A gradual reduction of female structures in the pistillate flowers ofRicinus communis L. (castor-bean) with chlorflurenol (morphactin)

Chlorflurenol (morphactin) EMD 7301 W (60, 120 and 240 mg I^?1) when applied at five to seven leaf and 10–12 leaf stage induced hermaphrodite flowers in the inflorescences ofRicinus communis. The hermaphrodite flowers were mostly apical in position unlike the apical female flower in the control. With an increase in the time gap between sowing and emergence of the inflorescence there was a reduction of the female structures in the hermaphrodite flowers. The last formed inflorescences had an apical male flower in place of a female. The largest number of inflorescences with an apical male or hermaphrodite flower were produced with 60 mg 1^?1 applied at five to seven leaf stage. The hermaphrodite flowers failed to set fruits.     

Floral display size in comfrey, Symphytum officinale L. (Boraginaceae): relationships with visitation by three bumblebee species and subsequent seed set

The fecundity of insect-pollinated plants may not be linearly related to the number of flowers produced, since floral display will influence pollinator foraging patterns. We may expect more visits to plants with more flowers, but do these large plants receive more or fewer visits per flower than small plants? Do all pollinator species respond in the same way? We would also expect foragers to move less between plants when the number of flowers per plant are large, which may reduce cross-pollination compared to plants with few flowers. We examine the relationships between numbers of inflorescence per plant, bumblebee foraging behaviour and seed set in comfrey, Symphytum officinale, a self-incompatible perennial herb. Bumblebee species differed in their response to the size of floral display. More individuals of Bombus pratorum and the nectar-robbing B.?terrestris were attracted to plants with larger floral displays, but B. pascuorum exhibited no increase in recruitment according to display size. Once attracted, all bee species visited more inflorescences per plant on plants with more inflorescences. Overall the visitation rate per inflorescence and seed set per flower was independent of the number of inflorescences per plant. Variation in seed set was not explained by the numbers of bumblebees attracted or by the number of inflorescences they visited for any bee species. However, the mean seed set per flower (1.18) was far below the maximum possible (4 per flower). We suggest that in this system seed set is not limited by pollination but by other factors, possibly nutritional resources.     

The mating consequences of sexual segregation within inflorescences of flowering plants

Many co-sexual plants segregate female and male function among flowers on an inflorescence through dichogamy or the production of unisexual flowers. Sexual segregation may reduce self-pollination among flowers within inflorescences (geitonogamy), thereby increasing the pollen available for export to other plants. To assess these complementary roles we manipulated the simultaneously hermaphroditic (adichogamous) flowers of Eichhornia paniculata to produce ten-flowered inflorescences with either female above male flowers (female/male inflorescences) or male/female inflorescences, which competed for mating opportunities with five-flowered adichogamous inflorescences. Because of the upward movement of bumble-bees, selfing increased upward in adichogamous inflorescences (overall female selfing rate s+/-s.e.=0.320+/-0.026). Female flowers of male/female inflorescences selfed less than flowers in corresponding positions in adichogamous inflorescences so s fell to 0.135+/-0.027. In contrast, all-female flowers of female/male inflorescences selfed similarly to upper flowers on adichogamous inflorescences, elevating s (0.437+/-0.043). During 1997, male/female inflorescences sired more outcrossed seeds than female/male or adichogamous inflorescences, whereas during 1994 flowers on male/female inflorescences received fewer visits than those of adichogamous inflorescences, reducing their outcross siring success. Hence, sexual segregation limits geitonogamy and enhances outcross siring success when it does not affect pollinator behaviour, illustrating the importance of both female and male function in inflorescence design.     

