The effect of ethephon on the growth and development of Liatris spicata

Summary

The first experiment studied the effect of applying ethylene biosynthesis regulating compounds (ethephon 1000 ppm, silver thiosulphate 0.4 mM and cobalt chloride 5 mM) on the growth and development of Liatris spicata cv. Callilepis. The results pointed to the important growth retardant properties of ethephon and the increased number of flowering stems per corm which could be obtained by pre-planting application. A second experiment aimed to optimize ethephon treatment in Liatris by applying the growth retardant in different concentrations (100, 700, 1300, 1900 and 2500 ppm) at three stages of development: stage I (pre-planting), stage II (immediately after the formation of basal leaf rosette) and stage III (when the main shoot began its rapid longitudinal growth). Besides confirming the effects produced by ethephon in the first experiment, the results suggested that the application of high ethephon concentrations (1900 and 2500 ppm) during stage II of growth produced many miniature flowering stems coming from the principal or secondary shoot.     

Flowering in pineapple as influenced by ethephon and its combinations with urea and calcium carbonate

An investigation was carried out to increase the efficacy of ethephon by combining it with urea and calcium carbonate for induction of flowering in pineapple, with the main objective of lowering the concentration of ethephon. Ethephon at a concentration as low as 25 ppm in combination with urea (2%) and calcium carbonate (0.04%) was able to induce more than 90% flowering after 50 days of treatment. Addition of either urea or calcium carbonate increased the effectiveness of ethephon for induction of flowering. Ethephon treatments were found to be markedly superior to planofix and the control. In the case of the control, plants started flowering 250 days after treatment and completed it after 340 days. Apart from earlier flowering, ethephon treatments resulted in uniform ripening, and harvests were complete within 10 days, whereas in the control harvests continued for about 70 days. The increased efficacy of ethephon at a lower concentration for induction of flowering, with the addition of urea and calcium carbonate, is of great significance as this will lead to decreased costs and increased commercial use.     

Effects of temperature on fruit thinning with ethephon in ‘Golden Delicious’ apples

The effect of temperature on the ability of 2-chloroethylphosphonic acid (ethephon), when applied at 20 mm stage of fruit development, to induce ethylene evolution of fruit and leaves and abscission of fruit and leaves was determined using 9-year-old root-bagged ‘Golden Delicious’/M.27 apple (Malus domestica Borkh.) trees in environment-controlled growth rooms. Ethephon at 400 μL L⁻¹ effectively thinned apples, and its thinning effect was not affected by increasing day/night temperature from 21.1/10 to 32.2/21.1 °C. Fruit ethylene evolution was enhanced by application of ethephon. Peak fruit ethylene evolution occurred 1 day after application of ethephon when day/night temperature was 32.2/21.1 °C whereas it occurred 2 days after application of ethephon at a day/night temperature of 21.1/10 or 26.7/15.6 °C. Ethephon increased leaf ethylene evolution drastically but it did not induce leaf abscission regardless of temperature.     

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.     

Temperature effects on corm dormancy and growth of Zephyra elegans D.Don

Experiments were performed with the Chilean geophyte Zephyra elegans, a potential cut flower, to evaluate the effect of corm weight and storage temperature on corm dormancy, and to determine the effect of day and night growing temperatures on its growth and flowering. Z. elegans has a deciduous and synanthous growth habit and the corm is replaced annually. Dormant corms were stored at different constant temperatures or temperature combinations from 20 to 40 °C. Corms released from their dormancy were grown at 15/10, 20/15, or 25/20 °C day/night temperatures. Corms of various weights were planted at the same date after being stored dry at 25 °C for 22 weeks. They all emerged 19–38 days after planting, showing that dormancy release was not affected by corm weight. A 20-week corm storage treatment at a constant 25 °C resulted in the most rapid corm sprouting. Sprouting percentage was reduced at higher or lower storage temperatures. Temperature also affected plant growth. When plants were grown at 15/10 or 20/15 °C they emerged and flowered more rapidly than when they were grown at 25/20 °C. The latter growing temperature also resulted in poor flower quality.     

