An Analysis of the Influence of Plant Density on the Growth of Vicia faba: I. THE INFLUENCE OF DENSITY ON THE PATTERN OF DEVELOPMENT

The competitive effects of varying the density on the developmentof Vicia faba have been studied in a series of multifactorialexperiments where the spacing both between and within rows wassimultaneously altered. Over densities ranging from 11 to 67plants per metre² seed production on an area basis tended tobe maximal at 35–45 plants per metre² in the winter typeand at the highest density for the spring type. As the densityincreased the number of pods per plant and the extent of branchingfell progressively but there was no appreciable change in eitherseed size or the number of seeds per pod: thus seed productionwas solely governed by the number of mature pods formed. Thenumber of flowers per plant was more dependent on the numberof inflorescences than on the number of flowers per inflorescence.Increasing the population diminished the number of nodes bearinginflorescences particularly in the upper part of the shoot,while the size of the inflorescence was decreased to a lesserextent. The number of flowers forming mature pods was very small(9–14 per cent.). At the top of the shoot the flowerswere infertile, while above the middle node most of the podsformed were shed while still immature. Thus the primary effectof increasing density was to depress the number of nodes onthe lower half of the stems which produced mature pods. By thetime the flowering stage was reached plant height was alreadycorrelated with density due more to a change in internode lengththan an alteration in the number of differentiated nodes; atmaturity the differences in height were smaller due to the greaternumber of nodes in the widely spaced plants. For a given density,alterations in the distance between rows had little influenceon development. The possible physiological factors responsiblefor the changing pattern of development brought about by varyingdensity are discussed.     

Ovule Fertilization and Seed Number per Pod Determination in Oil Seed Rape (Brassica napus)

Ovule fertilization in relation to seed number determinationin spring rapeseed, Brassica napus var. Maris Haplana, was investigated.Failure of fertilization was found to be the major factor limitingthe number of seeds per pod in both the basally and apicallylocated pods on the terminal inflorescence. Sufficient pollengermination on a stigma did not guarantee full seed set andeven when pollen tubes were present at the micropyle regions,ovules were not penetrated. Some seeds aborted: in some, triplefusion did not take place while other seeds were small and deemedat disadvantage to compete for available nutrients. Brassica napus, fertilization, ovules, seeds     

DEMOGRAPHIC ASPECTS OF FLOWER AND FRUIT PRODUCTION IN BEAN PLANTS,PHASEOLUS VULGARIS L.

In this paper we assess the relative contributions to total pod yield of cohorts of flowers of known age. Bean plant (Phaseolus vulgaris L.) growth was monitored and 'births' of individual flowers were recorded and their fates followed. For every cohort of flowers an array of yield measures was calculated, including the mean and total cohort dry weight of fruits, and the numbers of viable and aborted seeds and completely undeveloped ovules. When mature, pods were removed from half of the plants. Plants whose mature pods were removed produced significantly greater numbers of flowers, ovules and viable seeds and a greater total weight of pods than did untreated plants. However, the proportion of ovules giving rise to viable seeds and to aborted seeds and undeveloped ovules was the same in plants of both groups. Approximately 50% of ovules of marketable pods, in all plants, yielded viable seeds. The 12 cohorts of flowers contributed markedly different amounts to plant yield. Early and later cohorts contributed much less than did middle cohorts in terms of marketable pod dry weight and numbers of fully developed seeds, aborted seeds, and undeveloped ovules. Peak productivity was therefore obtained from the middle phase of flowering in these annual bean plants. The lower pod yield of later cohorts is interpreted as a result of competition for limited resources between maturing pods and new flowers. We consider possible causes for the various fates of flowers and ovules and discuss flowers as plant modules suitable for demographic examination.     

Comparisons of Earlier- and Later-formed Pods of Chickpeas (Cicer arietinum L.)

