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.     

The effect of temperature on growth and dry matter production of lychee seedlings

In lychee (Litchi chinensis Sonn.), high day/night temperatures ($\text{30}\text{25}$, $\text{25}\text{20}$, $\text{20}\text{15}\text{°}\text{C}$ compared to $\text{15}\text{10}\text{°}\text{C}$) increased stem extension, node and leaf production and plant dry weight in seedling selections of 6 cultivars (‘Bengal’, ‘Haak Yip’, ‘Kwai May’, ‘Gee Kee’, ‘Tai So’ and ‘Wai Chee’). The mean daily base temperature for shoot growth (node production) was estimated by linear correlation to be 11.0°C for the seedlings. High temperatures also increased the proportion of leaf and decreased the proportion of root in the total dry weight. There was a strong effect of cultivar on all aspects of growth, but the responses to temperature were similar.This experiment shows that temperatures in many tropical and warm sub-tropical areas where lychees are grown are too high to induce satisfactory vegetative dormancy prior to floral initiation. The assessment of lychee seedlings for low vigour in a heated glasshouse appears to be a useful technique for the initial screening of adapted genotypes (which flower and fruit under warm conditions) prior to field evaluation.     

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.     

Effects of air temperature,soil temperature and soil moisture on growth and development of tomato itself and grafted on its own and egg-plant rootstock

The problem was studied whether tomatoes, grown in a hot and arid climate, benefit from grafting on egg-plant, which is highly efficient in water uptake. Growth and development of tomato (T), tomato grafted on its own rootstock ($\text{T}\text{T}$) and tomato grafted on egg-plant rootstock ($\text{T}\text{E}$) were compared at air temperatures of 28°C during the day and 18°C during the night ($\text{28}\text{18}$) and at 28°C constantly ($\text{28}\text{28}$), at soil temperatures of 14, 21 and 28°C with the following soil moisture regimes: wet (W₁), medium (W₂) and dry (W₃).At $\text{28}\text{18}$ and $\text{28}\text{28}$ water consumption was about equal, but the transpiration ratio at $\text{28}\text{28}$ was twice as high as that at $\text{28}\text{18}$. The latter conditions gave a much stronger plant with more fruits. At a soil temperature of 14°C water use was strongly reduced. The transpiration ratio increased with the soil temperature. Differences in plant type were small. At the highest soil temperature of 28°C fruit growth was strongly reduced. At lower soil moisture levels less water was used and the transpiration was lower. Plant type was correlated herewith.Vegetative growth of $\text{T}\text{T}$ was weaker than of T, but generative growth was stimulated. The strong E rootstock stimulated vegetative growth at high air and soil temperature, but fruit growth was very poor under these conditions; at a low soil temperature of 14°C vegetative growth was also reduced.The hope that the E rootstock would be beneficial for fruit growth at high temperatures was not fulfilled.An additional experiment in a growth-room at 23°C showed that under conditions of moisture stress there was no difference in water potential between leaves of $\text{T}\text{T}$ and $\text{T}\text{E}$.     

Prevention of hot-water treatment damage in narcissus bulbs by pre-warming

Summary

Hot-water treatment (HWT) used to control stem nematode in narcissus bulbs can lead to yield loss through damage to flower, leaf and root initials. Warm storage of bulbs, usually at 30°C, reduces this damage. The effects of two pre-warming treatments (18°C for two weeks or 30°C for one week before HWT) were investigated in bulbs hot-water treated at a range of dates (from early-July to late-September). Experiment 1 was conducted on bulbs of cv. Carlton lifted on three dates. In the year after HWT, flower numbers were much reduced when HWT was applied after mid-August following storage at ambient temperatures, or after late-August following storage at 30°C, but numbers were only slightly reduced even with late-September HWT when given after 18°C storage. Pre-warming was somewhat more effective after early lifting. Late HWT reduced yields of bulbs harvested after two years' growth, but 18°C treatment largely prevented these losses. In Experiment 2, the beneficial effects of 18°C treatment were confirmed in cvs Carlton and Golden Harvest but not in cv. Barrett Browning. These findings are discussed in terms of growth retardation by warm temperatures.     

