The Morphology of the Inflorescence in Ranunculus bulbosus L.

This paper records the form variation of 750 inflorescencesof Ranunculus bulbosus L. collected randomly from each of twolarge colonies growing on permanent grassland. Each inflorescence has a terminal flower, 1–4 bracts onthe main axis and up to 8 flowers borne on cymes subtended bythese bracts. Over 75 per cent, of each sample consists of inflorecenceswith 2 or 3 bracts on the main axis and 2–4 flowers. Thenumber of flowers increases with the number of bracts on themain axis and evidence is given that the 4-bract 9-floweredinflorescence may be nearly the largest and most complex thatcan be produced under these conditions. The distribution of flowers in the axillary cymes is such thatthe inflorescences tend to be radially symmetrical and pyramidalin form. This is so even thought with increase in the numberof bracts on the main axis the proportion of axillary flowersdecreases in the lowest cyme and increases in the cyme above. It is considered that the form and size of the inflorescencecan be related to the vigour of the plant and to the mechanicaland nutritional problems involved. A comparison of the varioustypes of inflorescences found probably reflects the developmentalsequence of flower production. It also indicates that thereis competition between certain potential flower positions asthe inflorescence develops.     

Flowering patterns of long-lived Heliconia inflorescences: implications for visiting and resident nectarivores

Summary Flowering patterns of four Heliconia (Heliconiaceae) species in Trinidad, West Indies were examined for their predictability and availability to the nectarivores that rely on Heliconia floral nectar. Principal flower visitors are trapling hermit hummingbirds; inflorescences are inhabited by nectarivorous hummingbird flower mites that move between inflorescences by riding in the hummingbirds' nares. Heliconia inflorescences flower for 40–200 days, providing long-term sources of copious nectar (30–60 l per flower), but each Heliconia flower lasts only a single day. As an inflorescence ages the interval increases between open flowers within a bract; wet-season inflorescences produce open flowers more slowly than dry-season conspecifics.Estimated daily energy expenditures for hermit hummingbirds demonstrate that slow production of short-lived open flowers plus low inflorescence density preclude territorial defense of Heliconia by the hermits. Heliconia flowering patterns are viewed as a means of (i) regulating reproductive investment by the plants through staggered flower production over long periods of time, and (ii) maintaining outcrossing by necessitating a traplining visitation pattern by its hummingbird pollinators. I suggest that Heliconia exhibit a two-tiered pollination system by using hermit hummingbirds primarily for outcrossing and using hummingbird flower mites primarily for self-pollination.     

Thermal insulation and accumulation of heat in the downy inflorescences of Saussurea medusa (Asteraceae) at high elevation in Yunnan,China

Himalayan snowball plants, which are considered to be an extreme form of downy plants, have very dense trichomes on well-developed bracts that surround the inflorescences. It has been postulated that the downy inflorescences of these plants might serve to keep the interior of inflorescences warmer than the outside and, thus, to protect reproductive cells from low temperatures in their Himalayan habitat. In the present study, we examined the downy inflorescences of Saussurea medusa Maxim. in native habitats in the high alpine zone of the Henduan Mountains in Yunnan, China, and we analyzed the temperature within inflorescences after absorbance of light energy. S. medusa is pollinated by bumblebees and we found that its inflorescences accumulated heat not on the inside, but, rather, on the upper surfaces. The thick hollow stems and the overlapping bracts with obvious epinasty might serve not only to retain heat, but also as an insulator to protect the inside against overheating, with apparent local warming of flowers that are located at the tops of plants, which are cone-shaped. We made a model that mimicked the warming of inflorescences, providing support for the hypothesis that the downy bracts of S. medusa have two functions: thermal insulation to protect the inside of flowers and the accumulation of heat on the upper surfaces of the inflorescence. Such a system might be effective in attracting pollinators and also in protecting tissues from extreme variations in temperature. Electronic Publication     

