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.     

Effect of bulb storage temperature on leaf emergence and plant development during scale propagation of Lilium longiflorum ‘White American’

Effects of temperature and duration of bulb storage on leaf emergence of scale bulblets and on the type of plant development were investigated in Lilium longiflorum ‘White American’. After the parent bulbs had been stored for 0, 5, 10 or 15 weeks at 30, 20, 10, or 0°C, scales collected from different parts of a bulb were scale-propagated at 25 or 14°C, or under the temperature regimes normally used in The Netherlands. Independently of the scale position, a higher storage temperature promoted leaf emergence from scale bulblets, whereas a lower temperature delayed it. Higher storage temperatures produced more epigeous type plants, especially from outer and middle scales. Sprouting of the parent bulb had no effect on leaf emergence from the scale bulblets nor on the type of plant development.     

Effects of N–P–K deficiency and temperature regime on the growth and development of Lilium longiflorum ‘Nellie White’ during bulb production under phytotron conditions

One-year-old scale bulblets of Lilium longiflorum Thunb. ‘Nellie White’ (Easter lily) were grown under a combination of six constant day/night temperature regimes and five N–P–K nutrient treatments under short days for 107 d (growing period 1 or GP-1) to compare the effects on growth and development and bulb production. Results during GP-1 were as follows: failure of bulblets to produce a shoot (“no-shows”) was found at high temperatures (30/26 and 26/22 °C) and not influenced by the nutrient treatments. Flower bud abortion was observed in the minus-N, minus-P, and minus-N–P–K treatments at high temperatures (30/26 or 26/22 °C), but not observed at any temperatures in the complete and minus-K treatments. The loss of bulb fresh weight in minus-N treated bulblets was less than in the other treatments resulting in less root and shoot growth in the minus-N treatment. At the intermediate temperatures where growth was highest, omission of N, P, K, or all three resulted in losses in stem bulb fresh weight, stem plus leaf fresh weight, number of flowers, and stem root fresh weight. Omission of N, P, or all three nutrients resulted in lowest basal root fresh weight. Bulb N and K concentrations were lowest in plants grown with complete nutrient solution at the two coldest temperature regimes (14/10 and 10/6 °C). Bulb P concentration was lowest at the three coldest (18/14, 14/10 and 10/6 °C) and the warmest (30/26 °C) temperature regimes. Stem length was shorter when P was omitted. Omission of any of the three nutrients resulted in lower concentrations of the other nutrients. The one exception was where low K did not affect N concentration. In the second phase of the experiment, plants grown at 18/14 °C and irrigated with the complete nutrient solution for 107 d (GP-1) were continued at this day/night temperature regime and five N–P–K nutrient treatments for another 89 d under long days (growing period 2 or GP-2). Results during GP-2 were as follows. Basal bulb yield was not impacted by omission of N, P, or K, or all three. Of all growth measurements, only stem plus leaf fresh weight was lower and only when all three nutrients (minus-N–P–K) were omitted. At the end of GP-2, basal bulb concentrations of N and P did not differ from the concentrations in bulbs at the beginning of GP-1; however, K concentration was lower at the end of GP-2. Omission of N or P further resulted in lower bulb K concentration, suggesting that a moderate supply of N, P, and K be applied during GP-2 since an additional year of bulb production is needed to produce forcing-sized bulbs.     

In vitro flowering of Lilium rubellum Baker

Scales excised from in vitro cultured bulblets of Lilium rubellum were cultured on MS medium supplemented with 0.044 or 4.4 μM BA in the dark for 300 days, the culture period of which was divided into three stages, with temperatures in each stage as follows: 25 °C in stage 1 (days 0–60); 25 °C or 8 °C in stage 2 (days 61–210); 20 °C in stage 3 (days 211–300). Numbers of bulblets per scale and bulblets with elongated stem (the transition from juvenile to vegetative adult phase) depended on the culture condition. The highest number of bulblets and the percentage of bulblets with elongated stems were obtained in scales cultured in medium with 4.4 μM BA at 25 °C in stage 2. On the other hand, BA concentration (0.044 and 4.4 μM) and/or temperatures (25 and 8 °C) in stage 2 influenced flowering in the bulblets with elongated stems (the transition from vegetative adult to flowering phase). Flowering occurred in bulblets with elongated stems when bulblets on scale were cultured in medium with 4.4 μM BA at 8 °C in stage 2, whereas no flowering occurred in bulblets cultured in any other culture conditions. In conclusion, the concentration of BA affects the transition from juvenile to vegetative adult phase, and the exposure of in vitro developed bulblets to low temperature is indispensable to initiate the flowering process.     

