Environmental and genotypic effects on bulb development in onion – a review

Environmental and genetic factors influence growth and bulb development of onions by affecting their physiology. Photoperiod plays critical a role in bulb development and determines the suitability of a cultivar for a particular region. Long days and high temperatures promote onion bulbing. Bulbing is regulated more by temperature than photoperiod, as determined by growing degree days. Far-red light promotes bulbing most effectively. High-temperature storage of sets (above 20–25°C) results in increased total bulb yields, while very high temperature (25.5–31°C) or temperature below 0°C depresses yield. Plant density has an impact on bulb size: the higher the plant density the smaller the bulb size. Onion is more sensitive to water stress during bulb formation and enlargement than during the vegetative stage. Nitrogen improves bulb development, but too much nitrogen promotes excessive vegetative growth and delays maturity. Growth hormones (gibberellins and ethrel) promote the growth and development of bulbs. Flowering and bulb formation in onion is regulated by different (Flowering Locus T) FT genes. Two antagonistic FT-like genes regulate bulb formation. AcFT1 promotes bulb formation, while AcFT4 prevents AcFT1 up-regulation and inhibits bulbing. There is a need to link our research with the genetics and physiology of onions, to enhance bulb yield.     

High-Temperature Treatment (Blindstoken) of Bulbs of Tulip cv Rose Copland for Flower Killing and Yield Improvement

A three-year experiment on the high-temperature treatment of tulip bulbs established that yield could be increased by between 8 and 31 % for bulb weight or between 14 and 29 % for numbers of large bulbs, depending upon season, associated with a near-complete flower kill. The optimum pre-treatment storage temperature was 17°C, and the best date (of the five tested) for starting blindstoken at 33°C for one week was 20th-21st September.

Yield increases were greater when the blindstoken treatment was applied to bulbs whose shoots were short; later treatment, or treatment after pre-treatments which allowed faster shoot growth, were less effective. For optimum flower kill and yield increase the shoot should be about 1 cm high at treatment. Bulb weight and large bulb number were correlated, suggesting that the treatment increases total bulb weight by increasing bulb size rather than by differentially affecting the growth of daughter bulbs.

No adverse effects of the treatments were observed when the bulbs were forced in a glasshouse the following season.     

Optimization of agrotechniques in the cultivation of Luffa acutangula

Germination requirements, flowering pattern, planting density and growing regimes were examined for Luffa acutangula (L.) Roxb. Maximum germination (50%) was obtained at 35°C, and at 8, 12, and 45°C germination was completely inhibited. Partial removal of the seed coat increased the percentage of germination while vernalization and exposure to salinity 5=50 mM NaCl reduced it. Planting season influenced flowering pattern, with significantly more female flowers being produced in spring-summer (long days and high temperatures) than in autumn-winter (short days and low temperatures). A high yield of 44.5-47.3 Mg ha 1 was obtained for plants trained on trellises at planting densities of 10,000 and 20,000 plants ha-1. Fruits kept at low temperatures showed the least deterioration during storage, a shelf life of about two weeks being demonstrated at 4°C.     

Bulbing responses of two cultivars of red tropical onions to photoperiod,light integral and temperature under controlled growth conditions

