‘西伯利亚’百合花香随开花进程变化及日变化规律

 采用动态顶空套袋-吸附技术,采集东方百合‘西伯利亚’不同花期和一天不同时间点释 放的花香,并利用自动热脱附-气质联用（ATD–GC/MS）技术分析花香成分和释放量。结果表明：‘西 伯利亚’百合花香成分主要包括萜烯类、醇类、醛类、酮类、酯类、芳香族类和烷烃类7 大类;其释放 量和化合物数量在初开期较少,半开期逐渐增加,盛开期最高,衰败期急剧下降。在4 个时期分别检测 出12、46、55 和20 种成分,其中萜烯类化合物最多,释放量最大;在一天当中其释放量和化合物数量从 早到晚同样表现出先增加后减少的变化,15：00-16：00 时间段总释放量最高,成分最多,而在7：00- 8：00 和19：00-20：00 这两个时间段成分及释放量明显减少;从7：00 到20：00 的7 个时间段释放的 花香中分别检测出27、42、51、57、45、40 和16 种化合物,萜烯类化合物最多,释放量最大。花香成 分中含量最高的芳樟醇、β–罗勒烯和β–月桂烯等萜烯类化合物可能是‘西伯利亚’百合花香的主要致 香成分,而光强的变化是引起‘西伯利亚’百合花香日变化的重要原因。     

Early flower initiation allows ample manipulation of flowering time in cherimoya (Annona cherimola Mill.)

Flower initiation date and readiness to flowering in buds of different age were studied in ‘Fino de Jete’ cherimoya (Annona cherimola) cultivar in order to establish the limits for the manipulation of its flowering date. Flower initiation was analyzed by light and scanning electron microscopy (SEM) collecting axillary buds from May to the following February, whereas the bud readiness to produce perfect flowers was determined by forcing buds of different age to sprout by means of leaf removal and tipping the new growth. SEM images confirm that cherimoya buds are differentiated into flowers almost a year before blooming. In this regard, axillary buds have already formed the sepals when the subtending leaf has just begun unfolding (week 0), while the petals are clearly visible in 1-week-old buds. Sectioning of paraffin-embedded buds illustrate that cherimoya buds are in fact a bud complex that 1 week after its inception comprises 4–5 buds of different size of which the two largest ones are reproductive, while the 2–3 smallest buds often remain undifferentiated at that time. The high capacity of flowering expressed by young buds that have been forced to grow proves that cherimoya meristems are early competent for flowering. No differences in fertility or in the time needed to reach anthesis after leaf removal were found among buds of different ages. Node position had no effect on bud break and flowering potential. The early flower initiation in cherimoya deduced from this work opens a wide temporal window for the experimental manipulation of flowering and harvest dates in this crop.     

Deferring flowering of nobile dendrobium hybrids by holding plants under low temperature after vernalization

Orchids are currently the most valuable potted crop in the United States. To date, no studies focused on making possible the year-round greenhouse production of flowering nobile dendrobium orchids. This experiment was aimed at developing a strategy to defer flowering of nobile dendrobium orchids by holding them under low temperature. Mature Den. Red Emperor ‘Prince’ and Den. Sea Mary ‘Snow King’ were held at 10 °C for various durations (0, 4, 8, 12 or 16 weeks) after vernalization (4 weeks at 10 °C). Plants were forced in a greenhouse after holding. Time to flower, flower differentiation (flowering node percentage, number of aerial shoot and aborted bud) and flower quality (total flower number, flower diameter, flower number per flowering node and flower longevity) were determined. Increase of low temperature holding duration from 0 to 16 weeks extended time to flower up to 3 months and did not affect parameters of flower except producing larger flowers and reducing flower number per flowering node for Den. Red Emperor ‘Prince’. Notably, the flower longevity was not adversely affected. Defoliation was aggravated in Den. Red Emperor ‘Prince’ by longer duration of cooling and was considered a detrimental effect of low temperature holding.     

