Flowering performance and yield of established and recent strawberry cultivars (Fragaria × ananassa) as affected by raising temperature and photoperiod

Plants of six strawberry cultivars were raised under controlled conditions and tested for flowering and yield potential. Short days (SD) at intermediate temperatures for 4 weeks in August induced profuse flowering in subsequent long days (LD) in all cultivars except the late-flowering ‘Malwina’. LD conditions induced flowering only in ‘Nobel’, which has an everbearing parent. ‘Nobel’ and ‘Saga’ exhibited broad temperature adaptation for SD floral induction, which was generally reduced or suppressed at 9 and 27°C. After autumn planting, all cultivars flowered most abundantly in plants raised in SD and intermediate temperatures. Flowering was earliest in ‘Nobel’ and ‘Rumba’. Plants that did not reach floral commitment after 4 weeks in SD continued and completed induction under subsequent natural SD conditions after planting in the field, demonstrating the capability of fractional induction. Berry yield varied in parallel with flowering in the field and was always higher in plants raised under SD conditions. The traditional cultivars ‘Florence’ and ‘Sonata’ out-yielded the more recent cultivars. Some cultivars lost more than two thirds of their initiated flowers during the winter with obvious consequences for their yields. With proper raising management, acceptable yields were obtained after autumn planting even in a cool Nordic climate.     

Quantitative long-day flowering response in the perpetual-flowering F1 strawberry cultivar Elan

Summary

Perpetual-flowering strawberry cultivars are commonly classified as photoperiodically day-neutral, even though early investigations demonstrated long-day (LD) regulation. An important reason for this inconsistency is that these freely flowering plants are difficult to establish in a true vegetative state, and experiments have therefore often been started using runner plants with pre-formed inflorescences. In order to circumvent this problem, we have used the perpetual-flowering F₁-hybrid ‘Elan’ that is propagated by seed, and is thus not pre-conditioned by its earlier life history. The results demonstrated a marked quantitative LD response across a range of temperatures from 9° – 27°C. Seedlings were responsive to the LD stimulus at an early stage, and early flowering required LD exposure almost from germination. The critical daylength for the early flowering response was about 15 h at 18°C. Because of this threshold LD response, it is concluded that regulation of flowering is truly photoperiodic in nature, and not merely an effect of additional light. Flower development was also slightly advanced by LD conditions. Stolon formation was strongly enhanced by short-day conditions in combination with high temperature. Thus, not only flowering, but also runnering, was oppositely affected by photoperiod in ‘Elan’ compared with mono-flowering cultivars. The results are discussed in relation to the photoperiodic classification of strawberries.     

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 photoperiods before,during and after vernalization on flower initiation and development and its varietal difference in Japanese bunching onion (Allium fistulosum L.)

Summary

To control the bolting of Japanese bunching onion (Allium fistulosum L.) photoperiodically, the effect of photoperiods before, during and after vernalization on flower initiation and development and the varietal differences were investigated using the two mid-season flowering cvs Kincho and Asagi-kujo, and a late-season flowering cv. Cho-etsu. A long-day photoperiod (LD, 16 h) given before vernalization inhibited flower initiation. Especially, the bolting rate of ‘Asagi-kujo’ decreased by about a half, compared with the short-day photoperiod (SD, 8 h). The interaction between the effect of night temperature (3°C, 7°C, 11°C or 15°C) and the effect of the photoperiod (SD and LD) during vernalization was also investigated. In ‘Kincho’, LD did not affect flower initiation at 3°C, but inhibited flower initiation at 7°C, 11°C and 15°C. In ‘Asagi-kujo’, flower initiation was significantly inhibited by LD under all temperature conditions. This inhibitory effect was stronger at 11°C and 15°C than at 3°C and 7°C. In ‘Cho- etsu’, LD significantly inhibited flower initiation at 3°C and 7°C, and flower initiation rarely occurred at 11°C and 15°C. In this study, generally, LD during vernalization inhibited flower initiation in all cultivars. Thus Japanese bunching onion required a short-day photoperiod in flower initiation, which was stronger in ‘Asagi-kujo’ and ‘Cho-etsu’ than in ‘Kincho’. From these results, we conclude that low temperature and a short-day photoperiod complementarily induce flower initiation in Japanese bunching onion. Varietal differences exist in the requirement of low temperature and a short-day photoperiod: the primary requirement in ‘Kincho’ is low temperature and that in ‘Asagi-kujo’ is a short-day. After flower initiation, the early stage of flower development is day-neutral, and after the floret formation stage, a long-day photoperiod promotes flower development and elongation of the seedstalk.     