The influence of fruiting on the bud sprouting and flower induction responses to chilling in Citrus

Summary

The effect of chilling temperatures on bud sprouting and flower formation was compared on fruiting and non-fruiting ‘Owari’ satsuma mandarin (Citrus unshiu Marc) trees. On non-fruiting trees, bud dormancy was weak, and a significant proportion of buds were able to sprout at high temperatures without being chilled. Separate effects of low temperatures on bud sprouting and flower induction were demonstrated. On fruiting trees these two effects of low temperatures were also demonstrated on summer-flush buds, but not on older (spring-flush) buds. The spring-flush buds from fruiting trees scarcely sprouted without being chilled. These buds required a longer chilling period for dormancy release than for flower induction, and it was not possible to separate the effect of low temperature on flower induction from the effect on dormancy release. The presence of fruit reduced flower formation by reducing bud sprouting. Furthermore, fruit had a direct inhibitive effect on vernalization which resulted in increased formation of vegetative shoots. The effect of fruit and low temperature on flowering was unrelated to carbohydrate accumulation in the leaves or the roots.     

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 mode of action of ethephon in increasing health of gladiolus corms

Gladiolus corms and cormels were treated with various combinations of ethephon and the fungicides methylethyl mercury benzoate, benomyl, thiobendazole and methylmercury dicyandiamide either before or after storage at 10 °C and 30 °C for 6 weeks. The treated corms were examined for germination, splitting and rot symptoms caused by Fusarium oxysporum f. sp. gladioli.

Ethephon increased corm splitting in all treatments; it also increased germination in corms stored at 30 °C, and it increased the proportion of corms showing typical Fusarium rot symptoms by stimulating the growth of latent internal Fusarium. The effectiveness of the fungicides tested against F. oxysporum f. sp. gladioli was enhanced by the addition of ethephon. Permeability of corms to methylethyl mercury benzoate was increased by ethephon, and it is concluded that ethephon improves the efficiency of this fungicide, and probably of other fungicides as well, by increasing their penetration into gladiolus corms.     

Manipulating Regular Bearing in ‘Golden Delicious’/M9 Apple Trees using GA4+7 and Ethephon

Control of regular cropping in apple is considered critical for fruit growers to ensure their economical sustainability. Irregular flowering can be mitigated by plant growth regulators thanks to their promotion or inhibition effects. In this study, responses of GA₄₊₇ and ethephon on alternate bearing in ‘Golden Delicious’/M9 were examined. GA₄₊₇ and ethephon were applied on the same trees during three consecutive years (2010–12). Flowering, yield, shoot growth, and also some fruit quality parameters were assessed. GA₄₊₇ appeared to be more effectual to regulate alternate bearing. The alternate bearing index calculated with yield in successive years was high in control (0.91), moderate in ethephon (0.71), and low in GA₄₊₇ treated trees (0.41). Modified alternate bearing index, based on cluster number, indicated moderate intensity in GA₄₊₇ (0.53) and high intensity in the others. Although GA₄₊₇ reduced crop density at about 50%, there was little variation in yield per tree and crop efficiency due to increasing of fruit size. GA₄₊₇ did not increase shot length after establishment of equilibrium between vegetative and generative growth in 2012. Ethephon slightly reduced vegetative growth and relatively increased fruit size due to the decrease of fruit set.     

Effects of temperature and plant growth regulators on anthocyanin synthesis and phenylalanine ammonia-lyase activity in chicory (Cichorium intybus L.)