贮藏温度对黄瓜花粉活力的影响

研究了不同贮藏温度对黄瓜新鲜雄花和花蕾花粉活力的影响。结果表明:5～25℃范围内,随着贮藏温度的降低黄瓜花粉寿命延长,5、10、15℃分别较常温(25℃)的花粉寿命长60、44、34h;低温贮藏花蕾能有效地延长花粉寿命,以在傍晚(约18:00)采摘第2天将开放的大花蕾为贮藏材料较好;5℃低温下花粉活力持续时间最长,但因低温不利于雄花开放和散粉,所以在授粉前将5℃低温贮藏的花蕾放在常温(25℃)下1～2h以加速雄花的开放和散粉。     

Promotion of Globularia sarcophylla flowering by Uniconazol,an inhibitor of gibberellin biosynthesis

Globularia sarcophylla, originating from the Canary Islands, was recently introduced as a new cut flower in Israel. Two major problems have prevented its commercialization: the late-summer blooming and the low quality of its flowering shoots. In the present work we studied the factors affecting G. sarcophylla flowering. We found that long-day (LD) conditions slightly promote flowering but artificial photoperiodic illumination does not enable the manipulation of flowering time. On the other hand, treatment with the gibberellin (GA)-biosynthesis inhibitor, Uniconazol, had a dramatic promotive effect on flowering time. Application of Uniconazol in autumn or winter induced flowering in winter or early spring, respectively. The inhibitor did not advance flowering during the summer or in the phytotron under high temperatures. When plants were grown in the spring/summer under heavy shading, they did not flower unless they were treated with Uniconazol. Uniconazol treatment also improved flower quality by reducing the length of inflorescence pedicles. This effect was found in all seasons. Based on our results, we raise the hypothesis that Uniconazol treatment induces flowering by diverting assimilates to the apex. Inhibition of GA biosynthesis under conditions limiting photosynthetic activity reduces vegetative growth and increases the availability of assimilates to the apex, leading to flower initiation. However, under high irradiance and/or high temperatures, when the levels of assimilates are sufficient to induce natural flowering, the inhibitor has no further effect.     

Effect of photoperiod and light integral on flowering and growth of Eustoma grandiflorum (Raf.) Shinn.

The aim of the study was to examine the effects of different photoperiod and light integral on floral initiation, development and subsequent growth of Eustoma grandiflorum (Raf.) Shinn. Six-weeks-old seedlings of ‘Echo Blue’ and ‘Fuji Deep Blue’ were placed under short day (SD, 10 h) and were transferred to long days (LD, 20 h) at 2-week intervals from 6 to 14 weeks after seeding. Plants initiated flower buds regardless of light regimes. Flower bud initiation was delayed by SD compared to LD; plants transferred after 6 weeks from seeding initiated flower buds at least 21 and 10 days earlier at LD at high (HL) and low (LL) daily light integral, respectively, compared to those at SD. Light regimes had little or no effect on time to flower bud development after initiation. Thus, it seems likely that LD and HL affected the initiation rather than development. Both the photoperiod and light integral strongly influenced the subsequent growth after initiation. SD delayed the time to visible bud (VB), increased the number of nodes to first open flower, number of branches, stem diameter and shoot dry weight compared to LD. HL promoted flowering and increased several shoot characteristics and flowering compared to LL.The results indicate that Eustoma is a quantitative long-day plant. LD, and more specifically HL, enhanced flower bud initiation, development and subsequent growth. An initial SD period is preferred to increase the number of branches, number of flowering buds and flowers, stem diameter and shoot dry weight.     

The effect of various environmental factors on flowering of gladiolus. I. Light intensity

Light intensity is an important factor affecting the flowering of Gladiolus. Insufficient illumination from sprouting to the 4-leaf stage decreased flowering percentage. However, the inflorescences of those plants which did flower under conditions of low light intensity were normal and developed the full number of florets per spike. Plants at the 4–6 leaf stage were most sensitive to prevailing light conditions. Low light intensity during this period decreased both the percentage of flowering and the number of florets per spike. After this stage only the number of florets per spike was affected by insufficient light.     