Induction of bulb maturity of Ornithogalum thyrsoides

The influence of bulb maturity at bulb harvest on growth and flowering response of Ornithogalum thyrsoides Jacq. ‘Chesapeake Starlight’ was investigated. Experiments were designed to determine if bulb maturity can be induced by bulb storage temperatures and whether bulb maturity can be evaluated by flowering responses. Bulbs with all senesced leaves at harvest were considered “mature” or with emerging young leaves and re-growing young roots were considered “immature”. Bulbs were potted after 0, 3, and 6 weeks of 30 °C or 2 weeks of 10 °C given either in the middle or at the end of 6 weeks of 30 °C. Mature bulbs, as compared to immature bulbs, took longer for leaves to emerge when control bulbs that did not receive any temperature treatment after harvest were planted upon harvest. Leaf emergence of the immature bulbs was significantly earlier than that of the mature bulbs. Mature bulbs which received 30 °C for 3 weeks (30 °C/3 week) flowered 31 days faster than immature bulbs and all bulbs flowered. Leaf emergence and flowering of mature and immature bulbs that received 30 °C/6 weeks or 2 weeks of 10 °C in the middle of 6 weeks of 30 °C (30 °C/2 weeks–10 °C/2 week–30 °C/3 weeks) did not differ from each other. Maturity can be induced by storing immature bulbs at 30 °C/6 weeks. Maturity, as evaluated by flowering percentage and days from leaf emergence to flowering, can be induced in O. thyrsoides. Immature bulbs can, therefore, be harvested for later forcing as long as bulbs are treated with 30 °C/6 weeks. It is proposed that maturity can be correlated with the speed of flowering and bulbs can be harvested at immature physiological state for forcing. Postharvest high-temperature treatment can be used to force immature bulbs that were harvested before the senescence of the leaves.     

Changes in endogenous abscisic acid and soluble sugars levels during dormancy-release in bulbs of Lilium rubellum

Changes in endogenous abscisic acid and soluble sugars levels during dormancy-release of lily bulbs of Lilium rubellum were investigated. Shoot emergence and flowering of the bulbs stored for 14 weeks at 4 °C occurred more synchronously, and the time span from first to last flower in the plants was shorter than those of bulbs stored for 10 weeks at 4 °C. Longer duration of bulb storage showed accelerating effects of increasing leaf number and stem length but negatively affected flower size. Flower number per plant was not much influenced by bulb storage duration. Concentration of endogenous abscisic acid (ABA) level in the bulbs during bulb storage decreased as storage duration increased, and it remained at a constant level after being stored for 10 weeks. This result suggests that the decrease in the endogenous ABA level during bulb storage is correlated with dormancy-release. Concentrations of soluble sugars also changed during bulb cold storage. Sucrose concentration increased as the chilling term increased to 10 weeks but decreased afterward. Glucose and fructose increased from the beginning of chilling to the end of a 14-week cold storage.     

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.     

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

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

Effect of photoperiod and temperature on inflorescence appearance and subsequent development towards flowering in onion raised from sets

The plants of two onion cultivars Sturon and Stuttgarter were raised from sets and placed in a growth room at 12 °C, a light flux density of 120 μmol m⁻² s⁻¹ and a 16 h photoperiod. Cultivar Stuttgarter took 195 days to initiate, whereas time for initiation in cv. Sturon was 201 days. After initiation the plants were transferred to wide range of photo-thermal regimes consisting of six set point temperatures (6, 10, 14, 18, 22 and 26 °C) and four photoperiods (8, 11, 14 and 17 h day⁻¹). An overall mean temperature for all developmental stages under each photo thermal combination was 12.2, 12.4, 15.9, 17.8, 23 and 24.4 °C. Time to inflorescence appearance, spathe opening and floret opening decreased linearly as temperature and photoperiod increased. At low to mild temperatures (12.2–17.8 °C), longer photoperiod enhanced florets per umbel, whereas at higher temperatures (23–24.4 °C), the floret number declined with lengthening photoperiods. As the photoperiod extension in each temperature advanced inflorescence appearance, spathe opening and floret opening and this would be beneficial in a programme to accelerate seed production in onion.     

