Temperature integration of Hederahelix L.: Quality aspects and growth response

Reducing energy use in greenhouses contributes to the profitability of horticulture. Important energy savings can be realized through the use of temperature integration. However, such a greenhouse heating strategy is only acceptable for commercial purposes if there are no adverse effects on plant growth and quality. During this 3-month study, Hedera helix ‘Green Ripple’ and H. helix ‘Shamrock’ were subjected to a day/night temperature regime of 20/20 °C (control) and two treatments with temperature integration over 24 h and 4 d, respectively, based on a DIF of 13.5 °C, maintaining the average temperature at the same level of the control. Temperature treatments resulted in a promotion of stem elongation. After 3 months, shoot length rose up to maximum 37.3% when temperature integration was applied. However, temperature integration reduced total dry weight and particularly root dry weight was negatively affected. In addition, assessments of relative growth rate, shoot extension rate, specific leaf area, total leaf area and pigment concentrations were performed and it was concluded that dynamic temperature regimes with longer integration periods support commercial production of English ivy.     

Different mechanisms to obtain higher fruit growth rate in two cold-tolerant cucumber (Cucumis sativus L.) lines under low night temperature

One cold-sensitive cultivar (Jinyan 4) and two cold-tolerant inbred lines (NY-1 and XC-1) of cucumber (Cucumis sativus L.) were subjected to temperatures of 28 °C/22 °C (day/night, control) or 28 °C/12 °C (day/night, cold treatment) in a 10 h photoperiod (7:00–17:00). Under control conditions, cucumber fruits grew fast during afternoon and early night, and slow during late night and morning. Under 28 °C/12 °C conditions, the two cold-tolerant inbred lines maintained relatively higher fruit growth rates than the cold-sensitive cultivar by different mechanisms. Compared to Jinyan 4, NY-1 fruits had higher growth rates during cold nights while XC-1 fruits grew faster during the next day. Under the 28 °C/12 °C temperature regime, the assimilate accumulation in the fruits of all tested genotypes followed a similar trend with the corresponding fruit growth rates. After a cold night treatment, the net CO₂ assimilation rates of one- and two-fruit plants, which had increased sink demand, were higher than that of plants without fruits in all tested genotypes. This response indicates that feedback inhibition might be an important reason for the reduction of photosynthesis on the next day. In addition, after a cold night treatment, the levels of exportable sugars (sucrose and stachyose) in mature leaves of XC-1 were higher than those measured in Jinyan 4 and NY-1, which might explain why XC-1 fruits had faster assimilate accumulation rates in the next morning. Higher activity of sucrose-phosphate synthase, a key enzyme of sucrose and stachyose biosynthesis, constituted an additional evidence that faster sucrose and stachyose biosynthesis in mature leaves may occur in XC-1 than in Jinyan 4 and NY-1 at that time. In conclusion, our results showed that cucumber genotypes may use different mechanisms to enhance their cold tolerance.     

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.     

Effect of high temperature stress on the reproductive growth of strawberry cvs. ‘Nyoho’ and ‘Toyonoka’

High temperatures are known to reduce fruit size and fruit weight in strawberry, but cultivar differences in the response to high temperature stress during the reproductive stage up to the second inflorescence have not been sufficiently reported. We examined the effect of two day/night temperature regimes on fruit set and fruit growth in two cultivars, ‘Nyoho’ and ‘Toyonoka’. A high day/night temperature of 30/25 °C reduced the number of inflorescences, flowers, and fruits in both cultivars compared with plants grown at 23/18 °C. The percentage of fruit set in ‘Nyoho’ was not significantly different between the two temperature treatments, while that in ‘Toyonoka’ was much lower at 30/25 °C than at 23/18 °C. Days to ripening was shorter at 30/25 °C than at 23/18 °C, and no cultivar differences were observed. Fresh weight of primary, secondary, and tertiary fruits was greater at 23/18 °C than at 30/25 °C in both cultivars, and no cultivar differences were observed, except in tertiary fruits. The diameter of fruits from all positions was also reduced at 30/25 °C in both cultivars. Relative growth rates of fruits showed two peaks in both cultivars and in both temperature treatments. Both peaks appeared earlier at 30/25 °C than at 23/18 °C. Percentage of fruit set at 30/25 °C in the second inflorescence was also significantly lower in ‘Toyonoka’ than in ‘Nyoho’. These results indicate that high temperature stress negatively affects the reproductive process in strawberry and that plant response to high temperature stress is cultivar-related in such responses.     