Expression of IAA-Lysine Synthetase Gene Caused Variations of Flower Develop ment in Transgenic Tobacco

The indoleacetic acid-lysine synthetase (iaaL) gene of Pseudornonas syringae subsp. savastanoi was fused to a rice Rchl0 promoter and introduced into tobacco plants. The expression pattern of this chimeric Rchl0-iaaL gene in the transgenic plants was studied, and the endogenous levels of indoleacetic acid (IAA) were assayed with the high-performance liquid chromatography (HPLC) method. The results showed that the Rchl0 promoter could direct the high level expression of the iaaL gene in young inflorescences, fully bloomed flowers, and immature fruits, resulted in a decrease of the IAA levels by 32%–82%. The transgenic plants displayed decreased apical dominance, enlongated stamens, abnormal inflorescences and fruits. The transgenie plant pYL614-T14, in which the endogenous IAA levels in inflorescences were reduced by 82 %, displayed extremely abnormal inflorescence with only two flowers and a much higher potential of vegetative growth than that of the controls after flowering. These Rchl 0-iaaL gene transgenic tobacco plants would pro- vide valuable materials for further studies of physiological functions of IAA in reproductive development.     

REPRODUCTIVE SUCCESS AND INFLORESCENCE SIZE OF CALOPOGON TUBEROSUS (ORCHIDACEAE)

Reproductive success of Calopogon tuberosus, which produces no nectar, was investigated in relation to inflorescence size and dispersion pattern. Mean inflorescence size was 2.56 (range 1–10). A bagging experiment showed that insects are required for pollen transfer and that fruits are produced from self-, geitonogamous, and cross-pollinations; fruit set was not 100%. Fruit set of nonmanipulated plants was limited by the number of pollinator visits. Reproductive success increased with increasing inflorescence size, although not above theoretical predictions. However, the probability of producing no fruit or contributing no pollinia decreased with increasing inflorescence size since sequential flowering increased the probability of a pollinator visit to the inflorescence over the blooming period. Large inflorescences did not provide a greater pollinator attraction than small ones, because inflorescences only presented a few open flowers at a time. In addition, flowers on plants growing in clumps of 2–8 plants had a higher probability of setting fruit, apparently because of increased pollinator attraction. Although there are obvious selective advantages for large inflorescences, the sequential flowering habit, and low resource availability may reduce the advantages of large inflorescence size at our study site.     

Adaptive plasticity of floral display size in animal-pollinated plants

Plants need not participate passively in their own mating, despite their immobility and reliance on pollen vectors. Instead, plants may respond to their recent pollination experience by adjusting the number of flowers that they display simultaneously. Such responsiveness could arise from the dependence of floral display size on the longevity of individual flowers, which varies with pollination rate in many plant species. By hand-pollinating some inflorescences, but not others, we demonstrate plasticity in display size of the orchid Satyrium longicauda. Pollination induced flower wilting, but did not affect the opening of new flowers, so that within a few days pollinated inflorescences displayed fewer flowers than unpollinated inflorescences. During subsequent exposure to intensive natural pollination, pollen removal and receipt increased proportionally with increasing display size, whereas pollen-removal failure and self-pollination accelerated. Such benefit-cost relations allow plants that adjust display size in response to the prevailing pollination rate to increase their attractiveness when pollinators are rare (large displays), or to limit mating costs when pollinators are abundant (small displays). Seen from this perspective, pollination-induced flower wilting serves the entire plant by allowing it to display the number of flowers that is appropriate for the current pollination environment.     

Lying to Pinocchio: floral deception in an orchid pollinated by long-proboscid flies

Plants that lack floral rewards may nevertheless attract pollinators if their flowers sufficiently resemble those of rewarding plants. Flowers of the South African terrestrial orchid Disa nervosa are similar in floral dimensions and spectral reflectance to those of a sympatric nectar-producing irid ( Watsonia densiflora s.l. ). Observations showed that the orchid and Watsonia share the same pollinator, a long-proboscid tabanid fly Philoliche aethiopica . These flies visited inflorescences of both species during their foraging bouts and most (64%) observed or captured on Watsonia inflorescences carried pollinaria of the orchid on their proboscides. They probe an average of 6.3 flowers on Watsonia inflorescences, but just 1.9 flowers on the Disa inflorescences, a behaviour which would strongly promote cross-pollination in the self-compatible orchid. The orchid generally achieves high levels of pollination success, with approximately 50% of flowers receiving or exporting pollen at some sites. Pollination success was also high at one site that lacked Watsonia plants, suggesting that the orchid does not have an obligate dependence on Watsonia . Its pollination system may therefore be characterized as intermediate between generalized food deception and specific floral mimicry.  © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 152 , 271–278.     

