Floral morphogenesis in Sinofranchetia (Lardizabalaceae) and its systematic significance

The floral organs of Sinofranchetia chinensis Hemsl. (Lardizabalaceae) are all spiral in initiation. Stamen and petal (nectar‐leaf) primordia initiate independently and are different in shape. The petals and three stamens in the first whorl are retarded in the early developmental stages. The carpel primordia are conduplicate; the stigma is formed around the upper part of the ventral slit and the style is not differentiated. The functionally unisexual flowers are bisexual in organization in the early developmental stages. The development of the flowers on the inflorescence is spiral and centripetal. Some floral characteristics of Sinofranchetia appear to be plesiomorphic in Lardizabalaceae. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 160 , 82–92.     

Pollen-ovule ratios in some Neotropical Araceae and their putative significance

The correlation between pollen-ovule (P/O) ratio and breeding system has generally been analysed with respect either to pollination efficiency, or in terms of sex allocation theory. Pollen/ovule ratios were measured in nine species of Araceae belonging to two genera with bisexual flowers (Anaphyllopsis, Monstera) and three genera with unisexual flowers (Dieffenbachia, Philodendron, Montrichardia). The family Araceae with its unique inflorescence morphology allows the analysis of variations of the P/O ratio with respect to two basal morpho-functional pollination units: the flower or the inflorescence. We found a relationship between the value of the P/O ratio and the breeding system that is partially different from Cruden's results (1977). Some facultative xenogamous species have a higher P/O than the obligatory xenogamous species. A link was found between the P/O and the type of inflorescence, the floral cycle, and the mode of growth.     

濒危植物庙台槭生殖生物学研究1.花序和花的形态及发育

庙台械的花序为有限花序,由一顶花和6—9枝侧花枝组成,属圆锥状聚伞花序。一个花序共有14—29朵花,包括两性花、雄花和无性花三类花。根据花在花序上着生的位置,可分为三级。7月初,花序原基形成,在花序轴伸长的同时,侧面形成侧花枝轴原基。花序的顶花最早进行个体发育,随后是侧花枝顶花;侧花枝上同一级花的发育顺序则是从花序的下面向上进行。花器官发生时,花萼原基最先形成,然后是花瓣、雄蕊、心皮和胚珠。     

HELICAL FLORAL ORGANOGENESIS IN GLEDITSIA,A PRIMITIVE CAESALPINIOID LEGUME

In order to determine the extent of floral ontogenetic differences among species of a genus, six species of Gleditsia were studied. Gledilsia is one of only two leguminous genera known in which there is completely helical succession of floral organs. Floral ontogeny was compared in three species (Gleditsia amorphoides, G. aquatica, and G. triacanthos), and late stages in six species (including the first three plus G. caspica, G. delavayi, and G. japonica). Other unusual primitive developmental features include the unequal-sized flower primordia which produce flowers of variable merosity. Order of floral development is also loosely controlled, so that flowers of different growth stages are intermixed in the inflorescence. Variable features include the occurrence of floral bracts, merosity of flowers, number of organs, and position of the first organ (sepal) initiated. The inflorescence type, while usually a raceme, often has lateral branches near the base, or fascicles of flowers at some points. A terminal flower often is present, although not in all species. Sex of flowers and inflorescences also varies, although floral initiation tends to include both stamens and carpel primordia. Suppression of one or the other may occur at different stages of development. Carpel orientation also varies; the cleft may be tilted or inverted occasionally. It is proposed that absence of subtending floral bracts influences development so as to favor radial symmetry and establishment of other “chaotic” characters seen in Gledilsia flowers.     