Summary

The effects of photoperiod, light intensity and temperature on bulb formation and bulb structure of two tropical onion cultivars were investigated. From an initial experiment it was observed that the number of true scales and sheath scales differed significantly between the cultivars ‘Red Creole’ and ‘Agrifound Dark Red’. When these two cultivars were given 11, 12 and 13 h photoperiod treatments, it was found that both cultivars needed at least 12 h photoperiod for bulb formation. Modify the R/FR ratio from 1.22 to 1.16 in the final hour of the 11 h light period did not induce bulbing. The 13 h photoperiod increased the number of true scales and decreased the number of sheath scales compared with the 12 h photoperiod in both cultivars but total scale + leaf sheath numbers remained nearly constant. When onion plants were grown under 0%, 25%, 50% and 75% shading treatments, (12 h photoperiod), only plants receiving 0% and 25% shading bulbed. Low light intensity decreased the number of true scales and increased the number of sheath scales. Four temperature regimes were compared in a growth room experiment. Plants under the 29°348C treatment bulbed within two weeks and matured within six weeks. However, plants receiving the 25°308C treatment delayed bulb initiation more than those plants receiving 17°228C and 21°268C treatments. At the lowest temperature, bigger bulbs with thick necks were produced. This may be due to changes in bulb structure since at low temperature, the number of sheath scales was increased, however the number of true scales remained relatively constant in both cultivars. Dormant leaf initials decreased with decreasing temperature while the number of secondary meristems significantly increased. The results suggest that ‘Red Creole’ was more responsive to shorter photoperiods, bulbing earlier than ‘Agrifound Dark Red’. There was no significant difference in time to bulbing in response to temperature between the two cultivars if measured by bulbing ratio however there were differences in bulb structure which suggested that ‘Red Creole’ bulbed earlier. These effects may be due to the breeding histories of the two cultivars. It is suggested that studying bulb structure may provide a useful method of interpreting onion bulbing responses.     

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.     

Increases in ethylene and carbon dioxide production by Tulipa gesneriana L. ‘Prominence’ after completion of the cold-requirement

Bulbs of Tulipa gesneriana L. ‘Prominence’ were either specially pre-cooled at 5 ± 0.5°C or held at 17 ± 0.5°C in a flow-through system equipped for atmospheric sampling. Bulbs at 17°C had low CO₂ and C₂H₄ production rates until January when they began to increase. An initial peak of C₂H₄ production occurred during the 2nd week of pre-cooling, followed by a major increase after 12 weeks. In addition, bulbs were specially pre-cooled for periods of 2–16 weeks (2-week increments). The bulbs were then transferred to 17 ± 0.5°C, where initial periods of special pre-cooling of greater than 12 weeks resulted in a dramatic increase in respiration rate over bulbs cooled for less than 12 weeks. These increases in C₂H₄ and CO₂ liberation appeared to be related to completion of the bulb cold-requirement. However, no surge of shoot elongation occurred after 12 weeks of pre-cooling and transfer to 17°C.     

Effect of set-size and storage temperature on bolting,bulbing and seed yield in two onion cultivars

The effects of three set-sizes (12.5, 17.5 and 22.5 mm in diameter) and seven storage temperatures (0, 5, 10, 15, 20, 25 and 30 °C) on bolting, bulbing and seed yield in two onion (Allium cepa L.) cultivars ‘Hygro’ and ‘Delta’ were investigated. The incidence of bolting increased linearly with set-size and curvi-linearly with decreasing storage temperature. Time to inflorescence emergence and floret opening showed a curvi-linear response to storage temperature with the earliest inflorescence emergence and floret opening occurring at 5 °C and the latest at 30 °C for ‘Hygro’ and at 25 °C for ‘Delta’. Seed yield per umbel also showed a curvi-linear response to storage temperature with the lowest seed yield occurring at 30 °C for ‘Hygro’ and at 25 °C for ‘Delta’ and the highest seed yield at 5 °C. For a seed crop, storage of large sets (22.5 mm) of these cultivars at 5 °C for 120 days appeared to be optimum with 5–12% higher seed yield per umbel than that of 90 days storage. Bulb yield showed a curvi-linear response to storage temperature with the highest bulb yield occurring at 25 °C and the lowest at 5 °C.     

