Timing of reproductive and vegetative development in Saxifraga oppositifolia in an alpine and a subnival climate

Morphogenesis of floral structures, dynamics of reproductive development from floral initiation until fruit maturation, and leaf turnover in vegetative short-stem shoots of Saxifraga oppositifolia were studied in three consecutive years at an alpine site (2300 m) and at an early- and late-thawing subnival site (2650 m) in the Austrian Alps. Marked differences in the timing and progression of reproductive and vegetative development occurred: individuals of the alpine population required a four-month growing season to complete reproductive development and initiate new flower buds, whereas later thawing individuals from the subnival sites attained the same structural and functional state within only two and a half months. Reproductive and vegetative development were not strictly correlated because timing of flowering, seed development, and shoot growth depended mainly on the date of snowmelt, whereas the initiation of flower primordia was evidently controlled by photoperiod. Floral induction occurred during June and July, from which a critical day length for primary floral induction of about 15 h could be inferred. Preformed flower buds overwinter in a pre-meiotic state and meiosis starts immediately after snowmelt in spring. Vegetative short-stem shoots performed a full leaf turnover within a growing season: 16 (+/-0.8 SE) new leaves per shoot developed in alpine and early-thawing subnival individuals and 12 (+/-1.2 SE) leaves in late-thawing subnival individuals. New leaf primordia emerged continuously from snowmelt until late autumn, even when plants were temporarily covered with snow. Differences in the developmental dynamics between the alpine and subnival population were independent of site temperatures, and are probably the result of ecotypic adaptation to differences in growing season length.     

Soil Patches of Inorganic Nitrogen in Subtropical Brazilian Plant Communities with Araucaria angustifolia

One-year old tubers of two hybrid calla lily (calla) cultivars (Zantedeschia ‘Pot of Gold’ and ‘Majestic Red’) were inoculated with the arbuscular mycorrhizal fungus (AMF), Glomus intraradices, or not, and grown at three different rates of phosphorus (P) supply to asses the effects of AMF-inoculation on plant development (time of shoot emergence and flowering), flowering (number, length and rate of flowering), and tuber biomass and composition over two growing cycles (2002, 2003). Tubers and flowers of calla responded differently to AMF inoculation. Differences in mycorrhizal responsiveness between cultivars was related to differences in P requirements for flower and tuber production, and the influence of P supply on resource allocation to different reproductive strategies. Inoculation increased shoot production and promoted early flowering, particularly in 2003. Inoculated plants also produced larger tubers than non-inoculated plants, but only increased the number of flowers per plant in 2003. High P supply also increased tuber biomass, but decreased the number of flowers per plant in 2002. Plants grown at a moderate P-rate, produced the most flowers in 2003. For ‘Majestic Red’, benefits from AMF were primarily in terms of tuber yield and composition, and AMF effects on marketable flower production could potentially have negative impact on production strategies for growers. Inoculation of ‘Pot of Gold’ primarily influenced flower production and aspects of tuber quality that caused detectable enhancement of tuber yield and flowering in the second growing cycle following inoculation (2003). The results of this study show that the responses of calla to AMF are partially a function of how nutrient supply alters resource allocation to sexual and vegetative reproduction. Whether AMF-induced changes in resource allocation to flowering and tubers significantly alters commercial productivity and quality of calla depends on the crop production goals (e.g. tubers, cut flowers or potted plants). The U.S. Government’s right to retain a non-exclusive, royalty free licence in and to any copyright is acknowledged.     

Management of below-ground biomass of <Emphasis Type="Italic">Typha angustifolia</Emphasis> by harvesting shoots above the water surface on different summer days

