Changes in carbohydrate contents in shoot tips,leaves and roots of strawberry (Fragaria × ananassa Duch.) during flower-bud differentiation

Flowering is an important step in crop production. Under flower-inducing conditions, biochemical or physiological changes can be recognized. Changes in carbohydrates have an important role in flower development in plants; however, carbohydrate changes during flower bud differentiation in strawberry have not been thoroughly investigated. In this study, runner plants potted in 18 cm diameter pots and grown under non-inducing conditions (28 ± 3/22 ± 3 °C day/night; 16 h day length). When the plants were established, half of the plants then were put under inducing conditions (23 ± 3/13 ± 3 °C day/night; 8 h day length). After the induction period of 21 short-day cycles, plants were brought to non-inductive conditions again. In order to evaluate the carbohydrate changes during flower differentiation, shoot tips, leaves and roots were sampled from four replicated plants collected weekly for the period of 7 weeks. Sucrose, glucose and fructose contents were determined by HPLC, and starch by the anthrone method. The results obtained indicated that the most abundant soluble sugar in all organs tested was sucrose. Sucrose in the shoot tips of induced plants at 42, 56 and 70 days after the start of the short-day treatment were significantly higher than corresponding time in non-induced plants. However, the glucose, fructose and starch contents in shoot tips, leaves and roots of non-induced plants in most sampling dates were greater than those of induced plants. In other words, the shoot tips (bud) of induced plants acted as strong ‘utilizing sink’ and preferentially metabolized carbohydrates rather than storing them. It seems that non-structural carbohydrate contents in shoot tips, leaves and roots of strawberry may have an important role in flower-bud differentiation.     

Interactions of photoperiod,temperature, duration of short-day treatment and plant age on flowering of Fragaria x ananassa Duch. cv. Korona

The effects of photoperiod (10, 12, 16, 20 or 24 h), day-temperature (12, 15, 18, 24 or 30 °C), the number of short days (14, 21 or 28 days), plant age (4, 8 or 12 weeks) and their interactions on flower and inflorescence emergence were investigated in strawberry cv. Korona. No flowers emerged in plants exposed to photoperiods of 16, 20 or 24 h or to a short-day treatment for 14 days. All plants exposed to short days at daily photoperiods of 10 or 12 h for 21 days or longer, emerged flowers at temperatures between 12 and 18 °C. A further increase in temperature led to a drastic decrease in the total number of flowers per plant. A short-day treatment (10 or 12 h photoperiod) of 28 days resulted in highest numbers of inflorescences and flowers per plant, while a short-day treatment of 21 days resulted in the highest numbers of flowers per inflorescence. Complete flower induction was observed in only 4-week-old runner plants. The number of inflorescences and the number of flowers per inflorescence increased with plant age. However, the start of flowering was delayed with increasing plant age.     

Prolonged high-temperature exposure differentially reduces growth and flowering of 12 Viola × wittrockiana Gams. cvs

Many cool season garden crops, including Viola × wittrockiana Gams. (pansy), exhibit reduced flowering outdoors during the warm summer months. Twelve pansy cultivars varying in summer garden performance were grown under either 20 ± 1.5 or 30 ± 1 °C (air temperature) to determine growth and flowering responses to prolonged high-temperature exposure and to identify selection criteria to screen pansies for flowering heat tolerance. Increasing temperature from 20 to 30 °C increased leaf number below the first flower on ‘Crystal Bowl Primrose’ and ‘Skyline White’ only. Flower bud number reduction at 30 °C versus 20 °C varied from 20% for ‘Crystal Bowl Purple’ to 77% for ‘Majestic Giants Red and Yellow’. Flower diameter reduction at 30 °C versus 20 °C ranged from 14% for ‘Skyline Beaconsfield’ to 44% for ‘Super Majestic Giants Ocean’. The percentage reduction in total color (flower number × estimated flower area) ranged from 60% for ‘Crystal Bowl Primrose’ to 88% for ‘Majestic Giants Rose Shades’. Based on a weighted base selection index, ‘Super Majestic Giants Canary’ and ‘Delta Yellow’ were identified as the most heat-tolerant cultivars, while ‘Super Majestic Giants Ocean’ and ‘Majestic Giants Rose Shades’ were identified as the most heat-sensitive. In a second experiment, root and shoot dry mass were determined after 10, 20, or 30 d when grown at 20 or 30 °C. Relative growth rate and root:shoot ratio were also calculated. After 30 d, ‘Crystal Bowl Primrose’, ‘Crystal Bowl Sky Blue’ and ‘Skyline White’ relative growth rates were lower at 30 °C versus 20 °C. Root:shoot ratio on day 30 was lower at 30 °C compared to 20 °C for six cultivars, but similar across temperature for five cultivars and higher for ‘Crystal Bowl Primrose’. Flower bud number at first flower was positively correlated with branch number, shoot dry mass at flowering, but not correlated with root dry mass at flowering, and negatively correlated with flower diameter and root:shoot ratio (either at flowering, or after 10, 20 or 30 d at 30 °C), suggesting that these traits may be useful when screening pansies for flowering heat tolerance.     

