Changes in Dormancy and Sensitivity to Vernalization in Axillary Buds of Satsuma Mandarin Examined in vitro During the Annual Cycle

Effect of season and the presence of fruit on bud-endodormancyand the flowering response to low temperature treatments weredetermined using bud cultures of Owari satsuma mandarin (Citrusunshiu Marc). Bud dormancy was deeper in fruiting as comparedto defruited trees. In fruiting trees, the intensity of buddormancy was highest in spring, decreased to a low value byearly Jul. and then increased until early winter. This increasein dormancy during summer and early autumn did not occur innon-fruiting trees. No flowers formed in buds cultured betweenMay and Sep. Both in fruiting and defruited trees, buds becamecompetent to show a vernalization response to chilling by theend of Oct., at the time they also became capable of sproutingin vitro at low temperature (15/10 °C). There was a directeffect of fruit on the buds which persisted long after fruitremoval and resulted in a reduction of the flowering responseto chilling.Copyright 1995, 1999 Academic Press Citrus flowering, Citrus unshiu Marc., dormancy, flower induction, flowering, in vitro flowering, satsuma mandarin, vernalization     

The effect of LAB 173711 and ethephon on time of flowering and cold hardiness of peach flower buds

Peach flowers are often killed during bloom by spring frosts. LAB 173711, a compound with abscisic (ABA)-like activity, and ethephon delayed flowering in peach trees. In greenhouse experiments, LAB 173711, at concentrations of 10^?3–10^?2 M, was most effective in delaying bloom when applied after a 5°C cold storage period, rather than before the dormancy breaking treatment. In contrast, ethephon delayed bloom most effectively when applied before 5°C cold storage; ethephon caused flower bud abscission when treatments were made after the chilling requirement had been satisfied. In field experiments, ethephon delayed flowering by 6–7 days, which reduced bud injury after a spring frost during bloom. No flower bud injury was found on ethephon-treated trees after temperatures of ?4.3°C; whereas without ethephon 25% of the flower buds were frost damaged. LAB 173711 delayed the time to 50% bloom by 2–3 days. However, this was not long enough to avoid low-temperature injury to the flower buds.     

Influence of different temperatures on bud break and 1-aminocyclopropane-1-carboxylic acid content of young peach trees

Effects of different temperatures on bud break and 1-aminocyclopropane-1-carboxylic acid (ACC) content were determined by using potted two-year-old ‘Akatsuki’ peach trees. One group of trees were subjected to 1°C for four weeks and then transferred to a growth chamber at 24°C, while the other was kept at 24 °C throughout the experiment. After four-week temperature treatments floral and vegetative bud break were evaluated weekly and bud break percentage was calculated. Bud break was greater under 1 °C than 24 °C in both November and December. The time required to release buds from dormancy was shorter in December than November. In November ACC content in peach buds increased after one and two weeks, then decreased in the forth week under both treatments. However, in December ACC content after two and four weeks showed a similar trend under 1 °C and a reverse trend under 24 °C. It was higher under low temperature treatment. These data indicate that chilling requirements for bud break of peach seems to be associated with the promotion of ethylene biosynthesis caused by low temperature stress.     

The effect of LAB 173711 and ethephon on time of flowering and cold hardiness of peach flower buds

Peach flowers are often killed during bloom by spring frosts. LAB 173711, a compound with abscisic (ABA)-like activity, and ethephon delayed flowering in peach trees. In greenhouse experiments, LAB 173711, at concentrations of 10^–3–10^–2 M, was most effective in delaying bloom when applied after a 5°C cold storage period, rather than before the dormancy breaking treatment. In contrast, ethephon delayed bloom most effectively when applied before 5°C cold storage; ethephon caused flower bud abscission when treatments were made after the chilling requirement had been satisfied. In field experiments, ethephon delayed flowering by 6–7 days, which reduced bud injury after a spring frost during bloom. No flower bud injury was found on ethephon-treated trees after temperatures of –4.3°C; whereas without ethephon 25% of the flower buds were frost damaged. LAB 173711 delayed the time to 50% bloom by 2–3 days. However, this was not long enough to avoid low-temperature injury to the flower buds.     

