Long-day control of flowering in everbearing strawberries

Summary

Photoperiod and temperature control of flowering in a number of perpetual-flowering or everbearing strawberry cultivars of widely varying pedigree has been studied in controlled environments. Flower bud initiation in the cultivars ‘Flamenco’, ‘Ridder’, ‘Rita’ and ‘Rondo’ was significantly advanced by long-day (LD) conditions at temperatures of 15°C and 21ºC; while, at 27ºC, flowering took place under LD conditions only. Some plants of the seed-propagated F₁-hybrid ‘Elan’, raised at 21°C, also flowered under short-day (SD) conditions at 27°C, but reverted to the vegetative state after a few weeks when maintained under these conditions. When vegetative plants growing in SD at 27°C were transferred to LD conditions at the same temperature, they consistently initiated flower buds and started flowering after about 4 weeks. At such a high temperature, flowering could thus be turned on and off by switching between SD and LD conditions. This applied to all the cultivars studied. Also the cultivar ‘Everest’, which was tested only at 21°C, produced similar results. Night interruption for 2 h was effective in bringing about the LD response. At 9°C, flowering was substantially delayed, especially in ‘Flamenco’ and, at this temperature, flowering was unaffected by photoperiod. Runner formation was generally promoted by high temperature and SD conditions, but the photoperiodic effect varied between experiments. We conclude that everbearing strawberry cultivars, in general, whether of the older European-type or the modern Californian-type originating from crosses with selections of Fragaria virginiana ssp. glauca, are qualitative (obligatory) LD plants at high temperature (27°C), and quantitative LD plants at intermediate temperatures. Only at temperatures below 10°C are these cultivars day-neutral.     

The physiology of hyacinth bulbs. XI. The effect of gibberellic acid on the growth and flowering of variously chilled bulbs

The effect of gibberellic acid, GA₃, on the growth and flowering of hyacinth cultivars ‘Pink Pearl’, ‘Delft Blue’ and ‘Carnegie’, chilled in a cold room at 5°C or a garden frame for 28, 42 or 81 days, and either rooted or dry, unrooted, was investigated. GA, was applied to the basal plates of the bulbs in a lanolin paste on 10 October 1975.The growth of the inflorescence and leaves of plants originating from dry-chilled bulbs was generally the same as that of those grown from rooted plants. A similar response to GA₃ treatment was observed in all cultivars. Treatment of bulbs with GA₃ decreased the number of days to flowering, stimulated the growth of inflorescences and leaves, and its effect was most pronounced in the plants chilled for shorter periods.     

Short days and temperature effects on growth and flowering in strawberry (Fragaria × ananassa Duch.)

Summary

‘Korona’, ‘Elsanta’, ‘Bounty’ and ‘Senga Sengana’ strawberry (Fragaria × ananassa Duch.) plants, were placed at constant temperatures of 9, 15 or 21°C and daylengths of 8 h (short day) or 24 h (long day). The plants were given different numbers of short-day (SD) cycles, and flowering and growth were studied. ‘Korona’ and ‘Elsanta’ were responsive to both short-day treatment and temperature, with optimum flowering at 15°C and 24 SD. ‘Bounty’ was more responsive to temperature, inducing flowers independently of the number of SD cycles at 9°C and 15°C. In ‘Senga Sengana’ flowering was induced independently of temperature and the number of SD cycles, indicating that it had a stronger dependence on other environmental effects. The effect of the number of short-day cycles and the temperature on vegetative growth variâtes such as the number of stolons and daughter plants, the length of flower trusses and petiole length were also studied.     

Effect of chilling on runner formation and flower initiation in the everbearing strawberry

Fresh and cold-stored plants of the everbearers ‘Rabunda’ and ‘Ostara’ were placed for 90 days, from the end of August, in glasshouses of the IVT phytotron at 14, 20 and 26°C and a daylength of 16 hours.In the fresh plants hardly any runners were formed at 14 and 20°C, but flowers were initiated, while at 26°C both runners were formed and flowers initiated. In the cold-stored plants, runners were formed first and thereafter flowers were initiated at all temperatures.It was concluded that (1) chilling induces runner formation, but can be replaced by high temperature, and (2) chilling delays flower initiation.     