Observations on the Varietal Resistance of the Apple to Scab (Venturia Inaequalis,Aderh.) with Special Reference to its Physiological Aspects.

Summary

A biologically based phenology model is proposed to simulate the flowering of the female kiwifruit `Hayward'. The heart of the model is a phenological sub-model describing the distribution of buds and flowers between several phenological stages. It is based on the model of Dennis et al. (1986) with temperature as driving variable, assuming that the development of a flower bud is a stochastic process consisting in accumulated small increments of development time, expressed in degree-hours. Another sub-model integrates quantitative elementary components which allows the simulation of the number of flowers. The model parameters have been estimated for the female cv. Hayward and have been fitted on a data set from 1991. Validation has been done on data sets from 1990 and 1992. Under the climatic conditions of Corsica, this model gives a good representation of the variability of delay in and intensity of flowering, and it fits well to the distribution of canes for flower number.     

The effect of temperature and light on flower development in Pelargonium × domesticum

Factors influencing the number of flowers produced in Pelargonium × domesticum cultivar ‘Lavender Grand Slam’, and their rate of development after the plants had been given a period of low-temperature flower induction, were studied.Under short days progressive abortion reduced flower numbers as the temperature regime during the forcing-period was increased. Under long days this effect was less marked and the high-temperature regime advanced flowering by over a month. When long days and high temperatures were used for forcing, it was necessary to maintain a high light intensity, 335 J/cm²/day giving the best results in terms of earliness of flowering and the number of flowers produced. At lower irradiance there was some risk of flower abortion, particularly in the first inflorescence.     

Identification of differentially expressed genes in fragrant rose Jinyindao with suppressive subtraction hybridization

To investigate the floral fragrance new genes, scent mutant of rose was used here. The suppressive subtraction hybridization (SSH) technique and micoarray analysis of the clones were used to isolate the cDNA fragments, which showed differential expression between the rose scent mutant ‘Wangriqinghuai’ and wild type ‘Jinyindao’ (Rosa × hybrida), and RT-PCR was used to identify up-regulated expressed genes. 16 positive contigs of JSSH were obtained. Some ESTs such as RcOMT1, RcOMT2, RhMYB92 and RhGP1 were known to regulate scent metabolism, and 5 ESTs with no homology in NCBI may represent new genes involved in rose flower fragrance metabolism. SSH technique combined with cDNA micoarray would be useful for analysis and isolation of the genes related to rose floral scent.     

Temperature and photoperiod control of morphology and flowering time in two greenhouse grown Hydrangea macrophylla cultivars

Knowledge of the factors involved, and tools to control morphology and flowering are important in intensive and cost-efficient greenhouse production. Hydrangea macrophylla is an important flowering pot plant in Norway and is produced year-around in greenhouses. Due to problems in scheduling, a study was conducted to compare floral transition and morphology of two commercially important cultivars of Hydrangea (‘Early Blue’ and ‘Schneeball’) under different flower initiating treatments in growth chambers. Plants were grown with high pressure sodium lamps (HPS) at moderate temperature (17 °C) (MT) and high (24 °C) temperature. At high temperature, the effect of (1) irradiance under long day conditions (16 h lighting with 70 or 200 μmol m⁻² s⁻¹), and (2) short day (8 h lighting) was investigated. The short day treatment had similar light integral as the low irradiance long day treatment (SD: 8 h × 140 μmol m⁻² s⁻¹ and LD: 16 h × 70 μmol m⁻² s⁻¹ = 4.0 mol m⁻² d⁻¹). The intention was to test the effect of irradiance and SD on flower transition and morphology under high temperatures. The results clearly showed that MT is the strongest signal for floral transition. MT resulted in a rapid floral transition of the terminal buds and lateral flower buds. A short forcing period was required and the plants became short and compact without any use of chemical growth retardants. At high temperatures only SD had a promotive effect on flower transition and the response was found to be stronger in ‘Schneeball’ than ‘Early Blue’. In general, all the treatments under high temperatures required a long forcing time and the plants tended to be very tall with a low number of lateral flower buds.     

