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.     

Bee-pollination inHibbertia fasciculata (Dilleniaceae)

In direct contrast to mostHibbertia spp., the flowers ofH. fasciculata R. Br. ex D. C. bear only a single whorl of stamens and these stamens are arranged separately (not in typical bundles). The short filaments are appressed to the three carpels so that the inflated, porose and introrsive anthers form a centralized cluster obscuring the three ovaries. The three slender styles emerge at right angles from between the filaments. These styles curve upward and the stigmas form the three points of a triangle; each stigma is approximately one millimeter outside the centralized cluster of anthers. The flowers are nectarless and bear a bright yellow corolla. A pungent and unpleasant fragrance appears to be concentrated within the pollenkitt. When native bees attempt to forage for the pollen, within the cluster of anthers, the ventrally deposited loads of pollen, on the bees' abdomens, contact the outer triangle of stigmas. The major pollinators ofH. fasciculata are female bees in the polylectic genera,Lasioglossum (subgenusChilalictus, Halictidae) andLeioproctus (Colletidae). These bees carry an average of more than two pollen taxa when they are caught foraging onH. fasciculata. 78% of the 47 bees, captured onH. fasciculata carried the pollen from at least one sympatric taxon bearing nectariferous flowers (e.g., genera in theMyrtaceae, Compositae, andEpacridaceae). The pollination biology ofH. fasciculata is assessed in relation to the known radiation of bee-pollinated flowers in the genusHibbertia, and within theDilleniaceae s. l.     

Dioecy in the endemic genusDendrocacalia (Compositae) on the Bonin (Ogasawara) Islands

Dendrocacalia crepidifolia Nakai (Compositae, Senecioneae), the only species of this arboreal genus endemic to Haha Island in the Bonin Islands, was found to be dioecious. Male flowers differ from female ones in having a stunted style (style in female exserted from corolla and deeply bifurcating) and anthers filled with fertile pollen (anthers in the female lacking pollen). The size of the corolla and number of florets per head were similar between male and female flowers. The crown area of this arboreal species was also similar in male and female plants. The sex ratio was 0.55 male, not significantly different from 0.5. Both sexes produced nectar of similar sugar concentration (ca. 50%). The flowers are pollinated by feral honeybees (Apis mellifera), but they are thought to have been pollinated by small, lesshairy, endemic solitary bees before honeybees were introduced and subsequently became the dominant bee species on the island. The evolution of dioecy ofDendrocacalia on the island is thought to stem from the deleterious effects of inbreeding that are inherent in plants with geitonogamy. The increased geitonogamy on the island has resulted from increased woodiness (i.e., increased number of flowers per plant) and the original dependence on endemic bee pollinators, which are now endangered.     

Bees assess pollen returns while sonicating Solanum flowers

Summary Can bees accurately gauge accumulating bodily pollen as they harvest pollen from flowers? Several recent reports conclude that bees fail to assess pollen harvest rates when foraging for nectar and pollen. A native nightshade (Solanum elaeagnifolium Cavanilles) that is visited exclusively for pollen by both solitary and social bees (eg. Ptiloglossa and Bombus) was studied in SE Arizona and SW New Mexico. The flowers have no nectaries. Two experiments were deployed that eliminated pollen feedback to the bees by experimentally manipulating flowers prior to bee visits. The two methods were 1) plugging poricidal anthers with glue and 2) emptying anthers of pollen by vibration prior to bee visitation. Both experiments demonstrated that bees directly assess pollen harvest on a flower-by-flower basis, and significantly tailor their handling times, number of vibratile buzzes per flower and grooming bouts according to the ongoing harvest on a given flower. In comparison to experimental flowers, floral handling times were extended for both Bombus and Ptiloglossa on virgin flowers. Greater numbers of intrafloral buzzes and numbers of times bees groomed pollen and packed it into their scopae while still on the flower were also more frequent at virgin versus experimental flowers. Flowers with glued andreocia received uniformly brief visits from Bombus and Ptiloglossa with fewer sonications and virtually no bouts of grooming. Curtailed handling with few buzzes and grooms also characterized visits to our manually harvested flowers wherein pollen was artificially depleted. Sonicating bees respond positively to pollen-feedback while harvesting from individual flowers, and therefore we expect them to adjust their harvesting tempo according to the currency of available pollen (standing crop) within Solanum floral patches.     