Study of homeosis in the flower of Philodendron (araceae): a qualitative and quantitative approach

This study deals specifically with floral organogenesis and the development of the inflorescence of Philodendron squamiferum and P. pedatum. Pistillate flowers are initiated on the lower portion of the inflorescence and staminate flowers are initiated on the distal portion. An intermediate zone consisting of sterile male flowers and atypical bisexual flowers with fused or free carpels and staminodes is also present. This zone is located between the sterile male and female floral zones. In general, the portion of bisexual flowers facing the male zone forms staminodes, and the portion facing the female zone develops an incomplete gynoecium with few carpels. The incomplete separation of some staminodes from the gynoecial portion of the whorl shows that they belong to the same whorl as the carpels. There are two levels of aberrant floral structures in Philodendron: The first one is represented by the presence of atypical bisexual flowers, which are intermediates between typical female flowers and typical sterile male flowers. The second one is the presence of intermediate structures between typical carpels and typical staminodes on a single atypical bisexual flower. The atypical bisexual flowers of P. squamiferum and P. pedatum are believed to be a case of homeosis where carpels have been replaced by sterile stamens on the same whorl. A quantitative analysis indicates that in both species, on average, one staminode replaces one carpel.     

THE DEVELOPMENTAL BASIS FOR SEXUAL EXPRESSION IN CERATONIA SILIQUA (LEGUMINOSAE: CAESALPINIOIDEAE: CASSIEAE)

The flowers of Ceratonia siliqua, an anomalous caesalpinioid legume in the tribe Cassieae, are unusual in being unisexual and in lacking petals. Inflorescence development, organogeny, and flower development are described for this species. All flowers are originally bisexual, but one sex is suppressed during late development of functionally male and female flowers. Ceratonia siliqua is highly plastic in sexuality of individuals, inflorescence branching pattern, racemose or cymose inflorescences, bracteole presence, terminal flower presence, organ number per whorl, missing floral organs, pollen grain form, and carpel cleft orientation. Order of initiation is: five sepals in helical order, then five stamens in helical order together with the carpel. Each stamen is initiated as two alternisepalous primordia that fuse to become a continuous antesepalous ridge; in some flowers, the last one or two stamens of the five may form as individual antesepalous mounds. Petal rudiments are occasional in mature flowers. Position of organs is atypical: the median sepal is on the adaxial side in Ceratonia, rather than abaxial as in most other caesalpinioids. This feature in Ceratonia may be viewed as a link to subfamily Mimosoideae, in which this character state is constant.     

Sex expression in fruiting male vines of kiwifruit

Summary In three canes on each of five fruiting male kiwifruit vines (A. deliciosa var. deliciosa (A. Chev) Liang and Ferguson), staminate and bisexual flowers were interspersed, so that staminate, bisexual and mixed inflorescences were found. Further variation in inflorescence composition resulted from the abortion of flower buds prior to anthesis. These two sources of variation, in combination, resulted in 19 inflorescence patterns, which varied substantially in frequency among and within vines. Some tendencies were determined. In particular, most of the inflorescences had retained their terminal flower, whereas just over half had retained one or both primary lateral flowers, and in two-thirds of the inflorescences retaining a terminal flower, this was bisexual. The five vines ranged in bisexual flower frequency from 40% to 70%. Phenotypic Gender (P) estimates are given for each vine, based on the frequencies of staminate and bisexual flowers from three canes per vine. Flower development, lability in sex expression and the use of P estimates as part of a selection index in breeding for hermaphrodite kiwifruit cultivars are discussed.     

Homeosis, morphogenetic gradient and the determination of floral identity in the inflorescences ofPhilodendron solimoesense (Araceae)

A comparative developmental study of the inflorescence ofPhilodendron solimoesense was conducted using scanning electron microscopy. The spadix ofP. solimoesense is characterized by unisexual flowers. Staminate flowers are initiated on the upper portion of the spadix while pistillate flowers develop on the lower portion of the spadix. An intermediate zone located between the upper male and lower female portion of the inflorescence consists of sterile male flowers. Within this intermediate zone a row of flowers exhibit polarity with respect to the identity of sexual organs. Stamens are initiated on the flank of the floral meristem facing the upper male zone and carpels are initiated on the portion of the floral meristem facing the lower female zone. The resulting flowers therefore assume a bisexual identity. At the level of the inflorescence, all floral buds are initiated along a series of contact parastichies and the continuity of these parastichies is not disrupted at any level in the male, intermediate, and female zones on the spadix. Results from this study support the presence of a morphogenetic gradient acting at the level of the inflorescence and appears to be independent of the boundaries of floral primordia.     