Environmental control of growth and flowering of Rubus idaeus L. cv. Glen Ample

Environmental control of the annual growth cycle of ‘Glen Ample’ raspberry has been studied in order to facilitate crop manipulation for out-of-season production. Plants propagated from root buds were raised in long days (LD) at 21 °C and then exposed to different temperature and daylength conditions at varying ages. Shoot growth was monitored by weekly measurements and floral initiation by regular sampling and examination of axillary bud #5. Under natural summer daylight conditions at 60°N shoot growth was nearly doubled at 21 °C compared with 15 °C, while at 9 °C one half of the plants ceased growing and formed flower buds at midsummer. Developing shoots have a juvenile phase and could not be induced to flower before the 15-leaf stage. No significant reduction in induction requirements was found in larger plants. Plants exposed to natural light conditions from 10th August, had an immediate growth suppression at 9 and 12 °C with complete cessation after 4 weeks (by September 7). This coincided with the first appearance of floral primordia. At 15 °C both growth cessation and floral initiation occurred 2 weeks later (by September 21), while at 18 °C continuous growth with no floral initiation was maintained until early November when the photoperiod had fallen below 9 h. The critical photoperiod for growth cessation and floral initiation at 15 °C was 15 h. Plants exposed to 10-h photoperiods at 9 °C for 2–4 weeks had a transient growth suppression followed by resumed growth under subsequent high temperature and LD conditions, while exposure for 5 or 6 weeks resulted in complete growth cessation and dormancy induction. The critical induction period for floral initiation was 3 weeks although no transitional changes were visible in the bud before week 4. When exposed to inductive conditions for marginal periods of 3 or 4 weeks, an increasing proportion of the plants (20% and 67%, respectively), behaved as primocane flowering cultivars with recurrent growth and terminal flowering. It is concluded that growth cessation and floral initiation in raspberry are jointly controlled by low temperature and short day conditions and coincide in time as parallel outputs from the same internal induction mechanism.     

Effect of photoperiod on flower bud initiation and development in myoga (Zingiber mioga Roscoe)

Selection of suitable production locations in Australia and New Zealand for production of myoga (Zingiber mioga Roscoe) has been limited by lack of information on climatic influences on flowering. This study focused on photoperiod as potential production sites within Australia differ considerably in daylength due to the geographical range. The two cultivars available in Australia (Inferior and Superior) were examined in this trial due to previously observed differences in vegetative and reproductive development.Plants grown under long-day conditions (16 h) and short-day conditions (8 h) with a night break produced flower buds, while those under short-day conditions (8 h) did not. The failure of plants under short-day conditions to produce flower buds was due to abortion of developing floral primordia rather than a failure to initiate inflorescences. It was concluded that for flower development in myoga a qualitative long-day requirement must be satisfied, but that flower initiation was day-neutral.Short-day conditions resulted in abortion of flower primordia, premature senescence of foliage and reduced foliage dry weight in both cultivars. Early senescence and low flower bud yield of the Inferior cultivar, but not the Superior cultivar have been observed in crop evaluation trials in Southern Australia and New Zealand. Differences in critical photoperiod between the two cultivars may explain this observation and therefore photoperiodic requirements may be an important consideration in site and planting date selection for different cultivars.     