Optimal foraging in bumblebees and coevolution with their plants

Summary The aims of this paper were to consider the coevolution between bumblebee movement patterns within plants and various properties of the plants such as the spatial distribution of their flowers, and to determine the extent to which the bumblebees and the plants can be considered to be maximally adaptive or optimal. Attention was restricted to plants which have flowers arranged on vertical inflorescences and to the bumblebees which visit these plants.It was found that the bumblebees tend to commence foraging at the bottom of each infloresence, that they tend to move from one flower to the closest vertically higher flower, that they miss flowers as they move upwards and that they tend to leave each inflorescence before reaching the top. It was also found for the four common plant species considered that nectar abundance per flower decreases with flower height on an inflorescence, that the flowers with receptive stigmas are restricted to the bottoms of the inflorescences while the flowers shedding pollen occur above them, and that the flowers are arranged approximately in spirals on the inflorescences.The pattern of movements of the bumblebees and the various properties of the plants appear to represent coevolved adaptations. Furthermore the bumblebees' movement patterns appear to be optimal in the sense that they result in the maximum net rate of energy gain to the bumblebees. Further studies are necessary, however, to determine whether or not the plants can be considered to be optimal.An exception to the above scheme is provided by a plant which is quite uncommon in the study area. This plant also has flowers on vertical inflorescences and appears to be pollinated by bumblebees. However, while the pattern of movements of the bumblebees on this plant species are extremely similar to those on the four common species, this plant species exhibits quite different properties from the other four. Two possible explanations for this exception are presented.     

Prevention of flower formation in dicotyledons

Prevention of flower formation is important, for example for preventing the spread of transgenes from genetically modified plants or the spread of non-native species, for increasing vegetative growth or preventing the formation of allergenic pollen. The aim of this study was to determine whether flowering of dicotyledonous plants can be prevented by genetic manipulation without harmful effects on vegetative growth. Here we describe isolation of the BpMADS1 gene (similar to SEP3, formerly AGL9) from birch and show that it is expressed only in the inflorescences. In tobacco and Arabidopsis, the expression of BpMADS1::GUS was also virtually inflorescence-specific. Transgenic tobacco and Arabidopsis containing a BpMADS1::BARNASE construct grew well. In one tobacco line the formation of the inflorescence was completely prevented; in several other lines the flowers lacked stamens and carpels and therefore were sterile. The final dry weights of the shoots of the sterile tobacco lines were 140–200% of those of controls. In Arabidopsis, some of the transgenic lines containing the BpMADS1::BARNASE construct formed inflorescences. Some of these lines formed never flowers and some others formed occasionally single fertile flowers. Some other lines did not form inflorescences, but formed up to about one hundred leaves, even in long-day conditions. These results suggest that formation of flowers or inflorescences in widely different dicotyledonous plants could be prevented using the BpMADS1::BARNASE construct and that prevention of flowering may lead to increased vegetative mass.     

Variation in fruit- and seed set among and within inflorescences of Melampyrum roseum var. japonicum (Scrophulariaceae)

Abstract Variations in fruit set and seed set among and within inflorescences of the annual herb, Melampyrum roseum var. japonicum, were studied. Under natural conditions, although the mean fruit set was slightly different among inflorescences, the mean seedset was not significantly different among inflorescences within the plants. In constrast, within the inflorescences, the flowers located at a lower position of the inflorescence and which opened earlier showed higher fruit set than those at a higher position and which opened later. However, the seed set of matured capsules were not significantly different from each other, regardless of the position of flowers within the inflorescences. Patterns of the fruit- and seed set under open pollination indicated that variation in seed reproduction of M. roseum is due to variation in fruit production. The results of clipping experiments of flowers revealed that there was no functional limitation in seed production among flowers located at various positions within the inflorescence. It seemed that the variation in the fruit set within the inflorescences of M. roseum was not attributable to 'architectural effects'. Reduction of the number of flowers within the inflorescences resulted in an increase of fruit set and seed weight, indicating that the flowers in an inflorescence compete for resources. This phenomenon supports the 'resource competition hypothesis', and variation in fruit set within the inflorescence is attributable to competition among flowers within the inflorescence for limited resources. Consequently, it was concluded that, under natural conditions, the early blooming flowers located at lower positions of the inflorescences obtain more resources and produce more fruits than the late blooming flowers located at higher positions in M. roseum .     