In chickpeas (Cicer arietinum L.) flowering and pod developmentproceed acropetally. In plants grown under normal field conditionsat Hyderabad, in peninsular India, and at Hissar in north India,at successively apical nodes of the branches there was a declinein pod number per node, weight per pod, seed number per podand/or weight per seed. The percentage of nitrogen in the seedswas the same in earlier and later-formed pods at Hyderabad;at Hissar the later-formed seeds contained a higher percentage.Earlier- and later-formed flowers contained similar numbersof ovules. The decline in seed number and/or weight per seedin the later-formed pods of 28 out of 29 cultivars indicatedthat pod-filling was limited by the supply of assimilates orother nutrients. By contrast, in one exceptionally small-seededcultivar there was no decline in the number or weight of seedsin later-formed pods, indicating that yield was limited by ‘sink’size. Cicer arietinum L., chickpea, flowering, pod development, seed number, seed weight, nitrogen content     

Gender variation in Actinidia deliciosa,the kiwifruit

Summary Flower and fruit characters were measured in ten female, five male and five fruiting male selections of A. deliciosa var deliciosa (A. Chev) Liang and Ferguson. Flowers from female vines had functional pistils, which contained many ovules. Stamens appeared to be fully developed but produced only empty pollen grains. Flowers from male vines had functional stamens that produced high percentages of pollen grains with stainable cytoplasmic contents. Pistils did not contain ovules and were generally small with vestigial styles. Fruiting male vines had both staminate and bisexual flowers. Staminate flowers were similar to those found on strictly male vines. Bisexual flowers produced ovules and stainable pollen. Pistils were smaller than in pistillate flowers. Although the three flower sexes differed in style length, ovary dimensions and ovules per carpel, staminate and bisexual flowers were similar in number of flowers per inflorescence, stamen filament length, pollen stainability, inflorescence rachis length and carpel number, and differed from pistillate flowers in these characters. The three flower sexes had similar sepal and petal numbers. The fruit of fruiting males were considerably smaller than those of females. Low ovule number appears to be the major factor limiting fruit size in the fruiting males studied. Prospects for developing hermaphroditic kiwifruit cultivars through breeding are discussed.     

Patterns of fruit and seed production inBauhinia ungulata (Leguminosae)

Patterns of seed and fruit production ofBauhinia ungulata, a small tree legume indigenous in tropical America, were studied in Costa Rica. Only about 8% of flowers produced fruits. The average pod had 19 ovules and about two thirds of these began seed development, with mature pods containing an average of 9.7 mature undamaged seeds. About half of the mature pods were damaged by herbivores and within these, 27% of ovules or seeds had been eaten. Among trees there was no significant variation in pod production, but the number of ovules per pod and seed production per pod varied significantly. Within infructescences most pods were retained at middle positions. Within pods, the probability of an ovule developing into a seed increased toward the distal end. The pattern of seed and fruit production in this species agrees well in general with that reported for other neotropical legumes. The abortion of seeds and fruits can be regarded as a way of controlling maternal investment, and as a response to herbivory.     

Plasticity of reproductive components at different stages of development in the annual plant Thlaspi arvense L.

Summary This study examines the effect of different densities and the removal of all neighbours at different stages of development on all components of reproduction in the inbreeding annual Thlaspi arvense L. A 64-fold increase in density significantly reduced all repooductive components. The number of flower buds per plant was decreased most strongly; the order of decreasing plasticity among the other components was number of capsules per flower, individual seed weight, ovule number per capsule, flowers per flower bud and seeds per ovule. Removing neighbours at all stages of development increased seed yield of plants in comparison to the control without density reduction, but patterns of plasticity depended strongly on time of treatment. The main effect of the removal of neighbours at the vegetative stage was to increase the number of flowers per plant, but the number of ovules per capsule and seed weight increased also, and abortion of capsules decreased. Removing neighbours at the onset of flowering initially failed to affect flower number per plant, instead it resulted in a strong reduction of capsule abortion and an increase in seed weight. However, several weeks after flowering had initially ceased, fresh lateral inflorescences were produced, resulting in a second flush of reproduction. Removing neighbours at the stage of fruit ripening resulted at first only in an increase in seed witht, but later a second reproductive phase occurred. Fresh lateral branches were produced, but the apical meristem was also reactivated. The overall pattern of plasticity among all reproductive components in response to a removal of neighbours was the same as in response to density. The position of a capsule along the inflorescence influenced its number of ovules, the rate of seed abortion and the mean weight of seeds, with the type of effect depending on the developmental stage at which neighbours were removed. Significant negative correlations were found between the mean weight of seeds and the number of seeds in a capsule under all treatments.     