Effect of temperature on growth and flowering of litchi (Litchi chinensis Sonn.) cultivars

Summary

Moderate day/night temperatures (20/15° v. 15/10°C) increased vegetative growth and reduced flowering in the seven litchi cvs Tai So, Bengal, Souey Tung, Kwai May Pink, Kwai May Red, Salathiel and Wai Chee. At higher temperatures (25/20° and 30/25°C), vegetative growth was promoted further and flowering eliminated. Temperature also influenced the type of inflorescence formed. More leaves were formed on the panicles of trees growing at 20/15° than at 15/10°C. All terminal shoots on all cultivars produced panicles at 15/10°C. The relative order for the amount of flowering at 20/15°C was: ‘Wai Chee’>‘Salathiel’>‘Kwai May Pink’>‘Tai So’>‘Bengal’>‘Souey Tung’>‘Kwai May Red’. Cultivars which were vigorous at high temperatures produced fewer panicles at 20/15°C and fewer leafless panicles at 15/10°C. Only small differences were observed in the leaf water potential and the nutrient status of the shoots at different temperatures. Vigour and flowering of the cultivars in the glasshouse generally reflected field performance in subtropical Australia (Lat. 27°S). Low vigour could be useful for selecting litchi cultivars for good fruiting in environments with warm autumns and winters.     

Crown branching and cropping potential in strawberry (Fragaria ananassa Duch.) can be enhanced by daylength treatments

Summary

When strawberries (Fragaria ananassa Duch.) are produced in a greenhouse, usually two crops a year are obtained; in the fall and in the spring. To increase productivity, new cultivation techniques are needed. The aim of this study was to examine the effect of daylength treatments on the performance of strawberry plants to improve plant production protocols. The possibility of obtaining two successive crops during forcing was explored by exposing plants of cultivar Korona to two successive short day (SD) treatments followed by cold storage. The following daylength treatments were studied: 3 wk SD + 2 wk long day (LD) + 3 wk SD (3SD2LD3SD), 3 wk SD + 4 wk LD + 3 wk SD (3SD4LD3SD), and 10 wk SD (10SD). In addition, crown branching was studied in plants subjected to SD treatments. Two successive SD treatments enabled two successive flowering and cropping periods during greenhouse forcing after eight weeks of cold storage.The first SD treatment caused crown branching and induced flowering in the apical meristem of the main-crown and in the oldest axillary meristem(s), whereas younger axillary meristems were induced during the second SD treatment. Marketable yield and the number of inflorescences were comparable in 3SD4LD3SD and 10SD, but considerably lower in 3SD2LD3SD. However, this study demonstrated the high cropping potential of artificially SD treated plants, which makes them a potential alternative for greenhouse strawberry cultivation. Multi-crowned plants of ‘Korona’ can be produced by subjecting young plants to a three week SD treatment, and crown branches can be induced to flowering by a new SD treatment resulting in a very high cropping potential. Induced plants can be stored at –1°C for later forcing.     

Effect of temperature on dormancy in strawberry

Early in autumn, at the end of September or at the beginning of October, strawberry plants of the cultivars ‘Glasa’ and ‘Tioga’ were transferred from outdoors to separate phytotron glasshouses at constant temperatures of 10° and 14°C. In November a number of these plants were chilled at 3°C for 0 to 4 weeks and subsequently forced; the rest remained at 10° and 14°C until June.The plants kept at 10°C and subsequently chilled and forced, grew faster and more vigorously than those pretreated at 14°C. The 14° plants showed more pronounced growth differences resulting from the length of the chilling treatments than did the 10° plants. Those remaining continuously at 10° developed vigorously from March onwards, while those at 14°C retained their flat appearance into June. These results showed that a continuous temperature as high as 10°C was still able to break dormancy in the strawberry plants, while 14°C was ineffective.     

Environmental factors affecting flowering of rice flower (Ozothamnus diosmifolius,Vent.)

Rice flower (Ozothamnus diosmifolius, Vent.), native to east Australia, is a spring flowering perennial shrub. It is a new cut flower plant, recently introduced into cultivation in Australia and in Israel. Its response to environmental conditions, which affect growth and flowering, are not yet known. The purpose of the present study was to evaluate the effects of growth temperature, photoperiod and total solar energy on flowering. Experiments were conducted with plants of the cv. Cook’s Snow White. Plants were grown in three cycles under controlled conditions in the phytotron, at four day/night temperature regimes: 17/9, 20/12, 23/15 and 26/18°C. Two photoperiods — short day (SD) of 10 h natural day light and long day (LD) of 10 h natural light plus 10 h incandescent light — were employed. High temperatures enhanced vegetative growth but blocked flowering under both LD and SD. Under medium–moderate temperatures plants were absolute LD plants and did not flower under SD conditions. Under lower temperatures plants flowered under both LD and SD, but SD delayed flowering. High total solar radiation under LD did not affect flowering time but greatly promoted the number of flowering stems.     