A dynamic model of regrowth in Typha angustifolia after cutting shoots above the water surface was formulated by characterizing the phenology and mobilization of resources from below-ground to above-ground organs after the cutting. The model parameters were determined by two cutting experiments to investigate the different strategies with flowering and non-flowering shoots after cutting in 2001 and by four cutting experiments to elucidate the regrowth characteristics after cutting on different days from June to September in 2002. A difference was evident both for flowering and non-flowering shoots and for each cutting day. From June to August, non-flowering shoots regrew immediately after cutting, but flowering shoots did not. The shoot regrowth height, number of leaves and shoot biomass were higher with the earlier cutting. The model was validated using the below-ground biomass observed in December 2002 and below-ground dynamics observed in 2003. In the low-flowering shoot zone of the stands, in which the percentage of flowering shoots was small (around 10%), the decrease in below-ground biomass became larger from June (20%) to August (60%). Cutting the high-flowering shoot zone (flowering shoots: 78%) in July 2001, just 1 week after peduncle formation, decreased the below-ground biomass by about 50%. In the low-flowering shoot zone, cutting just before senescence is better for decreasing below-ground biomass with a smaller rate of flowering shoots. The difference of below-ground biomass reduction in non-flowering shoots is mainly due to the decrease in downward translocation (DWT) of above-ground material to below-ground organs during senescence, because of the decrease in regrowth biomass. As for flowering shoots, the decrease in the photosynthate transportation from above-ground to below-ground organs and that of DWT are closely related because they cannot grow again within the season.     

Bi-directional inflorescence development inArabidopsis thaliana: Acropetal initiation of flowers and basipetal initiation of paraclades

In this study we investigated Arabidopsis thaliana (L.) Heynh. inflorescence development by characterizing morphological changes at the shoot apex during the transition to flowering. Sixteen-hour photoperiods were used to synchronously induce flowering in vegetative plants grown for 30 d in non-inductive 8-h photoperiods. During the first inductive cycle, the shoot apical meristem ceased producing leaf primordia and began to produce flower primordia. The differentiation of paraclades (axillary flowering shoots), however, did not occur until after the initiation of multiple flower primordia from the shoot apical meristem. Paraclades were produced by the basipetal activation of buds from the axils of leaf primordia which had been initiated prior to photoperiodic induction. Concurrent with the activation of paraclades was the partial suppression of paraclade-associated leaf primordia, which became bract leaves. The suppression of bract-leaf primordia and the abrupt initiation of flower primordia during the first inductive photoperiod is indicative of a single phase change during the transition to flowering in photoperiodically induced Arabidopsis. Morphogenetic changes characteristic of the transition to flowering in plants grown continuously in 16-h photoperiods were qualitatively equivalent to the changes observed in plants which were photoperiodically induced after 30 d. These results suggest that Arabidopsis has only two phases of development, a vegetative phase and a reproductive phase; and that the production of flower primordia, the differentiation of paraclades from the axils of pre-existing leaf primordia and the elongation of internodes all occur during the reproductive phase.     

Seasonal patterns of carbon assimilation and allocation of a summer-green forest herb, <Emphasis Type="Italic">Parasenecio</Emphasis> <Emphasis Type="Italic">auriculata</Emphasis> (Senecioneae; Asteraceae)

Summer-green herbs inhabiting deciduous forests often put out aerial shoots under bright conditions before tree-canopy closure and grow until late summer under the closed canopy. Some of them produce leaves continuously even after the initiation of canopy closure, indicating an exploitation of the low light period. The manner of carbon assimilation during bright and shade periods within a growth season should reflect the seasonal patterns of vegetative growth and reproductive allocation of individual species. We examined the seasonal patterns of assimilation, partitioning of photosynthate between reproduction and storage, and the budget of reproduction of a perennial understory herb, Parasenecio auriculata. Although photosynthetic rates per unit leaf area decreased with the seasonal reduction in light level, net assimilation at the whole-plant level was maintained at a high level even after canopy closure owing to the increase in the total leaf area. Stored resource in tubers contributed to the rapid development of aerial shoots in the early season, and annual tuber growth was completed before flowering. Instant photosynthetic products considerably contributed to the maintenance of flowers but not to fruit development because of low assimilation rate during fruiting. These findings indicated that carbon assimilation during flowering contributes to sexual reproduction without influencing the development of storage organs. Stable carbon assimilation over summer by shade-acclimatized leaves enabled the maintenance of high productivity associated with high sexual reproduction.     