SURVEY OF SHOOT ORGANIZATION IN THE ARACEAE

Shoot organization is examined in 87 species from 29 genera representing all six subfamilies of the Araceae and of Acorus, which has been placed in a separate family. Within each taxonomic group examined, the details of shoot organization are presented, including the types of segments and articles which make up the shoot, the degree of expansion of leaf blades, and the placement of buds along the shoots. Literature on shoot organization of the 29 genera is reviewed. The degree of correlation between shoot organization characteristics and systematic groupings is examined, and the utility of these characteristics for systematics is evaluated. It is found that within the taxa observed, the pattern of shoot organization provides a distinctive “fingerprint” at the generic or sectional level, sufficient for determination of the group. Some patterns which appear are pointed out: taxa with bisexual flowers usually produce a single inflorescence at the terminus of a vegetative article. A few taxa with bisexual flowers produce pairs of inflorescences at the ends of articles. Multiple inflorescences (more than two) at an article terminus occur only among taxa with unisexual flowers. Multiple inflorescences are associated with anisophyllous or homeophyllous sympodial growth, while single or paired inflorescences are associated with homeophyllous or intermittent homeophyllous sympodial growth. These patterns might be understood as the result of selection for flexibility of reproductive effort and of seasonal reproduction.     

Batesian mimicry in the non-rewarding orchid Disa pulchra, and its consequences for pollinator behaviour

The non-rewarding flowers of the South African orchid Disa pulchra are remarkably similar in morphology and spectral reflectance to the flowers of a sympatric nectar-producing iris, Watsonia lepida. Field observations indicated that both D. pulchra and W. lepida are pollinated by the long-tongued fly, Philoliche aethiopica (Tabanidae). The hypothesis that D. pulchra is a floral mimic of W. lepida was supported by choice experiments, which showed that, in terms of visits to inflorescences, flies do not discriminate between the two species. However, flies probed fewer flowers and spent less time on D. pulchra inflorescences than on Watsonia inflorescences. Thus the absence of nectar in the flowers of D. pulchra may reduce the risk of geitonogamy and pollen discounting. A breeding system experiment showed that fruits of D. pulchra that arise from self-pollination contain relatively few viable seeds compared with outcrossed fruits. These findings support the hypothesis that deception in orchids evolved under selection for more efficient mating systems.     

Multi-cycle synchronous protandry in raceme-like inflorescences of a bumblebee-pollinated herb Aconitum grossedentatum

Multi-cycle synchronous dichogamy is expected to be a mechanism for reducing self-pollination and sexual interference. It is often found in plants with umbellate inflorescences where pollinator movement is unpredictable, but not in plants with raceme inflorescences that are pollinated by bumblebees. Plants with raceme inflorescences often acropetally open flowers, resulting in an arrangement of females at lower level and males at upper level. This is good enough to preclude geitonogamy because bees tend to move upwardly within the inflorescences. Furthermore, although the degree of segregation of sexes varies among species, their intraspecific variations within a population have rarely been examined. Here, we present a synchronous protandry in bee-pollinated Aconitum grossedentatum, which has a raceme-like inflorescence and opens flowers basipetally. To evaluate the functional significance of synchronous dichogamy in mating, we firstly observed the distribution of sex phases of open flowers. Then, we assessed the effect of each phase flower on foraging behavior by pollinators and seed-set success. The inflorescences tended to exhibit either male- or female-phase flowers at any moment early in the flowering season, but the degree of segregation of sexes declined over time within a population. The degree of the segregation did not affect bumblebee visits to flowers, but it decreased seed-set success of female-phase flowers at that time. Our results demonstrated that synchronous protandry was beneficial for pollination success in A. grossedentatum by avoiding geitonogamy. Nevertheless, we also found asynchronous protandry late in the season, suggesting that the benefits by synchronous protandry decreased over the season.