ORGAN INITIATION AND DEVELOPMENT OF INFLORESCENCES AND FLOWERS OF ACACIA BAILEYANA

Inflorescence and floral ontogeny are described in the mimosoid Acacia baileyana F. Muell., using scanning electron microscopy and light microscopy. The panicle includes first-order and second-order inflorescences. The first-order inflorescence meristem produces first-order bracts in acropetal order; these bracts each subtend a second-order inflorescence meristem, commonly called a head. Each second-order inflorescence meristem initiates an acropetally sequential series of second-order bracts. After all bracts are formed, their subtended floral meristems are initiated synchronously. The sepals and petals of the radially symmetrical flowers are arranged in alternating pentamerous whorls. There are 30–40 stamens and a unicarpellate gynoecium. In most flowers, the sepals are initiated helically, with the first-formed sepal varying in position. Petal primordia are initiated simultaneously, alternate to the sepals. Three to five individual stamen primordia are initiated in each of five altemipetalous sectorial clusters. Additional stamen primordia are initiated between adjacent clusters, followed by other stamens initiated basipetally as well as centripetally. The apical configuration shifts from a tunica-corpus cellular arrangement before organogenesis to a mantle-core arrangement at sepal initiation. All floral organs are initiated by periclinal divisions of the subsurface mantle cells. The receptacle expands radially by numerous anticlinal divisions in the mantle at the summit, concurrently with proliferation of stamen primordia. The carpel primordium develops in terminal position by conversion of the floral apex.     

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.

     

Homeosis in Araceae Flowers: The Case of Philodendron melinonii

The early stages of development of the inflorescence of Philodendronmelinonii were examined using scanning electron microscopy.Pistillate flowers are initiated on the lower portion of theinflorescence and staminate flowers are initiated on the distalportion. The male flowers have four to five stamens. The femaleflowers have a multilocular ovary consisting of four to sixlocules. A transition zone consisting of sterile male flowersand bisexual flowers with fused or free carpels and staminodesis also present on the inflorescences. This zone is locatedbetween the male and female flower zones. Generally, the portionof the bisexual flower facing the male zone forms stamens, andthe portion facing the female zone develops an incomplete gynoeciumwith few carpels. In P. melinonii, the incomplete separationof staminodes from the gynoecial portion of the whorl showsthat the staminodes and carpels belong to the same whorl. Thebisexual flowers of P. melinonii are believed to be a case ofhomeosis where carpels have been replaced by sterile stamenson the same whorl. At the level of the inflorescence, pistillateand staminate flowers are inserted on the same contact parastichiesalong the inflorescence; there is no discontinuity between thefemale zone, the bisexual zone, and the male zone. The presenceof bisexual flowers is believed to correspond to a morphogeneticgradient at the level of the inflorescence as a whole. Copyright2000 Annals of Botany Company Flower, development, gradient, inflorescence     

Morphological correlates of nectar production used by honeybees

Abstract.  1. Honeybees foraging on lavender have been shown to choose inflorescences that are larger and have more flowers. If they are selecting optimally then these inflorescences should yield higher net rates of energy gain. The number and distribution of flowers within inflorescences is a complex function of age, however, which might itself influence nectar quality and availability.
2. Sampling of the overnight nectar secretion of visited and unvisited inflorescences showed that younger inflorescences with more flowers produced more sugar per flower and had fewer unproductive flowers than other inflorescences, but the size of the inflorescence had no effects.
3. Overall display size attracted bees to inspect inflorescences, as inflorescences that were inspected but rejected were larger and/or had larger or more bracts than those that were ignored. Bees, however, accepted more productive inflorescences based on different cues: inflorescence age and number of flowers.
4. Inflorescence choice thus appeared to reflect a two-stage decision process based on different morphological criteria at each stage.     

