Effect of photoperiod and light integral on flowering and growth of Eustoma grandiflorum (Raf.) Shinn.

The aim of the study was to examine the effects of different photoperiod and light integral on floral initiation, development and subsequent growth of Eustoma grandiflorum (Raf.) Shinn. Six-weeks-old seedlings of ‘Echo Blue’ and ‘Fuji Deep Blue’ were placed under short day (SD, 10 h) and were transferred to long days (LD, 20 h) at 2-week intervals from 6 to 14 weeks after seeding. Plants initiated flower buds regardless of light regimes. Flower bud initiation was delayed by SD compared to LD; plants transferred after 6 weeks from seeding initiated flower buds at least 21 and 10 days earlier at LD at high (HL) and low (LL) daily light integral, respectively, compared to those at SD. Light regimes had little or no effect on time to flower bud development after initiation. Thus, it seems likely that LD and HL affected the initiation rather than development. Both the photoperiod and light integral strongly influenced the subsequent growth after initiation. SD delayed the time to visible bud (VB), increased the number of nodes to first open flower, number of branches, stem diameter and shoot dry weight compared to LD. HL promoted flowering and increased several shoot characteristics and flowering compared to LL.The results indicate that Eustoma is a quantitative long-day plant. LD, and more specifically HL, enhanced flower bud initiation, development and subsequent growth. An initial SD period is preferred to increase the number of branches, number of flowering buds and flowers, stem diameter and shoot dry weight.     

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.     

Gibberellin substitution for the high night temperatures required for the long-day promotion of flowering in Gypsophila paniculata L.

Gibberellic acid (GA) promoted flowering of Gypsophila paniculata plants grown under long-day (LD) conditions at low night temperatures, which otherwise prevented the realization of the LD induction. GA did not induce flower formation of plants grown in short-days (SD), either under low winter temperatures or at the relatively high night temperatures of spring and summer, which allow flowering under LD. GA had only a marginal promotive influence under fully inductive conditions of LD and high temperatures. Thus, in gypsophila, GA substitutes for the high night temperature which is required as a background for the photoperiodic induction, but not for the long photoperiod itself.     

The responses of early-flowering chrysanthemums to daylength

In a study of photoperiod response 30 early (summer)-flowering chrysanthemum cultivars from Britain and Japan reacted as quantitative short-day plants. Both flower bud initiation and development occurred more rapidly in short days (SD) as compared with long days (LD). The early-flowering cultivars differed from late-flowering chrysanthemums in that lateral flower buds, and often the terminal flower buds, develop to anthesis in LD. Internodes were shorter in SD and flowers had fewer florets. There was an increased number and proportion of disc florets in SD in all cultivars except one. Two cultivars, ‘Mezame’ and ‘Pennine Yellow’, closely approached day-neutrality.All cultivars produced fewer leaves in LD on upper lateral shoots than on main stems. Either the presence of the terminal flower bud induces earlier flowering of the upper lateral shoots, or the change which causes the terminal apical meristem to initiate a flower in LD influences the axillary meristem also.SD could be used to speed up the flowering of glasshouse-grown crops of early-flowering cultivars. The advantages and disadvantages which may be associated with treatment at different stages of growth are discussed.     

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 effect of various environmental factors on flowering of gladiolus. I. Light intensity

Light intensity is an important factor affecting the flowering of Gladiolus. Insufficient illumination from sprouting to the 4-leaf stage decreased flowering percentage. However, the inflorescences of those plants which did flower under conditions of low light intensity were normal and developed the full number of florets per spike. Plants at the 4–6 leaf stage were most sensitive to prevailing light conditions. Low light intensity during this period decreased both the percentage of flowering and the number of florets per spike. After this stage only the number of florets per spike was affected by insufficient light.     