A Developmental Pattern of Flowering in Colored <Emphasis Type="Italic">Zantedeschia</Emphasis> spp.: Effects of Bud Position and Gibberellin

The restricted flowering of colored cultivars ofZantedeschia is a consequence of developmental constraints imposed by apical dominance of the primary bud on secondary buds in the tuber, and by the sympodial growth of individual shoots. GA₃ enhances flowering inZantedeschia by increasing the number of flowering shoots per tuber and inflorescences per shoot. The effects of gibberellin on the pattern of flowering and on the developmental fate of differentiated inflorescences along the tuber axis and individual shoot axes were studied in GA₃ and Uniconazole-treated tubers. Inflorescence primordia and fully developed (emerged) floral stems produced during tuber storage and the plant growth period were recorded. Days to flowering, percent of flowering shoots and floral stem length decreased basipetally along the shoot and tuber axes. GA₃ prolonged the flowering period and increased both the number of flowering shoots per tuber and the differentiated inflorescences per shoot. Activated buds were GA₃ responsive regardless of meristem size or age. Uniconazole did not inhibit inflorescence differentiation but inhibited floral stem elongation. The results suggest that GA₃ has a dual action in the flowering process: induction of inflorescence differentiation and promotion of floral stem elongation. The flowering pattern could be a result of a gradient in the distribution of endogenous factors involved in inflorescence differentialtion (possibly GAs) and in floral stem growth. This gradient along the tuber and shoot axes is probably controlled by apical dominance of the primary bud. Online publication: 7 April 2005     

二型花柱植株金荞麦繁殖特征

开花物候及繁殖分配是植物适应环境的重要因素。对金荞麦开花物候、繁殖分配及策略进行了研究。结果如下:金荞麦的花果期为每年的8—11月,9月集中开花,其集中开花模式有助于吸引昆虫传粉,提高繁殖成功率;金荞麦单花开花持续时间为1—2 d,种群花期均为85d。L型花序花期为15—26d,S型花序花期为14—27d,两者没有显著差异;L型单花序开花数为26—131朵,S型单花序开花数为36—147朵,两者没有显著差异。L型和S型花序开花动态呈现单峰曲线,在花序开花后第11天L型和S型都达到最大值,分别为7.30%和7.20%,且两种花型具有较高的开花同步性,这有助于其繁殖适应性的提高。同一个花型中,雌蕊长、雄蕊长之间存在极显著负相关,但雌雄总长不存在显著差异,表明雌蕊长、雄蕊长可能存在权衡关系;金荞麦的繁殖器官和营养器官生物量在L型和S型间不存在显著差异,但其花生物量与植株生物量表现出极显著正相关关系。金荞麦L型花生物量分配极显著大于S型,而总生物量不存在显著差异,说明金荞麦植株的营养生长与有性繁殖间存在权衡关系。     

Specification of chimeric flowering shoots in wild-type Arabidopsis

Within wild-type Arabidopsis populations, a subset of the plants were found to have a single chimeric shoot on their primary shoot axes. The chimeric shoots were located below the lowest primary-axis flower; and they exhibited features of both flowers and paraclades (lateral flowering shoots). Morphological analyses of chimeric shoots indicated that they developed from single primordia. In each chimeric shoot, the side furthest from the apical meristem was specified as 'flower'—while the side closest to the meristem was specified as 'paraclade'—suggesting that a stimulus from outside the apical meristem can directly induce primordia to develop as flowers. It is concluded that the development of the teratological chimeric shoots resulted from the overlap of the vegetative and floral specification processes within single primordia.     

The Morphogenesis of Apple Buds: III. The Inception of Flowers

The early stages in the change from vegetative to reproductivedevelopment of apple spur terminal buds were followed by dissectionof buds from untreated trees, and from trees defoliated at differenttimes in the season. A change in the development of the leafprimordia occurred when there were approximately eight in thebud. This was followed by the development of bracts, which appearedto be necessary for the formation of actual flower parts. Leafprimordia tend to inhibit this process. Whereas their effectupon the apical meristem was subsequently reduced by the formationof bracts, so that eventually a terminal flower formed, theireffect upon the lower lateral meristems was unaltered. Thesemeristems therefore remained in a vegetative state. In addition to the number of leaf primordia in the bud, thedegree of dormancy may be an important factor in determiningthe onset of flowering. Since the number of leaf primordia invegetative buds at the end of the season is eight, the spatialdistribution of primordia on the main axis of the bud and theirvascular connexions might have a decisive effect on bud development.This was related to the effect of older primordia in the budupon the development of younger ones. In buds in which theseolder primordia were inhibited by foliage, etc., i.e. thosewith a long plastochrone, no effects were observed upon thedevelopment of younger primordia and the buds remained vegetative. Whilst correlative inhibition of buds thus affected their abilityto form flowers, there is no evidence of a critical leaf areafor flowering. Flowering in apple buds is more likely to bedue to the removal of factors inhibiting reproductive developmentthan to the synthesis of a specific flower inducing substanceas such.     