     

Studies on the Growth, Flowering, and Production of Female Sterile Flowers as Affected by Different Levels of Foliar Potassium in Solanum sisymbrifolium Lam.: I. EFFECT OF POTASSIUM CONTENT OF THE PLANT ON VEGETATIVE GROWTH AND FLOWERING

As compared to a high level of foliar potassium, a low but nota deficient level promotes shoot elongation and flowering inS.sisymbrifolium.This is accompanied by formation of flowers with rudimentaryovaries in which the megagametophyte in the ovules aborts atthe two- or the four-nucleate stage. Plants having a higherK content do not bear the female sterile flowers. Inflorescencesof the high-K plants with 20 per cent fewer buds have 23 percent higher dry weight than inflorescences of low-K plants.The ratio of organic nitrogen to dry weight is not affected,indicating that the inflorescences of the high-K plants arebetter supplied with metabolites in general.     

Effects of some natural and synthetic growth regulators on sex-expression of Myrica esculenta Buch-Ham. ex D. Don

Gibberellic acid (GA,), chlorflurenol and ethrel were applied at different concentrations to either male or female trees of Myrica esculenta. GA₃ induced intersexual flowers both on the male and female trees whereas chlorflurenol and ethrel induced similar (intersexual) flowers but only on the male plants. When GA₃ was applied in combination with chlorflurenol, fewer intersexual inflorescences appeared on the male plants along with a significant decline in the number of flowers per inflorescence. In combination, chlorflurenol and ethrel induced copious female and intersexual inflorescences per male plant, especially when two successive treatments of 100 mg/I of chlorflurenol and 1920 mg/l of ethrel were applied. The induced female inflorescences later bore fruits.     

How floral displays affect geitonogamy in an upward foraging bumblebee‐pollinated protandrous plant

Reducing geitonogamy (pollen transfer among flowers within the same plant) has been suggested as a major selective force for plants with multiple flowers. The occurrence of geitonogamy is generally different among flowers within inflorescences; however, no researchers have examined whether plants enlarge their display size without increasing the possibility of geitonogamy by presenting more flowers at positions where they are less likely to be geitonogamously pollinated. We observed that bumblebee pollinators foraged upward within the tower‐shaped inflorescences of protandrous Megacodon stylophorus (C. B. Clarke) Harry Sm. Because M. stylophorus did not strictly bloom bottom‐up, there were substantial frequencies of geitonogamous pollination resulting from upward and horizontal pollen transfer. Although there was a strong correlation between total numbers of flowers plants produced and numbers of flowers presented on single days, proportions of flowers possibly geitonogamously pollinated were weakly correlated with total numbers of flowers. This might have been because plants with more resources enlarged their display size by producing more flowers on lower floors where flowers had a low probability of being geitonogamously pollinated. This study shows that the tower‐shaped inflorescences of M. stylophorus enlarge their size without more cost of geitonogamous mating, suggesting that geitonogamy acts as an important selective agent in the evolution of inflorescence architectures.     