Stamen movements in flowers ofOpuntia (Cactaceae) favour oligolectic pollinators

Opuntia brunneogemmia andO. viridirubra occur sympatrically in the Serra do Sudeste, Rio Grande do Sul, Brazil. Their flowers have 450–600 thigmonastic stamens and provide large amounts of pollen and nectar for bees. Bees of 41 species were registered at the flowers ofO. brunneogemmia and 30 at the flowers ofO. viridirubra. Females of three oligolectic species are the only effective pollinators:Ptilothrix fructifera (Anthophoridae),Lithurgus rufiventris (Megachilidae), andCephalocolletes rugata (Colletidae). During their visits inOpuntia-flowers, bees touch the filaments and stimulate the movement of the stamens to the centre of the flower. At the end of this movement, the anthers are densely packed around the style. As a consequence the pollen is presented in an easily accessible upper layer of anthers and various, nearly inaccessible lower layers. The lower layers contain about 80% of the pollen reward. Only females of the three oligolectic pollinators exploit the pollen from the lower layers and reach the nectar furrow. Therefore, through their stamen movements,Opuntia flowers hide most of their pollen from flower visitors but favour effectively pollinating, oligolectic bees.     

Notes on the pollination mechanisms ofMoraea inclinata andM. brevistyla (Iridaceae)

Individual flowers ofMoraea inclinata are nectariferous and last about six hours. They appear to be pollinated largely by bees in the familyHalictidae (Lasioglossum spp.,Nomia spp.,Zonalictus) and to a lesser extent by bees in the familyAnthophoridae (Amegilla). The mechanism of bee-pollination inM. inclinata is the Iris type; i.e., each flower consists of three pollination units (an outer tepal, a partly exserted anther, and the opposed style branch which terminates in a pair of petal-like crests). Bees rarely visit more than one pollination unit per flower. Transferral of pollen to the bee is passive and nototribic although all bees collected on the flowers were female and 55% of the bees carried pollen loads with 2–5 pollen taxa in their scopae.Moraea brevistyla flowers are nectariferous but lack scent and last two days. They are visited infrequently by bees and only one femaleLasioglossum spec. carried the pollen ofM. brevistyla. Unlike flowers ofM. inclinata those ofM. brevistyla deposit pollen only on the head and thorax. Bee-mediated autogamy in both species is avoided due to the erratic foraging patterns of the bees and the flexibility of each stigma lobe as the bee backs out of the flower. Approximately 2–4 flowers in the inflorescences of both species (6–8 flowers/infloresence) develop into capsules.     

The pollination biology ofHibbertia stricta (Dilleniaceae)

The exines of pollen grains ofHibbertia stricta (DC.)R. Br. exF. Muell. (Sect.Pleurandra) wear an oily, yellow pollen coat that stains positively for lipids. The pollen is collected by asocial bees, exclusively. The most common floral foragers are members of the genusLasioglossum (subgenusChilalictus;Halictidae) and they harvest pollen via thoracic vibration. As these bees cling to the inflated anthers their pollen smeared bodies come in contact with either of the two wet, nonpapillate stigmas. The stigmas respond positively to cytochemical tests for the presence of esterase immediately following expansion of the corolla, indicating the effective pollination period. The foraging patterns of the bees are narrowly to broadly polylectic. AsH. stricta flowers are nectarless, it is not surprising that bees bearing mixed pollen loads always carry the pollen of at least one nectariferous, coblooming plant. The pollination biology ofH. stricta is compared with otherHibbertia spp. and with pollen flowers in general.     

Mutual reproductive dependence of distylic Cordia leucocephala (Cordiaceae) and oligolectic Ceblurgus longipalpis (Halictidae, Rophitinae) in the Caatinga

Background and Aims

The close relationship between distylic Cordia leucocephala and the bee Ceblurgus longipalpis, both endemic to the Caatinga, north-east Brazil, was investigated, emphasizing reproductive dependence, morphological adaptations of the partners, and pollen flow.