Promotion of Globularia sarcophylla flowering by Uniconazol,an inhibitor of gibberellin biosynthesis

Globularia sarcophylla, originating from the Canary Islands, was recently introduced as a new cut flower in Israel. Two major problems have prevented its commercialization: the late-summer blooming and the low quality of its flowering shoots. In the present work we studied the factors affecting G. sarcophylla flowering. We found that long-day (LD) conditions slightly promote flowering but artificial photoperiodic illumination does not enable the manipulation of flowering time. On the other hand, treatment with the gibberellin (GA)-biosynthesis inhibitor, Uniconazol, had a dramatic promotive effect on flowering time. Application of Uniconazol in autumn or winter induced flowering in winter or early spring, respectively. The inhibitor did not advance flowering during the summer or in the phytotron under high temperatures. When plants were grown in the spring/summer under heavy shading, they did not flower unless they were treated with Uniconazol. Uniconazol treatment also improved flower quality by reducing the length of inflorescence pedicles. This effect was found in all seasons. Based on our results, we raise the hypothesis that Uniconazol treatment induces flowering by diverting assimilates to the apex. Inhibition of GA biosynthesis under conditions limiting photosynthetic activity reduces vegetative growth and increases the availability of assimilates to the apex, leading to flower initiation. However, under high irradiance and/or high temperatures, when the levels of assimilates are sufficient to induce natural flowering, the inhibitor has no further effect.     

Factors Controlling Flowering in Seed-Raised Freesia Plants

The effect of plant age, temperature and day-length on flower initiation and development in “ K. & M. Super ” freesias has been studied.

The flowering response decreased with increasing temperature and the critical temperature for flower initiation was found to be about 21°C. An interaction of plant age, temperature, and duration of treatment was present. Short days (9 hrs.) slightly stimulated flower initiation in“ Yellow K. & M. Super” but delayed it in “ Blue K. & M. Super” freesias. Short-day treatment in the open during the summer had no significant effect, whereas shading markedly hastened flowering.

Flowering could be initiated at an early stage, but older plants were more responsive, especially those of “Blue K. & M. Super”. Optimum temperatures for flower initiation were 12-15°C., applied for 6-9 weeks after the plants had formed about seven visible leaves.

Abnormal inflorescences in freesias, recognized by enlarged bracts and irregular spacing of the florets (so-called “gladiolus-like flowers”), appeared to result from incomplete flower initiation. In extreme cases flower stalks without any flowers were formed. In order to avoid such abnormal flowering it was important that the first floret in the inflorescence should have reached a certain stage (P₂) of development before low-temperature treatment was discontinued.     

Promotion of floral initiation in ‘Fuerte’ avocado by low temperature and short daylength

Potted avocado (Persea americana Mill., cv. ‘Fuerte’) plants were maintained in growth cabinets for up to 32 weeks and new growth observed for flower formation. Flowers were formed if temperatures were 20°C or below, but with 25° or 30°, even if only for 1 hour per day, flower formation was inhibited. Time to flowering was accelerated, but number of flowers reduced, if daylength was shortened from 15 h to 9 h. With low temperature and short days, full bloom was about 4 months after starting experiments. Spring flowering of cv. ‘Fuerte’ in the field could follow flower induction about 4 months previously with the onset of winter temperatures and daylengths.     

Effects of photoperiod,light source and growth regulators on the growth and flowering of Trachelium caeruleum

Summary

Experiments were conducted to determine the appropriate photoperiod, light intensities and sources, and growth regulators, necessary to produce Trachelium caeruleum as a commercially acceptable potted plant. T. caeruleum behaved as an LDP with a critical photoperiod of 14 h necessary for flower initiation but was day neutral for subsequent flower development (from macroscopic bud visibility to anthesis). Providing long days by daylength extension using metal halide (MH) lamps to provide high irradiance resulted in significantly earlier flowering and more flowers than using either MH or incandescent lamps at low irradiance. The use of incandescent lamps to extend the day resulted in slower flowering and fewer flowers than using MH lamps at the same irradiance. Daminozide was effective for controlling plant height but ancymidol and chlormequat were ineffective. Removal of the terminal bud resulted in more compact plants, and more blooms per plant, but delayed flowering by approximately one week.     