Application of a probabilistic model for analysing the abortion of seeds and pods in winter oilseed rape (Brassica napus)

In winter oilseed rape (WOSR), only a subset of ovules can develop into seeds in the majority of pods. Any difficulty during the process of seed production may result in seed or pod abortion. This study aimed to reproduce the process of seed development in WOSR based on a limited number of parameters. As a result of the complexity of the developmental patterns of WOSR, it is challenging to identify the roles of various factors that influence seed production using an experimental approach. Here, we present a stochastic probabilistic model of seed development. The generalised least squares method was implemented to estimate the model parameters using the experimental data. Experiments were done in Grignon (France) in 2008 and 2009. The variations in the parameters were analysed according to the following four factors: year, pod rank, inflorescence position and ramification‐clipping treatment. The year had no effect on the number of ovules per ovary (μ) and the probability of seed viability (p). The proportion of effective pollen grains (k) significantly decreased with pod rank at the end of the main stem. Inflorescence position influenced the number of ovules per ovary (μ: 30.8–33.8 from top to bottom) and the parameter k. The mean number of seeds per pod on the main stem and the bottom ramification along the stem was larger than the other ramifications within one plant. Ramification‐clipping treatment increased the number of ovules per ovary (μ: 31 for control plants and 32 for clipped plants), the parameter k and the number of seeds per pod (p). This effect could be due to the competition for assimilates between the pods and seeds. Furthermore, the distribution parameters of the pollen number per stigma (m) remained stable, and the probability of pod survival (Bo) varied with different factors, including the year, pod rank and inflorescence position. Our results indicate that pollen germination is a factor that determines final seed number. This model can identify the impact of each of the factors that lead to the abortion of seeds and pods in WOSR, which include the position effect, assimilate competition and pollination limitation. However, further studies on the pollination process in WOSR should help to refine this model.     

Evolution of floral display in Eichhornia paniculata (Pontederiaceae): genetic correlations between flower size and number

The evolution of floral display is thought to be constrained by trade‐offs between the size and number of flowers and inflorescences. We grew in the glasshouse 60 maternal families from each of two Brazilian populations of the annual herb, Eichhornia paniculata. We measured flower size, daily flower number, and total flower number per inflorescence, and two indices of module size, leaf area and age at flowering. We also assessed the size and number of inflorescences produced over 6 weeks. All floral traits exhibited significant heritable variation, some of which was due to genetic variation in module size. Genetic (maternal family) correlations between daily and total flower number did not differ from 1.0, indicating that display size (daily flower number) cannot evolve independently from total flower number per inflorescence. Genetic correlations between flower size and daily flower number ranged from negative to positive (r=–0.78 to +0.84), depending on population and inflorescence. Positive correlations occurred when variation in investment per inflorescence was high so that some families produced both larger and more flowers. These correlations became zero when we controlled for variation in module size. Families that flowered later produced fewer, larger inflorescences (r=–0.33, –0.85). These data support theoretical predictions regarding the combined effects of variation in resource acquisition and allocation on traits involved in trade‐offs, and they emphasize the hierarchical organization of floral displays. Our results imply that patterns of resource allocation among inflorescences influence evolutionary changes in flower size and number per inflorescence.     

ECOLOGICAL ASPECTS OF SEX EXPRESSION IN SUBDIOECIOUS SCHIEDEA GLOBOSA (CARYOPHYLLACEAE)

The importance of ecological factors such as sex lability, spatial segregation, and resource allocation in the evolution of dioecy were examined in Schiedea globosa. S. globosa is a subdioecious species with equal numbers of plants possessing strictly male or female function and a small proportion of hermaphrodites. The propensity for labile sex expression was under both environmental and genetic control; some plants with male function became hermaphroditic (by producing female flowers) under better growing conditions in the field and in the greenhouse. There was some spatial segregation of the sexes. Because of sex lability, more hermaphrodites than males occurred on moister slopes. Although there were not measurable sex-related differences in mortality within or between two flowering seasons, more females than males and hermaphrodites occurred at the bottom of slopes. Males and females produced the same number of ramets and inflorescences, but females had a greater number of flowers per inflorescence. Males and females had the same number of ovules (vestigial in males), but females had larger ovules and longer stigmas. Hermaphrodites and males had the same amount of pollen per flower despite the production of fruit by the hermaphrodites. In hermaphrodites, there was no apparent tradeoff within flowers between pollen production and ovule production. These results indicate that spatial segregation, sex lability, and environmental conditions influence allocation patterns of S. globosa, and in combination with high inbreeding depression and selling rates, may promote the further evolution of dioecy in S. globosa.     