Effect of precooling at 5 or −1°C on shoot growth,flowering and carbohydrate metabolism in tulip bulbs

Precooling of dry tulip bulbs at ?1°C may be advantageous, compared with precooling at 5°C. Increasing the duration of precooling enhanced the growth of the shoots after planting, improved flower quality, and reduced the number of days to flower. The positive benefit of a stepwise precooling (5°C for 3 weeks, then ?1°C) was evident.Shoot elongation was promoted, and number of days to flower was reduced when the bulbs were precooled at ?1°C for less than 12 weeks. Extension of precooling beyond 12 weeks, however, was more effective with 5°C precooling. With few exceptions, sufficient precooling at either 5 or ?1°C gave a high percentage of flowering plants with first-quality flowers. Short durations (6–8 weeks) of precooling sometimes promoted flower blasting.Precooling at 5 or ?1°C had a similar effect upon the carbohydrate interconversion in scales and shoots of the bulbs, which as a rule is more pronounced at the lower temperature. The shoots accumulated sucrose, and to some extent fructosyl sucroses, during the 15 weeks precooling. Starch was also accumulated, the highest concentration being obtained at 5°C. The amount of starch was reduced in the scales during precooling, while the concentration of sucrose and fructosyl sucroses increased to a maximum value and then slowly diminished after about 9 weeks of precooling. The monosaccharides, glucose and fructose showed very small variations.     

Partitioning of 14C-assimilate in Easter Lily as affected by growth stage and flower removal

Three weeks before anthesis, flower buds of Easter Lily plants received 47 and 12% of ¹⁴C translocated from Leaf 5 (upper) and 25 (middle), respectively, whereas the bulb received 5 and 52%, respectively. Flower bud removal increased the fraction in the bulb to 52% (Leaf 5) and 63% (Leaf 25). At anthesis, the flowers received 78% (Leaf 5) and 65% (Leaf 25) of translocated ¹⁴C-assimilate, nearly all of which was in the second flower which was still expanding. Less than 5% of the ¹⁴C from either leaf moved to the bulb in intact flowering plants, but upon flower removal, the bulb received 26 and 59% of the labelled assimilate from Leaf 5 and 25, respectively. Five weeks after anthesis, nearly 85% of the ¹⁴C-assimilate from either leaf was in the bulb. The fraction of ¹⁴C moving into the daughter bulb increased from less than 10%, 3 weeks before, to over 50%, 5 weeks after anthesis. Regardless of treatment, sink activity of the daughter scales was 2- to 12-fold higher than that of the mother scales. Although much of the current assimilate from the upper half of the intact lily shoot moves to flowers before anthesis, flower-bud removal is an effective way to increase carbon supply to the bulb.     

Inhibition of flowering of Mexican- and Guatemalan-type avocados under tropical conditions

Avocado trees of a range of cultivars growing in Darwin, northern Australia (average yearly maximum 33°C, minimum 23°C), were observed for flower and shoot development. Terminal buds of the cultivars ‘Fuerte’, ‘Rincon’ and ‘Edranol’ sampled in July were not floral. Buds which did not burst were sampled in September and they contained developing flowers with perianth primordia. Vegetative extension growth resulted from laterals proximal to the inhibited terminal buds.Avocado trees of the cultivars ‘Fuerte’ and ‘Hass’ which had initiated floral buds were transferred to controlled environment chambers with 33°C day, 23°C night ($\text{33}\text{23}$) or 25°C day, 15°C night ($\text{25}\text{15}$) with a 12-h photoperiod and photon flux density of 400 μmol m^?2 s^?1 (400–700 nm). At $\text{33}\text{23}$ the trees had fewer flowers and a shorter flowering period than at $\text{25}\text{15}$. Inhibited floral buds and lateral vegetative extension resulted at $\text{33}\text{23}$, as observed in northern Australia. The unburst buds had developing flowers with perianth and stamen primordia.The controlled environment experiments showed that the abnormal flushing behaviour of Mexican- and Guatemalan-type avocados growing in northern Australia was due to high temperature. Floral development was inhibited at the stage of stamen differentiation.     

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.     

Interactions between root-zone temperature and light levels on growth,development and photosynthesis of Lycopersicon esculentum Mill. cultivar ‘Vendor’

Six-week-old tomato plants were subjected to 5 root-zone temperatures, ranging from 12 to 36°C, and 4 light levels in a factorial design. Large increases in shoot dry weight, leaf area and fruit development resulted from soil warming to 24°C when plants were grown under high light conditions. Shoot growth and fruit weight were reduced at 24°C root temperature under low light conditions. Total plant photosynthesis, leaf area index, net assimilation rates and leaf chlorophyll content were related to plant growth and flower development for the various treatments. Our experiments have shown an interaction between root-zone temperature and light levels for greenhouse tomatoes. Soil warming caused large increases in shoot dry weight and fruit development when light was not limiting plant growth, but had deleterious effects on flowering and fruit set under shaded conditions.     