Temperature responses,flowering and fruit yield of the June-bearing strawberry cultivars Florence,Frida and Korona

The effect of night temperature on short day (SD) floral induction has been studied in three June-bearing strawberry cultivars of different geographic origin and compared with yield performance in the cool Nordic environment. At the optimum day temperature of 18 °C, the SD flowering response of the cultivars ‘Florence’ and ‘Korona’ increased significantly with increasing night temperature from 9 to 18 °C, while an optimum was reached at 15 °C in the cultivar ‘Frida’ that is selected under cool-environment conditions in Norway. Also, while saturated flowering response was obtained with 3 weeks of SD treatment at all temperatures in ‘Frida’, several plants of ‘Florence’ and ‘Korona’ failed to initiate flowers at 9 °C night temperature even with 5 weeks of SD. The effect of extended SD period was particularly pronounced in ‘Florence’. The slow SD floral induction response of ‘Florence’ was associated with a 2 week delay of anthesis in subsequent long day (LD) conditions at 21 °C. Yield performance of the same cultivars during 2 years under field conditions at Nes Hedmark and in North Norway also demonstrated that the yield potential of ‘Florence’ was not realized under the climatic conditions prevailing at these locations. In both years the yields varied significantly among the cultivars, ‘Frida’ having the highest yields followed by ‘Korona’, with ‘Florence’ far below. It is concluded that, in the Nordic environment, autumn (September) night temperatures are obviously sub-optimal for yield performance of some June-bearing strawberry cultivars, and that this effect is mediated by autumn temperature effects on flower initiation responses.     

Interacting effects of temperature integration and light intensity on growth and development of single-stemmed cut rose plants

Energy conservation in horticulture can be achieved by allowing temperatures to fluctuate within predefined bandwidths instead of using rigid set points for heating and ventilation. In temperature integration, plants are supposed to compensate effects of temporarily deviations of the average temperature some time later by deviations in the opposite direction. However, little is still known on the effects of integration periods exceeding 1 day. In this study, effects of temperature integration on growth and development of single-stemmed cut rose plants were determined. Pruned rose shoots were placed in climate chambers in which light levels switched daily (2 days integration period) or weekly (14 days integration period) from high light intensity (300 μmol m⁻² s⁻¹) to low light (150 μmol m⁻² s⁻¹). Temperatures were kept continuously at 20 °C (control) or changed with the light intensity (phase, high temperature at high light intensity, low temperature at low light intensity) or changed opposite to the light intensity (counter phase). Bandwidths of temperature integration were 0, 6 or 10 °C. Under these conditions, buds grew out to harvestable shoots in approximately 45 days. At both integration periods, shoot length was significantly reduced with increasing bandwidths of temperature integration. Shoot dry weights were reduced when a bandwidth of 10 °C was applied. At both integration periods, rates of photosynthesis were primarily determined by light intensity. However, in the counter phase treatments, photosynthesis rate at high light and low temperature was reduced compared to the high light condition of the control. Under these conditions, starch content increased to approximately 10%, suggesting a feedback inhibition of the rate of photosynthesis. However, this did not (yet) affect plant growth or development.     

Growth and development of Lilium longiflorum ‘Nellie White’ during bulb production under controlled environments : I. Effects of constant,variable and greenhouse day/night temperature regimes on scale and stem bulblets