COMPARATIVE REPRODUCTIVE BIOLOGY OF HERMAPHRODITIC AND MALE-STERILE IRIS DOUGLASIANA HERB. (IRIDACEAE)

A comparative study of the reproductive biology of male-sterile and hermaphroditic plants in a gynodioecious population of Iris douglasiana Herb. (Iridaceae) was conducted at the University of California's Marine Laboratory at Bodega Bay, California, between 1976–1979. Each year of the study, there were 11.1% male-sterile plants in the population, some of which began blooming at the same time as the earliest blooming hermaphrodites. Male-sterile flowers made up between 7–21% of the flowers produced during the male-sterile flowering period. Male-sterile flowers had smaller sepals and petals than hermaphrodites, there were fewer of them per square meter, and they had fewer pollinated stigmas than did hermaphroditic flowers. In a test to determine pollinator preference, intact hermaphroditic flowers tended to have more pollinated stigmas than did hermaphrodites with their stamens removed or those flowers with shortened sepals made to resemble the smaller male-sterile flowers. Floral phenology and nectar-flow patterns were similar in both types of flowers as were the kinds of amino acids and sugar rewards in the nectar. Male-sterile flowers, however, produced much less nectar per flower. There were no significant differences in the number of ovules per flower or the number of seeds produced per capsule between the two flower types, but the loss of seeds through larval predation was much greater in capsules from hermaphroditic flowers. Early flowering and setting of seed by plants with male-sterile flowers could give them a reproductive advantage over plants with hermaphroditic flowers which experience higher levels of larval predation later in the growing season.     

The evolution of ovule number and flower size in wind-pollinated plants

In angiosperms, ovules are "packaged" within individual flowers, and an optimal strategy should occur depending on pollination and resource conditions. In animal-pollinated species, wide variation in ovule number per flower occurs, and this contrasts with wind-pollinated plants, where most species possess uniovulate flowers. This pattern is usually explained as an adaptive response to low pollen receipt in wind-pollinated species. Here, we develop a phenotypic model for the evolution of ovule number per flower that incorporates the aerodynamics of pollen capture and a fixed resource pool for provisioning of flowers, ovules, and seeds. Our results challenge the prevailing explanation for the association between uniovulate flowers and wind pollination. We demonstrate that when flowers are small and inexpensive, as they are in wind-pollinated species, ovule number should be minimized and lower than the average number of pollen tubes per style, even under stochastic pollination and fertilization regimes. The model predicts that plants benefit from producing many small inexpensive flowers, even though some flowers capture too few pollen grains to fertilize their ovules. Wind-pollinated plants with numerous flowers distributed throughout the inflorescence, each with a single ovule or a few ovules, sample more of the airstream, and this should maximize pollen capture and seed production.     

Intra-inflorescence variation in floral traits and reproductive success of the hermaphrodite Silene acutifolia

BACKGROUND AND AIMS: Intraspecific variation in floral components and reproductive success is often located at the intra-individual level. The arrangement of flowers within inflorescences may explain a great deal of this variation. The variation in number of ovules, fruit set, number of seeds per fruit, seed set, seed weight and seed germination is investigated at different positions within the inflorescence of Silene acutifolia. METHODS: Data were obtained in natural populations, and germination experiments were conducted in a germination chamber. KEY RESULTS: The number of ovules, fruit set, number of seeds, seed set and seed weight, showed a significant decline from early (primary) position to later (tertiary) position. The patterns of intra-inflorescence variation were consistent in different populations and years of study. Seed germination showed an opposite pattern, seeds from primary position showed the lowest germination percentages and seeds from tertiary position the highest, although the effect of position on germination was only marginally significant. There was significant among-population variation in number of ovules per flower. Fruit set also varied significantly among populations, with lower fruit set in the smaller and more isolated population. No significant among-population differences were detected in number of seeds per fruit and seed set. Seeds from the smallest and more isolated population (Arnado) were the lightest. Seed germination showed strong differences between populations, seeds from Arnado started to germinate later, and showed the lowest final germination percentages. CONCLUSIONS: Architectural effects or resource competition are the most commonly proposed hypothesis to explain these patterns. Data suggest that there is less pollen available to pollinate tertiary flowers, and that there is not enough outcross pollen in Arnado. The germination percentages suggest that there is variation in the source of pollen within inflorescences, with high probability of receiving outcross pollen in flowers from primary position, and higher probability of geitonogamous crosses in tertiary flowers.     