Methods

In the municipality of Pedra, in the Caatinga of Pernambuco, the breeding system and reproductive success of C. leucocephala, its interaction with flower visitors and inter- and intramorph pollen flow were determined.

Key Results

The bee Ceblurgus longipalpis, the unique flower visitor and effective pollinator of self-incompatible Cordia leucocephala, presents morphological features adapted to exploit hidden pollen and nectar in the long and narrow corolla tubes. Pollen of low-level anthers is collected with hairs on prolonged mouthparts and pollen of high-level anthers with clypeus, mandibles, and labrum, showing pollen removal from both levels with the same effectiveness. In both morphs, this results in similar legitimate, i.e. intermorph cross-pollen flow. Illegitimate pollen flow to stigmas of pin flowers, however, was much higher than to stigmas of thrum flowers. Moreover, more illegitimate pollen was transported to stigmas of pin and less to those of thrum flowers when compared with legitimate pollen flow.

Conclusions

The study reveals a one-to-one reproductive inter-dependence between both partners. Data indicate that this relationship between bee species and plant species is one of the rare cases of monolecty among bees. Monotypic Ceblurgus longipalpis, the only rophitine species of Brazil, evolved prolonged mouthparts rare among short-tongued bees that enable them to access pollen from flowers with short-level anthers hidden for bees of other species, and nectar at the base of the flower tube.     

Breeding system and pollination by mimicry of the orchid Tolumnia guibertiana in Western Cuba

The mimicry of malpighiaceous oil‐flowers appears to be a recurrent pollination strategy among many orchids of the subtribe Oncidiinae. These two plant groups are mainly pollinated by oil‐gathering bees, which also specialize in pollen collection by buzzing. In the present study, the floral ecology of the rewardless orchid Tolumnia guibertiana (Oncidiinae) was studied for the first time. The orchid was self‐incompatible and completely dependent on oil‐gathering female bees (Centris poecila) for fruit production. This bee species was also the pollinator of two other yellow‐flowered plants in the area: the pollen and oil producing Stigmaphyllon diversifolium (Malpighiaceae) and the polliniferous and buzzing‐pollinated Ouratea agrophylla (Ochnaceae). To evaluate whether this system is a case of mimetism, we observed pollinator visits to flowers of the three plant species and compared the floral morphometrics of these flowers. The behavior, preferences and movement patterns of Centris bees among these plants, as well as the morphological data, suggest that, as previously thought, flowers of T. guibertiana mimic the Malpighiaceae S. diversifolium. However, orchid pollination in one of the studied populations appears to depend also on the presence of O. agrophylla. Moreover, at the two studied populations, male and female pollination successes of T. guibertiana were not affected by its own floral display, and did not differ between populations. The results are discussed in relation to the behavior and preferences of Centris bees, as well as the differential presence and influence of each of the two floral models.     

The perfume flowers ofCyphomandra (Solanaceae): Pollination by euglossine bees,bellows mechanism,osmophores, and volatiles