Postharvest sprouting of onion bulbs grown in different temperature and C02 environments in the UK

Summary

The effects of different mean growing season temperatures and C0₂ concentrations during bulb production on postharvest bulb sprouting in a common storage environment at Reading, UK, was examined in two cultivars of the Rijnsburger type of onion (Allium cepa L.). Crops were grown in the field in temperature gradient tunnels maintained at either 374 or 532 ppm C0₂. At crop maturity, cohorts of bulbs were harvested, transferred to a constant temperature room (at an average of 11.6°C) and the subsequent duration to sprouting recorded. The duration to the onset of sprouting (expressed as days in storage until the first bulb sprouted) was not affected by cultivar, mean growing season temperature or CO₂ concentration, and was 165 d. The subsequent rate of sprouting (expressed as bulbs per day) was a positive linear function of mean growing season temperature, but no effects of CO₂ or cultivar were detected. Mean rate of sprouting increased from an average of 0.036 bulbs per day at 12.3°C to 0.093 bulbs per day at 18.6°C. Rapid sprouting in storage was associated with lower levels of total non-structural carbohydrate in the bulbs at the time of harvest. Thus, postharvest susceptibility of onion bulbs to sprouting in storage is expected to increase in warmer crop production temperatures.     

The growth and flowering of Hymenocallis × festalis

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

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

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

Influence of temperature,soil moisture and CCC on the flowering of Euphorbia fulgens

In the short-day plant Euphorbia fulgens under short-day conditions the flower induction in the shoot apex is delayed more and more nodes are formed beneath the final cyathium, the higher the temperature up to 28°C. The delay of induction is greater with plants growing in a moist soil than in a dry soil. The difference between moist and dry soil is greater, the higher the temperature. There are slight temporal differences in the induction of the lateral shoots in the temperature range between 15°C and 25°C, but the number of nodes formed at the lower paracladia is greater at the higher temperature. The development of the cyathia is enhanced at high temperatures. At temperatures above 28°C induction is prevented. The temperature limit for induction is some degrees higher for plants in dry soil than for those in moist soil. Cycocel causes effects similar to those caused by water deficiency, although the newly formed internodes become shorter.     

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.     

Flowering and fruit-set response to temperature in the avocado cultivar ‘Hass’

Avocado plants, cultivar ‘Hass’, were kept in growth cabinets at 33°C day, 28°C night ($\text{33}\text{28}$); 25°C day, 20°C night ($\text{25}\text{20}$); and 17°C day, 12°C night ($\text{17}\text{12}$), with a 12-h photoperiod and photon flux density of 400 μE m^?2 s^?1 (400–700 nm). At $\text{33}\text{28}$ and $\text{25}\text{20}$ flowers opened in the morning in the female stage and again in the afternoon of the following day in the male stage (Type A floral cycle). At $\text{17}\text{12}$ the flowers opened in the afternoon in the female stage and started to reopen in the male stage 2 days later during the afternoon. They remained open overnight and started to close the following morning. Pollen tube growth and ovule penetration occurred at all temperatures. Pollen tube growth was fastest at $\text{33}\text{28}$, but the pistils had lost the ability to support pollen tube growth by the second week of the experiment. A lower proportion of the ovules at $\text{17}\text{12}$ had an embryosac penetrated by a pollen tube. Embryo development occurred at all temperatures, but fruitlets were abscissed at $\text{33}\text{28}$ and embryo growth was very slow at $\text{17}\text{12}$. The most suitable temperature regime for floral behaviour, pollen tube growth and embryo development was $\text{25}\text{20}$.     

Environmental and chemical control of growth and flowering of Chamelaucium uncinatum Schauer

The main factor affecting floral initiation of Geraldton Wax-Flower (Chamelaucium uncinatum) is the photoperiod, while temperature is the major factor affecting flower development. Four weeks of short days (SD) are generally required for obtaining full flowering. The number of flowers produced per plant increases with increasing the number of SD. Under mild temperatures of $\text{20}\text{14°}\text{C}$ (day/night), plants initiated flowers even in long days (LD). However, fewer flowers were produced and on higher nodes as compared to SD plants. Chlormequat promoted flowering under prevailing summer conditions of high temperatures and LD. Under prevailing autumn conditions favourable for flower initiation, LD treatment or weekly sprays with gibberellic acid (GA) reduced the number of flowers per plant. Combined treatment of LD and GA reduced both the flowering percentage and the number of flowers per plant. Discontinuing the LD or the GA treatments caused a resumption of full flower initiation.     

The Effects of Adding Soluble Salts to the Casing Layer on The Yield and Size of Cultivated Mushrooms

The yield results of six field experiments with bulb onions are presented and it is concluded that : (1) The total yield of ripe bulbs increased with increasing number of plants per sq. ft. until an optimum was reached and thereafter the yield declined.