PATTERNS OF PRE- AND POSTFERTILIZATION RESOURCE ALLOCATION WITHIN AN INFLORESCENCE: EVIDENCE FOR INTEROVARY COMPETITION

I investigated the distribution of ovules and seeds on the inflorescence of Solanum Carolinense L. (Solanaceae). Ovules did not appear to vary in size, but the number of ovules per ovary and the size of ovaries decreased significantly along the inflorescence (from basal to distal positions). Experimental removal of basal ovaries at an early stage resulted in increased ovary size and number of ovules in distal ovaries, suggesting a dynamic system of control. Mature fruits displayed a similar pattern of decreasing mass and seed number with position along the infructescence. It is not clear whether the patterns of allocation to fruits are related to the patterns of allocation to ovaries in a simple cause-and-effect relationship. However, a satisfying hypothesis that explains these and other patterns of allocation is that they are all manifestations of, or adaptations to, interovary competition along the inflorescence.     

INTRASEASONAL VARIATION IN SEED PRODUCTION AMONG FLOWERS AND PLANTS OF THALICTRUM THALICTROIDES (RANUNCULACEAE)

Intraseasonal variation in ovule and seed production per flower and per plant of the perennial herb Thalictrum thalictroides (L.) Eames and Boivin was documented at three sites during three spring flowering seasons. Shading and pollen-addition experiments were used to assess the impact of variation in pollination and light availability on seed production. Mean seed number and percent seed set were lower in flowers open late in the season than in those open earlier. The lower percent seed set occurs primarily in flowers that are positioned laterally on the inflorescence and which open later than center flowers. Plants flowering early in the season produce more flowers, ovules and seeds than those flowering later. Mean percent seed set per plant did not change, however, indicating that temporal differences in total seed output can be traced largely to variation in total ovule number. Seed production may be limited by lack of pollination during periods of inclement weather. At least late in the season, seed output may also be resource-limited: the decline in percent seed set among flowers coincided with the decline in light availability, and hand-pollination of late-opening flowers did not increase percent seed set to earlier levels. Artificial shading led to a significant reduction in percent seed set of lateral flowers, and decreased the probability of flowering again the following year. Thus, the relative selective roles of resource and pollination limitations may vary during the flowering season.     

Differential self‐fertilization rates in response to variation in floral traits within inflorescences of Aquilegia buergeriana var. oxysepala (Ranunculaceae)

To assess variation in the proportion of self‐fertilized seeds among flowers within inflorescences and the relationship between floral traits and the rate of self‐fertilization, the proportion of self‐fertilized seeds among individual flowers was estimated using ten microsatellite markers in self‐compatible plants of Aquilegia buergeriana var. oxysepala. Within‐inflorescence variation in floral traits, such as the duration of the male and female phases, flower size, herkogamy and the number of pollen grains and ovules in two natural populations, were investigated. The first flower in an inflorescence produced more seeds and a higher proportion of self‐fertilized seeds than the second flower. The higher proportion of self‐fertilized seeds in the first flowers was accompanied by a higher number of pollen grains and ovules in the bud stage and the female phase. These results indicate that the high proportion of self‐fertilized seeds in the first flowers in an inflorescence may be due to the high number of remaining pollen grains in the female phase. This suggests that variation in floral traits within inflorescences affects seed quality and quantity among flowers within inflorescences.     