Pollination and reproductive success of two colour variants of a deceptive orchid, Dactylorhiza maculata (Orchidaceae)

Polymorphism in petal colour is common in deceptively pollinated plant species. Most of the deceptively pollinated orchids are food frauds, and in most of them, the deception is not mimetic. These plants have conspicuously coloured flowers which they use as the main attractant of naive pollinators. In a field experiment, we studied the response of bumblebees and other types of flower visitors to colour differences between experimentally paired plants of Dactylorhiza maculata , a nectarless food-deceptive species. In addition, pollen removal, an estimate of male fitness, and fruit production, an estimate of female fitness, were measured in the two colour variants. We found a trend of bumblebee preference for the dark-coloured flowers, but other flower visitors (as a group) showed no preference for any colour variant. No difference was found in the reproductive success between the two colour variants of D. maculata. The lack of a difference in reproductive success between plants with pale and dark inflorescences, despite the observed trend of bumblebee preference for dark inflorescences, suggests that there is some balancing factor in the pollination of the pale inflorescences. An excess of visits by some nocturnal species (or a group of species) which favours the pale colour of D. maculata inflorescences or an excess of visits during day time by some flower visitors other than bumblebees preferring the pale inflorescences over dark ones may form such a balancing factor.     

Sexual dimorphism and sex ratios of two Australian dioecious species of alpine pineapple grass, Astelia alpina var. novaehollandiae and Astelia psychrocharis (Asteliaceae)

Sexual dimorphism and male biased sex ratios have been predicted for dioecious plants experiencing the limited conditions for growth and reproduction found in many alpine environments. To test these predictions, the reproductive ecology of two congeneric, co-occurring, dioecious, clonal, species was examined in the subalpine and alpine zones of Kosciuszko National Park, southeastern Australia. Specifically, plant size (vegetative cover of plants in quadrats), floral display (number of flowers per inflorescence, number of inflorescences per quadrat) and sex ratios (proportion of females in quadrats with flowers) were examined in ten populations of Astelia psychrocharis (Asteliaceae) and nine populations of Astelia alpina var. novae-hollandiae (Asteliaceae). Sexual dimorphism did occur, with males having more flowers per inflorescence (106% more flowers for A.alpina males and 12% more for A.psychrocharis males compared to females) and more inflorescences per quadrat than females (78% more inflorescences for A.alpina males and 46% more inflorescences for A.psychrocharis males compared to females). Plant size did not differ between male and female quadrats of either species, nor were there male biased sex ratios. However, plant size was related to flowering status in A.psychrocharis with the 65 quadrats that did not flower having lower vegetative cover than the 175 flowering quadrats indicating that there may be a minimum size/ cover required prior to flowering in this species. For A.alpina, all but two of the 185 quadrats randomly sampled flowered. There was no effect of altitude on plant size and very little effect of altitude on floral display for either species, apart from a slight increase in the number of inflorescences per quadrat with increasing altitude for A.psychrocharis, and slight decrease in number of flowers per inflorescence with increasing altitude for A.alpina females.     

Impact of floral herbivory by <Emphasis Type="Italic">Coleotechnites eryngiella</Emphasis> Bottimer (Lepidoptera: Gelechiidae) on the reproductive output of <Emphasis Type="Italic">Eryngium yuccifolium</Emphasis> Michaux (Apiaceae): a test of the reserve ovary model

The reserve ovary model is a key hypothesis proposed to explain why plants produce surplus flowers and posits that plants may utilize surplus flowers to compensate for losses from floral herbivory. We tested this hypothesis in the prairie plant Eryngium yuccifolium and its floral herbivore Coleotechnites eryngiella. At five Illinois tallgrass prairie sites, we collected central, primary lateral, and secondary lateral inflorescences from E. yuccifolium to determine whether damage by the larvae of C. eryngiella to the flowers in earlier developing inflorescences would be compensated for in later developing inflorescences. Coleotechnites eryngiella does extensive damage to the central and primary inflorescences and little damage to the secondary inflorescences. Later maturing inflorescences did not compensate for early damage by increasing seed production in later inflorescences. The secondary inflorescences of E. yuccifolium may only compensate for catastrophic damage done to the central and primary inflorescences early on in development, serve as additional advertisements for pollinators, act as pollen donors, or allow the plant to take advantage of “ecological windows” of high pollinator and low herbivore abundance. Our findings were spatially and temporally consistent and did not support the predictions of the reserve ovary model in the E. yuccifolium–C. eryngiella system suggesting that in this system, alternate, proximate, and ultimate causes need to be explored for the production of surplus flowers.     

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.