Efficient in vitro multiplication in Ornithogalum ulophyllum Hand.-Mazz. from twin scale explants

Ornithogalum ulophyllum Hand.-Mazz. with beautiful white flowers is an important medicinal and ornamental plant of the Middle Eastern countries and need exploitation for commercial propagation. The study reports in vitro mass proliferation of bulblets achieved from twin scales and “in vitro regenerated bulblet” explants on MS medium supplemented with various concentrations of BAP–NAA. The best regeneration on twin scales and “in vitro regenerated bulblets” was obtained on MS medium containing 2 mg l⁻¹ BAP–0.5 mg l⁻¹ NAA and 2 mg l⁻¹BAP–1 mg l⁻¹ NAA, respectively. However, bulb scales seemed to be more potent for bulblet regeneration. A large number of the developing bulblets rooted on the regeneration medium. Remaining non-rooting bulblets were rooted on MS medium containing 1 mg l⁻¹ NAA. All plants were acclimatized in the environmental chamber for 4 weeks and were transferred to the greenhouse for flowering. Regenerated bulblets developed into morphologically normal plants.     

Propagation of Lilium hybrids. I. Dependence of bulblet production on time of scale removal and growth substances

Production of bulblets from bulb scales of 12 Lilium Oriental hybrid clones indicated that an approximately threefold range in regenerative capacity existed within this group. The cultivar ‘Empress of India’ was the highest producer and provided 10 bulblets per bulb scale during a six-month period. This could provide an estimated yield of 500 bulblets per bulb. Propagation from bulb scales of most of the clones was equally effective with scales which were removed from the plants either immediately after cold treatment of the dormant bulbs, at the cessation of flowering, or at the cessation of growth of the aerial stems (post-senescence). Only ‘Empress of India’ and ‘American Eagle’ deviated, in that they produced fewer bulblets at the post senescence stage.When bulb scales were removed for propagation immediately after flowering, and treated with a combination of BAP and NAA (both 5 μM), bulblet production of the low producing clones was significantly increased, while that of the high producing ‘Empress of India’ was significantly decreased. These effects were less pronounced when the bulb scales were removed at the post-cold stage and virtually absent at the post senescence stage.     

Modeling plant morphology and development of petunia in response to temperature and photosynthetic daily light integral

The effects of mean daily temperature (MDT) and mean photosynthetic daily light integral (MDLI) on flowering during the finish stage of two petunia (Petunia × hybrida) cultivars were quantified. Petunia ‘Easy Wave Coral Reef’ and ‘Wave Purple’ were grown in glass-glazed greenhouses at 14–23 °C or 14–26 °C and under 4–19 mol m⁻² d⁻¹ with a 16-h photoperiod. The flower developmental rate was predicted using a model that included a linear MDT function with a base temperature multiplied by an exponential MDLI saturation function. The flower developmental rate increased and time to flower decreased as MDT increased within the temperature range studied. For example, under a MDLI of 12 mol m⁻² d⁻¹, as MDT increased from 14 to 23 °C, time to flower of ‘Easy Wave Coral Reef’ and ‘Wave Purple’ decreased from 51 to 22 d and 62 to 30 d, respectively. Flower developmental rate increased as MDLI increased until saturation at 14.1–14.4 mol m⁻² d⁻¹. Nonlinear models were generated for effects of MDT and MDLI on flower bud number and plant height at flowering. The number of flower buds at flowering increased as MDT decreased and MDLI increased. For example, at an MDT of 14 °C with 18 mol m⁻² d⁻¹, plants had 2.5–2.9 times more flower buds than those grown at 23 °C and 4 mol m⁻² d⁻¹. Models were validated with an independent data set, and the predicted time to flower, flower bud number, and plant height were within ±7 d, ±20 flowers, and ±4 cm, respectively, for 96–100%, 62–87%, and 93–100% of the observations, respectively. The models could be used during greenhouse crop production to improve scheduling and predict plant quality of these petunia cultivars.     

Study and prediction of quality changes in garlic cv. Perla (Allium sativum L.) stored at different temperatures

White and purple garlic is harvested in the Bajio region of Mexico from February to August and then stored at room temperature. A complete study of quality changes under different conditions and how these conditions interact to determine the shelf life of the product has been lacking, nor have objective parameters to predict shelf life been determined. Six batches of 360 bulbs of garlic (Allium sativum L.) cv. Perla were stored for 190 days at 0 °C, 0 °C and 70% relative humidity (RH), 5, 20, 30 °C, and at room temperature (RT) (17.7 ± 7 °C). The weight loss, subjective firmness of the bulbs, clove penetration resistance, hue value, internal sprouting index, soluble solids and dry matter content of the cloves were recorded periodically. The weight loss and internal sprouting index had a negative correlation on the subjective firmness, penetration resistance, and hue of the cloves. Storage at 5 °C, 20 °C, and RT induced sprouting, and subsequent growth had an effect on a loss of firmness and color. Complete sprouting (>100%) induced a weight loss of 9–11% at these temperatures. In order to maintain an adequate safety margin for marketing, we propose an internal sprouting index of 50% to determining the effective shelf life of garlic cv. ‘Perla’. In accordance with this criterion and in conditions studying, shelf life at 0 °C was 155 days; at 5 °C and RT it was 80 days; and at 20 °C it was 60 days. These results lead us to conclude that it is possible to estimate the shelf life of garlic using the internal sprouting index.     