One-year-old scale and stem bulblets of Lilium longiflorum Thunb. ‘Nellie White’ (Easter lily) were grown under constant and variable growth chamber conditions and greenhouse conditions to compare growth and development and bulb production. Eight temperatures regimes were established using the following: six growth chambers set to provide day/night temperature regimes of 30/26, 26/22, 22/18, 18/14, 14/10 and 10/6 °C; a seventh growth chamber (VAR) programmed to begin at 22/18 °C, then decline in three 4–5 week steps to 10/6 °C, and subsequently increase in three 4–5 week steps to 22/18 °C to simulate seasonal field temperatures in the coastal bulb production area of northern California and southern Oregon; and a double layer polyethylene greenhouse (GH) set to begin cooling at 22 °C and heating at 18 °C. Ten percent of the scale bulblets and 35% of the stem bulblets failed to develop shoots (“no-shows”). “No-shows” increased with increasing temperature with a significant number starting at 18/14 °C. The moderately high GH temperature also induced “no-shows”. Maximum basal bulb (the main planted bulb) weight occurred at 26/22 °C for both bulblet types. Scale bulblets not only produced heavier basal bulbs with a larger circumference than stem bulblets, but also produced heavier stem bulbs. Stem bulb formation and production was maximized in the range of 18/14–26/22 °C and in the GH for scale bulblets. Stem bulb production from stem bulblets did not differ from zero. Scale bulblets produced more basal and stem roots than the stem bulblets at the end of the early growth period, but there was no significant difference at the end of the study. Root fresh weight was greatest in the range of 14/10–18/14 °C and declined at higher or lower temperatures. The VAR and GH treatments had similar root weights to those at 18/14 °C. Shoot length was maximized at 22/18 °C for stem bulblets and in the GH and at 22/18 °C for scale bulblets. Stem plus leaf (shoot) fresh weight was not statistically different between bulblet types with the exception of an increased weight for stem bulblets grown at 22/18 °C. Scale bulblets in the GH had greater stem plus leaf weights than scale bulblets in the other temperature regimes. Shoot leaf number was highest in stem bulblets at 22/18 °C and in the GH. In these two temperature treatments, more leaves were produced by stem bulblets than scale bulblets. In all other treatments, there was no significant difference in leaf number. Bulblet type had no effect on number of flowers produced. Flower number was maximum in the range 10/6–22/18 °C, decreased at 26/22 °C and in the GH, and was absent at 30/26 °C. For bulb production, reduced flowering is desired since flowers are generally removed during the outdoor bulb production period. Meristem abortion, which also causes a desirable reduction in flowers, was greater in scale bulblets. It occurred at 26/22 °C and was greater at 30/26 °C. Scale bulbs produced the largest main bulbs, with a maximum yield at 26/22 °C.     

Gas exchange and antioxidant response of sweet pepper to foliar urea spray as affected by ambient temperature

This paper analyses the effect of different air temperatures (10, 20 and 30 °C) on the response of sweet pepper plants (Capsicum annuum L. cv. Herminio) to foliar urea applications after growing plants for 20 day with and without nitrogen (N) applied to the growing substrate. Leaf CO₂ assimilation, chlorophyll fluorescence, root respiration, lipid peroxidation and antioxidative enzymes were analysed. Spraying plants with urea increased leaf CO₂ assimilation of N-deficient plants when applied at 20 or 30 °C, compared with non-sprayed plants. When plants were sprayed with urea at 10 °C chlorophyll fluorescence of leaves was similar to that of plants that were supplied with full N in the nutrient solution. Root respiration was not affected by urea sprays whilst leaf NO₃⁻ concentration was increased by urea but only when it was sprayed at 10 or 20 °C. Lipid peroxidation and ascorbate peroxidase in N-deficient plants were reduced significantly by urea sprays, especially when plants were sprayed at 20 °C with N-limitation in the growing substrate. This study shows that N-limitation in the growing substrate induces a temperature-dependant increase in the activities of antioxidant enzymes in leaves of pepper and applications of foliar urea can be optimised, when applied at the appropriate temperature, to partly replace the N supplied to the roots of sweet pepper.     

Production protocol development for greenhouse cut Linaria, Lupinus, and Papaver flowers

Linaria maroccana Hook. f. Ann., ‘Lace Violet’, Lupinus hartwegii ssp. cruikshankii Lindl. ‘Sunrise’ and Papaver nudicaule L. ‘Meadow Pastels’ seeds were directly sown into 105 cell plug trays and received either ambient light or supplemental high intensity discharge (HID) lighting. For each species, a 2 × 3 × 3 factorial was used with two light intensities during propagation, three transplant stages, and three night temperatures. Seedlings were transplanted at the appearance of 2–3, 5–6, or 8–9 true leaves. Transplanted Linaria and Papaver seedlings were placed at 5/11, 10/16, or 15/21 ± 1 °C night/day temperatures and Lupinus seedlings were placed at 15/24, 18/25, or 20/26 ± 2 °C night/day temperatures. For this study, the optimum production temperature for Linaria was 10/16 °C as the cut stems produced at 15/21 °C were unmarketable and production time was excessively long at 5/11 °C. At 10/16 °C, Linaria seedlings should be transplanted at the 2–3 leaf stage to maximize stem number, stem length and profitability. For Lupinus the optimum temperature was 15/24 °C due to long stems and high profitability per plant. Lupinus seedlings should be transplanted at the 2–3 leaf stage when grown at 15/24 °C to obtain the longest and thickest stems; however, $/m² week was higher for plants transplanted at the 8–9 leaf stage due to less time in finishing production space. For Papaver, the 15/21 °C temperature was optimal as that temperature produced the longest stems in the shortest duration, resulting in the highest $/m² week. At 15/21 °C Papaver plants should be transplanted at the 2–3 leaf stage. Supplemental HID lighting had no effect on any of the species.     

