The effect of day length,source of light and growth regulators on growth and flowering of Clerodendrum thomsonae Balf

The formation of flower buds in Clerodendrum seems not to be affected by day length, but the development of the buds is delayed in long days. When long days were established by means of low-intensity illumination with incandescent lamps, few flowers developed and the stems elongated considerably even at a day length of 16 hours. When fluorescent lamps were used for day-length extension, short shoots with many flowers were obtained even in 24-hour days. Flower development was also delayed by gibberellic acid (GA₃), but promoted by chlormequat both in short and long days. Shoot elongation was retarded by chlormequat and promoted by GA₃.Plants obtained from commercial greenhouses varied considerably with respect to growth and flowering. By selection a clone was obtained which flowered richly on short shoots. Shoot elongation stopped when flowering began. A ‘negative’ selection gave rise to a clone which flowered sparsely and in which shoot elongation was not influenced by flowering.     

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.     

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.     

Environmental and chemical control of growth and flowering of Chamelaucium uncinatum Schauer

The main factor affecting floral initiation of Geraldton Wax-Flower (Chamelaucium uncinatum) is the photoperiod, while temperature is the major factor affecting flower development. Four weeks of short days (SD) are generally required for obtaining full flowering. The number of flowers produced per plant increases with increasing the number of SD. Under mild temperatures of $\text{20}\text{14°}\text{C}$ (day/night), plants initiated flowers even in long days (LD). However, fewer flowers were produced and on higher nodes as compared to SD plants. Chlormequat promoted flowering under prevailing summer conditions of high temperatures and LD. Under prevailing autumn conditions favourable for flower initiation, LD treatment or weekly sprays with gibberellic acid (GA) reduced the number of flowers per plant. Combined treatment of LD and GA reduced both the flowering percentage and the number of flowers per plant. Discontinuing the LD or the GA treatments caused a resumption of full flower initiation.     

The impact of photoperiod and irradiance on flowering of several herbaceous ornamentals

Forty-one herbaceous species were grown under short-days (8 h photoperiod, ambient irradiance averaged 12–13.2 and 6.4–8.3 mol m⁻² day⁻¹ for Experiments I and II, respectively) with or without supplemental high-pressure sodium lighting (+50, 100, or 150 μmol m⁻² s⁻¹); or under long-days delivered using natural day lengths and irradiance with night interruption lighting (2200–0200 h at 2 μmol m⁻² s⁻¹ from incandescent lamps) or under ambient daylight plus supplemental irradiance during the day and as a day extension to 18 h (0800–0200 h) with supplemental high pressure sodium lighting (+50, 100, or 150 μmol m⁻² s⁻¹) to identify the impact of photoperiod and irradiance on flowering of each species. Days to first open flower, leaf number below first flower, and mean dry weight gain per day (MDWG) were measured when the first flower opened. Twenty-seven species were photoperiodic with examples of five photoperiodic response groups represented: obligate short-day (2), facultative short-day (5), obligate long-day (16), facultative long-day (4); 13 were day neutral (no photoperiod response in flowering). One species, Salvia sclarea L., did not flower. A facultative irradiance response was observed with 10 species; 28 species were irradiance indifferent; 2 had delayed flowering as irradiance increased. Photoperiod affected MDWG of 30 species. Increasing irradiance affected MDWG with 14 species. Photoperiod interacted with irradiance to affect MDWG of 11 species. Cobaea scandens had the greatest MDWG (0.40 g day⁻¹) while Amaranthus hybridus had the least MDWG (0.01 g day⁻¹) across photoperiod and irradiance levels.     

Growth of Rhododendron cultivars as affected by temperature and light

Summary

The purpose of this study was to investigate the adaptation of four Rhododendron cultivars to contrasting light and temperature conditions. Two evergreen rhododendron cultivars and two deciduous azaleas were grown for 112 d under short day (14 h) and long day (20 h) photoperiods combined with temperatures of 15 and 24°C. Additionally, these cultivars were compared for daylength extension at 24°C/long day under two irradiation treatments (incandescent lamps and fluorescent tubular lamps). The number of flushes of growth increased with increasing photoperiod and temperature in both evergreen cultivars and in R. canadense; azalea #89132 made only one flush in all treatments. In the evergreen cultivars the number of leaves per shoot in the first flush did not differ significantly between treatments, indicating that this character was predetermined by conditions during bud development. The number of leaves in later flushes increased with increasing photoperiod and temperature. The elongation growth of most flushes was also enhanced by longer photoperiod and higher temperature. High irradiation during photoperiodic extension further enhanced the growth. Azalea #89132 made more flower buds under high than low irradiation. The two evergreen cultivars differed in their growth habit. ‘Pohjola’s Daughter’ tended to continue growth in long days or at very high temperatures, and is thus predicted to thrive best in a maritime or semi-maritime cool climate. ‘Helsinki University’ responded to short daylength by ceasing growth regardless of temperature, and could be expected to perform successfully also in continental climates at latitudes around 45° N. R. canadense seemed to do best in a cool climate, but azalea #89132 should in time acclimatize in all kinds of climates within the limits of this study.     