Incidence and severity of hardcore in sweet potatoes as affected by genetic line,curing, and lengths of 1°C and 21°C storage

The effects of genetic line, curing, length of 1°C storage, and length of subsequent 21°C storage on hardcore in sweet potato roots (Ipomoea batatas) were studied. Both incidence (percent roots affected) and severity (amount of affected tissue per root) were measured. ‘Centennial’ and NC 320 (= ‘Caromex’) were found to be susceptible to the disorder, ‘Jewel’ and NC 625 were resistant, and NC 327 was intermediate. Cured roots showed a trend toward less hardcore than uncured roots. Hardcore increased as roots were chilled from 1 to 14 days. A post-chilling 21°C storage period of 2 days resulted in the highest amount of hardcore, with 6 days less was present, and with 0 days least. Significant interactions were present between all factors.     

Some physiological changes in strawberry (Fragaria × ananassa ‘Camarosa’) plants under heat stress

Summary

The effects of heat injury induced by long exposures were evaluated in strawberry (Fragaria × ananassa ‘plants’) Camarosa in this study. Seedlings were grown in 14 × 12 cm pots using perlite for three weeks at 25/10°C day/night temperature, and watered daily by modified 1/3 Hoagland nutrient solution. Half of the plants were transferred to a growth chamber with a constant 25°C, 16/8 h (light/dark) photoperiod regime and 1200 lux light intensity for a week to acclimate the plants. Temperature was increased stepwise (5 K per 48 h) to 30, 35, 40°C and finally to 45°C. In addition to others, plants were transferred from the outside to the growth chamber, at each temperature step to impose a heat shock. Leaf relative water content (RWC, %), loss of turgidity, chlorophyll content (Spad value) and heat-stress tolerance (HTS; LT₅₀) were measured in control and stressed plants. Total soluble proteins and total DNA were extracted from the leaves following the above treatments using standard procedures and total protein contents were determined using a Bradford assay. In general, effects of gradual heat stress (GHS) and shock heat stress (SHS) on the variables studied were mostly significant, except for chlorophyll content, while the effect of temperatures was significant for all the variables. Interaction between the heat stress type and temperature treatments was not significant for leaf RWC, loss of turgidity and chlorophyll content. Data also indicated that total protein and DNA contents were changed significantly by heat stress types (GHS and SHS) and/or temperature treatments. The plants exposed to GHS exhibited a significant increase in HST compared with the plants exposed to SHS (LT₅₀ of 41.5°C and 39°C, respectively). Consequently, gradual heat stress increased HST in strawberry leaves. Increased HST may be associated with the accumulation of several heat-stable proteins in GHS plants.     

Temperature effects on dormancy,bud break and spear growth in asparagus (Asparagus officinalis L.)

Summary

The effects of the length of chilling, chilling temperature and growing temperature on dormancy of asparagus crown buds and subsequent rates of spear growth were examined. The results showed that prior chilling enhanced bud break at low growing temperatures and stimulated the growth of spears.Thus, chilling should facilitate commercial production by hastening bud break and spear growth rates at lower temperatures. If sufficient chilling was given, the minimum temperature for rapid bud break was approx. 12.5°C for ‘Rutgers Beacon’ and ‘Jersey Giant’, and around 10°C for ‘UC 157’ and ‘Apollo’. The optimum chilling temperature appeared to be closer to 5°C than to 10°C or 2°C for ‘Rutgers Beacon’ plants grown at 12.5°C. Increasing the growing temperature had a significant effect on the relative spear growth rate (RSGR) in all cultivars. Prior chilling had no effect on the RSGR for ‘Dariana’ and ‘Apollo’; but, for ‘UC 157’, chilling plants at 5°C for 5 or 10 weeks increased growth rates at 12.5°C and at 20°C. These results demonstrate that release of bud dormancy and spear growth rates depended not only on the growing temperature, but also, at least in some cultivars at some temperatures, on the duration and temperature of chilling during the previous Winter.     

Chilling requirements of Paeonia cultivars

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

Flower-bud formation in apple under various day and night temperature-regimes

Starting at full bloom, 4 temperature treatments were applied to 3-year-old ‘Golden Delicious’ and ‘Cox's Orange Pippin’ trees. Either 17 or 24° C were applied in 3 successive periods of 5–6 weeks each.In ‘Golden Delicious’, exposure to 24° C during the first 5 weeks after full bloom enhanced shoot growth and reduced flower-bud formation in spur buds. The difference in temperature-regime during the third period did not affect either growth or flowering. Almost all apical shoot buds became floral, irrespective of treatment.‘Cox's Orange Pippin’ trees maintained at 24° C throughout grew more vigorously than did those kept at 17° C continuously, but flowering-abundancy was the same. Lowering of the temperature in the last period before harvest did not influence shoot growth, but markedly reduced flowering of both spur buds and apical shoot buds.In a second experiment, a night temperature of either 20 or 10° C was applied in 2 successive periods to 3-year-old ‘Cox's Orange Pippin’ trees kept at a day temperature of 20° C throughout. Lowering of the night temperature in the middle of the season reduced flower-bud production, but there was no difference in growth vigour compared with 20° C continuously.It is postulated that temperature affects flowering in two opposite ways, whose relative importance determines the net result.     