The perfume syndrome and pollination by fragrance-collecting euglossine bees in the neotropic solanaceous genusCyphomandra was confirmed by field observations. In SE Brazil,C. sciadostylis was visited byEufriesea violaceae, andC. diploconos byEuglossa mandibularis; C. hartwegii was pollinated byEulaema meriana in Costa Rica. The primary attractant, fragrant droplets that ooze from the dorsally bulged connectives, is mopped up by the males with the forebasitarsi. Thereby, the poricidal thecae are inadvertently pushed causing the dry pollen to dust the bee's sternum. The number and direction of the pollen jets are related to pollinator size and stigma structure. The flowers are homogamous, selfsterile, and last three days. The androecium is optically non-contrasting or has cryptic colour. Flowers ofC. sciadostylis andC. diploconos undergo a colour change and an almost three-fold increase in corolla size when scent production and visits cease. The dorsal papillar epidermis of the connective is underlain by a glandular parenchyma typical of osmophores. GC techniques revealed germacrene D as the main component in the mentholic scent ofC. sciadostylis, ipsdienol, heneicosane, and tricosane as dominant in the nutmeg-like scent ofC. diploconos, and benzyl acetate and benzyl alcohol in the sweet fragrance ofC. hartwegii. In all cases, these were accompanied by numerous minor components of heterogeneous chemical nature.—Pollen release by means of a peculiar pneumatic bellows mechanism appears as a necessary and probably ubiquitous feature ofCyphomandra. Even a slight pressure exerted upon the thin, elastic thecal walls blows pollen jets through the pores. Unusual anatomic changes accompany anther maturation. Initially voluminous parenchymatic locular intumescences (placentoids) contract completely during meiosis, then expand once more when the pollen is ripe, pushing the grains against the locular wall, and contract a second time, allowing air to enter the thecae.—Cyphomandra pinetorum was found to be exceptional in exhibiting a pollen flower syndrome, and not cryptical but optically contrasting yellow anthers, as known forSolanum.     

Contrasting breeding systems in twoEriotheca (Bombacaceae) species of the Brazilian cerrados

The pollination biology and breeding systems ofEriotheca pubescens andE. gracilipes have been studied. These two species occur as trees in cerrado vegetation, the neotropical savannas of Central Brazil, with partially sympatric distributions. They have similar phenology and floral structure, although the flowers ofE. pubescens are larger. Both species have nectar flowers pollinated by largeAnthophoridae bees but the main pollinators of each species differ in size. The species have markedly different breeding systems: late-acting self-incompatibility inE. gracilipes and apomixis stimulated by pollination inE. pubescens.     

TheMoegistorhynchus longirostris (Diptera: Nemestrinidae) pollination guild: long-tubed flowers and a specialized long-proboscid fly pollination system in southern Africa

A guild of 20 late spring- and early summer-flowering species ofIridaceae, Geraniaceae andOrchidaceae is pollinated partly or exclusively by the long-proboscid flyMoegistorhynchus longirostris (Nemestrinidae). This large-bodied fly, active in late spring and early summer, has mouthparts 40–70 (90) mm long and forages for nectar from a variety of species. These plants share a suite of convergent floral features including a straight or weakly curved floral tube usually 50–70 mm long but sometimes to 90 mm, relatively short petals or tepal lobes coloured white, cream or salmon with reddish nectar guides, and often violet or red anthers and pollen. Flowers of most species with these characteristics are zygomorphic with the stamens either arcuate (mostIridaceae) or declinate (Geraniaceae and someIridaceae). The flowers are odourless and typically secrete large amounts of nectar of relatively constant sugar concentration, mostly 24–29%, with a high sucrose:hexose ratio. Guild members utilize five separate sites of pollen deposition on the body of the fly, typically utilizing different deposition sites when two or more co-occur, indicating strong selection to aviod pollen contamination.M. longirostris is restricted to the west coast of southern Africa and at least 8 species appear to depend exclusively on the insect for pollination. The remaining species in the guild are pollinated by one or both of the long-proboscid fliesPhiloliche gulosa andP. rostrata (Tabanidae) over other parts of their range. Species and races pollinated entirely byM. longirostris have longer floral tubes which makes nectar unavailable to other insects, including other species of long-proboscid fly. The only insect with mouthparts long enough to forage effectively on these long-tubed flowers isM. longirostris and this fly must be considered a keystone species in the ecosystems in which it occurs.Dedicated to emer. Univ.-Prof. DrFriedrich Ehrendorfer on the occasion of his 70th birthday     

Pollination system and its significance on isolation and hybridization in JapaneseEpimedium (Berberidaceae)