Summary

This study addresses the effects of air temperature and plant growth regulators on anthocyanin synthesis, sugar content and phenylalanine ammonia-lyase (PAL) activity in chicory (Cichorium intybus L.). Anthocyanin in chicory was synthesised at the highest level under 15°/10°C (day/night) temperatures, followed by 20°/15°C, and 25°/20°C; while synthesis was inhibited > 90% at 30°/25°C, resulting in an almost green colour. Sugar contents paralleled anthocyanin development under the same temperatures. The plant growth regulators, abscisic acid (ABA), ethephon and uniconazole all stimulated anthocyanin synthesis, with uniconazole treatment showing the greatest effect. Gibberellic acid (GA₃) inhibited anthocyanin development, while GA₃ in combination with uniconazole alleviated this inhibition.

PAL activity was higher at 15°/10°C or 20°/15°C (day/night) temperatures when plants were treated with ABA, ethephon or GA₃, than at 25°/20°C and 30°/25°C (day/night) temperatures. These results suggest that, under lower temperatures, plant growth regulators may play an important role in anthocyanin synthesis and PAL activity in chicory.     

Thinning ‘Red Fuji’ apples with ethephon or NAA

Summary

A series of trials in Tasmania examined the thinning effects of ethephon and NAA on ‘Red Fuji’ apple. In the ethephon trials, concentrations from 25 to 600 ppm were applied at full bloom (FB) or 14 days after full bloom (AFB) to trees on either seedling or M.M.106 rootstocks. The NAA trial involved spraying concentrations of 5, 10 or 15 ppm at FB or 14 days AFB to trees on seedling rootstocks. Ethephon thinning of ‘Red Fuji’ was similar at FB and 14 days AFB. The dependence of fruit thinning on ethephon concentration was described by fitting non-linear response curves. These relationships were stronger and less variable for M.M.106 than seedling trees. Ethephon proved a satisfactory thinner for trees on both rootstocks. At the high spray volume used, the preferred concentrations at both FB and 14 days AFB would be 25 or 50 ppm for seedling and 100 or 200 ppm for M.M.106 rootstocks. NAA under-thinned at 5 ppm and over-thinned at 10 and 15 ppm at both FB and 14 days AFB. No firm recommendation can be given for NAA as a thinner of ‘Fuji’ at this stage.     

The effects of low temperatures on the vegetative growth and flowering of the primocane fruiting raspberry ‘Autumn Bliss’

Summary

The effects of low temperatures on subsequent vegetative growth and flowering in the raspberry ‘AutumnBliss’ were investigated. In the first experiment, a number of lifting dates were used to determine the seasonal pattern of dormancy and the effect of natural chilling on plant development. In the second, different durations of artificial chilling(0, 2, 4, 6, 8 and 10 weeks at 0?C) were combined with two lifting dates to investigate the effect of natural and artificial chilling. In these experiments, plants which received little chilling grew slowly and failed to develop beyond short rosettes of leaves but as chilling increased, the rate of vegetative growth increased. This coincided with a decline in the time toflowering. These two responses, however, were distinct. In a third experiment, the effect of vernalization of actively growing canes was tested in an attempt to separate the effects of cold on time to flowering, and on the removalof dormancy. The plants responded significantly to cold treatment and flowering was advanced, indicating a distinct vernalizing effect     

The response of bud break and flowering to cool winter temperatures in kiwifruit (Actinidia deliciosa)

Summary

A range of temperatures (7°C, 10°C or 13°C mean) were imposed under controlled conditions on four year old, container-grown ‘Hayward’ kiwifruit vines. The treatments were applied for periods of from one to four months during the dormant period from May to September (Southern Hemisphere). Following these treatments the vines were held at a “forcing” temperature of 16°C mean until flowering. The objective was to define the response of bud break and flowering in spring to temperatures experienced during the preceding winter. Cool winter temperatures dramatically increased flower numbers, increased the proportion of bud break, advanced the day of bud break, and increased the duration from bud break to flowering. These responses were much larger between 13°C and 10°C than they were between 10°C and 7°C. For any treatment duration, the temperature imposed during dormancy had no effect on the time of flowering. Two months at cool temperatures produced the greatest number of flowers per winter bud, with reduced numbers at three and four months. The proportion of winter buds that produced shoots showed a similar response. The Richardson chill unit is frequently used to describe the effects of winter chilling on kiwifruit. It proved unreliable as an index to integrate the effects of temperature and time on any of the developmental variables monitored in this experiment.     