Early forcing of narcissus: The effects of lifting date and stage of floral development at the start of cooling

Early Narcissus flowers may be obtained if bulbs are lifted early from the field, warm-stored (35°C) and then cool-stored (9°C) before forcing in a glasshouse. The earliest satisfactory forcing was investigated, in ‘Carlton’ and ‘Fortune’, by lifting weekly from 27 May to 22 June, and storing at 17°C for 0–7 weeks between warm- and cool-storage. Storage at 17°C is usually intercalated to allow the completion of flower differentiation prior to the start of cool storage.After warm-storage, the bulbs lifted on 27 May and 22 June had reached Stages Sp and A2 of flower differentiation, respectively; 5–7 weeks of 17°C-storage were then needed to reach complete flower differentiation (Stage Pc). Cool storage was therefore begun with bulbs ranging from Stage Sp to Stage Pc. The earliest cooled bulbs had progressed only to Stage A2, and all others to Stage Pc, after 14–16 weeks of cool storage. No floral defects (e.g., split paracorolla) were noted in any treatment, but in ‘Carlton’, about half the bulbs lifted on 27 May and stored for 0 or 1 week at 17°C did not yield a flower, due to failure of the scape to elongate and death of the flower bud within the spathe.Duration of the glasshouse period was reduced by later lifting and by longer 17°C-storage, but following lifting on 15 or 22 June and 2 or more weeks at 17°C, differences were trivial. For flowering within 30 days in the glasshouse, 5 or 6 weeks' 17°C-storage was needed with 27 May lifting, reducing to 1 week at 17°C after 22 June lifting. Flowering within 21 glasshouse days was achieved only after 15 or 22 June lifts followed by 4–5 weeks at 17°C. The earliest flowers in ‘Fortune’ (7 November) were produced following 3–5 weeks at 17°C after lifting on 27 May or 1 June, or following 1–2 weeks at 17°C after later lifting. In ‘Carlton’, the earliest flowers (23 November) followed 2–3 weeks at 17°C after lifting between 1 and 15 June, or 0–1 weeks at 17°C after the last lifting date (22 June). Following the use of 3 weeks' 17°C-storage, flowering date was about equal, irrespective of lifting date. However, further extension of 17°C-storage resulted in a delay in flowering date. Scape length increased irregularly with longer storage at 17°C; scapes were taller following later lifting (8–22 June) than following earlier lifting. Differences in flower diameter between treatments were relatively small.     

Possible role of non-structural carbohydrates in flower induction in strawberry

Summary

Flower-induction is the event that initiates the transition of a vegetative apex into a floral apex in response to an environmental or developmental cue. Under flower-inducing conditions, biochemical or physiological changes can be recognised. One possible change that could occur is in sugar content. In this study, levels of non-structural carbohydrates (e.g., sucrose, glucose, fructose and starch) were measured in shoot tips, leaves and roots of strawberry (Fragaria ananassa cv. ‘Kordestan’) under flower bud-inducing conditions, and compared with non-induced plants. Runner plants were potted and grown for 4 weeks under non-inducing conditions (31º/25°C day/night; 16 h daylength). Half of the plants were then put under flower-inducing conditions (25°/15°C day/night; 8 h daylength) for 3 weeks. Samples for carbohydrate analysis were taken from induced and non-induced plants every 3 d over 3 weeks, and sucrose, glucose and fructose contents were determined by HPLC, and starch concentrations by the anthrone method. The most abundant soluble sugar, in all organs tested, was sucrose. Sucrose levels in shoot tips and leaves decreased at the beginning of the induction treatment, but soon increased to the levels recorded in non-induced plants. Fructose increased markedly in shoot tips of induced plants 3 d after the start of the short-day treatment, and declined thereafter. Starch contents in shoot tips, leaves and roots of non-induced strawberry plants were higher than those in induced plants on most sampling dates. From the results of this study, it appears that soluble carbohydrate contents in different organs of June-bearing strawberry may have a decisive role on flower-bud induction.     