Photoperiodic reaction of sexual and asexual reproduction in Fragaria chiloensis L. CHI-24-1 plants grown at various temperatures

Floral initiation of a wild strawberry strain, Fragaria chiloensis CHI-24-1, is strongly induced by a 24 h day-length (DL) treatment for 40 days consisting of natural daylight and continuous lighting at night by an incandescent lamp. To use the characteristics of floral initiation in CHI-24-1 as a genetic resource for breeding of cultivated strawberries, the photoperiodic reactions of sexual and asexual reproductive growth under various temperature conditions should be clarified. For that purpose, we examined: (1) floral initiation, inflorescence emergence and runner production seasons of CHI-24-1 plants grown under natural climatic conditions in an open field at the Faculty of Agriculture, Kagawa University and (2) the effects of various DLs and temperatures on floral initiation and runner production of CHI-24-1 plants. When the CHI-24-1 plants were grown under natural conditions, the floral initiation, inflorescence emergence and runner production were observed, respectively, in late autumn, spring, and from spring to autumn. Floral initiation of CHI-24-1 plants was induced strongly by 24 h DL at mean temperatures greater than 20 °C. The maximum floral initiation rates were 90% in the parent plant and 94% in the daughter plants, which were linked by runners to the parent plant. The floral initiation of the daughter plants occurred under 20, 22, and 23 h DL at mean temperatures greater than 20 °C, but not for the parent plants. Floral initiation was induced in 100% of the parent plants by the 8 h DL and the lowest mean-temperature conditions. Results of those experiments indicated that CHI-24-1 was an absolute long day plant having critical DL of about 20 h at mean temperatures greater than 20 °C, even though it was a June-bearing strawberry plant. In addition, CHI-24-1 was a facultative short-day plant at mean temperatures of less than 15 °C.     

Comparative forcing of Hydrangea macrophylla ‘Bailer’ as a florist's hydrangea

‘Bailer’ (Endless Summer™) is a new, pink- or blue-flowered hydrangea that flowers on new wood continuously throughout the growing season. It is also winter-hardy in northern, temperate climates (USDA Z4). Use of Endless Summer as a florist's potted hydrangea would provide consumers with a dual-use product (flowering potted plant, landscape shrub). The objectives were to determine if Endless Summer could be forced as a florist's hydrangea using two forcing regimes (immediate, standard), two soil pH regimes, and two pinching treatments. ‘Merritt Supreme Pink’ (pink), ‘Blue Danube’ (blue), and Endless Summer (blue, pink) were forced under immediate (no cold treatment, short- and long-day photoperiods) and standard (6 weeks cold, 4 °C to overcome dormancy) conditions. Since commercial liners were not yet available, cuttings of Endless Summer were used in the immediate forcing experiment. Days to visible flower bud, first color, full flower were recorded, as well as height, no. of branches, no. of flowers, and flower size. In the immediate forcing experiment, only Endless Summer produced flowers. Cultivars differed significantly (P < 0.001) for days to visible flower bud, days to first color, days to full flower, and height. The number of flowers and flower size were not significantly different among pink cultivars. In the standard forcing experiment, Endless Summer reached days to visible flower bud, days to first color, and days to full flower significantly earlier than either comparison, although it exhibited weaker stems and less intense flower pigmentation. Pinching (blue pH) had a significant effect on all traits except the days to full flower and flower size, although no pinching treatment was significant for pink pH. Photoperiod was significant only for the days to visible flower bud (pink pH), days to full flower (blue pH), and final height (blue pH). Further research is needed before Endless Summer can be grown as a dual-use florist's potted hydrangea with acceptable quality.     

Light quality of continuous illuminating at night to induce floral initiation of Fragaria chiloensis L. CHI-24-1