The effect of temperature and light on flower development in Pelargonium × domesticum

Factors influencing the number of flowers produced in Pelargonium × domesticum cultivar ‘Lavender Grand Slam’, and their rate of development after the plants had been given a period of low-temperature flower induction, were studied.Under short days progressive abortion reduced flower numbers as the temperature regime during the forcing-period was increased. Under long days this effect was less marked and the high-temperature regime advanced flowering by over a month. When long days and high temperatures were used for forcing, it was necessary to maintain a high light intensity, 335 J/cm²/day giving the best results in terms of earliness of flowering and the number of flowers produced. At lower irradiance there was some risk of flower abortion, particularly in the first inflorescence.     

Interactions of photoperiod,temperature, duration of short-day treatment and plant age on flowering of Fragaria x ananassa Duch. cv. Korona

The effects of photoperiod (10, 12, 16, 20 or 24 h), day-temperature (12, 15, 18, 24 or 30 °C), the number of short days (14, 21 or 28 days), plant age (4, 8 or 12 weeks) and their interactions on flower and inflorescence emergence were investigated in strawberry cv. Korona. No flowers emerged in plants exposed to photoperiods of 16, 20 or 24 h or to a short-day treatment for 14 days. All plants exposed to short days at daily photoperiods of 10 or 12 h for 21 days or longer, emerged flowers at temperatures between 12 and 18 °C. A further increase in temperature led to a drastic decrease in the total number of flowers per plant. A short-day treatment (10 or 12 h photoperiod) of 28 days resulted in highest numbers of inflorescences and flowers per plant, while a short-day treatment of 21 days resulted in the highest numbers of flowers per inflorescence. Complete flower induction was observed in only 4-week-old runner plants. The number of inflorescences and the number of flowers per inflorescence increased with plant age. However, the start of flowering was delayed with increasing plant age.     

Flower production in Gerbera: I. Correlations between shoot,leaf and flower formation in seedlings

Flower production of seedling plants of Gerbera was shown to be positively correlated with the number of lateral shoots and with the number of leaves per flower. The most productive plants were those which formed 2–5 lateral shoots during the first year and had a $\text{leaf}\text{flower}$ ratio of 2–4. The number of lateral shoots at the moment the first flower bud became visible was strongly correlated with the number of lateral shoots after 1 year.There was a positive correlation between the number of lateral shoots and total number of leaves, but hardly at all between total leaf number and flower production, as the $\text{leaf}\text{flower}$ ratio increased with the number of lateral shoots.     

Flower and corm development in gladiolus as affected by photoperiod

Gladiolus plants cultivar ‘Spick and Span’ were grown in winter under natural short day (SD) or under long day (LD), with 4 hours low intensity light at midnight. Growth of the various organs was followed by periodic sampling. SD promoted flower development and advanced anthesis but reduced the final size of the flower. LD increased weight and size of leaves and flowers.Initial growth of the corm was similar under both photoperiods, but while corm growth continued throughout the growing-period under SD, it was checked under LD when flowers were developed at an enhanced rate and until anthesis. At this stage, the allocation of assimilates was directed towards the flower sink and away from the corm sink.Final corm weight was also promoted by LD. This is interpreted as an indirect effect due to increased photosynthesis of the larger LD plants. In non-flowering plants raised from cormels, SD specifically promoted corm growth, although no competing flower sink was present.It is concluded that photoperiod affects growth and development of gladiolus in two ways: directly — by affecting the partitioning of assimilates between the flower or the corm; and indirectly — by affecting the total photosynthates available to the plants by influencing foliage size and the total growth period.     

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.     