Benzyladenine Treatment Significantly Increases the Seed Yield of the Biofuel Plant Jatropha curcas

Jatropha curcas, a monoecious perennial biofuel shrub belonging to the family Euphorbiaceae, has few female flowers, which is one of the most important reasons for its poor seed yield. This study was undertaken to determine the effects of the plant growth regulator 6-benzyladenine (BA) on floral development and floral sex determination of J. curcas. Exogenous application of BA significantly increased the total number of flowers per inflorescence, reaching a 3.6-fold increase (from 215 to 784) at 160 mg/l of BA. Furthermore, BA treatments induced bisexual flowers, which were not found in control inflorescences, and a substantial increase in the female-to-male flower ratio. Consequently, a 4.5-fold increase in fruit number and a 3.3-fold increase in final seed yield were observed in inflorescences treated with 160 mg/L of BA, which resulted from the greater number of female flowers and the newly induced bisexual flowers in BA-treated inflorescences. This study indicates that the seed yield of J. curcas can be increased by manipulation of floral development and floral sex expression.     

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

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

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.     

Characterization of unisexual flower development in the endangered mahogany tree Swietenia macrophylla King. (Meliaceae)

The selection of candidate plus trees of desirable phenotypes from tropical forest trees and the rapid devastation of the natural environments in which these trees are found have created the need for a more detailed knowledge of the floral and reproductive biology of tropical tree species. In this article, the organogenic processes related to unisexual flower development in tropical mahogany, Swietenia macrophylla , are described. Mahogany inflorescences at different developmental stages were evaluated using scanning electron microscopy or optical microscopy of histological sections. The unisexual flowers of S. macrophylla are usually formed in a thyrse, in which the positions of the female and male flowers are not random. Differences between male and female flowers arise late during development. Both female and male flowers can only be structurally distinguished after stage 9, where ovule primordia development is arrested in male flowers and microspore development is aborted in female flower anthers. After this stage, male and female flowers can be distinguished by the naked eye as a result of differences in the dimensions of the gynoecium. The floral characteristics of S. macrophylla (distribution of male and female flowers within the inflorescence, and the relative number of male to female flowers) have practical implications for conservation strategies of this endangered species.  © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society , 2008, 156 , 529–535.     

Floral and inflorescence morphology and ontogeny in Beta vulgaris, with special emphasis on the ovary position

Background and Aims

In spite of recent phylogenetic analyses for the Chenopodiaceae–Amaranthaceae complex, some morphological characters are not unambiguously interpreted, which raises homology questions. Therefore, ontogenetic investigations, emphasizing on ‘bracteoles’ in Atripliceae and flowers in Chenopodioideae, were conducted. This first paper presents original ontogenetic observations in Beta vulgaris, which was chosen as a reference species for further comparative investigation because of its unclarified phylogenetic position and its flowers with a (semi-)inferior ovary, whereas all other Chenopodiaceae–Amaranthaceae have hypogynous flowers.

Methods

Inflorescences and flowers were examined using scanning electron microscopy and light microscopy.

Key Results

Floral development starts from an inflorescence unit primordium subtended by a lateral bract. This primordium develops into a determinate axis on which two opposite lateral flowers originate, each subtended by a bracteole. On a flower primordium, first five tepal primordia appear, followed by five opposite stamen primordia. Simultaneously, a convex floral apex appears, which differentiates into an annular ovary primordium with three stigma primordia, surrounding a central, single ovule. A floral tube, which raises the outer floral whorls, envelops the ovary, resulting in a semi-inferior ovary at mature stage. Similarly, a stamen tube is formed, raising the insertion points of the stamens, and forming a staminal ring, which does not contain stomata. During floral development, the calyces of the terminal flower and of one of the lateral flowers often fuse, forming a compound fruit structure.