A wild strawberry strain, Fragaria chiloensis CHI-24-1, produced inflorescences from both parent and asexually propagated daughter plants linked with runners when grown at 23 °C/20 °C (day/night) under a 24 h day-length (DL) of daylight plus nightly lighting by an incandescent lamp, but not under 8 or 16 h DLs. In the present study, the effect of light quality for continuous illuminating at night on floral initiation of CHI-24-1 plants grown under a 24 h DL was examined. The CHI-24-1 plants were grown under a 24 h DL consisting of natural daylight and continuous lighting at night by an incandescent, a blue fluorescent, a red fluorescent or a far-red fluorescent lamp for 40 days in summer and autumn. Also, the CHI-24-1 plants were grown for 40 days in a growth chamber at 25 °C/20 °C (day/night) with natural daylight and continuous lighting at night by red- and four types of far-red light-emitting-diodes (LEDs with peak wavelengths of 660, 700, 735, 780 and 830 nm). In both experiments, floral initiation of the parent and daughter plants was observed under a stereomicroscope. Although more than 50% of the parent and daughter plants initiated flower buds under the incandescent and far-red fluorescent lamps, about 15% and 0% of those initiated flower buds under blue and red fluorescent lamps, respectively. Floral initiation of the parent and daughter plants occurred under the far-red LED light source whose peak wavelength was 735 nm, but not under the red or the other far-red LEDs. From these results, it can be concluded that the effective light wavelength range of nightly continuous illuminating for floral induction in the CHI-24-1 plants is 735 nm in the far-red light region. Hence, the induction of floral initiation by nightly continuous far-red light (735 nm) appeared to be a response mediated by phytochrome.     

Cryopreservation of shoot apices of hawthorn in vitro cultures originating from East Asia

The objective of this study was to establish a cryopreservation protocol for hawthorn shoot apices (Crataegus pinnatifida Bge.). Cryopreservation was carried out via encapsulation–dehydration, vitrification, and encapsulation–vitrification on shoot apices excised from in vitro cultures. We began by showing that cold-acclimation enhanced the regrowth of cryopreserved apices from 10.0 to 65.5% in encapsulation–dehydration. We then decided that the encapsulation–dehydration method was an optimal cryopreservation method for hawthorn shoot apices in terms of its high recovery after cryopreservation as well as its ease of use compared with vitrification and encapsulation–vitrification. In encapsulation–dehydration, the protocol leading to optimal regrowth was as follows: after cold-acclimation at 5 °C in the dark for 2 weeks, excised shoot tips were pretreated for 24 h at 25 °C on hormone-free Murashige and Skoog [Murashige, T., Skoog, F., 1962. A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol. Plant. 15, 473–497] (MS) basal medium with 0.4 mol/L sucrose, then encapsulated and precultured in liquid MS medium with 0.8 mol/L sucrose for 16 h at 25 °C. Precultured beads were dehydrated for 6 h at 25 °C in the dessicator containing 50 g silica gel to a moisture content of 15.3% (fresh-weight basis) before cryostorage for 1 h. In addition, we examined the effect of adding glycerol to both the alginate beads and loading solution to enhance regrowth after cryopreservation in encapsulation–dehydration. In the present study, it was shown that adding 0.5 mol/L glycerol resulted in high regrowth percentages (82.5–90.0%) in four Crataegus species.     

Changes in morphological phenotypes and essential oil components in lavandin (Lavandula × intermedia Emeric ex Loisel.) transformed with wild-type strains of Agrobacterium rhizogenes

Hairy roots were induced from leaf-derived calli of lavandin (Lavandula × intermedia Emeric ex Loisel.) by infection with wild-type strains of Agrobacterium rhizogenes, A-5 (MAFF 02-10265) and A-13 (MAFF 02-10266). A-5-inoculated calli formed hairy roots more efficiently than A-13 ones. The transgenic shoots could be obtained from hairy root segments mediated by each Agrobacterium strain. However, different plant growth regulators were required for efficient adventitious shoot formation in each strain. In A-5, the most efficient adventitious shoot formation rate of 23.8% was observed in a medium with 4.4 × 10⁻⁶ M of 6-benzylaminopurine. On the other hand, a significantly higher rate of 13.2% was detected in a medium with 4.0 × 10⁻⁷ M of N-(2-chloro-4-pyridyl)-N′-phenylurea in A-13. Most of the regenerated plants showed dwarfism with closed internodes and extensive lateral branching, which were typical characteristics of ‘hairy root syndrome’. On the other hand, only nine of the 45 regenerated plants formed flower buds in early June, a delay of about one month compared with nontransgenic regenerated plants. The floral stalks and spikes of these plants were very short, resulting in a compacted form. Many regenerants showed a significantly lower productivity of essential oil than nontransgenic regenerants. Moreover, the relative percentage of the linalyl-cation-derived compounds, linalool and linalyl acetate, decreased in most of the regenerated plants. Compact plants with the ability of flower bud formation are assumed to be valuable not only for lavandin breeding, but also for clarifying the interaction between rol genes expression and essential oil production.     