Observations on native populations of JapaneseEpimedium have revealed that two types of effective pollinators can be recognized. One of the two types, which consists of small bees (mainlyAndrena spp. andLasioglossum spp.), is characterized by nondiscriminating behavior for collecting pollen and is commonly found inEpimedium. The other type, which comprises medium sizedTetralonia nipponensis and largerBombus diversus queens as main components, showed flower-dependent foraging fidelity associated with nectar-sucking behavior.T. nipponensis with a shorter proboscis pollinated flowers with a shorter spur ofE. trifoliatobinatum and of a part ofE. s sempervirens, while the queen ofB. diversus with a longer proboscis pollinated longer spurred flowers ofE. grandiflorum andE. sempervirens. In the populations of putative hybrid-derivatives which show gradational variations of spur length, bees of the pollencollecting type pollinated any flower non-discriminately while bees of the nectar-foraging type tended to visit the flowers with spur lengths corresponding to their proboscis length. These observations suggest that the pollen-collecting bees play an important role for gene flow among theEpimedium species, and the nectar-foraging bees reinforce the isolation between the species by their selective pollination. Reproductive isolation between species ofEpimedium is discussed in relation with some practical behavior, such as flying power, of the pollinators.     

Corolla wilting facilitates delayed autonomous self-pollination in Pedicularis dunniana (Orobanchaceae)

Structural changes associated with corolla wilting may serve as a mechanism for effecting self-pollination. Low pollinator visitation, high seed production and a corolla that persists after anthesis indicates that Pedicularis dunniana is autogamous. Delayed autonomous self-pollination is facilitated by corolla wilting. Wilting of the upper lip (galea) brought the pollen laden anthers into contact with the stigma resulting in the deposition of self pollen on the stigma. The seed set of flowers either emasculated, or with restrained galeae thus preventing anthers brushing against the stigma, was significantly lower than that of open-pollinated flowers. This demonstrates that autogamy occurs in this species through corolla wilting. Germination experiments indicated that outcross seedlings were more vigorous than selfed seedlings as a result of inbreeding depression. It is likely that autogamy provides reproductive assurance for P. dunniana under conditions of pollinator scarcity.     

The flower biology ofCephalanthera longifolia (Orchidaceae)—pollen imitation and facultative floral mimicry

Solitary bees (Halictus sp.) were found to be the effective pollinators ofCephalanthera longifolia. In the same foraging flight the bees also visit flowers ofCistus salviifolius which has a similar colour pattern.Cephalanthera offers no reward to its pollinators, but orange papillae on its labellum successfully imitate pollen ofCistus. AsCephalanthera also attracts pollinators in the absence ofCistus, this is regarded as facultative floral mimicry.     

Pollination ofEchinocereus fasciculatus andFerocactus wislizenii

One of the most common types of cactus flower in the southwestern United States is the large, colorful, cup-shaped flower.Echinocereus fasciculatus var.boyce-thompsonii in Arizona is a representative of this class of flowers. Its flowers are visited by three common types of insect visitors: medium-sized bees, small solitary bees, and beetles. All three types of visitors come into contact with the pollen, but only the mediumsized bees regularly touch the stigma in their visitations. The main effective pollinators are therefore the medium-sized bees (Megachile, etc.).Ferocactus wislizenii has a similar floral mechanism and is likewise pollinated mainly by medium-sized bees (Megachile, Lithurge, Diadasia, etc.).Pollination of North American Cacti, 1.     

The production of floral oils byMonttea (Scrophulariaceae) and the function of tarsal pads inCentris bees

Plant species that secrete oil as their primary floral reward are rare and sporadically found in the angiosperms. We report here thatMonttea, a genus previously unsuspected of being an oil-plant, produces lipids from trichome elaiophores on the inside of the lower (anterior) lip. The discovery of the production of oils by species of this S. American genus explains the occurrence of unusual dual-function collecting structures in ArgentineCentris (Hymenoptera: Anthophoridae) and explains the presence of oil-collecting bees in regions where oil-secreting flowers were previously thought to be absent. The behavior of these centridine pollinators onMonttea flowers parallels that of oil-collecting bees onDiascia (Scrophulariaceae) in S. Africa.     