Leaf production and curd initiation of winter cauliflower in response to temperature

Summary

In experiments in 1994 and 1995 a range of transplanting dates and thermal crop covering treatments were used to produce different environmental conditions for the growth of two Roscoff cauliflower selections ‘December/January’ and ‘March’. In 1994 non-covered plants of ‘March’ initiated on average 19 d later and with 19 leaves more than ‘December/January’. In the two seasons, covering the crops gave delays in curd initiation of up to 93 d, depending on planting date, and increased the number of leaves produced by up to 50 compared with non-covered crops. Leaf production was best described by an accumulated effective day-degree scale using day-degrees <17°C for ‘December/ January’ and day-degrees <16°C for ‘March’. This shows that both light and temperature are concerned with controlling leaf production. During the juvenile phase of growth, apex diameters expanded linearly with temperature up to a diameter of about 0.2 mm. After this there was a different response to temperature suggesting that a phase change had occurred at an apex diameter of 0.2 mm. When this occurred numbers of leaves ranged from 23 to 28. Vernalization appeared to occur most rapidly in ‘December/January’ between 12 and 16°C with an optimum at about 14°C while in ‘March’ the optimum appeared to be slightly lower than this. Any increase in time spent at temperatures in excess of 16°C delayed curd initiation.     

Verfrühung von Süßkirschen im Folienhaus

Early ripening sweet cherry cvs ‘Burlat’, ‘Earlise’, ‘Samba’, ‘Souvenir des Charmes’ and clone M, which are all characterised by large fruit size and dark red fruit, on GiSelA 5 rootstock were forced – by closing a polytunnel from 24 March to 20 April 2006 – at Klein-Altendorf research station of Bonn University. A portable gas heater was used for automated frost protection in April. An adjacent uncovered planting at the same spacing of 3.8?m?×?1.75?m served as control. Forcing resulted in a 16–18 days earlier flowering in April relative to the 12–16 days earlier harvest at the beginning of June, resulting in a 2–4 days longer fruit development and retarded ripening. PAR was reduced in the polytunnel by 40% on sunny and 30% on overcast days with a concurrent drop in the humidity to 30% on sunny and 40% on overcast days and nearly 100% relative humidity at night. Polytunnel air temperatures on sunny days were increased – during ventilation – by up to 6?°C relative to the outside, e.g. 33?°C versus 27?°C outside. Forced cherries saved one spray application against aphids compared to those outside. Fully-grown cherry leaves contained 40–60?mg chlorophyll/g FM sufficient for photosynthesis with commensurate chlorophyll contents when grown in the polytunnel compared with those outside, and were deficient in calcium (0.5% DM) and magnesium (0.2% DM), but with a surplus in both nitrogen (3.5% DM) and phosphorus (0.42% DM). The surplus leaf nitrogen was due to excessive nitrogen mineralization in the rich soil under the higher temperatures in the polytunnel which caused the vigorous vegetative growth despite the dwarfing rootstock. Great fluctuations in fertilisation – despite strong flowering and sufficient pollination with honey bees – of between 4–71% may be due to the combination of S-alleles of the cherry varieties, infrequent water supply, nutrient imbalance and microclimate. Trees of cv. ‘Burlat’, ‘Earlise’ and clone M in their fourth leaf yielded an average of 2.5–7.5?kg fruit with 15?kg/tree in one case. Fruit of forced cvs. ‘Burlat’, ‘Souvenir’ and ‘Samba’ were larger compared with those of cv. ‘Earlise’ and clone M, which were smaller as a result of increased fruit load on the tree than those from uncovered control trees. For all five cvs tested, except forced cv. ‘Earlise’, a fruit mass of between 10?g (28?mm ) and 12?g (30?mm) and a sugar content of 12–17% with sugar:acid ratios of 20–37:1 made their fruit suitable for marketing as superior or premium fruit at higher farm-gate prices of 4.5–8?€/kg. Fruits were sufficiently dark red or black and firm for short distance transport and rapid sale. An economic evaluation showed financial gains, when yields exceed 8?kg fruit per tree per year at a farm-gate price of 4.50?€/kg.     