Conclusions

In Beta vulgaris, the inflorescence is compound, consisting of an indeterminate main axis with many elementary dichasia as inflorescence units, of which the terminal flower and one lateral flower fuse at a later stage. Floral parts develop starting from the outer whorl towards the gynoecium. Because of the formation of an epigynous hypanthium, the ovary becomes semi-inferior in the course of floral development.Key words: Beta vulgaris, Chenopodiaceae, floral ontogeny, gynoecial development, epigynous hypanthium, semi-inferior ovary, inflorescence ontogeny, LM, SEM     

The effect of flower position on male and female reproductive success in a deceptively pollinated tropical orchid

In many plants, including orchids, differential fruit set along the inflorescence has been attributed to pollinator behaviour. For instance, the pollinator, moving up the inflorescence, becomes satiated with the resources and leaves before visiting the upper flowers. Consequently, the pollinators do not visit flowers as frequently higher up the inflorescence. Alternatively, flower size may vary along the inflorescence, making pollination ineffective as flowers decrease in size. I tested for the presence of differential pollination along the inflorescence in a pollinator-limited tropical epiphyte, Lepanthes rupestris Stimson, and determined the likely cause of the observed pattern. As this species has inflorescences with sequential flowering, pollinator behaviour, moving up the inflorescence as in synchronous multiflowering inflorescences, can be discounted as an explanation for differential fruit set. Fruit set is shown to be more frequent at the base of the inflorescence, but male reproductive success through pollinarium removal is basically independent of flower position. Moreover, cross-pollination by hand at variable flower positions along the inflorescence results in equal fruit set, suggesting that resources are not limiting and cannot explain the cause of differential fruit production along the inflorescence in natural populations. Furthermore, flower size is shown to diminish along the inflorescence, suggesting that the pollinator(s) may be ineffective at depositing the pollinarium in the smaller higher flowers. Consequently, pollinator behaviour and its interaction with flower size, and not resource limitation, is likely to be the main cause of differential fruit set along the inflorescence in L. rupestris .  © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 151 , 405–410.     

Fruit production and floral traits: correlated evolution in <Emphasis Type="Italic">Govenia</Emphasis> (Orchidaceae)

The most common estimate of reproductive success in orchids is usually fruit set. Factors such as resource limitation and certain floral traits may influence reproductive success in animal-pollinated plants. Correlated evolution of reproductive success vs. seven floral traits (inflorescence length, flower number, flower distribution along inflorescence, dorsal sepal length, lateral sepal length, flower color, and column position) was studied in eight species of Govenia. Taxa represented three lineages in the genus. Independent contrasts were calculated on a phylogeny inferred from chloroplast (trnL-F IGS) DNA sequences, and a correlation test and multiple regression were then performed. Two data sets were evaluated, one including all eight species and another excluding G. utriculata, which is autogamous. The historical analyses showed that there is a correlation between reproductive success and dorsal sepal length, column position, and flower number, these correlations suggest that changes in these floral traits usually accompany evolutionary shifts in reproductive success. Multiple regression tests suggest that changes in reproductive success can be explained by shifts in flower number, inflorescence length, column position and by dorsal sepal length. When phylogeny is taken into account, our analyses showed that evolutionary shifts in these floral traits were correlated with changes in reproductive success. Evolutionary correlation between reproductive success and floral traits might be explained by the natural selection of certain floral phenotypes by pollinators.     

地质时期樟科植物花化石及其系统演化意义

该研究对地质时期樟科植物花化石的主要类群,即Androglandula、Lauranthus、Mauldinia、Neusenia、Perseanthus和Potomacanthus属分别从属和种的形态特征、分布、地层以及系统意义进行了论述,并结合现代樟科植物从地层和分布、花序类型、花部形态特征和显微构造特征进行了分析。结果表明:(1)樟科植物在中晚白垩纪期,已经起源于劳亚古陆的中纬度区域。(2)樟科植物的花序类型为Mauldinia属的侧生花序类型和假伞形花序类型。(3)花为3基数的两性花,花被片6枚排列为2轮,雄蕊12或6,排列为4、3或2轮,最内轮雄蕊不育,第三轮雄蕊基部常见一对附属腺体,雄蕊药室瓣裂,4或2药室,雌蕊为单心皮。(4)花被片上常有大量的油细胞、并列型气孔器和单细胞毛。该研究结果中樟科花化石的发现,为樟科植物的系统演化提供了古生物学的证据和资料。     