Effects of shoot size,number of continuous-light cycles and solar radiation on flower initiation in the carnation

Carnation plants (Dianthus cary ophyllus L.) cultivar ‘White Sim’, were grown in containers in a glasshouse under short (8 h) days. When the primary shoots had 4, 8 or 12 pairs of visible leaves, the plants were moved to a continuous-light area, lit by tungsten lamps for 5, 10, 15 or 30 days, and then returned to short days. This was repeated with several sets of plants at different times of year to obtain a range of radiation flux densities.The number of continuous-light cycles required to initiate a given proportion of shoots was dependent upon the radiation integral, a generalised linear model gave quantitative relationships between the proportion of responding shoots, the number of cycles of continuous light (CL) and the radiation integral. For shoots with 4 visible leaf pairs the model

$\text{keta;=μ+∝X}{}_1\text{+βX}{}_2$

accounted for 83% of the deviance, where η is the linear predictor, μ, α and β are parameters, X₁ = log_e (number of CLs + 1) and X₂ = log_e mean radiation (calories cm^?2 day^?1). For shoots with 8 visible leaf-pairs, 76% of the deviance was removed.Under low radiation integrals, intra-plant competition resulted in only a small proportion of shoots on a plant initiating flowers; increasing the number of CL cycles only partially mitigated this effect. At low radiation integrals, shoots that failed to initiate flowers in CL were often delayed by this treatment and initiated flowers later than shoots in short days. Both the CL-requirement and the limiting effect of the radiation integral on the proportion of shoots that initiated flowers decreased as shoot size increased.It is concluded that competition for photosynthetic assimilates under low radiation conditions can severely limit flower initiation in the carnation.     

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 of cacao under controlled temperature conditions

The relationship between flowering and day and night temperatures in cacao has been studied over a period of nine months in controlled environment rooms, with clonal trees which were 13 months old at the start of the experiment.

All the plants started to flower at the same time, but thereafter there was a marked response to temperature. Flowering was greater at day temperatures of 80° and 86° F. (26 .7°, 30° C.) than at day temperatures of 74° F. (23–3° C.) and, at each level of day temperature, flowering was greater at a night temperature of 80° F. than at one of 74° or 86° F. The relative effects of temperature were similar on numbers of flowering cushions per plant and of flowers per cushion.

There was no apparent relationship bfetween the amount of flowering and new leaves (flushes) produced, either at the time of flowering or at any period before. Neither was there a quantitative relationship between flowering and leaf area of the plants, though, in general, the treatments that resulted in the greatest leaf areas also resulted in the greatest numbers of flowers. A possible relationship was suggested between the number of flowering cushions and the total extension growth of the branches.     

Variation among Kalanchoe species in their flowering responses to photoperiod and short-day cycle number

Summary

Our objectives were to identify the critical daylength and number of short-day (SD) cycles necessary for flowering in Kalanchoe glaucescens, K. manginii, and K. uniflora. In Experiment I, plants were grown for 20 weeks under 9, 10, 11, 12, 13, 14, or 15 h photoperiods at 300 µmol m^–2 s^–1 for 8 h 55 min (9 h photoperiod), or 9 h and extended with dayextension (3 µmol m^–2 s^–1) lighting (10 – 15 h photoperiods). All species flowered when grown under photoperiods ranging from 9 – 12 h. The percentage of flowering plants decreased for all species as the photoperiod increased from 12 h to 14 h. No flowering occurred on plants grown under a 15 h photoperiod. Node numbers below the terminal inflorescence increased from 18 nodes to 28 nodes on K. glaucescens, from 12 nodes to 14 nodes on K. manginii, and from 12 nodes to 16 nodes on K. uniflora as the photoperiod increased from 12 h to 14 h, from 10 h to 12 h, and from

12 h to 13 h, respectively. Total flower numbers on K. uniflora decreased from 45 flowers to 13 flowers as the photoperiod increased from 9 h to 13 h. In Experiment II, plants were exposed to 0, 1, 2, 3, 4, 5, 6, 7, or 8 weeks of SD (8 h photoperiod) before being placed under night-interruption lighting (2 µmol m^–2 s^–1; between 22.00 – 0.200 h). One-hundred percent of K. glaucescens, K. manginii, and K. uniflora plants flowered when they received more than 1, 3, or 6 weeks of SD, respectively. The node number below the terminal inflorescence in each species was not affected by SD cycle-number. Total flower numbers per plant, and days to first open flower, were unaffected as the number of SD cycles exceeded the number required to induce flowering for all species.     

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.