Effect of the plant raising environment,transplant weight and date of transplanting on the subsequent growth and development of leeks (Allium porrum L.) grown for early production

Leek transplant weight at planting was greater for a given period of growth at 23°C than at 9°C but was unaffected by nutrition. A single line fitted to all the data, using a time-scale based on ‘effective day-degrees’ (with a base of 4°C and an upper limit of 23°C) accounted for over 76% of the variance in transplant weight at planting. Plant weight at harvest was positively related to transplant weight and fitting straight lines to each of the early and late harvest data sets from all the experiments accounted for 75% of the variance in plant weight at harvest. There were no ‘carry-over’ effects of temperature or nutrition from the plant-raising phase other than those on transplant weight. It was calculated, using data from two of the experiments where transplanting date was a factor, that yields fell by between 0.4 to 1.61 ha“1 for each week’s delay in planting over the period early April to mid-June. This loss in yield could be compensated by planting larger plants; 300 g plants could be produced in early August by planting 0.6 g, 0.9 g and 1.7 g plants in mid-April, mid-May and early/mid-June, respectively. The number of plants with flower initials at harvest increased with an increase in transplant weight and exceeded 10% with transplants of 0.5 g fresh weight or more and, for comparable transplant weights, was substantially greater from plants raised at 9° than 12°C. Flower initials were present even in crops from plants raised at 23°C. Transplants raised at 9°C produced up to 30% bolters at harvest but bolters were almost completely absent in crops established from plants raised at 12°C, 18°C or 23°C. Small plants (<0.4 g fresh weight) with 2-3 visible true leaves responded to cold.     

The influence of temperature on photosynthesis of different tomato genotypes

Net photosynthesis and dark respiration from whole plants of various tomato genotypes were measured in a closed system. At low irradiance (27 W m^?2) and low external CO₂ concentration (550 mg m^?3), net photosynthesis of 10 genotypes was found to vary between 0.122 and 0.209 mg CO₂ m^?2 s^?1. Correlation was observed between net photosynthesis, net uptake on a daily basis (8 h photoperiod at 20°C and 16 h nyctoperiod at 10°C), specific leaf weight and leaf area ratio. At high irradiance (243 W m^?2), high external CO₂ concentration (1480 mg m^?3) and ambient temperatures of 10, 18, 20 and 26°C, four genotypes were analysed. ‘F6 I.V.T.’ had the highest rate of photosynthesis at 10°C, while ‘Sonatine’ ranked high at 26°C. Dark respiration increased with temperature, except in the case of ‘Bonabel’ where the effect of temperature was slight.     

Effects of Runner Tip Size and Plugging Date on Fall Flowering in Short-Day Strawberry (Fragaria × ananassa Duch.) Cultivars

Abstract

Producing strawberry transplants from runner tips that were plugged ～1 month earlier (early July) than the standard time (early August) promoted fall flowering in some short-day strawberry cultivars. In 2002,100% of ‘Chandler’ transplants produced in early July flowered in the fall, but none of the August-plugged ‘Chandler’ transplants flowered in the fall. In 2003, 73% of ‘Chandler’ transplants produced in mid-July from average-size runner tips and less than half of transplants from small-size runner tips flowered in the fall. Again, August-plugged plants did not flower in the fall. Flowering was absent in ‘Northeaster’ plants. Under protected cultivation, July-plugged ‘Sweet Charlie’ plants bloomed earlier and produced more fruit in November and December than those plugged in August. This study showed that fall flowering in ‘Chandler’ and ‘Sweet Charlie’ strawberry is possible if the transplants are prepared by plugging runner tips in early July. This novel technique for propagating strawberry transplants for annual plasticulture combined with production under high tunnels creates an opportunity for strawberry production in early winter and again in the spring (double cropping) in the mid-Atlantic coast region.     

Growth responses of some greenhouse plants to environment. II. The effect of soil temperature on Chrysanthemum morifolium Ramat

The effect of a wide range of soil temperatures (6–26°C) on growth and flowering of Chrysanthemum morifolium Ram. ‘Horim’ were studied at the favourable air temperature of 18°C. Shoot growth was severely reduced at soil temperatures below 10°C which may be explained by poor root growth, while flowering was enhanced by approximately 2 days compared to higher soil temperatures. Increasing the soil temperature to 18°C was beneficial. Further increase had no positive effect on growth. Measurements of net photosynthetic rates revealed no effect of lowering soil temperatures from 18 to 6°C.Mother plants grown at 18°C air temperature revealed no effect of soil temperatures ranging from 13 to 21°C on number and fresh weight of the cuttings. Neither did mother plants grown at the less favourable air temperatures of 12 or 15°C. Cutting production was, however, affected by air temperature.     