Dynamics of flower development and vegetative shoot growth in the high mountain plant Saxifraga bryoides L.

Saxifraga bryoides L. is an abundant species in the subnival and nival zone of the European mountains. First flowering occurs, at the earliest, 6 weeks after snowmelt. This is a remarkably long prefloration period in an environment with a short growing season. To gain more information about the developmental strategies of this species, the timing and the dynamics of flower bud formation and vegetative shoot growth were studied at sites with growing seasons of different lengths at two subnival locations (2650 and 2880 m a.s.l.) in the Tyrolean Alps. At an early, mid and late thawing site, individuals emerging from the winter snow were labelled. Reproductive and vegetative shoots were sampled at regular intervals throughout the growing season and analysed, using different microscopic techniques. Flower buds of S. bryoides develop in three cohorts. Provided the growing season is long enough, cohorts 1 and 2 come into flower, whereas cohort 3 buds remain primordial and continue to develop after winter. New flower primordia appear as day-length decreases from August on, which suggests a short-day requirement for floral initiation. At the end of the growing season, flower buds of different stages are present, but only primordial stages survive winter. Thus, flower buds of S. bryoides develop largely or even completely in the year of anthesis. Developmental dynamics were quite similar at the different sites. Time from flower initiation until anthesis took about 2 months, independently of whether flowers were formed within one or two seasons. All of the leaves on vegetative short-stem shoots turnover within a growing season. Leaves having passed winter continuously decline and are replaced by newly formed ones (21±3 at the mid-thawing site and 18±1 leaves at the short-season site). An individual leaf functions therefore, on average, about 12 months. In most years the seed crop of S. bryoides results mainly from the first cohort of flowers in an individual. In a changing climate with a prolonged growing season, the chance of two cohorts to develop mature seeds from flower cohorts 1 and 2 would increase.     

展毛翠雀花期繁殖特征和生物量分配对放牧的响应

生物量分配影响植物生长和繁殖,是植物生活史研究的重要内容。为了了解植物生活史性状对放牧的响应,该研究以青藏高原高寒草甸毒杂草展毛翠雀为对象,分析了放牧干扰对展毛翠雀的花期繁殖分配和性分配的影响。结果表明:放牧显著降低了展毛翠雀的总生物量、个体大小和繁殖投入; 放牧未改变展毛翠雀的营养部分与繁殖部分的等速生长关系,但显著增加了繁殖部分的生物量分配和总花数; 展毛翠雀的个体大小与总花数呈显著的正相关关系,但与性分配呈显著的负相关关系; 展毛翠雀的总花数与单花大小、单花的花瓣比例均表现出负相关关系,表明总花数与单花大小之间、总花数与单花的花瓣比例之间均存在权衡。因此,在放牧条件下,展毛翠雀的繁殖分配和性分配均表现出显著的可塑性。     

Which stem parts of Slender speedwell (<Emphasis Type="Italic">Veronica filiformis</Emphasis>) are the most successful in plant regeneration?

Regeneration of Slender speedwell (Veronica filiformis) from small parts of stem without using stimulative agents was the focus of the investigation. Four different short fragments of shoot (main terminal, secondary terminal, nodal segment and internodal segment) were cultivated under greenhouse and natural conditions. All tested vegetative segments induced roots, rooted in a soil substrate and in a semi-natural lawn, survived winter, and flowered. Multiplication of clonal plants was confirmed for both the main and secondary terminal segments. These terminal segments had the best response in number of growing individuals, flowering stems, and weight of dried biomass. The manipulative experiment revealed that clonal success of speedwell is connected with possibilities to hive off of all tested above-ground segments. Establishment of plantlets from the segment in natural condition was not successful when accompanied by certain grass species.     