Influences of day and night temperatures on flowering of Fragaria x ananassa Duch., cvs. Korona and Elsanta,at different photoperiods

The effects of photoperiod (12, 13, 14, 15 or 16 h), day temperature (12, 15, 18, 24 or 27 °C) and night temperature (6, 9 or 12 °C) and their interactions on flower and inflorescence emergence were investigated by exposing 4 week old runner plants of strawberry cvs. Korona and Elsanta during a period of 3 weeks. A daily photoperiod of 12 or 13 h resulted in the highest number of plants with emerged flowers. A photoperiod of 14 h or more strongly reduced this number, while no flowers emerged at a photoperiod of 16 h. Plants exposed to photoperiods of 12 or 13 h flowered earlier and had longer flower trusses. A day temperature of 18 °C and/or a night temperature of 12 °C were optimal for plants to emerge flowers and resulted in the shortest time to flowering. A night temperature of 6 °C strongly reduced the number of plants that emerged flowers, especially when combined with lower day temperatures. Photoperiod and temperature had no effect on the number of inflorescences, all flowering plants produced on average one inflorescence. The number of flowers on the inflorescence increased with decreasing day temperature and when photoperiod was raised from 12 to 15 h. In general, ‘Korona’ was more sensitive to photoperiod and temperature as ‘Elsanta’, and had a lower optimal day temperature for flower emergence. Results of this experiment may be used to produce high quality plant material or to define optimal conditions when combining flower induction and fruit production.     

‘秀丽’蒲包花光周期反应特性的研究

 采用迁光试验研究长日照植物蒲包花‘秀丽’的限界性诱导光周期,不同发育阶段对光周期的敏感性和光周期处理对盆花品质的影响,并推测了童期长度。连续短日照和经7 d长日照后移至短日照的蒲包花,从处理到开花的天数显著长于长日照14 ~ 42 d后移至短日照的处理,而14 ~ 42 d长日照转移的处理之间差异不显著,表明14 d的长日照处理足以促进蒲包花开花,其限界性诱导光周期在7 ~ 14 d之间,长日照14 d以后蒲包花的花芽发育对光周期不敏感。长日照7 d后转到短日照,从处理到现蕾的天数减少而从现蕾到开花的天数增加,顶花芽败育,侧芽萌发开花,表明长日照7 d促进了花芽分化,但此时花芽发育对光周期仍敏感。本试验条件下,生长至3对叶片时蒲包花已结束童期。长日照促进株高和主枝长度的增加,21 d长日照后转移到短日照的处理,株高、主枝长度显著大于14 d时转移的处理,开花整齐,盆花品质显著提高。长日照转到短日照时,地上部鲜质量、根鲜质量、总质量均随着迁光天数的延迟而下降;短日照转到长日照时则相反。9月上旬播种育苗,在3对叶片时开始长日照处理21 d,蒲包花‘秀丽’可在1月上旬始花,保证春节上市。     

Variation among Kalanchoe species in their flowering responses to photoperiod and short-day cycle number

Summary

Our objectives were to identify the critical daylength and number of short-day (SD) cycles necessary for flowering in Kalanchoe glaucescens, K. manginii, and K. uniflora. In Experiment I, plants were grown for 20 weeks under 9, 10, 11, 12, 13, 14, or 15 h photoperiods at 300 µmol m^–2 s^–1 for 8 h 55 min (9 h photoperiod), or 9 h and extended with dayextension (3 µmol m^–2 s^–1) lighting (10 – 15 h photoperiods). All species flowered when grown under photoperiods ranging from 9 – 12 h. The percentage of flowering plants decreased for all species as the photoperiod increased from 12 h to 14 h. No flowering occurred on plants grown under a 15 h photoperiod. Node numbers below the terminal inflorescence increased from 18 nodes to 28 nodes on K. glaucescens, from 12 nodes to 14 nodes on K. manginii, and from 12 nodes to 16 nodes on K. uniflora as the photoperiod increased from 12 h to 14 h, from 10 h to 12 h, and from