Effect of temperature and daylength on flower initiation and runner formation in two everbearing strawberry cultivars

Plants of the everbearing cultivars ‘Revada’ and ‘Rabunda’ were placed at constant temperatures of 14, 20 and 26°C and daylengths of 8, 16 and 24 hours, consisting of 8 hours daylight prolonged with 0, 8 or 16 hours in can descent light, light intensity 0.8 W/m² visible radiation.Flower initiation and runner formation occurred irrespective of temperature and daylength. The duration of runner formation depended on temperature and daylength and was longer at 20 and 26°C than at 14°C and longer at 16 and 24 hours than at 8 hours.The results are discussed.     

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.     

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.     

Flowering of Primula malacoides in response to photoperiod and temperature

Primula malacoides Franch. ‘Prima Lilac’ was grown at 16 or 20 °C in combination with short days (SD, 8 h) or long days (LD, 16 h). In addition to uninterrupted growing conditions, plants within each temperature were moved at weekly intervals to the other photoperiod and left until termination. Temperature, but not photoperiod, significantly affected the rate of development from start of treatments (51 days from seeding) to 2 mm visible flower bud (VB). At 16 °C, VB averaged 30 days and at 20 °C, 48 days. Time to flower (first horizontal petals) at 16 °C increased from 56 to 64 days as SD increased from 1 week to continuous conditions while LD decreased time to flower from 64 to 56 days. Time to flower at 20 °C varied from 73 to 87 days with additional SD exposure resulting in slower and LD in faster flowering. These observations of the flowering response in ‘Prima’ are contrary to the photoperiodic classification of P. malacoides as a SD plant.     

Flower-bud formation and shoot growth in apple as affected by temperature

Under controlled conditions, 3-year old ‘Golden Delicious’ and ‘Cox's Orange Pippin’ trees were exposed to 2 temperatures (high: 24° and low: 17° or 19° C) in various treatments in a 4-month period starting at full bloom. In general, shoot growth was reduced at the low temperature. For ‘Golden Delicious’ flowering did not respond to the various treatments; in ‘Cox's Orange Pippin’ it was stimulated at the low temperature.A rise in temperature from 17° to 24° C seven weeks before harvest, given to ‘Cox's Orange Pippin’ trees kept at 17° C from full bloom, reduced flower-bud formation and stimulated growth. A similar temperature increase applied to trees maintained at 24° C for 4–5 weeks after full bloom favoured flower-bud formation, but did not affect growth.The inhibitory effect of the high temperature on flowering is discussed in terms of an increase of the plastochron under the influence of gibberellins produced by the growing shoot tips.     

Characterisation of the thermodormancy response in the everbearing strawberry ‘Everest’.

Summary

Temperature regimes that induce and ameliorate cropping troughs (“thermodormancy”) were evaluated over two seasons for the everbearing strawberry ‘Everest’. When plants were exposed to 26°C for 5, 10, 20 or 30 d in July, heat-induced troughs in cropping were observed in August. An important discovery was that cool (13°C) night temperatures ameliorated the severity of thermodormancy. In this study, thermodormancy appeared to be due principally to flower abortion post-anthesis, as large numbers of flowers emerged in mid-July, during the high temperature treatments, but went on to produce low fruit numbers in mid-August. Flower initiation itself (monitored by crown dissection) was not reduced by high temperatures. The observation that night-time temperature is critical for thermodormancy has significance for commercial production, in which protected cropping tends to increase average temperatures throughout the season, and venting tends to focus on day-time temperatures.     

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.     