Growth and development of Lilium longiflorum ‘Nellie White’ during bulb production under controlled environments : II. Effects of shifting day/night temperature regimes on scale bulblets

One-year old scale bulblets of Lilium longiflorum Thunb. ‘Nellie White’ (Easter lily) were grown for 107 days during growth period 1 (GP-1) in six growth chambers under constant day/night temperature regimes of 30/26, 26/22, 22/18, 18/14, 14/10 and 10/6 °C. Subsequently, half of the plants in each temperature regime were transferred to 18/14 °C and the other half continued at the six constant temperature regimes. Both groups of plants were grown for an additional 89 days in growth period 2 (GP-2). Continuous temperatures of 26/22, 26/22–22/18 and 26/22–18/14 °C produced the greatest increase in basal bulb fresh weight (the main planted bulb), basal bulb circumference and stem bulb fresh weight, respectively. However, shifting these optimal temperatures to 18/14 °C during GP-2 resulted in a lower increase in basal bulb fresh weight and circumference. The optimum range for stem bulb production was expanded to 30/26–14/10 °C by shifting to 18/14 °C. The greatest increase for basal root growth occurred at 14/10–10/6 °C and for stem root growth at 14/10 °C. The temperature shift did not affect either root type. Maximum increase for stem length was at 26/22 and 22/18 °C and for stem plus leaf weight at 14/10 °C under constant temperature regimes. Transferring the plants from 10/6 to 18/14 °C resulted in the greatest increase in stem length and from 10/6 and 14/10 to 18/14 °C in the greatest increase in stem plus leaf weight. The greatest increase in the number of leaves occurred at 26/22 and 10/6 °C, but this growth parameter was unaffected by shifting to 18/14 °C, indicating that leaf number was determined in GP-1. Bulbils developed only when bulbs at high GP-1 temperature regimes (30/26 and 26/22 °C) were transferred to 18/14 °C during GP-2. Lower temperatures tended to favor an increase in flower bud production under continuous temperature regimes, while shifting to 18/14 °C increased flower bud production after initially high and low temperatures. Meristem abortion was greatest at 30/26 °C followed by 26/22 °C, but was not affected by temperature shifts in GP- 2. Thus, it is concluded that the abortion was induced or initiated during GP-1.     

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.     

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.     

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.     

In vitro proliferation and minimum growth storage of fraser photinia: Influences of different medium,sugar combinations and culture vessels

Protocols for the in vitro proliferation and storage of fraser photinia were developed by comparing 6-benzyladenine (BA) concentrations (0.5–4 mg/L) together with different media formulations [Murashige and Skoog (MS) media and Quoirin and Lepoivre (QL) media], sugar combinations (sucrose and mannitol), culture vessels (baby food jars and vitrovents) and methods (synthetic seed technology and slow growth storage). The best responses in terms of both proliferation percentage and multiple shoot formation were obtained in QL medium containing 1 mg/L BA. Synthetic seed production was optimized by encapsulating shoot apices in 3% sodium alginate. Encapsulated shoot apices could be maintained up to 6 months at 4 °C in dark with 91.6% sprouting in MS medium. Microshoots were stored at 4 °C up to 15 months on sucrose and mannitol containing QL medium in both baby food jars and vitrovents without subculture. The stored material could be recovered and multiplied normally in 1 mg/L BA supplemented QL medium. Both in vitro propagated and conserved microshoots were rooted (∼75%) on QL medium with 1 mg/L indole butyric acid (IBA). Optimized synthetic seed and slow growth storage system can be used for short and medium-term storage of fraser photinia germplasm.     

‘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。     

Effects of photoperiod on shoot elongation and endogenous gibberellins in the glasshouse carnation

Plants of glasshouse carnation were grown in photoperiodic cycles comprising 8 h natural daylight followed by either 16 h of darkness (short-day treatment) or by 16 h of low-intensity lighting from tungsten filament lamps (continuous-light treatment). When plants were transferred from short days to the continuous-light treatment, rates of shoot elongation were increased and flower initiation was promoted. Shoot tips of plants grown in continuous light yielded greater amounts of diffusible gibberellin-like substances than shoot tips of plants grown in short days. Yields of diffusible gibberellins increased with increases in the duration of the continuous light treatment up to 28 days, by which time flower initials were present. Application of GA₃ to the plants resulted in increased rates of shoot elongation, but no effect on flowering was observed.     