The Effects of Some Growth Regulators on Peach Flower Bud Abscission

Applications of growth regulators to detached peach laterals in winter had variable effects on flower bud abscission. GA₃ and GA₄₊₇ increased bud abscission while IAA, BA and ABA inhibited abscission. Ethephon had a variable effect. Interactions were obtained between the compounds generally with IAA or GA playing the major role. GA had a peak of activity during a critical period in late winter indicating a variation in responsiveness. Variations in sensitivity to GA were obtained for different cultivars. Field applications of GA₃, GA₄₊₇, and ethephon to Elberta peach trees in winter, alone and in various combinations, promoted bud abscission.     

Physiology of flowering and dormancy regulation in annual- and biennial-fruiting red raspberry (Rubus idaeus L.) – a review

Summary

Recent research on how the structure and physiological development of red raspberry (Rubus idaeus L.) plants are controlled by genotype and the climatic environment is reviewed. Some older work, especially on plant structure relations, is also included. Physiological differences between annual- and biennial-fruiting plant types are highlighted. One major difference is the different requirements for flower formation. While biennial-fruiting cultivars have an absolute low temperature (≤ approx. 15°C) requirement for floral initiation, annual-fruiting cultivars readily initiate floral primordia at temperatures as high as a constant 30°C. Also, while biennial-fruiting cultivars are facultative short-day plants with a critical photoperiod of 15 h at intermediate temperatures, flowering is promoted by long photoperiods in at least some annual-fruiting cultivars. However, the essential difference that determines whether the shoot life-cycle becomes annual or biennial is that, in biennial-fruiting genotypes, floral initiation is linked to the induction of bud dormancy; whereas, in annual-fruiting cultivars, floral initiation is followed by direct flower development. Although this is genetically determined, it is a plastic trait that is subject to modification by the environment. Thus, at low temperatures and under short photoperiods, the majority of initiated buds also enter dormancy in annual-fruiting cultivars, with tip-flowering as a result. Practical applications are discussed, and it is concluded that our present physiological knowledge-base provides excellent opportunities for the manipulation of raspberry crops for out-of-season production and high yields. It also provides a firm platform for further exploration of the underlying molecular genetics of plant structures and response mechanisms.     

Flowering in six clones of the Andean root crop arracacha (Arracacia xanthorrhiza Bancroft)

Summary

The effect of dehydration on arracacha (Arracacia xanthorrhiza Bancroft) cormels was investigated and found to have a positive effect on flowering for some accessions and a negative or negligible effect on others. The clear difference in flowering response between accessions is attributed to genetic variation and suboptimal growth conditions. The unclear results indicate that the treatments used were suboptimal and that factors other than drought stress are involved in flower induction. However, the dehydration treatments had a positive effect on the production of hermaphrodite flowers in all accessions, and dehydration is therefore considered an important factor in the flower-inducing treatment. The high temperatures and low humidity during the current experiment had a negative effect on pollen release and thus seed production, indicating that a moderate temperature is needed during the arracacha growth period. There are clear morphological differences between the accessions, with ABS 5516 as the most vigorous and with the highest measured values in all variables except percentage of hermaphrodite flowers.     

Effects of ethephon and 2,4,5-T on fruit size,rind pigments and alternate bearing of ‘Imperial’ mandarin

Ethephon and 2,4,5-T were used on ‘Imperial’ mandarin to study their effects on fruit thinning, fruit size, rind pigments and alternate bearing.Ethephon at 250 p.p.m. produced the largest and heaviest fruits. Pigment levels were not affected by 2,4,5-T, but ethephon increased carotenoids and reduced chlorophyll a and b levels. The effectiveness of a colouring agent seems to be related to its ability to reduce both levels of chlorophyll a and b provided that carotenoid levels do not decrease.Treated trees exhibited less tendency towards alternate bearing than control trees. Ethephon had a greater thinning-effect than 2,4,5-T. It also evened cropping for 2 successive years. One spray of ethephon in an “on” year would be effective in reversing and leveling cropping of ‘Imperial’ mandarin for at least 4 years under Mildura conditions.     