Flowering and changes in respiration in Asiatic hybrid lilies as influenced by bulb vernalization

Asiatic hybrid lilies, Lilium × elegans Thunb., ‘Red Carpet’ and ‘Sunray’ were used to investigate the effect of bulb vernalization at 2.5 °C on plant growth, flowering, and CO₂ production (respiration), and to use the CO₂ production pattern to monitor the time of flower bud initiation and development. Lily shoot emergence and flowering were accelerated when bulbs received 2.5 °C bulb vernalization; however, flowering was delayed when bulbs were stored at 20 °C before treatment at 2.5 °C; this indicated that bulbs were de-vernalized. The maximum CO₂ level, and the minimum level, reached in 78 h in non-vernalized bulbs and in 110 h in 6 weeks of 2.5 °C (6 weeks/2.5 °C) treated bulbs, was increased as the 2.5 °C duration was increased; this indicated that CO₂ level can be an useful parameter to measure the cold stimulus (i) accumulated in bulbs following bulb vernalization. The respiration rate higher than the predicted values of the best-fit curves derived from the quadratic equations was designated as Blip A and this was correlated to the time of flower bud initiation and development. Shoot elongation may follow the rise in carbon dioxide levels after reaching the minimum level. It is proposed that increased carbon dioxide levels higher than the predicted levels (Blip A), was correlated to the time of flower bud initiation and development. Measurement of carbon dioxide production upon receipt of bulbs may be a useful technique to provide important information for optimum vernalization treatments for bulbs that have accumulated different levels of low temperature stimulus after bulb vernalization.     

Flowering induction of Guzmania by ethylene

Ethylene exposure time required to induce flowering of Guzmania lingulata Mez. ‘Anita’ was investigated by exposing plants to ethylene at 100 μl l⁻¹ for 4, 6, 8, 10, 12, 16, or 24 h. Plants were also exposed to ethylene-free air for the same lengths of time. Plants exposed to ethylene for 4 h did not flower, but exposure for 6 h or longer resulted in 100% flowering. Suppression of endogenous ethylene synthesis by aminoethoxyvinylglycine (AVG) resulted in a longer exposure time of 20 h being required to obtain 100% flowering. This result suggests that endogenous ethylene production contributes substantially to floral induction. Ethylene treatment on a single young leaf induced flowering as well. Application of a protein synthesis inhibitor, cycloheximide, prevented flowering induced by ethylene, indicating that activation of ethylene responsive genes is followed by synthesis of new proteins involved in flowering.     

Environmental factors affecting flowering of rice flower (Ozothamnus diosmifolius,Vent.)

Rice flower (Ozothamnus diosmifolius, Vent.), native to east Australia, is a spring flowering perennial shrub. It is a new cut flower plant, recently introduced into cultivation in Australia and in Israel. Its response to environmental conditions, which affect growth and flowering, are not yet known. The purpose of the present study was to evaluate the effects of growth temperature, photoperiod and total solar energy on flowering. Experiments were conducted with plants of the cv. Cook’s Snow White. Plants were grown in three cycles under controlled conditions in the phytotron, at four day/night temperature regimes: 17/9, 20/12, 23/15 and 26/18°C. Two photoperiods — short day (SD) of 10 h natural day light and long day (LD) of 10 h natural light plus 10 h incandescent light — were employed. High temperatures enhanced vegetative growth but blocked flowering under both LD and SD. Under medium–moderate temperatures plants were absolute LD plants and did not flower under SD conditions. Under lower temperatures plants flowered under both LD and SD, but SD delayed flowering. High total solar radiation under LD did not affect flowering time but greatly promoted the number of flowering stems.     