Early inflorescence and floral development in Cocos nucifera L. (Arecaceae: Arecoideae)

Palms are generally characterized by a large structure with a massive crown that creates difficulties in anatomical studies. The flowering behaviour of palm species may be a useful indicator of phylogenetic relationships and therefore evolutionary events. This paper presents a detailed histological study of reproductive development in coconut (Cocos nucifera L.), from initiation up to maturation of staminate and pistillate flowers. Reproductive development in coconut consists of a sequence of individual events that span more than two years. Floral morphogenesis is the longest event, taking about one year, while sex determination is a rapid process that occurs within one month. The inflorescence consists of different ultimate floral structural components. Pistillate flowers are borne in floral triads that are flanked by two functional staminate flowers. The staminate flowers are born in floral diads towards the base of the rachilla followed by solitary flowers in the middle to top of the rachilla. Three primary phases were identified in reproductive development, namely, transition of axillary bud into inflorescence bud, formation of floral buds, and sexualisation of individual flower buds. All developmental events with respect to stage or time of occurrence were determined.     

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.     

INFLORESCENCE AND FLORAL DEVELOPMENT IN HOUTTUYNIA CORDATA (SAURURACEAE)

The inflorescence of Houttuynia cordata produces 45–70 sessile bracteate flowers in acropetal succession. The inflorescence apical meristem has a mantle-core configuration and produces “common” or uncommitted primordia, each of which bifurcates to form a floral apex above, a bract primordium below. This pattern of organogenesis is similar to that in another saururaceous plant, Saururus cernuus. Exceptions to this unusual development, however, occur in H. cordata at the beginning of inflorescence activity when four to eight petaloid bract primordia are initiated before the initiation of floral apices in their axils. “Common” primordia also are lacking toward the cessation of inflorescence apical activity in H. cordata when primordia become bracts which may precede the initiation of an axillary floral apex. Many of these last-formed bracts are sterile. The inflorescence terminates with maturation of the meristem as an apical residuum. No terminal flowers or terminal gynoecia were found, although subterminal gynoecia or flowers in subterminal position may overtop the actual apex and obscure it. Individual flowers have a tricarpellate syncarpous gynoecium and three stamens adnate to the carpels; petals and sepals are lacking. The order of succession of organs is: two lateral stamens, median stamen, two lateral carpels, median carpel. The three carpel primordia almost immediately are elevated as part of a gynoecial ring by zonal growth of the receptacle below the attachment of the carpels. The same growth elevates the stamen bases so that they appear adnate to the carpels. The trimerous condition in Houttuynia is the result of paired or solitary initiations rather than trimerous whorls. Symmetry is bilateral and zygomorphic rather than radial. No evidence of spiral arrangement in the flower was found.     

Large flowers tend to be short-lived in Mediterranean ecosystems: Insights from three Cistus species

Larger and longer lived flowers receive more pollinators, but may also involve increased water maintenance costs under hot, dry environments. Hence, smaller and/or short-lived flowers may buffer such costs. We surveyed floral longevity in three large-flowered Mediterranean Cistus species. We hypothesize that: (1) in Cistus, floral longevity decreases with increasing air temperature and flower size; (2) in C. ladanifer, flower size and longevity increase along an altitudinal gradient; (3) floral longevity is differentially affected by temperature rather than flower size along the gradient; (4) under similar temperature, floral longevity decreases with flower size. For each species, we evaluated the effects of flower size and air temperature on floral longevity. Specifically, floral longevity was surveyed along an altitudinal gradient in the largest flowered species Cistusladanifer. Floral longevity in Cistus species lasted < 1 d and was affected by air temperature, independently of flower size. In C. ladanifer, flower size increased along the gradient but floral longevity decreased. Still, floral longevity decreased with increasing air temperature and, to a lesser extent, with flower size. Together, our findings show a triangular relationship among air temperature, flower size and floral longevity with margins for plasticity to accommodate pollinator attraction with the costs of large-flowered Mediterranean plants.