Alleviative effects of calcium acetate on defoliation and fruit drop induced by 2-chloroethylphosphonic acid in citrus

Experiments were conducted to evaluate the effects of calcium acetate on defoliation and fruit drop of ponkan (Citrus reticulata Blanco) and Meiwa kumquat (Fortunella crassifolia Swingle) trees treated with 2-chloroethylphosphonic acid (ethephon). Ethephon at 200 or 300 p.p.m. caused about 20% defoliation of ponkan trees, while this defoliation was materially alleviated by an addition of 0.05 M calcium acetate to the ethephon solution. Acceleration effects on fruit color did not differ with ethephon or ethephon + calcium acetate treatments. Ethephon at 400 p.p.m. caused about 30% fruit drop in kumquat trees, and an addition of 0.05 M calcium acetate to the solution almost completely prevented the fruit drop. Fruit color of kumquat was most advanced by the use of ethephon alone, and the addition of calcium acetate decreased the effect slightly.     

Effects of growth retarding treatments on apple tree growth,fruit maturation and fruit abscission

SUMMARY

Eight days after petal fall in 1991, mature 'Delicious'/MM. 106 apple trees and four days after petal fall in 1992, mature 'McintoshVMM. 106 were ringed, scored, root pruned (1 m from the trunk, two sides, 30 cm deep), or treated with ethephon (500 mg 1¹). Only ringing and scoring reduced vegetative growth. Ethephon advanced fruit maturation and fruit abscission, but root pruning did not affect the trees or fruit significantly. Mature 'Cort-land'/M.7a apple trees were root pruned 8 d after petal fall in 1991 and/or at full bloom in 1992. Root pruning reduced shoot growth, even in the year after treatment. Fruit abscission was reduced in 1991 and 1992 by root pruning in 1991, but root pruning in 1992 had no impact on abscission, in 1992. In an additional experiment, mature 'Mcintosh'/ MM.106 were root pruned 4 d after petal fall in 1991 or root pruned both in 1991 and at full bloom in 1992. Growth and preharvest fruit abscission were reduced in both the year of root pruning and the year after.     

Influence of sub-optimal temperature on tomato growth and yield: a review

Summary

The effects of temperature on growth, development and yield of tomato (Lycopersicon esculentum) are reviewed with special emphasis on cultivar differences. The focus is on sub-optimal temperatures, above the level where chilling injury occurs. Temperature has a large effect on all aspects of development. Leaf and truss initiation rates decrease linearly with decreasing temperature. Although these rates may be different for different cultivars their response to temperature is the same. Young plants grown at sub-optimal temperatures produce thicker leaves, so they intercept less light and therefore have a lower relative growth rate. There was no interaction between temperature and cultivar for relative growth rate and related traits. In a crop producing fruits, this aspect is less important as most of the light is intercepted anyway. At sub-optimal temperatures, fruit set is reduced as a result of poorer pollen quality. The period between anthesis and ripening of the fruit increases and, as the growth rate of the fruit at a certain developmental stage is independent of temperature, fruits become larger at sub-optimal temperature. Higher temperature leads to an increase in early yield, at the cost of vegetative growth, but may also cause a delay in later trusses. Total yield over a whole season might be equal at lower temperatures, but higher tomato prices early in the season do not make it economically profitable to reduce the temperature in the greenhouse. Short-term effects might thus be different from long-term effects. In the literature, the link between yield and whole plant growth is often missing, limiting the possibilities of studying the underlying processes that contribute to changes in yield. Breeding for cultivars with equal production at lower temperatures is hampered by the limited variation for temperature response in cultivated tomato. Therefore breeders have to look for other sources of variation, as in related wild Lycopersicon species.