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.     

Levels and Aggregation of Ribosomes during Dormancy and Dormancy Break of Peach Flower Buds

The level of ribosomes and their aggregation state (monosomes-polysomes) have been investigated in relation to dormancy in peach flower buds (Prunus persica). The ribosomes were analysed by a linear sucrose gradient. The ribosomal content hardly changes in the bud before dormancy and until dormancy breaks; on the other hand after this period there is a remarkable increase in the ribosomal level strictly related to the increase in bud weight. The ribosomal content reaches the highest value at flowering. During dormancy break the largest portion of ribosomes is localized in flower primordia, not in scales. Polysomes, which are always present in buds, remain constant during dormancy (35%), increase at dormancy breaking, reaching the highest level at flowering.     

The Cold Awakening of <Emphasis Type="Italic">Doritaenopsis</Emphasis> ‘Tinny Tender’ Orchid Flowers: The Role of Leaves in Cold-induced Bud Dormancy Release

Massive flowering of tropical Phalaenopsis orchids is coordinated by the cold-induced release of reproductive bud dormancy. Light and temperature are the two key factors integrated by the dormancy mechanism to both stop and reactivate the meristem development of many other angiosperm species, including fruit trees and ornamental plants. It is well established that leaves and roots play a major role in inducing flower development; however, currently, knowledge of molecular events associated with reproductive bud dormancy release in organs other than the bud is limited. Using differential gene expression, we have shown that the leaves of a hybrid of Phalaenopsis species, Doritaenopsis ‘Tinny Tender’, undergo major metabolic modifications. These changes result in the production of sucrose and amino acids, both of which can sustain bud outgrowth, and auxin and ethylene, which may play important roles in awaking the dormant buds. Intake of abscisic acid and synthesis of the hormone jasmonate may also explain the inhibition of vegetative growth that coincides with bud growth. Interestingly, many genes that were upregulated by cold treatment are homologous for genes involved in flower induction and vernalization in Arabidopsis, indicating that processes regulating flowering induction and those regulating reproductive bud dormancy release may use similar pathways and effector molecules.     

Seasonal variation in the competence of the buds of three cultivars from different Citrus species to flower

The role of bud competence in the determination of flowering seasonality was studied in three Citrus cultivars, Bearss lime (Citrus latifolia Tan.), Fino lemon (C. limon [L.] Burm. f.) and Owari satsuma (C. unshiu (Mak.) Marc.), which differ in their adaptation to hot climates and their propensity to produce off-season blooms. Potted plants were kept in a greenhouse under non-inductive conditions (minimum temperature higher than 20°C), and periodically the flowering response was determined of a group of trees exposed for 30 days to an inductive temperature regime (15/8°C). A seasonal change in bud competence was demonstrated, and both bud sprouting and flower formation were highest when the low temperature regime was imposed during February and March. During the summer months, the low temperature regime resulted in a small increase in bud sprouting as compared to non-chilled trees, but only vegetative buds developed and no flowers were formed. The influence of environmental factors on the determination of bud competence was further studied. No effect of photoperiod was found, but raising the minimum air temperature above 25°C during 60 days, eliminated bud competence in Owari satsuma. In Bearss lime trees, the buds reacquired the competence after 4 months at 25/20°C, a temperature regime that does not induce flower formation. The reacquisition of competence was much faster at a lower temperature (15/8°C). A consistent relationship between the flowering response and DNA methylation in buds could not be demonstrated in all cultivars.     