COST OF REPRODUCTION IN POLEMONIUM VISCOSUM: PHENOTYPIC AND GENETIC APPROACHES

I measured the effect of early reproduction on subsequent growth and survival in the alpine perennial wildflower, Polemonium viscosum. Measurements were made over 4 yr on 34 maternal sibships under natural conditions. A significant phenotypic cost of early reproduction characterized the study population. Plants that flowered after only one year's growth had twice as many leaves and 25% more shoots than nonflowering individuals of equal age. However, early flowering decreased leaf number by 18% in the subsequent year and survivorship by 20% after two years relative to changes in leaf number and survival of nonflowering plants. For such trade-offs to shape the further evolution of reproductive schedules, flowering probability and those age-specific components of plant size that represent the energetic currency for reproductive costs must be heritable. Although families showed significant heterogeneity in the probability of early flowering, most (62%) entirely failed to flower. Moreover, phenotypic variation in vegetative size components at ages 1 and 2 had little genetic basis. Only at ages 3 and 4, after vegetative and demographic costs of early reproduction had been incurred, did vegetative size components (leaf length and number, and shoot number) vary significantly among families. Results of this study provide little evidence of a genetically based trade-off between early reproduction and subsequent survival in P. viscosum.     

Revisiting phase transition during flowering in Arabidopsis

Single-phase transition during flowering has been suggested by Hempel and Feldman (1994) [Planta 192: 276]. When early flowering ecotypes of Arabidopsis were microscopically observed, a long day signal simultaneously induced the acropetal (bottom to top) production of flower primordia and the basipetal (top to bottom) differentiation of paraclades (axillary flowering shoots) from the axils of pre-existing leaf primordia. However, this model could not account for the production of an extra number of secondary shoots in the TERMINAL FLOWER 1 overexpressor line or AGL20 overexpressor line in Columbia background with a functional allele of FRIGIDA. We report here that Columbia with a functional allele of FRIGIDA under long days and Columbia under short days show an inflorescence-producing phase between the vegetative and the flower-producing phases, supporting two-step phase transition during flowering. In addition, a late-flowering mutant, fwa shows an inflorescence phase but fca, fy and fve follow a single-phase transition, suggesting flowering time mutations have different effects on phase transition during flowering.     

Cryptic floral determination: stem explants from vegetative tobacco plants have the capacity to regenerate floral shoots

The developmental fates of shoots regenerated in culture and in situ by stem tissues of Nicotiana tabacum cv. Wisconsin 38 from different positions along the main axes of plants at different ages have been characterized. It was expected that explants from vegetative plants would not have the capacity to produce floral shoots. Contrary to the expected result, a small percentage (about 0.2%) of the shoots formed from cultured stem explants taken from young, vegetative plants were floral, i.e., produced a small number of nodes and then a flower. A larger percentage (about 2%) of the shoots formed by explants from the same region of plants which had flowered were floral. The largest percentage (76%) of floral shoots arose from explants taken from the inflorescence. Internode cells which were stimulated to divide and undergo organogenesis in situ after decapitation of the plant also produced few-noded, floral shoots with apical internode tissues producing many such floral shoots and basal internode tissues producing few such floral shoots. These results indicate that the capacity to form a flower is a visible expression of a cryptic developmental state which is quantitatively but not qualitatively controlled in time and space.     

The Influence of Ringing on Bud Development and Flowering in Satsuma Mandarin

Ringing of Satsuma mandarin (Citrus unshiu Marc.) trees showedincreased flowering in the following spring when performed duringSeptember and October, but not during November. Most of theeffect on flowering was due to an enhancement of both bud sproutingand the number of flowering shoots formed per node. In addition,a direct effect of ringing on flower initiation was demonstrated,since the number of vegetative shoots was reduced. The response of the buds to ringing was rapid as demonstratedby changes in bud weight, protein content, and electrophoreticpattern and behaviour when cultured in vitro. Buds from ringedtrees readily flowered in vitro when forced during the winterrest period and flower formation was enhanced by the additionof cytokinin. Buds from control trees formed a smaller numberof flowers in vitro, and flowering was much less enhanced bythe addition of cytokinin. It is concluded that ringing acceleratesflower initiation in the buds and this effect takes place beforethe winter rest period. Key words: Bud sprouting, Citrus unshiu Marc., flower initiation, flowering, in vitro flowering, Satsuma mandarin, ringing     