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.     

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.     

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.     

High temperatures and time to budbreak in low chill apricot ‘Palsteyn’. Towards a better understanding of chill and heat requirements fulfilment

The efficiency of different temperature cycles in inducing budburst of one-year-old shoots of the apricot cultivar ‘Palsteyn’ from dormancy was evaluated. Three replications of shoots were collected during two consecutive years from adult trees, following the accumulation of different amounts of chilling in the field. Thereafter, shoots were exposed to different temperature cycles in growth chambers, for 60 days. The temperature treatments included a continuous temperature of 5 °C; daily temperature cycles of 19/5 h at 5/15 °C, at 5/20 °C, and at 5/25 °C; and the same temperature cycles for the remainder of the 60-day period, after pretreatment at 5 °C for 30 or 45 days. After the temperature treatments, shoots were forced at 25 °C until budburst. The mean time to budburst (MTB) (in days) of lateral vegetative, terminal vegetative and reproductive buds was evaluated. The efficiency of the different treatments was greatly influenced by the date on which shoots were cut. High temperatures had a more positive effect on the reduction of MTB when chilling accumulation had occurred in the field instead of the growth chamber. After partial chilling accumulation in the field, high temperatures (25 °C) combined with low temperatures are more efficient than cycles of moderate temperatures (15 or 20 °C) to induce an earlier budburst. In view of these results, a parallel accumulation of both chilling and heat requirements after partial chilling accumulation is suggested. The application of these results could assist in the development of more accurate models for the prediction of the overcoming of dormancy and blooming.     

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.     

Effects of greenhouse cooling method on growth,fruit yield and quality of tomato (Solanum lycopersicum L.) in a tropical climate

A tomato (Solanum lycopersicum L.) crop was grown in four greenhouses during the dry season 2005/06 in Central Thailand. Sidewalls and roof vents of two greenhouses were covered with nets and these greenhouses were mechanically ventilated when air temperature exceeded 30 °C (NET). The other two greenhouses were covered with polyethylene film and equipped with a fan and pad cooling system (EVAP). Overall mean air temperature was significantly reduced by 2.6 and 3.2 °C (day) and 1.2 and 2.3 °C (night) in EVAP as compared to NET and outside air, respectively. Temperature maxima in EVAP averaged about 4 °C lower than in NET and outside. The relative humidity was around 20 and 30% (day) and 10 and 15% (night) higher in EVAP than in NET or outside, respectively. Vapour pressure deficit averaged 0.25 kPa in EVAP, 1.03 kPa in NET and 1.48 kPa outside. The crop water-consumption was significantly lower in EVAP (1.2) than in NET (1.8 L plant⁻¹ day⁻¹), which is ascribed to reduced transpiration in EVAP. Total fruit yield was similar in NET (6.4 kg plant⁻¹) and EVAP (6.3 kg plant⁻¹). The quantity of undersized (mostly parthenocarpic) and blossom-end rot (BER)-affected fruits was reduced in EVAP. However, the proportion of marketable yield was significantly higher in NET (4.5 kg plant⁻¹) than in EVAP (3.8 kg plant⁻¹), owing largely to an increased incidence of fruit cracking (FC) in EVAP. Higher FC but lower BER incidence coincided with higher fresh weight and Ca concentration in the fruits in EVAP. It is concluded that in regions with high atmospheric relative humidity evaporative cooling without technical modifications allowing dehumidification will not improve protected tomato production.     

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.     

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.     