The relationship between xylem differentiation and dormancy evolution in apricot flower buds (Prunus armeniaca L.): the influence of environmental conditions in two Mediterranean areas

Environmental and climatic conditions affect the flower bud growth, flowering and yield performance of fruit species. Temperature and water availability appear to be important factors for temperate fruit trees in mild climates. The aim of this research was to study the involvement of temperature regime on biological processes, such as xylem differentiation and dormancy evolution, in apricot flower buds (Prunus armeniaca L.). Over 3 consecutive years, biological and anatomical investigations were carried out in Tuscany (Italy) and Murcia (Spain) on two cultivars characterized by a different chilling requirement (CR): Currot, a traditional Spanish cultivar with a very low CR, and Stark Early Orange (SEO), a North American cultivar with a very high CR. Currot had a regular bearing, and was characterized by a synchronism between endodormancy release and xylem differentiation. On the other hand, SEO showed an irregular flower bud growth leading to flowering and fruit-set failure, even with a high level of chilling accumulation. No relationship was found in SEO between xylem development and flower bud growth reactivation. The de-synchronism between these processes could determine the poor adaptability to different environmental areas of SEO cultivar, and its very high CR is not the main hypothesised cause of the altered flower bud development.     

脱落酸在植物花发育过程中的作用

植物激素脱落酸(ABA)对植物的生长发育具有多方面的调节作用,比如种子休眠、萌发,营养生长,环境胁迫反应等。大量研究显示,ABA也参与了植物的成花调控。影响植物成花调控的环境因子,包括光周期变化、春化作用、干旱等均会导致植物体内ABA代谢的变化。本文从调控植物开花的4条主要途径与植物体内ABA代谢变化之间的相互关系,花芽分化时期ABA在植物叶芽和花芽中的动态分布以及离体培养条件下ABA对花芽分化的影响等方面总结了ABA与植物花发育这一领域的最新研究进展。对ABA在植物成花诱导和花发育中的作用进行了综合分析。     

Shoot bending promotes flower bud formation by miRNA‐mediated regulation in apple (Malus domestica Borkh.)

Flower induction in apple (Malus domestica Borkh.) trees plays an important life cycle role, but young trees produce fewer and inferior quality flower buds. Therefore, shoot bending has become an important cultural practice, significantly promoting the capacity to develop more flower buds during the growing seasons. Additionally, microRNAs (miRNAs) play essential roles in plant growth, flower induction and stress responses. In this study, we identified miRNAs potentially involved in the regulation of bud growth, and flower induction and development, as well as in the response to shoot bending. Of the 195 miRNAs identified, 137 were novel miRNAs. The miRNA expression profiles revealed that the expression levels of 68 and 27 known miRNAs were down‐regulated and up‐regulated, respectively, in response to shoot bending, and that the 31 differentially expressed novel miRNAs between them formed five major clusters. Additionally, a complex regulatory network associated with auxin, cytokinin, abscisic acid (ABA) and gibberellic acid (GA) plays important roles in cell division, bud growth and flower induction, in which related miRNAs and targets mediated regulation. Among them, miR396, 160, 393, and their targets associated with AUX, miR159, 319, 164, and their targets associated with ABA and GA, and flowering‐related miRNAs and genes, regulate bud growth and flower bud formation in response to shoot bending. Meanwhile, the flowering genes had significantly higher expression levels during shoot bending, suggesting that they are involved in this regulatory process. This study provides a framework for the future analysis of miRNAs associated with multiple hormones and their roles in the regulation of bud growth, and flower induction and formation in response to shoot bending in apple trees.     

Pear bud metabolism: seasonal changes in glucose utilization

Utilization of glucose, uracil and valine by flower and leaf buds of seedling pear trees (Pyrus calleryana Decne.) from the time of flower bud initiation to flowering was investigated. A very high rate of glucose utilization through the pentose phosphate pathway was observed throughout the development of buds. There was no difference in the type of glucose metabolism between flower and leaf buds except immediately before flowering, when the metabolism in flower buds was shifted toward the glycolytic pathway. Such a shift did not occur in leaf buds. The incorporation of uracil and valine into the nucleic acid and protein fraction of buds, respectively, was high throughout bud development, perhaps indicating a high rate of turnover in the resting buds. Incorporation of both compounds decreased when buds started to expand prior to flowering.     