SPIRAL DEVELOPMENTAL PATTERNS IN THE STEM AND INFLORESCENCE OF LILIUM TIGRINUM

Extensive correlations in spirality were observed among vegetative and floral organs in Lilium tigrinum Ker. Organs involved were vegetative leaves, bracts, and bracteoles. These correlations varied in their degree of constancy depending upon the organs involved. The mature inflorescences of L. tigrinum appeared to fit the common definition of a raceme. In 67.3% of the flowers at node 3 on the raceme, the bract-bracteole spirals reversed the spiral of vegetative leaves on the stem. These reversals resembled those observed on essentially cymose inflorescences of certain members of the Caryophyllaceae. Cymose branching was found to be an invariable feature of the inflorescence of L. tigrinum when secondary flowers appear. The apparently indeterminate tips of inflorescence main axes were interpreted as exhibiting stages in progression from a basically determinate (cymose) inflorescence. It was concluded that the ancestors of L. tigrinum had well-developed cymose branching patterns in the inflorescence. Reversal of stem spirals by the bract-bracteole spirals at the apices of many inflorescences was considered to be the result of complete utilization of the inflorescence meristem. Explanations for those reversals were provided by the field theory and by the theory of the first available space.     

Water Deficit and Inflorescence Development in Zea mays L.--The Role of the Developing Tassel

In the normal pattern of development of Zea mays (cv. Iochief)a single mature female inflorescence is produced at node 7.A brief episode of water deficit at the time of terminal maleinflorescence initiation induced the subsequent developmentof two to three mature female inflorescences at nodes 5–7.This growth of the inflorescences at lower nodes was accompaniedby a marked inhibition of the growth of the terminal male inflorescence.Removal of either the developing terminal inflorescence or ofthe axillary inflorescence at node 7 at this time also promotedthe growth of the lower axillary inflorescences. The growthof these inflorescences was further stimulated by a period ofwater deficit when only the inflorescence at node 7 was removed,but removal of the male inflorescence abolished the capacityof these inflorescences to respond to the water deficit Excisionof the male inflorescence immediately before or immediatelyafter the period of water deficit produced the same response.It is concluded that this response of the lower axillary inflorescencesto water deficit is mediated through an effect on the developingterminal male inflorescence. Zea mays, water deficit, inflorescence development, tassel, correlative inhibition     

Phenological regulation of opportunities for within-inflorescence geitonogamy in the clonal species,iris versicolor (iridaceae)

Opportunities for selfing through geitonogamy are possible if more than one flower within the same clone, inflorescence, or floral unit is open at the same time. In a total of 200 inflorescences in two natural populations of Iris versicolor, flowers were observed and classified daily on the basis of anther dehiscence and stigma receptivity. Analysis of the flowering phenology demonstrated that (1) protandry limits opportunities for autogamy, (2) flowers mature sequentially within a floral unit (defined as a cluster of flowers borne on a single branch within an inflorescence), preventing the opportunity for geitonogamous fertilization between flowers of the same floral unit, and (3) 77% of all flowers had no opportunity to be pollinated by another flower within the same inflorescence. Both the number and the proportion of flowers with opportunities for geitonogamy increased with the number of flowers open in each population, and opportunities for geitonogamy also increased with the number of floral units within inflorescences. These morphological and phenological controls suggest that when selfing occurs in this species, it is most likely to occur between flowers on different inflorescences within the same clone. Since the organization of whole inflorescences in space is determined primarily by rhizome placement, clonal architecture may play an important role in mating system regulation in this species.     

What makes a fig: insights from a comparative analysis of inflorescence morphogenesis in Moraceae

Background and AimsMoraceae, the family of mulberry and fig trees, displays small homogeneous flowers but extremely diverse inflorescences ranging from simple and branched to complex and condensed. Inflorescences also vary in flower organization in the receptacle, in the degree of flower condensation and in receptacle shape. Thus, the objective of the present study was to compare the inflorescence morphogenesis of Moraceae species, to investigate whether clades with a similar pollination mode share the same patterns of inflorescence development and the developmental stages at which we observe the key changes resulting in the diversified inflorescence architecture that culminates in the Ficus syconium.MethodsInflorescences at different developmental stages were sampled from Brosimum gaudichaudii, Castilla elastica, Clarisia ilicifolia, Ficus pertusa, Maclura tinctoria and Morus nigra and processed for surface and anatomical analyses.Key ResultsThe inflorescence morphogenesis of the studied species is highly variable. The shape of the inflorescence meristem (bulging, hemispheric or elongated), the initiation order and arrangement of flowers along the receptacle and the occurrence of bracts vary between related species. This diversity originates early during inflorescence development. Brosimum gaudichaudii, C. elastica and F. pertusa have flowers enclosed or immersed within the receptacle, although inflorescences begin their development as flat and open structures, as occurs in the other three study species.ConclusionComparison of the inflorescence morphogenesis in Moraceae species allows us to infer that evolutionary ontogenetic changes driven by pollinators culminate in the enclosure of flowers inside the receptacle, as occurs in the Ficus syconium.     