耐热耐贮番茄品种改良

利用Lima品种作为父本与冬季栽培的番茄品种 (413、4 5 2、4 99、5 14和 5 6 0 )进行杂交 ,改良冬季栽培番茄品种的产量和品质 ,通过对杂交后代自交纯化 ,获得 4 5 2×Lima自交系产量最高 ,为 4 4 .2 9t·hm-2 ,比对照Lima和VF134 1 2增产 33.0 %和 31.6 % ,大部分自交系的果实硬度与对照相同 ;将耐热品种 6 6 7(CL5 915 2 0 6D4 2 5 0 )和 6 6 9(CL5 915 2 2 3D4 2 1 0 )与耐热的冬季栽培番茄品种进行杂交 ,然后自交并对其自交系的耐热性和果实品质进行选择 ,其中 5 0 2× 6 6 9、5 74× 6 6 7的自交系产量分别为 6 9.16和 6 6 .16t·hm-2 ,比对照Lima和VF134 1 2增产 18.2 %和 38.7% ,果实硬度与对照相同 ;将耐热品种L2 2和含突变基因 (nor1、nor2 )材料进行杂交和回交 ,对L2 2的货架期进行改良 ,其中BC2 和BC3 产量比L2 2高 4 %～ 9% ,果实在室温下保存 30d ,其完好率为 18%～...     

The effect of day and night temperatures on the growth,development and yield of glasshouse cucumbers

The responses of January-sown cucumber cvs Farbio and Sandra to day and night temperature during the early post-planting stage (late February to mid-April) were examined in a glasshouse experiment. Three day temperatures (15°, 20° and 25°C) were combined factorially with three night temperatures (10°, 15° and 20°C). Comparisons were also made between two temperature regimes (21°C day: 19°C night and 24°C day: 17°C night) applied during the pre-planting stage (late January to late February) and between two mainstem cropping methods (restriction or retention of mainstem fruits). In the pre-planting stage the 24°C day: 17°C night temperature combination produced plants which were taller, heavier and leafier than those grown at 21°C day: 19°C night. During the first 12 weeks of harvesting the larger plants produced significantly more fruit and higher gross monetary returns than did their smaller counterparts. The difference then diminished and after 20 weeks of harvesting plants from the two pre-planting temperature treatments had produced similar weights of marketable fruit of equivalent value. In the early post-planting period increases in total leaf area and stem length were closely correlated with 24-h mean temperature. Earliness (first harvest) and total weight of fruit after four weeks of harvesting were also linearly related to mean post-planting temperature. Raising the 24-h mean air temperature (within the range 15.2° to 22.6°C) by 1°C during the early post-planting stage increased early (4 week) yield by 0.82 kg m^-2 and total (20 week) yield by 1.17 kg m^-2. There was no effect of day/night temperature amplitude. After 20 weeks of harvest, gross monetary returns and profitability were generally highest when mean temperature in the early post-planting period was high and fell progressively with reduced mean temperature. Restricting stem fruits to oné per leaf node produced no significant difference in either the yield or quality of fruit from plants of any of the temperature treatments. The results are discussed from physiological and practical viewpoints and a cost-benefit comparison of temperature treatments is presented.     

Warm Storage of Narcissus Bulbs in Relation to Growth,Flowering and Damage Caused by Hot-Water Treatment

Three experiments are described on the effects on flowering of warm storage of narcissus bulbs before (and in some cases after) hot-water treatment (h.w.t.) against eelworm infection. Almost complete loss of the flower crop occurs if the bulbs are not warm stored, compared with the production of about 90% marketable flowers following warm storage. Optimum temperatures and durations of warm storage are not clearly defined; there is very little difference between the two recommended treatments, 34° C. for 3 days and 30° C. for 7 days, with the latter giving slightly better results. In another experiment, best results were obtained following 32·5° C. for 8 days or 35° C. for 5 days, with some varietal differences. These combinations were superior to most at 30° C., and to all of only 2 days duration. Higher temperatures and longer durations generally result in earlier flowering, with no adverse effect on flower quality. Bulb yield in the field following h.w.t. is higher when the bulbs are warm-stored before h.w.t. and, when forced in the following season, they give more flowers. Post-h.w.t. warm storage reduces flower quality and bulb yield in the field; although some minor benefits were observed, this treatment cannot be recommended. The possible mechanism for the protection afforded by warm storage is discussed.     