Fruit Quality and Composition of Two Advanced North Carolina Strawberry Selections

ABSTRACT

The advanced selections, NCS 10-038 and NCS 10-156, from the North Carolina breeding program were compared to the traditionally used cultivars, Camarosa and Chandler, for storage life and fruit composition in 2014 and 2015. Postharvest quality of NCS 10-038 was similar to that of ‘Camarosa’ and ‘Chandler’ after 8 days storage at 4 °C. NCS 10-156 was significantly worse in overall appearance and had more fruit shrivel, calyx browning, and mold than the other genotypes. However, NCS 10-156 was highest in soluble solids content and was similar in total anthocyanin content and total phenolic content to ‘Camarosa’ and ‘Chandler’. Further analysis of flavonoids by high performance liquid chromatography showed that NCS 10-156 was much lower in total flavonols than the other genotypes and comparable in anthocyanin pigments to ‘Chandler’. NCS 10-038, while similar in pigment profile to ‘Camarosa’, had less total anthocyanin than the other genotypes. NCS 10-038 had a lighter red color than the other genotypes and was similar in postharvest quality to ‘Chandler’ and ‘Camarosa’ and may be suitable for long-distance markets. NCS 10-156 is slightly softer than the other genotypes and more prone to mold while the higher soluble solids content may make it suitable for direct market sales. Both selections show postharvest promise for strawberry production in the humid mid-South region.     

Factors affecting the quality and in vitro germination capacity of strawberry pollen

Summary

Poor pollen quality and germination capacity curtails early yield in strawberry. The aim of this study was to establish a reliable method for in vitro assessment of strawberry pollen germination ability and to investigate further the effects of photoperiod and gibberellin on pollen germination and quality. In the first part of the study, pollen from seven strawberry cultivars (Chandler, Selva, Tudla, Camarosa, Eris, Pajaro and Irvine) was collected and its germination capacity and incidence of deformed pollen grains assessed in vitro using the hanging-drop technique. Highest germination rates, in ‘Selva’, were observed in a nutrient medium of 10% sucrose. Addition of calcium nitrate to the medium decreased the germination percentages of all cultivars. There was no significant difference, on average, between the germination rate at 20° and 25°C. Genetic factors affected the incidence of deformed pollen grains significantly, with ‘Pajaro’ showing the highest percentage (76%). In the second part, groups of young strawberry plants, cultivar Seascape, grown either under natural early spring conditions or under long-day or short-day conditions were sprayed once with GA₃ at 0, 50, or 200 mg l^–1. Pollen germination and deformation and stamen length were assessed three months later. In plants of the first group, GA₃ at 50 mg l^–1 increased pollen germination and decreased the incidence of deformed pollen grains, while GA₃ at 200 mg l^–1 decreased pollen germination without affecting the formation of deformed pollen grains. Plants of the second group showed a higher rate of pollen germination under long than under short days. GA₃ at 200 mg l^–1 decreased pollen germination under either short- or long-day conditions compared with the controls but doubled the percentage of deformed pollen only under short days. Stamens in control plants grew four times as long under long- than short-day conditions. GA₃ did not affect stamen length under long days but significantly enhanced their growth under short days.     

Effects of pre- and post-bloom temperature regimes on development of Lilium longiflorum Thunb.

Glasshouse grown ‘Ace’ and ‘Nellie White’ Easter lily plants were subjected to different temperature regimes to determine temperature requirements during pre- and post-bloom development. Rate of leaf- and flower-bud development and stem elongation on the primary (mother) axis were directly proportional to the range of temperatures used (6–24°C), and were equally effective in predicting crop development. Scale initiation on the secondary (daughter) axis during pre-bloom phases was proportional to growing temperature, reaching maximum activity at 18°C in ‘Ace’ and at 12°C in ‘Nellie White’. The shift from scale to leaf initiation and development following anthesis was favored by 12 rather than 18°C with significant reductions in leaf initiation in both cultivars at 24°C. No difference in secondary meristem diameter occurred with temperature during pre-bloom, but large dome size was associated with 12°C or lower during the post-bloom phase. Primary scale weight increase (filling), reached a maximum 50 days following anthesis, and was greatest at 18°C. Secondary scale filling reached a maximum 80 days after anthesis at both 18 and 24°C. The secondary axis became increasingly responsive to sprout-inducing temperatures with increasing age and development. Fifty days after anthesis, 12 and 18°C were equally effective in sprouting ‘Ace’ bulbs, while 12°C was more effective with ‘Nellie White’. Early leaf senescence, associated with high (24°C) temperature, did not favor increased bulb size, daughter leaf primordia count and meristem diameter, or sprouting.