Factors controlling Flowering in the Chrysanthemum: II. DAY-LENGTH EFFECTS ON THE FURTHER DEVELOPMENT OF INFLORESCENCE BUDS AND THEIR EXPERIMENTAL REVERSAL AND MODIFICATION

1. Inflorescence buds, produced by vernalized Chrysanthemum plantsin long day, cease to grow, and die at an early stage if maintainedin long day, but will produce open flowers if transferred toshort day. Dissection of such buds reveals that developmentdoes not proceed beyond the formation of the bare receptacleand no florets are initiated, while inflorescence buds producedin short day have almost completed floret initiation when theybecome macroscopically visible.
2. Inflorescence buds producedin long day can be induced to completetheir development inlong day by:
   1. removal of all lateral shoots, and
   2. by re-rootingthe inflorescenceitself, leaving only a numberof bracts onits axis.
3. Inflorescence buds produced in short day canbe inhibited fromdeveloping by
   1. transfer to long day,
   2. transferto low light intensity in shortday, and
   3. application of auxinpaste.
4. All three methods of inhibition become progressivelyless effectivewith the advancing development of the bud.
5. Thelatest stage at which development was found to have beenarrestedwas that of ovule formation.
6. Heights of plants were determinedat budding and when the flowershad started to open; markeddifferences due to length of daywere found.
7. Teratologicaleffects noted in buds, exposed for extended periodsto longday, included formation of bracts on the receptacle(the absenceof which distinguishes the subtribe Chrysantheminaeof the Compositaeto which the Chrysanthemum belongs) as wellas secondary inflorescences,petaloid stamens, &c.
8. The results are discussed in relationto known effects of auxinon vegetative growth and reproduction.

     

BEETLE POLLINATION OF CYCLANTHUS BIPARTITUS (CYCLANTHACEAE)

The morphology, inflorescence phenology, and insect visitors of Cyclanthus were observed during two reproductive seasons at Finca La Selva in the Atlantic lowlands of Costa Rica. The inflorescence of Cyclanthus is an elongate spadix that is subtended and enclosed by four large, cymbiform bracts. Staminate and pistillate flowers are arranged in separate cycles along the length of the spadix and show marked dichogamy. Pollinators of Cyclanthus are beetles of the genus Cyclocephala (Scarabaeidae). The beetles arrive at the inflorescence while it is in the pistillate phase, during the first evening of the 2-day flowering period. They remain in the inflorescence for 24 hrs, until the end of staminate anthesis. The bracts of the inflorescence produce specialized tissue that the beetles consume along with pollen. Chemical analysis of the food tissue indicates that it is almost 50% lipid by dry weight. The scarabs use the inflorescence as an aggregation site for mating. Experiments with bagged inflorescences showed that no seeds are produced in the absence of pollinators, which suggests that Cyclanthus is obligately allogamous.     

Morphology and Anatomy of Stems and Pedicels of Spring Flush Shoots Associated with Citrus Fruit Set