Pleiotropic effects of flowering time genes in the annual crucifer Arabidopsis thaliana (Brassicaceae)

Variation in flowering time of Arabidopsis thaliana was studied in an experiment with mutant lines. The pleiotropic effects of flowering time genes on morphology and reproductive yield were assessed under three levels of nutrient supply. At all nutrient levels flowering time and number of rosette leaves at flowering varied among mutant lines. The relationship between these two traits depended strongly on nutrient supply. A lower nutrient supply first led to an extension of the vegetative phase, while the mean number of leaves at flowering was hardly affected. A further reduction resulted in no further extension of the vegetative phase and, on average, plants started flowering with a lower leaf number. At low nutrients, early flowering affected the timing of production of siliques rather than the total output, whereas late flowering was favorable at high nutrients. This may explain the fact that many plant species flower at a relatively small size under poor conditions. Flowering time genes had pleiotropic effects on the leaf length, number of rosette and cauline leaves, and number of axillary flowering shoots of the main inflorescence. Silique production was positively correlated with the number of axillary shoots of the main inflorescence; the number of axillary primordia appeared to have a large impact on reproductive yield.     

Effect of flowering on vegetative growth and further reproduction in

Flowering intensity and plant size were monitored in 155 Festuca novae-zelandiae individuals over four years to determine if trade-offs exist between inflorescence production and vegetative growth, and between inflorescence production in different years. Less than half of the population flowered in any one year, 36% of individuals did not flower at all, and only 17% flowered in all four years of the study. Mean number of inflorescences per individual per year varied from 1.54 to 5.53 (maximum = 85). No trade-offs were detected between flowering frequency and intensity; individuals that flowered more frequently also produced more inflorescences in each flowering episode. No trade-off was detected between current and future reproduction, rather flowering intensity was positively correlated between years. Growth, as measured by diameter increment, was positively related to flowering frequency and flowering intensity, both across all individuals studied and within 1m x 1m plots. The presence of a positive relationship between growth and reproduction within plots argues against meso-scale variability in environment factors being the cause of the results from analyses involving all individuals. Clearly reproduction in F. novae-zelandiae does not incur a marked cost in growth or future reproduction. The assumptions underlying theoretical expectations of such trade- offs may not be valid for long-lived clonal plants such as F. novae-zelandiae.     

Population biology of the rare military orchid (Orchis militaris L.) at an established site in Suffolk, England

In Britain, where it reaches the north-westerly limit of its European distribution, Orchis militaris L. is extremely rare. Well-established and persistent populations of O. militaris are known to exist at only two sites. The largest extant population of O. militaris occurs in a disused chalk pit in Suffolk. A preliminary demographic analysis of this population, covering the period 1975 to 1991, along with estimates of key life stage transition probabilities are presented here. From 1975 to 1986 the number of separate identifiable plants in the population declined substantially. Until 1986 recruitment of rosettes was poor. The largest cohort of new plants, recorded in 1976, was 35. Approximately 48% of new individuals recruited between 1976 and 1985 failed to flower. Of those flowering, approximately 55% flowered during their first year above ground. Of the original population recorded in 1975, 67.8% flowered at least once during the study. The reproductive performance, i.e. the frequency of flowering and the period between episodes of flowering, varied considerably between individuals. Some plants flowered every year while others only flowered once during the study. Few plants remained below ground for more than one year, while several apparently persisted below ground for more than 6 successive years. Although the number of plants that can be identified as separate individuals has declined, the total number of rosettes in the population has, from 1986, increased dramatically. Because of the dense clumping of these recruits it is not possible to determine whether they are derived from seed or vegetative propagation. When post 1986 recruitment is combined with the number of plants that established before 1986 and survive, the apparent number of plants present at the site has more than doubled between 1975 and1991.     

In vitro flowering of Bambusa edulis and subsequent plantlet survival

Bamboo shoots could be induced to flower in vitro, but there is very little information on the effect of growth components on flowering. In this study, multiple shoots grown from in vitro, spikelet-derived, somatic embryos of Bambusa edulis were used for in vitro flowering. Multiple shoots flowered on Murashige and Skoog medium (MS) with 0.5 mM thidiazuron (TDZ) and 30 g l sucrose. Different