Periodicity of response to abscisic acid in lateral buds of willow (Salix viminalis L.)

Aseptically cultured lateral buds of Salix viminalis L. collected from field-grown trees exhibited a clear periodicity in their ability to respond to exogenous abscisic acid (ABA). Buds were kept unopened by ABA only when the plants were dormant or entering dormancy. Short days alone did not induce bud dormancy in potted plants but ABA treatment following exposure to an 8-h photoperiod prevented bud opening although ABA treatment of buds from long-day plants did not. Naturally dormant buds taken from shoots of field-grown trees and cultured in the presence of ABA opened following a chilling treatment. In no cases were the induction and breaking of dormancy and response to ABA correlated with endogenous ABA levels in the buds.Abbreviations ABA abscisic acid - GA₃ gibberellic acid - HPLC high-performance liquid chromatography - LD long day - MeABA methyl ABA - PAR photosynthetically active radiation - SD short day     

The inhibitory effect of gibberellic acid on flowering in Citrus

The application of gibberellic acid (GA₃) at any time from early November until bud sprouting, resulted in a significant inhibition of flowering in the sweet orange [ C. sinensis (L.) Osbeck] and the Satsuma ( C. unshiu Marc.) and Clementine ( C. reticulata Blanco) mandarins. Two response peaks were evident: the first occurred when the application was timed to the translocation of an unknown flowering signal from the leaves to the buds. The second occurred during bud sprouting, at the time the flower primordia were differentiating. From the pattern of flowering, it appears that the mechanism of inhibition was similar irrespective of the timing of GA₃ application. There was an initial reduction in bud sprouting affecting selectively those buds originating leafless inflorescences. An additional inhibition resulted in a reduction in the number of leafy inflorescences with an increase in the number of vegetative shoots, suggesting the reversion of a floral to a vegetative apex. The inhibited buds sprouted readily in vitro but invariably vegetative shoots were formed. A continuous influence of the sustaining branch is necessary to keep the flowering commitment of the buds; irreversible commitment occurs when the petal primordia are well differentiated.     

The effect of photoperiod on flower formation in vitro in a quantitative short-day cultivar of Nicotiana tabacum

Superficial cell layers of a quantitative short-day tobacco plant ( Nicotiana tabacum L. cv. White Burley) were excised from different parts of the inflorescence (i.e. pedicels, branch internodes, rachises), and cultured in continuous darkness, continuous light or 8 h light/16 h dark daily. The flowering response in vitro of the different types of explants was investigated with respect to the effect of light on the post-evocation phases of the flowering process and explant commitment. Treatment effect was qualitatively and quantitatively influenced by explant origin. Three morphogenic features were observed: flower neoformation, caulogenesis and rhizogenesis (the latter on rachis explants only). Under all treatments, the highest flowering potential was shown by pedicels, while the highest vegetative potential was shown by rachises. Branch internodes showed an intermediate response, but with a tendency towards caulogenesis, which probably reflects their phylogenetic origin. Thus, opposite gradients of the neoformation of flowering and vegetative buds on explants were observed under all treatments. Pedicels formed new single flowers rather than inflorescences, while rachises regenerated mainly inflorescences. In darkness, flowering was limited mostly to pedicels. Vegetative bud formation was higher than floral bud regeneration in all types of explant. Continuous light enhanced the flowering response mostly in pedicel and branch internode explants. Short days enhanced flower bud formation in vitro on all types of explant. Results with respect to microsporogenesis, flower and inflorescence anomalies observed under darkness also seem to support the existence of a quantitative photoperiodic control on floral neoformation in vitro in this plant. These results suggest that in Nicotiana tabacum cv. White Burley in vivo floral induction, initiation and development are governed by the same photoperiodic requirements.     