12 h to 13 h, respectively. Total flower numbers on K. uniflora decreased from 45 flowers to 13 flowers as the photoperiod increased from 9 h to 13 h. In Experiment II, plants were exposed to 0, 1, 2, 3, 4, 5, 6, 7, or 8 weeks of SD (8 h photoperiod) before being placed under night-interruption lighting (2 µmol m^–2 s^–1; between 22.00 – 0.200 h). One-hundred percent of K. glaucescens, K. manginii, and K. uniflora plants flowered when they received more than 1, 3, or 6 weeks of SD, respectively. The node number below the terminal inflorescence in each species was not affected by SD cycle-number. Total flower numbers per plant, and days to first open flower, were unaffected as the number of SD cycles exceeded the number required to induce flowering for all species.     

Effects of supplementary light to mother plants on adventitious shoot formation in flower peduncle segments of Begonia × hiemalis Fotsch in vitro

Plants of two Begonia × hiemalis cultivars (‘Schwabenland’ and ‘Nixe’) were grown in a greenhouse and continuously illuminated (24 h a day) from late October to early March, with light from warm white fluorescent lamps (L“WW”), high pressure mercury lamps (HPI/T) or high pressure sodium lamps (SON/T), each at three irradiance levels (5, 10 or 15 W m^?2). The control received light continuously (0.8 W m^?2) from incandescent lamps (INC). Every third week, plant material (flower peduncles) was collected for in vitro culture. The adventitious shoot formation was strongly dependent on cultivar, length of mother plant illumination and light source. The use of L“WW”, HPI/T or SON/T improved the regeneration ability of flower peduncle segments compared to control. Prolonged irradiation lowered the regeneration in ‘Schwabenland’, especially when HPI/T lamps were used.     

Effect of light wavelength on growth and flowering of narcissi forced under short-day and low quantum irradiance conditions

Summary

Four narcissus cultivars were forced under artificial light using fluorescent lamps which emitted white (307 – 770 nm), blue (393 – 580 nm), red (540 – 760 nm), yellow (450 – 750 nm), or green (387 – 680 nm) light. The photosynthetic photon flux density was 12.5 μmol m^–2 s^–1, with a 6 h photoperiod. Light colour (wavelength) had no significant effect on flowering date, or on the number of flowers collected (P < 0.05). Narcissus bulbs exposed to blue light (393 – 580 nm) formed shorter, more rigid shoots of lower weight with 13 – 40% shorter leaves.     

Vernalization promotes flowering of a heat tolerant Calandrinia while long days replace vernalization for early flowering of Brunonia

The flowering responses of Brunonia australis (blue pincushion) and Calandrinia sp. to vernalization, photoperiod, temperature and plant age were investigated to provide a foundation for manipulating flowering in these potential potted plants. Plants were vernalized at 4.8 °C for 0, 3 or 6 weeks at the plant age of 1–4 or 8–14 leaves. Following vernalization, plants were grown at 25/10 or 35/20 °C (day/night) under short days (11 h, ambient daylight averaged 380 ± 44 μmol m⁻² s⁻¹) or long days (16 h) provided by an additional 5 h night break (21:00–2:00 h at <4.5 μmol m⁻² s⁻¹ from incandescent lamps), for 85 days. This is the first work to investigate flowering of these ornamental species. Both species showed enhanced flowering following vernalization and a quantitative requirement for long days. The reduction of the time until the first visible inflorescence (Brunonia) or flower (Calandrinia) buds by 8–13 days was affected by vernalization for 3 or 6 weeks, respectively. Long days were effective for reducing the time to first visible floral bud and increasing the number of inflorescence or flowers per plant for both species. For Brunonia, LDs replaced vernalization when applied to plants with 1–4 leaves. Raising temperature from 25/10 to 35/20 °C increased the number of flowers per plant of Calandrinia by 2–2.5-fold for plants with 1–4 or 8–14 leaves respectively.     

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.     

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.     

Effect of day and night temperatures during short photoperiods on growth and flowering of Chrysanthemum morifolium Ramat

The effect of day and night temperatures of 10, 14 and 18°C on growth and flowering under short days was studied with six cultivais of chrysanthemum. A high day temperature resulted in earlier flowering and taller stems, but did not influence flower number and final total fresh weight, and only slightly influenced the distribution of fresh matter over stem, leaves and flowers. A high night temperature resulted in earlier flowering, more flowers and reduced stem and leaf weight. It did not affect leaf number and it influenced height and total fresh weight only slightly. Except for height, the day temperature acted independently from the night temperature. The cultivars responded similarly, except for two cultivars which generally did not flower at 10/10,10/14 and 14/10°C D/N. One cul-tivar produced more flowers at 14 than at 18°C.     