Total phenolics and flavonoids and total antioxidant capacity in pistachio (Pistachia vera L.) nuts in relation to cultivars and storage conditions

The effects of cultivar, drying and storage conditions on total phenolics (TP), total flavonoids (TF) and total antioxidant capacity (TAC), measured with ferric reducing antioxidant power (FRAP) and radical scavenging capacity (2,2-diphenyl-1-picrylhydrazyl or DPPH) assays, of in-shell and unpeeled kernels of ripe pistachios were investigated. Drying was carried out at 45 °C for 34 h to approximately 5% moisture in kernels and storage of dried nuts in packaging atmosphere of dry air or N₂ at 1 °C or 20 °C for 6 or 12 months. At harvest, each cultivar showed its highest values for each measured variable and TP ranged from 16.2 to 7.9 mg gallic acid equiv. g⁻¹ d.w., TF from 7.2 to 3 mg catechin equiv. g⁻¹ d.w., FRAP from 132.5 to 58.8 μmol Trolox equiv. g⁻¹ d.w., and DPPH from 122.6 to 45.7 μmol Trolox equiv. g⁻¹ d.w. Drying resulted in losses in all cultivars that averaged approximately 14.2%, 14.1%, 11.9% and 12.2% for TP, TF, FRAP and DPPH, respectively, while during 12-month storage the corresponding losses in dried kernels averaged approximately 24.7%, 21.8%, 30.3% and 32.4%. Decreases in all measured variables were advanced by storage time, but prevented by low temperature and packaging in N₂ atmosphere. Among the studied cultivars, Pontikis, Aegina, Bronte and Cerasola showed higher values of TP, TF and TAC than Sirora, Kerman, Joley and Mumtaz in all cases, while Pontikis the highest in most cases. The effects of cultivar, time, temperature and packaging atmosphere during storage were all significant on TP, TF, FRAP and DPPH. Strong correlations were also found among the measured variables.     

Effects of diurnal temperature alternations and light quality on growth,morphogenesis and carbohydrate content of Cucumis sativus L.

The effects of the difference (DIF) between day/night temperature (DT/NT) and end-of-day (EOD) light quality on growth, morphology, dry matter (DM) content and carbohydrate status in cucumber (Cucumis sativus L.) were examined. Plants were grown under a 12 h high light intensity period and DT/NT of 25/19 °C (positive DIF) or 19/25 °C (negative DIF) in combination with an exposure of 30 min EOD-red (EOD-R) or far-red (EOD-FR) light. A significant interaction between DIF and EOD light quality was found on morphology, DM and carbohydrate content in axial plant organs like stems and petioles, but not in leaf blades and roots. Positive DIF induced taller stems, and higher DM and carbohydrate content than negative DIF when the plants were grown under EOD-R. The stems developed under EOD-FR were tall and accumulated the highest content of DM and carbohydrates and only small differences were found between positive DIF and negative DIF. Under EOD-R a higher content of glucose and fructose was found under positive than negative DIF, while EOD-FR light resulted in a high glucose and fructose content under both positive and negative DIF and thereby equalized the effect of the two temperature treatments. The results show that positive DIF can induce similar responses in elongation growth, DM and carbohydrate accumulation as EOD-FR, and further that phytochrome status interact with the responses to alternating DT and NT.     

Haploid plant production in Zantedeschia aethiopica ‘Hong Gan’ using anther culture

This report describes advances in the anther culture of Zantedeschia aethiopica. Important factors for improvement as compared to the earlier procedure were: (1) using flowers from inflorescences developed at relatively low temperature during winter, (2) high temperature stress treatment at 32 °C for 2 days in the beginning of the culture, (3) use of Gamborg B5 as anther culture medium, and (4) addition of sucrose at high concentration of 8% in the culture medium. Plants were obtained via a callus phase. Frequency of anthers producing calli was around 4–5%. About 87% of the calli gave regenerants, of which 52% were haploid, 36% were diploid and the rest had other ploidy levels. In addition to chromosome counting, cytological examination of the microspore development and amplified fragment length polymorphism (AFLP) analysis of the regenerants showed that haploid as well as diploid plants originated from the microspores. Finally, 12 doubled haploid (DH) plants could be produced from each inflorescence. One quarter of the DHs equaled the original cultivar in growth vigor, while more than one third showed good fertility, indicating that inbreeding depression was not so severe in this heterozygous species. The improved protocol now enables production of sufficient number of DHs for application of haploid technology in genetic improvement and breeding of Z. aethiopica.