Factors affecting twin-scale propagation of narcissus

The effects of several factors on bulbil yields obtained by twin-scaling were examined in 4 narcissus cultivars (representing poeticus, trumpet and large-cup types). Bulbils were initiated on twin-scales prepared at any time of year, but grew satisfactorily only if twin-scaling was carried out between June and September. Large twin-scales initiated more bulbils, but smaller twin-scales were also effective propagules and gave high rates of multiplication and bulbils with high relative growth rates. Twin-scales cut from the outer-most scales initiated most bulbils, but more of those bulbils produced from the more central scales were recovered after 1 year; those from intermediate scales produced most and heaviest bulbils after 1 year. Partial loss of the basal plate had no effect on bulbil initiation. Optimum bulbil initiation, emergence and first-year recovery rates occurred following incubation at 15 or 20°C; at 25°C these responses were cultivar-dependent. Bulbil yield after 1 year was greater following incubation for 16 weeks compared with 12 weeks. There was little effect on bulbil yield of cold (9°C) or warm (35°C) treatments of the parent bulbs prior to twin-scaling, except for a marked reduction in the numbers of bulbils initiated when the warm treatment immediately preceded twin-scaling. When the propagules were grown on in a frost-free greenhouse (minimum, 5°C) bulbil yields were higher than from those grown either in a warm glasshouse (minimum, 18°C) or in the open; an initial cold period (5°C) given before the propagules were placed in the frost-free house also reduced yield.     

An analysis of the growth of forced tulips. 1. Changes in plant fresh and dry weights during growth at two temperatures

Changes in the fresh and dry weights of the component parts of plants of tulip cv. ‘Apeldoorn’ were followed in bulbs kept at low and high temperatures (9 and 18°C respectively) from the time of completion of flower differentiation until anthesis.There were marked differences between shoot dry weights at the two temperatures. At 9°C the stem, leaves and flower grew exponentially throughout the whole period, but at 18°C the specific growth rate of the stem and leaves declined throughout the period of the experiment. At 9°C the proportion of total dry weight in shoots and daughter bulbs was higher than at 18°C, and the proportion in the mother bulb was correspondingly smaller.At both temperatures the $\text{fresh weight}\text{dry weight}$ ratios of the mother bulb, shoot and daughter bulbs declined during dry storage, the decline being greater at 9°C. After planting, the ratio for all plant parts increased at 9°C, but scarcely changed at 18°C.These results are discussed in relation to dormancy, to the low-temperature requirement for successful and rapid flowering and to flower quality.     

The controlled atmosphere storage of Conference pears

Conference pears from five sources in Kent were stored in 0.5%, 1% and 2% O₂ at — 1°C. Samples from one source were also stored in air at the same temperature. On ripening at 18°C in air there was a lag phase before softening commenced. The lag phase generally lasted 3 d for fruit from 0.5% O₂ storage, 2 d for fruit from 1% and 2% O₂ storage, and between 1 and 3 d for fruit from air storage. There was no lag phase before chlorophyll loss. The rate of decline of firmness at 18°C was higher for fruit from 0.5% O₂ storage than for fruit from 1% or 2% O₂ storage. There was no effect of source of fruit on the length of the lag phase or the rate of softening. It was concluded that the storage life of Conference pears at — 1°C was at least 40 weeks in 0.5%, 1% or 2% O₂ and 35 weeks in air.     

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.     

Propagation of black currants by single-noded cuttings

Single-noded cuttings were taken from four regions of one-year-old black currant shoots in September 1966, before winter chilling had begun, and stored at 1 °C for 0, 4, 8 or 12 weeks before being inserted in seed trays and placed in a growth room at 20 °C, with continuous illumination. Cuttings from the lower half of shoots rooted and grew well with or without chilling, but cuttings from the upper middle quarter of shoots rooted better after 8 or more weeks in cold storage. Few cuttings from the top region rooted, even after 12 weeks of cold. Cold storage accelerated subsequent bud burst, as did 2 minutes’ treatment with GA₃ at 100 ppm.

In the field, dormancy of buds on intact plants increased after September and was pronounced in December. However, cuttings from all regions of shoots taken from plants in the field in January and immediately placed in the growth room rooted and grew well     

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.     