Cold treatments enhance responsiveness to gibberellin in stock (Matthiola incana (L.) R. Br.)

Summary

Endogenous GAs have been suggested as regulators of stem elongation and flowering of cold-requiring plants. Here, the relationship between temperature conditions and responsiveness to GA₄ on stem elongation and flowering of stock (Matthiola incana) was investigated. The optimum temperature for induction of flower bud initiation was 10°C, and the minimum duration was 20 d in the late flowering cv. Banrei; the type of cold treatment effect on flowering was classified as a “direct effect”. Stem elongation was markedly promoted by cold treatment regardless of flower bud initiation. The cold treatment amplified the stem elongation response to GA₄. The GA₄ level necessary for flower bud initiation was lower in the 10°C treatment than in the 15°C treatment, and it became lower at longer durations of cold treatment. These results indicate that the cold treatments enhance responsiveness to GA₄ not only in the stem elongation process but also in the flower bud initiation process and that the development of responsiveness to GA₄ may correlate with the temperature and duration of cold treatment.     

Long-term effect of irrigation with saline water on the development and productivity of jojoba clones

Summary

Three commercial clones of jojoba (Simmondsia chinensis) (64, Q-106 and 879–154) were planted in June 1991 at the Ramat Negev Experimental Station (Israel) and fertigated with water at three salinity levels, 1.2, 3.4 or 6.2 dS m^?1. The effects of salinity over three and a half years on key metabolic activities, on plant growth and development, on flowering characteristics, and on yield were studied. Salinity barely inhibited the rate of net photosynthesis, although it did reduce stomatal conductivity by about 50%. Salinity also affected the water status of the plants by reducing water potential. Growth of the plants was not greatly affected by salinity. It was found that jojoba plants accumulate sodium and chloride ions in their leaves and use a strategy typical of many halophytes to cope with the salinity. The effect of salinity on flower development was also studied, since the vitality of flowers is a key factor in obtaining seeds. Salinity did not affect the timing of the breaking of flower bud dormancy in the 1992-93 season, although it did delay flower bud growth in clones Q-106 and 64. Salinity brought forward the flowering of clone 879–154 by about a fortnight in the 1993-94 season, but did not affect the flowering pattern of the other clones. Fruit set was not inhibited by salinity in the 1994 or 1995 season, and no significant effects were found on yield and wax content in 1994 season, but yield was reduced by salinity in the 1995 season.     

The influence of fruiting on the bud sprouting and flower induction responses to chilling in Citrus

Summary

The effect of chilling temperatures on bud sprouting and flower formation was compared on fruiting and non-fruiting ‘Owari’ satsuma mandarin (Citrus unshiu Marc) trees. On non-fruiting trees, bud dormancy was weak, and a significant proportion of buds were able to sprout at high temperatures without being chilled. Separate effects of low temperatures on bud sprouting and flower induction were demonstrated. On fruiting trees these two effects of low temperatures were also demonstrated on summer-flush buds, but not on older (spring-flush) buds. The spring-flush buds from fruiting trees scarcely sprouted without being chilled. These buds required a longer chilling period for dormancy release than for flower induction, and it was not possible to separate the effect of low temperature on flower induction from the effect on dormancy release. The presence of fruit reduced flower formation by reducing bud sprouting. Furthermore, fruit had a direct inhibitive effect on vernalization which resulted in increased formation of vegetative shoots. The effect of fruit and low temperature on flowering was unrelated to carbohydrate accumulation in the leaves or the roots.     

‘地平线’天竺葵的花芽分化及光周期特性

 为了研究‘地平线’天竺葵的花芽分化特性及光周期对其生长发育的影响,采用石蜡切片 方法观察了花芽分化的过程,探讨了7 种光周期处理对始花期及开花质量的影响。结果表明：（1）‘地平 线’的花芽分化过程可以划分为8 个时期,持续时间大约为9 周;（2）‘地平线’花芽分化时期与各生长 指标（株高、株幅、真叶数和播种周数）均极显著相关,通过回归方程判断其幼龄期在5 片真叶前结束; （3）‘地平线’为量性短日照植物,促其早花的最佳光周期为昼12 h/夜12 h;（4）较长日照下‘地平线’ 的株形高大松散,较短光周期下矮小紧凑。‘地平线’天竺葵在5 片真叶前,采用16 h 日照栽培,可得到 健壮幼苗;5 叶期后,12 h 日照诱导,可促进分枝开花。