(2) At the optimum plant densities for total yield the bulbs were too small for normal market purposes but were of a suitable size for pickling whole.

(3) Some varieties of onion would not produce large bulbs even when grown at low plant densities; thus the choice of varieties for ware bulb production is of paramount importance.

(4) The fitting of a mathematic model to the density/yield data showed that if varieties were ranked for yield at anyone plant density this ranking would remain the same at all other plant densities. Absolute yield differences between varieties were, however, greatest at low plant densities.

(5) Decreasing the distance between rows at a given plant density increased the total yield of bulbs. At 7 plants per sq. ft., a density suitable for commercial dry bulb production, reducing the row spacing from 18 in. to 9-12 in. increased yield by 10 to 30%.

     

Factors affecting the response of tulips to gibberellin

Gibberellic acid (GA₃) treatment of forced tulip crops has potential for producing faster growth to anthesis in the glasshouse, for reducing losses due to floral bud blasting, and for reducing the duration of cold storage needed to obtain satisfactory flowers. Using partly and fully cooled direct-forced tulips, cultivar ‘Apeldoorn’, several factors (relevant to the definition of GA₃ treatments) were studied. Experiments confirmed the previously recorded effects of gibberellins in tulips: GA₃ injections reduced the duration of the glasshouse period, enhanced flower survival and flower length, and reduced stem length at flowering.Following bulb storage at temperatures from ?2 to 20°C, GA₃ reduced the glasshouse period by 15–25% and increased flower length, compared to controls, irrespective of storage temperature. Stem length was also reduced by GA₃, this effect being greater following a storage temperature of 5°C or lower. When GA₃ was applied during the period of 17°C-storage which precedes cool storage, or during or after storage at 5°C, it was found that treatments during or at the end of cool storage were more effective in producing the characteristic effects of GA₃ than were pre-cooling applications. In partly cooled bulbs (but not fully cooled ones), the GA₃-induced earliness of flowering was about doubled when GA₃ injections were given repeatedly at 2-week intervals throughout storage. The responses to GA₃ injections were found to be unmodified by early-lifting and heat-treatment (for earlier forcing), by delaying the start of 5°C storage (for later forcing), by glasshouse temperature (16 and 18°C), and by shading treatments; there was little effect of bulb size.     

Effect of temperature on bulb growth capacity and sensitivity to summer sprouting in Lilium longiflorum Thunb.

The production of Lilium longiflorum bulbs in The Netherlands, with its cool climate, has been a problem because of unsatisfactory bulb growth and the risk of premature sprouting of the daughter bulbs (summer sprouting). To investigate the possibilities of breeding a type of L. longiflorum that can be grown under cool climatic conditions, a collection of 27 L. longiflorum cultivars from Japan, The Netherlands and the United States was tested, together with two Asiatic hybrids and a L. speciosum cultivar, under low phytotron temperatures (10, 14, 17°C) and in field experiments.‘Mount Everest’, ‘Saeki’, ‘Indian Summer’ and ‘White American’ were among the best L. longiflorum cultivars, with less than 20% summer sprouting and good bulb production. This was in contrast to ‘Hinomoto’, ‘Ace’ and some American introductions, which showed more than 60% summer sprouting and low bulb production. The lower the phytotron temperature, the more summer sprouting occurred. The differences observed between the cultivars in the field experiments were in agreement with those observed in the phytotron. The genetic variation proved large enough to start a breeding program for L. longiflorum adapted to cool climate conditions.     

A study of the effect of the environment during growth on sprouting of bulb onions in store

The partition of dry matter between leaf and bulb with sheath was studied in relation to the post-harvest physiology of cvs Bola and Robusta grown at three sites for two seasons and dried and stored under standardized conditions. Foliar fall-over was synchronous at all sites in each season but the effects of site showed that crops either partitioned dry matter to the bulb early, lost less fresh weight in drying and sprouted later in store, or partitioned dry matter late, lost more fresh weight in drying and sprouted sooner in store. Crops showing the former behaviour were associated with low rainfall and a high number of day degrees between 6° and 20°C during early growth. There was up to 10 days difference between the sites in 50% sprouting dates. Bulbs of cv Bola sprouted earlier than those of cv Robusta, and bulbs harvested when foliar fall-over was negligible sprouted before those from later harvests. There were no site effects on plant maturity, on bulb growth regulator content (cv Robusta one year only), on sugar content at harvest or during storage, on bulb respiration rates at the end of drying or in the spring, or on bulb weight loss during storage.