The growth and flowering of Hymenocallis × festalis

Bulbs of Hymenocallis (including Ismene) have showy, fragrant flowers. Little is known of the horticultural potential of these plants, and observations and trials on a stock of Hymenocallis × festalis are described.

In a stock of glasshouse-raised bulbs, bulb grade exerted a marked effect of the number of florets produced, which increased from 2 in 9–10-cm-circumference bulbs, to 7 in 18–19-cm-grade bulbs. Field-raised bulbs of the same grades produced fewer florets. Bulbs were usually planted for flower production in the glasshouse in April; earlier planting (February) leading to greater floret size but a longer period in the glasshouse before anthesis. Planting could be delayed at least until June, or later flowering could be achieved by storing the dry bulbs over winter at a low temperature (5°C), but the latter treatment reduced the percentage of bulbs which flowered. The long scapes could be dwarfed by ethephon (as Ethrel). Hot-water treatment, as a pest and disease control measure, did not result in damage to the flowers provided it was delayed until after the staminal cup initial had been formed.

In the field, growth of the main bulb was more vigorous than in the glasshouse, but pot culture in the glasshouse led to copious offset production. Data are presented for bulb increases for various grades of bulbs planted in outdoor beds at rates of 350–1050 g per metre row.     

Effect of differential soil moisture and nutrient regimes on postharvest attributes of onion (Allium cepa L.)

Studies were conducted to observe the effect of different soil moisture and nutrient regimes on postharvest attributes of onion irrigated with microsprinkler irrigation system under semi-arid climate for 3 consecutive years (2002–2004). Soil moisture regime consisted of four irrigation treatments based on pan evaporation replenishment (0.60, 0.80, 1.00 and 1.20 Ep). Similarly, three fertigation treatments were tried with nutrient application rates of 100 (50:25:25), 150 (75, 37.5, 37.5) and 200 (100:50:50) kg/ha of NPK. Irrigation and fertigation had marked effect on yield, postharvest attributes and storability of onion. Irrigation at 1.20 Ep and fertigation at 200 kg/ha produced higher bulb and dry matter yield, mean bulb size and weight, which decreased with the decrease in amount of irrigation and fertigation. The percentage of B-grade bulbs, which is considered commercially important, had been considerably higher at 1.20 Ep of irrigation and 200 kg/ha of fertigation. TSS increased up to 1.00 Ep and then declined slightly, whereas it varied with fertigation significantly. A decreasing trend for protein content was recorded with the increase in irrigation from 0.60 to 1.20 Ep, however, protein content increased with increase in fertigation. Irrigation at 0.80 Ep and fertigation @ 200 kg/ha resulted into minimum physiological loss in weight (%) for onion during 60 days of storage. But for extended storage period, increasing fertigation and decreasing irrigation had adverse effect on storability of bulbs. Theoretically, 416 mm irrigation water was found optimum for maximizing the dry matter yield of onion. Studies indicated that onion crop should be irrigated at 1.0 Ep under microsprinkler irrigation regime for better postharvest attributes. Similarly, fertigation @ 150 kg/ha is most desirable for micro sprinkler irrigated onion crop under semi-arid climate of India.     

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.     

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.     

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 cold temperature durations of onion sets in store on the incidence of bolting,bulbing and seed yield

The experiment was conducted at the experimental area of the School of Plant Sciences, University of Reading during 1996. The planting material comprised of sets (graded to 22.5 mm diameter) of two cultivars, Hygro and Delta. The sets were stored at 5 °C for nine chilling durations, between 10 and 90 days. A control treatment (sets stored at room temperature of 20 °C for days) was also included in the experiment for comparison. Sets of both cultivars treated for 90 days at 5 °C, produced nearly seven times more bolters than those treated for 20 days. Cool temperature treatment for 10 days was too short to induce bolting. Number of florets and percentage of seed bearing florets per umbel increased with lengthening cold durations and this resulted in higher seed yield per umbel. Mean bulb weight per plant was found to increase with shortening the period of low temperature treatment. For bulb crop, storage of sets at 20 °C for 90 days appears to be optimum, as it checked bolting and increased average bulb weight and bulb yields m⁻² in both cultivars.