桂花不同品种开花过程中香气活性物质的变化

以12个桂花品种盛花期的花瓣为材料,用气质联用法检测到59种挥发物,其中占主导地位的是萜烯类化合物。选择相对含量均高于0.05%的21种挥发性物质进行主成分分析,12个桂花品种可分成3类,花色为黄色或金黄色的金桂和四季桂(6个品种)为一类,花色为白色或浅黄色的银桂(3个品种)为一类,花色为橙色或红色的丹桂(3个品种)为一类。黄色桂花中以‘柳叶金桂’香气活性物质贡献率最高,达56.75%;白色桂花中以‘厚瓣银桂’贡献率最高,达51.91%;橙色桂花中以‘镉橙丹桂’贡献率最高,达58.88%。以此3个品种为代表材料,用气相色谱—嗅闻技术测定了其开放过程中香气活性物质的变化。结果表明,3个品种在铃梗期都以释放具有罗兰香/木香/果香型的物质为主。初花期到盛花期,橙色花的‘镉橙丹桂’以释放花香型物质为主,白黄色花的‘厚瓣银桂’以释放香草香型物质为主,黄色花的‘柳叶金桂’以释放紫罗兰香/木香/果香型物质为主;到了末花期,‘镉橙丹桂’与‘柳叶金桂’中都是青草香/清新香型的物质占主导地位,而‘厚瓣银桂’中依然是香草香型物质居多,这可能是银桂香气更持久的原因。     

Interaction of photoperiod and temperature in flowering-control of Gypsophila paniculata L

Long day promotes flowering of Gysophila paniculata L cultivar ‘Bristol Fairy’. Repeated treatments with GA₃ or GA_{4 + 7} in short days did not promote flowering. The long photoperiod is effective only at relatively high temperatures. At night temperatures below 12°C, the plants remain vegetative even in long days. Efficient artificial lighting is from incandescent lamps at 60–100 lux. Fluorescent lighting (Cool-White) is not effective. Lighting of 4 hours as a night-break or at the end of the night were equally effective, but 4 hours lighting as a day-extension was less effective. Whole-night lighting promoted flowering more than any of the 4-hour lighting regimes. Cyclic lighting of one third light in each cycle promoted flowering to the same extent as continuous lighting. Light intensity during the day has a decisive effect on flower production.     

Quantitative trait loci analysis of flowering-time-related traits in tomato

The regulation of flowering time has been studied mainly in photoperiod-sensitive model plants. Little is known about the environmental and genetic regulation of flowering time in photoperiod-insensitive plants. Here, we studied the genetic control of flowering time in day-neutral tomato using quantitative trait locus (QTL) analysis. We used a BC₁F₆ population developed from Solanum lycopersicum ‘M570018’ and its wild relative Solanum pimpinellifolium (PI124039) to measure days to flowering (DTF) and number of leaves preceding the first inflorescence (LN), as well as their underlying developmental processes, which include the number of leaves initiated (LI), percentage of flower-induced plants (reproductive index, RI), days to macroscopic flower bud appearance (DMB) and flower development duration (FDD: DTF − DMB). A composite interval mapping detected 12 QTLs for the six traits, which included two QTLs for DTF on chromosomes 1 and 6. The DTF QTLs explained 43% of the phenotypic variation of this trait. The presence of S. pimpinellifolium alleles in the detected QTLs increased the rate of leaf initiation, reduced LN and hastened flower induction, floral development and anthesis. Most QTLs for LN, LI, RI, DMB and FDD clustered with the DTF QTLs; dmb1, fdd1, li_14d1, li_19d1 and ri_19d1 clustered with dtf1 on chromosome 1, and ln6 and fdd6 clustered with dtf6 on chromosome 6. These results suggest that the QTLs on chromosomes 1 and 6 may form a functional “gene cluster” that drives tomato flowering in synergy. Alternatively, the two DTF QTLs may act as “master genes” that control flowering time through pleiotropic effects on multiple developmental processes.     