Effect of Photoperiod and Chlorogenic Acid on Morphogenesis in Leaf Discs of Streptocarpus Nobilis

Leaf discs from vegetative plants greatly increase their phenolic content when cultivated in vitro. Under long days the values remained constant, and were higher when compared with short days cultures. Under short days total phenolics decreased after 10 d, corresponding to the induction and expression of in vitro flowering. The effect of photoperiod and chlorogenic acid (0.01 mM) on leaf discs cultured from induced and non-induced plants, were analyzed regarding the neo-formation of roots, as well as vegetative and flower buds. Chlorogenic acid enhances the regeneration of roots in all treatments tested, with the highest stimulation on induced leaf discs cultivated in short days. The flowering was not affected by chlorogenic acid, but an inhibitory effect was observed on the neo-formation of vegetative buds in non-induced explants maintained in short days. Vegetative buds were reduced by 50% in flower-induced leaf discs cultivated under short days.     

几种化学药剂对‘NJ72’油桃休眠解除的影响

在进行果树温室栽培时,经常遇到萌芽率低,萌芽开花延迟,花器官发育差,座果率低的问题。本试验以‘NU72’油桃为试材,观察了3种药剂对解除芽休眠的影响。结果表明,2％（NH2）2CS能提早花期,但存在药害现象,6％KNO3不能提早花期,并且花期不整齐,5％NH4NO3效果与6％KNO3类似。同时化学药剂处理促进花芽内H2O2的积累,抑制了过氧化氢酶（CAT）活性但促进了过氧化物酶（POD）活性,超氧物岐化酶（SOD）活性变化较小,化学药剂使花芽的呼吸速率增加,其中磷酸戊糖途径（PPP）代谢增加,糖酵解（EMP）降低,而三羧酸循环（TCA）代谢波动较小,葡萄糖－6－磷酸脱氢酶（G6PDH）活性在化学药剂处理时也增加。     

几种化学药剂对‘NJ72’油桃休眠解除的影响

在进行果树温室栽培时,经常遇到萌芽率低、萌芽开花延迟、花器官发育差、座果率低的问题。本试验以‘NJ72’油桃为试材,观察了3种药剂对解除芽休眠的影响。结果表明,2%(NH2)2CS能提早花期,但存在药害现象。6% KNO3不能提早花期,并且花期不整齐,5% NH4NO3效果与6%KNO3类似。同时化学药剂处理促进花芽内H2O2的积累,抑制了过氧化氢酶(CAT)活性但促进了过氧化物酶(POD)活性,超氧物岐化酶(SOD)活性变化较小。化学药剂处理使花芽的呼吸速率增加,其中磷酸戊糖途径(PPP)代谢增加,糖酵解(EMP)降低,而三羧酸循环(TCA)代谢波动较小。葡萄糖_6_磷酸脱氢酶(G6PDH)活性在化学药剂处理时也增加。     

剥鳞和激素处理对大樱桃花芽休眠解除及内源激素变化的影响

采用高效液相色谱法(HPLC)分析了剥鳞与激素处理对大樱桃花芽休眠解除及内源生长素(IAA)、赤霉素(GAD、玉米素(ZT)和脱落酸(ABA)变化的影响。结果表明,花芽中的ABA主要分布于鳞片内,鳞片中的GA3和ZT含量远低于去鳞芽,也低于完整芽。剥鳞能明显增加休眠花芽中内源GA2和ZT的含量,降低ABA的含量,对IAA含量的影响不大。剥鳞降低了ABA／GA3、ABA／ZT的比值,使花芽向促进生长、抑制休眠的方向转化。同时,休眠前、后期剥鳞均能明显提高萌芽率,中期剥鳞效果不明显。剥鳞后施用外源激素随休眠时期不同而有不同的破眠效果,早期剥鳞GA3的效果最好,6-BA次之,IAA最差;中期破眠效果不如早期,GA。和6-BA没有明显差别;后期以6-BA效果最好,其次是GA3和IAA;3次处理中ABA均明显抑制花芽萌发。