ANDROMONOECY IN ZIGADENUS PANICULATUS (LILIACEAE): SPATIAL AND TEMPORAL PATTERNS OF SEX ALLOCATION

I describe patterns of sex allocation and gamete packaging in the andromonoecious lily Zigadenus paniculatus. In this species, pistil length was continuously, but bimodally, distributed within plants, and smaller pistils contained fewer mature ovules. In hermaphrodite flowers, ovule number per flower increased with blooming rank in small plants but decreased with blooming rank in large plants. Flowers with pistils less than three-fourths stamen length almost never produced fruits and were classified as males. The pedicel, tepals, stamens, and pistil of hermaphrodite flowers were all heavier than those of males. Hermaphrodite flowers were concentrated on the terminal raceme, males on the lower racemes. In combination with acropetal blooming, this spatial separation of flower types resulted in a seasonal decline in the proportion of open flowers that were hermaphrodite. However, individual flowers were protandrous, so that the population sex ratio, initially strongly male-biased, declined as the season progressed. Hand pollinations showed that plants were self-incompatible. Inflorescence size was positively correlated with bulb size, and plants with large inflorescences had a higher proportion of male flowers. Nutrient supplementation had no effect on inflorescence size, but increased the proportion of hermaphrodite flowers. Nutrient-supplemented plants also began blooming earlier than controls. I discuss these patterns in relation to the adaptive significance of andromonoecious breeding systems.     

Factors affecting the Abscission of Reproductive Organs in Yellow Lupms (Lupinus luteus L.): II. THE EFFECTS OF GROWTH SUBSTANCES, DEFOLIATION, AND REMOVAL OF LATERAL GROWTH

Abscission of flowers in Lupinus luteus L. (var. Weiko II) withoutgrowth of ovaries is followed by abscission of small pods (15–20mm. long). Normally flower abscission is much more pronouncedthan pod abscission. Abscission was delayed on plants from which laterals or theirterminal and axifliary buds were removed. Flower abscissionwas not affected, but pod abscission increased as a result ofdefoliation. When flowers at the base of the main inflorescence were replacedby auxins and anti-auxins flower abscission was induced in eitheran auxin pattern in which most of the flowers near the siteof application dropped, and pods developed on the apical whorls,or an anti-auxin pattern in which pods developed on basal whorlsnear the site of application but not higher up. The anti-auxinpattern was similar to the pattern of abscission normally inducedby developing pods on basal whorls. -Naphthylacetic acid (NAA) was much more effective in inducingabscission than ß-indolylacetic acid (IAA). 2:3:5-triiodobenzoicacid (TIBA), NAA, and IAA applied in mixtures at various concentrationsacted mainly antagonistically, i.e. the abscission-inducingeffect of NAA and LAA was depressed in basal whorls, and inapical whorls the effect of TIBA was less prevalent. Consequentlythe effect of the mixtures on the total number of pods was aboutequal to that of the most active component by itself. All growth substances seemed to move much more efficiently inacropetal direction than in basipetal direction in the flowerstalk. Transport in lateral direction was very limited. The effect of growth substances applied on laterals was enhancedby defoliating the main 8tem. The influence of assimilates on flower and pod abscission andtransport of growth substances is discussed.     

Some Effects of Light Intensity, Daylength and Temperature on Flowering and Pollen Tube Growth in the Watermelon (Citrullus lanatus)

The effects of light and temperature on flowering and pollentube growth were studied in watermelon [Citrullus lanatus(Thunb.)Matsum. and Nakai, cv. Early Yates] plants grown in controlledenvironment cabinets. All female flowers were pollinated inone group of plants; none was pollinated in the other group. Temperature increase from 25 ^°C to 35 ^°C with daylengthof 14 h and light intensity of 32 klx caused increase in flowernumber per plant, proportion of male flowers, ovary length anddiameter, ovule number per ovary, rate of pollen tube growthand percentage of penetrated ovules at 24 hand 48 h after pollination.Very few flowers were produced at 40 ^°C, but there was ahigh proportion of male flowers. Increase in daylength from14 h to 24 h at 25 ^°C with light intensity of 32 klx alsoincreased number of flowers per plant, ovary length and diameterand number of ovules per ovary but sex expression and rate ofpollen tube growth were unaffected. Reduction in daylength from14 h to 8 hat 25 °C and light intensity of 32 klx and reductionin light intensity from 32 klx to 8 klx at 25 ^°C and 14h daylength both produced an increase in the percentage of immatureovules. The presence of fruit on the vine resulted in fewerflowers per plant and in reduced ovary legnth and diameter underall conditions tested. The results are discussed in relation to the fruiting responseof the plant.     

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.