Floral biological observations onHeliamphora tatei (Sarraceniaceae) and other plants from Cerro de la Neblina in Venezuela

During 20 days in 1985, floral biological observations were made at 1 850–2 100m elevation on Cerro de la Neblina in Venezuela.Heliamphora tatei var.neblinae (Sarraceniaceae) is nectarless and has poricidal anthers.Heliamphora tatei, Graffenrieda fruticosa, G. polymera, G. reticulata, Tocca pachystachya, T. tepuiensis (Melastomataceae),Saxofridericia compressa, andStegolepsis neblinensis (Rapateaceae), are buzz-pollinated by ten species ofBombus, Eulaema, Melipona, Centris, Xylocopa, Dialictus, andNeocorynura. Additional observations of floral visits on tepui species ofGentianaceae, Loranthaceae, Malpighiaceae, Ericaceae, Orchidaceae, andAsteraceae are reported. Visitors include the hummingbirdCampylopterus duidae, the flower-piercerDiglossa duidae, the nectarivorous batAnoura geoffroyi, and various species ofCentris andBombus bees. Scent baits for euglossine bees attracted very few bees.Apis mellifera adansonii-scutellata, the africanized honey bee, was caught at 1 850m elevation.     

Floral mimesis inThelymitra nuda (Orchidaceae)

Insect pollination occurred inThelymitra nuda R. Br. on sunny days when the ambient temperature exceeded 20 °C. The flower buds on a raceme opened subsynchronously displaying the brightly-colored, actinomorphic perianth and exposed the contrastingly-colored, scented and ornamented column. InT. nuda the staminodes and the filament of the fertile stamen are fused to one another producing an inflated hood over the anther. This staminodal hood is terminated in two non-ornamental, but brightly-colored, central lobes and two terete lateral lobes bearing approximately 400 white trichomes. Each trichome bears a double chain of 30–40 spherical, rugulose cells. Female bees, in the genusLasioglossum (Halictidae), were observed to land directly on the hood and curled their bodies around the four lobed tip of the staminodal complex. The bees attempted to forage on the lobes as if they were collecting pollen from fertile, poricidal stamens. These bees applied thoracic vibration to the yellowish central lobes and actively scraped the trichome clusters (Pseudopollen) with their forelegs. Bees carried the pollinaria ofT. nuda dorsally on their abdomens. Abdominal contact with the rostellum appeared to occur when the female bee disengaged herself from the staminodal hood. Observations made of bees on co-blooming flowers, and analyses of pollen loads collected by bees suggested that the orchid flower mimics the guild of blue-purple flowers that lack floral nectar but offer pollen in poricidal anthers. The models ofT. nuda are co-bloomingLiliaceae in the generaDichopogon andThysanotus. However, nectarless, buzz-pollinated flowers are also extensively distributed over the orchid’s range. More than 30% of the flowers in theT. nuda population had their pollinaria removed, suggesting a high capacity for cross-pollination in an orchid genus usually considered to be self-pollinated via mechanical autogamy. This study confirmed previous predictions that column modifications represented a trend towards pseudanthery.     

A presumed case of functional convergence between the flowers of Schizolobium parahyba (Fabaceae) and species of Malpighiaceae

Flowers of Malpighiaceae have a flag petal with a sturdy base that Centridini bees clasp with their mandibles to free their legs and thus be able to harvest oil. We found that the yellow, nectariferous flowers of Schizolobium parahyba (Fabaceae) have a forward-flexed upper petal with a sturdy claw and an adnate filament. Two Centris species were among the most frequent bee visitors to S. parahyba flowers. These bees clasped the adnate filament and the claw of the upper petal with their mandibles and extended their mouthparts into the corolla to take nectar. During the visit they leaned on, or loosely grabbed, the stamens. Blooming in the same area and period were two yellow-flowered Stigmaphyllon species (Malpighiaceae) whose pollen was also found on loads carried by the Centris bees. The flexion and the sturdiness of the upper petal claw of Schizolobium parahyba flowers may be viewed as a trait that suits the mandible clasp of Centris bees. Although this clasp is not needed when the bees visit S. parahyba flowers, it is vital when the bees exploit flowers of the Malpighiaceae. We suggest that the sturdy claw and the adnate filament of S. parahyba may be viewed as an instance of presumed functional convergence with the upper petal of Malpighiaceae.