower part), suggesting no preference of pollinators for different parts of the inflorescence. Hand-pollination experiments highlighted low pollen limitation in A. coriophora subsp. fragrans but high limitation in O. italica and O. anthropophora. Reproductive success of deceptive orchids in experimental plots decreased significantly when flowers on the upper half of the inflorescence were removed leading to reduced floral display, while reproductive success of the nectariferous species did not differ significantly.
• Our data highlight that in the examined orchids there is no clear relationship between fruit formation and flower position along inflorescences. Thus we can affirm that, for orchids, the entire inflorescence plays a dominant role in insect attraction but the part of the flower spike does not influence the choice of the insect. This implies that all flowers have the same possibility of receiving visits from pollinators, and therefore each flower has the same opportunity to set fruit.