Flowering and vegetative shoots of ‘Shamouti’ orange[Citrus sinensis (L.) Osbeck] and ‘Marsh’ seedlessgrapefruit (Citrus paradisi Macf.) were examined for correlationof their morphology and anatomy with fruit set. Fruit set isfavoured on leafy inflorescences whereas abortion is nearlycomplete on leafless inflorescences. Leafless inflorescencesof ‘Shamouti’ with one flower were found to havea very thin stem which contained few vascular bundles, whereasthose with three flowers had better-developed vascular systems.The vascular system of leafy inflorescences is significantlydifferent from that of leafless ones and contains a distinctcentral xylem cylinder. The vascular area of leafless inflorescencesis only about one-quarter of that of the leafy ones. The vascularsystem of grapefruit resembles that of the ‘Shamouti’orange. This study emphasizes the importance of the dimensionof the vascular system for fruit set and provides a possibleexplanation for the better fruit set on both leafy and leaflessinflorescences with several flowers compared with single-floweredinflorescences. Anatomy; citrus; fruit set; leafless inflorescence; leafy inflorescence; pedicel; vascular system; vegetative shoot     

PHYLOGENETIC IMPLICATIONS OF INFLORESCENCE AND FLORAL ONTOGENY OF MIMOSA STRIGILLOSA

Ontogeny of the inflorescence and flower of Mimosa strigillosa has been studied in order to explore the developmental basis for variation in number of parts, patterns of organ arrangement, and inflorescence architecture. Each racemose inflorescence of M. strigillosa has an acropetal order of initiation of bracts and flowers. Although flowers are initiated in acropetal order, they develop synchronously except for the basal flowers, which are retarded. The ring meristem in the calyx may be considered an expression of precocious fusion, a specialized condition within the genus. Two patterns of organ arrangement (nonsagittal and median sagittal) are distributed among 4- and 5-merous flowers along the inflorescences. Variability in number of parts probably has evolved through reduction of a basic, pentamerous structure, through fusion or suppression. It is proposed that the number of parts and pattern of organ arrangement are correlated features.     

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.     

Density Studies on Lupins: I. Flower Development

In an August-sown experiment the pattern of flower developmentwas followed for cv. Ultra (Lupinus albus L.) and cv. Unicrop(L. angustifolius L.) grown at low (10 plants m^–2) andhigh (93 and 83 plants m^–2, Ultra and Unicrop respectively)densities. Dry weight increase of flowers on the main-stem inflorescenceand first lateral below the main-stem were compared at differentfloral stages. Maximum flower weight was reached just priorto the open flower stage and remained constant or declined untila pod formed or abscission occurred. The time period betweenmaximum flower weight and pod formation or abscission was upto 10 days. Emergence of the inflorescence was earlier and thefirst flower of Ultra opened 10 days before Unicrop. Developmentof each terminal raceme (inflorescence) was acropetal, withpods having formed on lower flower nodes when terminal flowerswere still quite immature. Laterals forming the next generationof inflorescences grew from axillary leaf buds below an inflorescencewhile it was in full flower. Sources of competition from connectedreproductive and vegetative metabolic sinks are discussed. Lupinus spp., lupins, flower development, planting density     

Flower-like heads from flower-like meristems: pseudanthium development in <Emphasis Type="Italic">Davidia involucrata</Emphasis> (Nyssaceae)

Flower-like inflorescences (pseudanthia) have fascinated botanists for a long time. They are explained as condensed inflorescences implying that the pseudanthium develops from an inflorescence meristem (IM). However, recent developmental studies identified a new form of reproductive meristem, the floral unit meristem (FUM). It differs from IMs by lacking acropetal growth and shares fractionation, expansion and autonomous space filling with flower meristems (FM). The similarity among FUMs and FMs raises the question how far flower-like heads originate from flower-like meristems. In the present paper, pseudanthium development in Davidia involucrata is investigated using scanning electron microscopy. D. involucrata has pincushion-shaped heads composed of densely aggregated, perianthless flowers and associated with two large showy bracts. Early developmental stages show a huge naked FUM. The FMs appear almost simultaneously and lack subtending bracts. With ongoing FUM expansion new space is generated which is immediately used by further FM fractionation. The heads have only staminate flowers or are andromonoecious with staminate and a single perfect flower in oblique position. All FMs lack perianth structures and fractionate a variable number of stamen primordia. The perfect FM is much larger than the staminate FMs and forms a syncarpous gynoecium with inferior ovary. Pseudanthium development in D. involucrata confirms the morphogenetic similarity to FMs as to acropetal growth limitation, meristem expansion and fractionation. It thus should not be interpreted as a condensed inflorescence, but as a flower equivalent. Furthermore as the FUM develops inside a bud, its development is considered to be influenced by mechanical pressure. The oblique position of the perfect flower, the developmental delay of the proximal flowers, and the variable number of stamens which were observed in the pseudanthium development, can be caused by mechanical pressure. Next to the Asteraceae, D. involucrata offers a further example of a pseudanthium originating from a FUM. More knowledge on FUMs is still needed to understand diversification and evolution of flower-like inflorescences.     