Diversity in environmental controls of flowering in Australian plants

In adapting their flowering to a particular season of the year, plants utilize a number of environmental inputs. Knowledge of these environmental controls of flowering is important for production in commercial horticulture. Such information is also relevant for assessing whether or not a species is threatened by global warming. Here, for five Australian plant species, we document ways in which the environment regulates their flowering. Spring flowering of Croweaexalata ‘Bindelong Compact’ reflects a response to increased daily light integral, these plants showing no hint of a true long day photoperiodic response. Higher temperatures not only cause earlier flowering of this Crowea cultivar but also depress flower production (5% loss per 1 °C increase). By contrast, another Crowea, ‘White Star’, flowers only if exposed to cool temperatures (15 °C) at the time of the increase in daily light integral. Thus, in commercial horticulture, synchronous and rapid flowering of Crowea will be possible by shifting plants from shade to high light conditions. In nature, light intensity will also have a major impact on flowering. By contrast, best flowering of Lechenaultia formosa in spring is a response to short photoperiods at high temperature while L. biloba prefers long days and has potentially spring to summer flowering. Whereas rising summer temperatures could have a deleterious effect on flowering of C.exalata, global warming may have little impact on L. formosa and L. biloba which flower more profusely in warmer conditions. Another spring flowering species, Verticordia chrysantha, responds both to short days and to exposure to cool temperatures so its survival could be threatened by global warming. For Calytrix fraseri its late summer flowering in nature is explained by its requirement for an exposure to long days. When combined with information previously published for Australian plants, it is clear that there are no simple generalizations to explain why a plant species flowers when it does.     

Chilling requirements of Paeonia cultivars

Dormant second year potted plants of Paeonia ‘Coral Sunset’, ‘Monsieur Jules Elie’, and ‘Sarah Bernhardt’ were placed into three chilling regimes (constant 1, 4, or 7°C) for different durations (3, 6, 9, or 12 weeks) to ascertain their chilling requirements for shoot and flower production. Chilling was followed by forcing for up to 5 weeks at 18°C, then plants were maintained in a controlled greenhouse until flowering had finished. Mean number of shoots and flowers per plant were recorded and the time taken for shoots to sprout was calculated.Control plants (forced immediately without chilling) produced no shoots or flowers. For all cultivars, the proportion of plants that sprouted, and the mean number of shoots and flowers increased as plants were subjected to colder chilling temperatures, or longer chilling durations. However, there were no significant within-cultivar differences between different treatments of 9 weeks or more. The time taken for sprouting to occur after the completion of each chilling treatment consistently decreased as the duration of the chilling treatment increased. In most cases, lower chilling temperatures lead to more rapid sprouting once plants were placed in the 18°C forcing conditions.When a simple model was fitted where the chilling temperature and duration of each treatment was described by a cumulative normal curve rising from zero to some maximum value (or potential) once adequate chilling had been received, we found that temperatures of 4 and 7°C provided only 83 and 59%, respectively, of the chilling accumulated per unit time at 1°C. ‘Coral Sunset’, an interspecific hybrid early flowering type, required the greatest amount of chilling to sprout consistently, while ‘Sarah Bernhardt’, a very late flowering type, required the least. Of the three cultivars, ‘Sarah Bernhardt’ also required the least amount of chilling to achieve its potential shoot and flower numbers, while ‘Monsieur Jules Elie’, a mid-season flowering type, required the most chilling to achieve the same end for these two variables. This suggests that the response to spring temperatures as well as chilling influences the time of flowering.     

Physiological and biochemical studies during flower development in two rose species

The present investigation was aimed to study the changes in various physio-chemical attributes in petals of two different rose species, Rosa damascena Mill and Rosa bourboniana Desport differing in flowering behaviour from small bud (stage 1) till full bloom (stage 8). In both rose species fresh weight, dry weight and moisture content were maximum during full bloom. Electrical conductivity of the petal diffusates reached maximum at full bloom with significantly higher values in R. damascena. In both the species, starch content declined as the flower reached its full bloom stage with maximum reducing sugar content during this period. With progressive increase in petal growth, total protein and RNA declined. The results showed that in both the species peroxidase (POX) and catalase (CAT) activity were lower during full bloom with high activity of invertase and lipoxygenase (LOX) at this period. The present study indicates that lipid peroxidation induced membrane permeability could partly be the result of higher lipoxygenase activity during full bloom. The possible significance of these findings is discussed in relation to flower development in the two diverse rose species.