Effect of short-term exposure to high-temperature on total gene expression in the leaves of four raspberry (Rubus idaeus L.) cultivars

Summary

The effect of high temperature stress (27ºC or 37ºC for 24 h) on total gene expression profiles in the annual-fruiting raspberry (Rubus idaeus L.) cultivars ‘Autumn Bliss’, ‘Autumn Treasure’, ‘Erika’, and ‘Polka’ were evaluated at the floral initiation stage using a customised Rubus microarray. Significantly affected genes were obtained by pairwise t-tests using ‘volcano plots’ for each cultivar × treatment. A 10ºC elevation in temperature altered levels of expression, in at least one cultivar, of 644 differentially expressed genes in total, with ‘Erika’ and ‘Autumn Treasure’ showing elevated expression of 38 genes compared to ‘Autumn Bliss’ and ‘Polka’. We identified 12 common candidate genes that were modulated differentially in ‘Autumn Bliss’ and ‘Erika’ at 37ºC compared to 27ºC. In addition, two aquaporin genes (PIP1 and TIP2) were down-regulated in ‘Autumn Bliss’, but up-regulated in ‘Autumn Treasure’, ‘Polka’, and ‘Erika’ at 37ºC. Other down-regulated genes from the list of 38 genes included those encoding major latex-like proteins, plasma membrane proteins, cysteine rich proteins, and other stress-related proteins. Validation by real-time quantitative RT-PCR (RT-qPCR) indicated subtle changes in differential gene expression, suggesting a mild response to heat stress. This study used molecular tools to increase our understanding of, and to identify candidate genes involved in, the heat stress response of four annual-fruiting raspberry cultivars.     

Growth of Vitis vinifera L. and Vitis aestivalis Michx. as Affected by Temperature

Abstract

Four European (Vitis vinifera L.) winegrape cvs., ‘Semillon’, ‘Pinot Noir,’ ‘Chardonnay’, and ‘Cabernet Sauvignon’, and one American (Vitis aestivalis Michx.) winegrape cv. ‘Cynthiana’, were subjected to three temperature regimes in growth chambers set at 20/15°C, 30/ 25°C, or 40/35°C, for 16/8 hr day/night to determine the influence of temperatures on vine growth and development. In general, the best temperature for shoot and root growth 28 days after temperature treatments was 20/15°C for ‘Semillon’, ‘Cabernet Sauvignon’, and ‘Cynthiana’, and 30/25°C for ‘Pinot Noir’ and ‘Chardonnay’. Although 40/35°C reduced number of leaves, shoots, tendrils, and internodes, total leaf area (LA), and total shoot biomass of all the cultivars, the reduction was more pronounced in ‘Cynthiana’ than in the European cultivars. The average reduction in number of leaves at 40/35°C for the European cultivars was 47%, compared with 92% for ‘Cynthiana’. The two types of grapes adapted differently to high temperature. Shoot growth in the European cultivars continued under high temperature, whereas growth ceased in ‘Cynthiana’. Roots of ‘Cynthiana’, however, were less susceptible to the adverse effect of high temperatures than were the shoots. This study shows that the European cultivars were relatively more tolerant to high temperature than the American cultivar and they have a potential for production of wine in the climate of south central Kansas.     

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.     

The physiology of hyacinth bulbs. XV. The effect of gibberellic acid and silver nitrate on dormancy release and growth

The effect of gibberellic acid (GA₃), supplied to dormant hyacinth bulbs of cultivars ‘Lady Derby’ and ‘L'Innocence’ by vacuum infiltration, on growth and flowering was investigated. Results showed that GA₃ in all applied concentrations (50, 500, 1000 and 5000 mg/l) accelerated growth and flowering in both cultivars, after chilling for 42 days in a garden frame in natural conditions or chilled dry in cold storage at 5°C. Bulb infiltration with 10 mg/l AgNO₃ resulted in the acceleration of flowering only in ‘L'Innocence’, but stimulated the growth of the inflorescence stalk and leaves in both cultivars regardless of the mode of chilling.The infiltration method was confirmed to be very promising.     

The effect of soil temperature on lateral shoot formation and flower-bud formation in apple in the first year after budding

Under controlled environment conditions the influence of four soil temperatures (7°, 14°, 21°, and 28°C) on vegetative development and flower-bud formation of apple trees (cvs ‘Rode Boskoop’ and ‘Elstar’) were evaluated in the first year after budding. Relative air humidity was high, air temperature was 20°C. Broadly speaking, for both cultivars shoot growth clearly increased with increasing soil temperature. The effects on growth were mainly reflected in the number (not length) of the lateral shoots; the growth of the main shoot was little influenced by soil temperature. At 7°C the lateral shoots usually occurred higher along the main stem than at the higher temperatures. Flowering on the parent stem and on the lateral shoots was little affected by the soil temperatures tested. In general, flower-cluster quality was rather poor. If only clusters having more than four well-developed flowers are considered, flowering was favoured by higher soil temperatures; at 28°C, especially, cluster quality was much better than at the other soil temperatures. It is concluded that soil temperature is important in controlling the degree of lateral shoot-formation as well as the formation of well-developed flower clusters.