Accelerated rooting of carnation ‘Red Baron’ by temperature pre-treatment

Rooting of carnation cuttings was promoted by storage temperatures above 0°C with an inverse relationship between the level of temperature and the duration of the treatment. The effect of temperature on root dry weight was far more important than the effect of duration of storage. A long storage and a high temperature increased the incidence of Fusarium. Storage at temperatures lower than 13°C gave better results with auxin applied after storage, while temperatures higher than 13°C gave better results with a pre-treatment of auxin. During storage for 14 days at 9°C, the position of the cuttings had no clear effect on rooting. Horizontal storage, however, appeared to be unfavourable. Removal of 0.5 cm of the base of the stem after storage nullified the storage effect. Carbohydrates in the removed pieces decreased during storage, more so at 13°C than at 0°C. Anatomically, an acceleration of cell division at the base of the cutting was observed during storage at 9°C as compared to 0°C.At a commercial nursery, storage of cuttings for 12 days at 14°C improved rooting by 84% compared to storage at 0°C. The presented technique tends to shorten the expensive and vulnerable period from planting to rooting.     

The effect of various storage temperatures on peroxidase activity and protein PAGE gel electrophoresis in ‘Queen’ pineapple fruit

Mature ‘Queen’ pineapple fruit were stored for 30 days at various temperatures and afterwards examined for internal quality. A storage temperature of 8°C is at present generally accepted as the optimum. It was found that peroxidase (PO) activity is correlated with storage temperature and the appearance of storage injury symptoms. High storage temperatures of 10°C, 12°C and 16°C resulted in a high PO activity with internal browning of the core and pulp whereas temperatures of 2°C, 4°C and 6°C resulted in a low PO activity and white watery pulp. To verify these results, polyacrylamide gel electrophoresis was carried out with the proteins in the fruit. The difference in the two extreme temperatures of 2°C and 16°C resulted in a high intensity of high molecular mass proteins at 2°C and an increase in intensity of low molecular mass proteins at 16°C. There is a distinct “change over” of these protein band intensities at 8°C to 12°C. It is presumed that the correct storage temperature will be within these two limits.     

Effect of temperature manipulation during storage and ripening on firmness,extractable juice and woolliness in nectarines

‘Independence’ nectarines were stored at — 0.5°C for three or four weeks or at 3°C for four weeks or kept at room temperature for 18 h prior to storage for four weeks at -0.5°C. After cold storage, fruit from all treatments was ripened at 10°, 15°or20°C. In all treatments the percentage woolly fruit initially increased to high values and thereafter decreased with further ripening. The rate of increase and decrease in woolliness depended on the ripening temperature. A storage period of four weeks at — 0.5°C resulted more woolliness during subsequent ripening. Woolliness persisted longer after a four-week cold storage period than after a three-week one. When fruit was delayed at room temperature prior to cold storage, woolliness generally developed earlier and to a lesser extent during ripening. At all ripening temperatures initial storage at 3°C resulted in most woolliness extending over the longest period. In addition, browning of the meso- carp tissue occurred only in fruit cold stored at 3°C.-The delay period before cold storage decreased fruit firmness by 15.7 to 17.6 N. Except for fruit subjected to the delay period, the extractable juice in fruit of all treatments first decreased during ripening to low values then increased.     

The Effect of Cold Storage and Treatment with Gibberellic Acid on Flowering and Bulb Yields of Dutch Iris

Iris bulbs of the varieties Wedgewood and Prof. Blaauvv were injected with 50 or 500 μg. gibberellic acid (GA) before or after cold storage (10° C.) of 18 or 35 days. GA injection accelerated flowering by up to 19 days ; it had little or no effect on length of leaves or flower stem. It was most effective when applied at an early stage after flower initiation.

GA injection reduced bulb yield of Wedgiwood plants, and had no effect on, nor increased bulb yield of, Prof. Blaauw plants.

GA spraying (seven times at 10^-2M of GA) accelerated flowering and increased foliage growth in both varieties. It increased flower stem elongation and reduced bulb yield in Wedgfcwood plants.