Quantitative developmental analysis of homeotic changes in the inflorescence of Philodendron (Araceae)

Background and Aims: The inflorescence of Philodendron constitutes an interestingmorphological model to analyse the phenomenon of homeosis quantitativelyat the floral level. The specific goals of this study were (1)to characterize and quantify the range of homeotic transformationin Philodendron billietiae, and (2) to test the hypothesis thatthe nature of flowers surrounding atypical bisexual flowers(ABFs) channel the morphological potentialities of atypicalbisexual flowers. Methods: Inflorescences of P. billietiae at different stages of developmentwere observed using SEM. The number of appendices in male, femaleand sterile flowers were counted on 11 young inflorescences(5–6 flowers per inflorescence). The number of staminodesand carpels on ABFs were counted on 19 inflorescences (n = 143).These data were used for regression and ANOVA analyses. Results: There was an average of 4·1 stamens per male flower,9·8 carpels per female flower and 6·8 staminodesper sterile male flower. There was an average of 7·3floral appendices per atypical flower. Staminodes and carpelsare inserted on the same whorl in ABFs. A negative exponentialrelationship was found between the average number of staminodesand the number of carpels in ABFs. If only the ABFs consistingof less than six carpels are considered, there is a linear relationshipbetween the number of carpels and the average number of staminodes.The value of the slope of the regression equation indicatesthat on average, in P. billietiae, 1·36 carpels are replacedby one staminode. Conclusions: In P. billietiae, the number of appendages in female flowersimposes a constraint on the maximum total number of appendages(carpels and staminodes) that can develop on ABFs. The quantitativeanalyses indicate that the average number of different typesof floral appendages on an ABF and the number of organs involvedin a homeotic transformation are two independent phenomena.     

A ballistic pollen dispersal system influences pollination success and fruit‐set pattern in pollinator‐excluded environments for the endangered species Synaphea stenoloba (Proteaceae)

The critically endangered Synaphea stenoloba (Proteaceae) has numerous scentless flowers clustered in dense inflorescences and deploys a ballistic pollen ejection mechanism to release pollen. We examined the hypothesis that active pollen ejection and flowering patterns within an inflorescence influence the reproductive success (i.e. fruit formation) of individual flowers within or among inflorescences of S. stenoloba in a pollinator‐excluded environment. Our results showed that: (1) no pollen grains were observed deposited on the stigma of their own flower after the pollen ejection system was manually activated, indicating self‐pollination within an individual flower is improbable in S. stenoloba; (2) fruit set in the indoor open pollination treatment and the inflorescence‐closed pollination treatment indicated that S. stenoloba is self‐compatible and pollen ejection can potentially result in inter‐floral pollination success; (3) fruit set in the inflorescence‐closed pollination treatment was significantly lower than that of indoor open pollination, indicating within‐ and between‐flower pollination events in an inflorescence are most likely limited, with pollination between inflorescences providing the highest reproductive opportunity; and (4) analysis of the spatial distribution of cumulative fruit set on inflorescences showed that pollen could reach any flower within an inflorescence and there was no functional limitation on seed set among flowers located at various positions within the inflorescence. These data suggest that the pollen ejection mechanism in S. stenoloba can enhance inter‐plant pollination in pollinator‐excluded environments and may suggest adaptation to pollinator scarcity attributable to habitat disturbance or competition for pollinators in a diverse flora. © 2012 The Linnean Society of London, Botanical Journal of the Linnean Society, 2012, 170 , 59–68.