Aneuploid strawberry (2n = 8x + 2 = 58) was developed from homozygous unreduced gamete (8x) produced by second division restitution in pollen

Unreduced gamete formation is significant in the evolutionary development of complex polyploidy series found in wild strawberry, genus Fragaria (Rosaceae). Also, it is important for genetics and breeding in strawberry plants to elucidate the mechanism of unreduced gamete formation. The objective of this study was to search for ploidy anomalies resulting from artificial diploid × octoploid crosses, and examine the mechanism through which these unreduced gametes were produced. Five everbearing cultivars of Fragaria vesca L. diploid (2n = 2x = 14) were crossed with pollen from six June-bearing cultivars of Fragaria × ananassa Duch., octoploid (2n = 8x = 56). A total of 3000 mature seeds, 100 from each of the 30 parental combinations were sown at 23 °C/20 °C (day/night) under artificial lighting with a 16 h day. The seedlings were transplanted to pots and grown in a greenhouse. Reproductive and morphological observations, flow cytometry analyses, chromosome counts and DNA analyses using CAPS markers were performed to identify the genetic background of the offspring. Most of the seed (79%) did not germinate or died soon after germination. Of the seedlings produced, 7% seemed to be pure F. vesca based on morphological characteristics, flow cytometry analyses and chromosome counts; 14% were pentaploids (2n = 5x = 35), 0.1% were hexaploids (2n = 6x = 42), and 0.03% (one individual) was aneuploid (2n = 8x + 2 = 58). Electrophoresis banding patterns obtained by CAPS marker analysis were heterozygotic in the 8x pollen parent but homozygotic in the aneuploid progeny. Judging from the chromosome counts and the CAPS marker analysis, the aneuploid was the result of a homozygous unreduced pollen grain (8x) crossed with an incomplete chromosome compliment from the egg. Because of the homozygosity, the unreduced male gamete must have been derived from second division restitution (SDR) in the octoploid pollen parent.     

cDNA macroarray analysis of genes expressed in plumules of Pharbitis nil after induction of flowering

SUMMARY

A cDNA library was constructed from mRNA extracted from plumules including shoot apical meristems, 24 h after a 16 h dark treatment, to clone genes preferentially expressed during flower evocation in a short-day plant, Pharbitis nil. We partially sequenced 768 randomly selected cDNAs. A database search for these expressed sequence tags (ESTs) revealed that 57.4% were similar to registered genes and the remaining 42.6% showed no significant similarity to known genes. By using a cDNA macroarray, cDNAs derived from the plumules of P. nil subjected to one short-day (SD) to induce flowering, or kept under long-day (LD) conditions as a control, were hybridised with these EST clones. Six of the 768 clones were preferentially expressed by the SD treatment. Three of these were clones similar to chlorophyll a/b binding protein 8 (CAB-8), ubiquitin and a 60 kDa chaperonin -subunit gene. The other three clones did not show similarity to any known genes. The preferential expression of these genes by SD treatment suggests possible roles in flower evocation in the shoot apical meristem.     

The effect of forcing temperature on peony shoot and flower development

Pre-chilled potted plants of Paeonia ‘Coral Sunset’, ‘Monsieur Jules Elie’, ‘Sarah Bernhardt’, and ‘Karl Rosenfeld’ were placed in a range of controlled temperature regimes to ascertain the effect of temperature on the timing of shoot emergence and floral development. For all cultivars, warmer temperatures up to 25 °C lead to more rapid shoot emergence and flower development. Linear temperature responses adequately described the rate of development from shoot emergence to flower bud appearance, and from bud appearance to flower opening, but a curvilinear response was required to describe the time taken for shoots to emerge. There were significant differences between cultivars in the number of heat units required for shoot emergence, with the shoots of the slowest-developing cultivar, ‘Monsieur Jules Elie’, taking 50% longer to emerge than those of the most rapid, ‘Coral Sunset’. No significant differences were found among cultivars in the time taken from shoot emergence to flower opening, although the ‘split’ stage (when the bud opens sufficiently for petal colour to be observed) was slightly earlier in ‘Karl Rosenfeld’.