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.     

The temperature and photoperiod regulation of flowering and runnering in the strawberries,Fragaria chiloensis,F. virginiana,and F. x ananassa

The temperature and photoperiod interactions of a number of elite genotypes of Fragaria virginiana, F. x ananassa, and F. chiloensis were studied in a series of growth chamber experiments. Several parameters were evaluated including: (1) the critical day-length (CDL) for flowering of short day (SD) genotypes under 8, 9, 10, and 11 h days at 18 °C, (2) the floral and runnering response of single and multiple cropping genotypes under 8 and 16 h days at 18 °C, and (3) the effect of temperature on flower bud formation in day-neutral (DN) genotypes held at 18, 22, 26, and 30 °C under 12 h day-lengths. The same number of flowers were initiated under 15 and 30 day induction periods, regardless of photoperiod. Frederick 9, LH 50-4 and RH 30 (F. virginiana), ‘Aromas’ and ‘Tribute’ (F. x ananassa) and CFRA 0368 of F. chiloensis flowered under both long days (LDs) and SDs; while Eagle-14 (F. virginiana), ‘Fort Laramie’ and ‘Quinalt’ (F. x ananassa) flowered only under long days. While those genotypes that flowered under both LD and SD can be considered day-neutral, they varied in the degree of floral response to the two photoperiods. CFRA 0368 and Frederick 9 produced the same number of flowers under both LDs and SDs, while ‘Aromas’ and ‘Tribute’ had more flowers under LDs and RH 30 had more under SDs. Of the DN genotypes, LH 50-4 and RH 30 were the only ones that produced runners under SDs. Flowering in ‘Fort Laramie’ was least affected of any genotype by high temperature, although its dry weight was negatively impacted. Based on these data, several genotypes show promise as breeding parents: CFRA 0368 and Frederick 9 to equalize flower production under LD and SD conditions, LH 50-4 and RH 30 to produce more freely runnering DNs, and ‘Fort Laramie’ for floral heat tolerance.     

Temperature effects on flower formation in saffron (Crocus sativus L.)

The temperature conditions for shoot growth and flower formation were characterised for saffron (Crocus sativus L.). Leaf withering occurred during late winter or spring depending on location, and coincided with a rise in temperature. No growth was detectable in the buds during the first 30 days after leaf withering, neither in underground corms nor in lifted corms incubated in the laboratory under controlled conditions. Flower initiation occurred during the first growth stages of the buds. The optimal temperature for flower formation was in the range from 23 to 27 °C, 23 °C temperature being marginally better. To ensure the formation of a maximum number of flowers, the incubation at these temperatures should exceed 50 days, although incubation longer than 150 days resulted in flower abortion. Flower emergence required the transfer of the corms from the conditions of flower formation to a markedly lower temperature (17 °C). Incubation of the corms after lifting at a higher temperature (30 °C), reduced flower initiation and caused the abortion of some of the initiated flowers. No flowers formed in corms incubated at 9 °C. A variable proportion (20–100%) of the corms forced directly at 17 °C without a previous incubation at 23–27 °C formed a single flower. The wide differences in the timing of the phenological stages in different locations we found in this study seemed related to the ambient temperature. Leaf withering was followed shortly by flower initiation, which occurred during late spring or early summer as the rising temperature reached 20 °C. A long hot summer delayed flower emergence which occurred in late autumn as the temperature fell to the range of 15–17 °C.     

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.     

Day and night temperatures,daily light integral,and CO2 enrichment affect growth and flower development of Campanula carpatica ‘Blue Clips’

Campanula carpatica Jacq. ‘Blue Clips’ plants were grown in a greenhouse under nine combinations of day and night temperatures created by moving plants every 12 h among three day/night temperatures (15, 20, and 25°C). At each temperature, there were three daily light integrals (DLI; 4.2, 10.8, and 15.8 mol m⁻² per day, averaged over the experimental period) created with varying supplemental light, and ambient (≈400 μmol mol⁻¹) and enriched (≈600 μmol mol⁻¹) CO₂ concentrations. Time to flower was closely related to average daily temperature (ADT), and was not significantly affected by the day or night temperatures delivered to achieve a specific ADT. Time to flower was not largely affected by DLI or CO₂ enrichment. As plant ADT increased between 15 and 25°C, flower diameter decreased about 1 mm per degree and was not related to the difference between day and night temperatures (DIF). Flower diameter was smallest and least sensitive to changes in temperature at lower DLI and at ambient CO₂ levels. There were 10 less flower buds and 0.3 g less dry mass per plant at first flower for every 1° increase in plant ADT at high and medium DLIs. Flower bud number and dry mass were relatively low and less sensitive to changes in ADT at low DLI, and increased slightly with CO₂ enrichment at medium and high but not at low DLI. Plant height was not related to ADT, but increased linearly as DIF increased from −6 to 12°C at all DLIs, but the response was stronger under low DLI than high and medium DLIs. Flower bud number and dry mass were correlated closely with the ratio of DLI to daily thermal time (base temperature of 0°C). Flower bud number and dry mass were highest when C. carpatica plants were grown at 15°C with a DLI of 10–15 mol m⁻² per day.     

Responses of native Lupinus varius (L.) to culture conditions: effects of photoperiod and sowing time on growth and flowering characteristics

The effects of photoperiod and sowing time on growth and flowering characteristics of Lupinus varius were investigated during two growing periods to determine its responses to culture conditions as a potential native cut-flower crop. The seeds were sown in an unheated plastic greenhouse on 28 September, 28 October and 28 November under natural, 14- and 16-h day-length treatments. 14- and 16-h day-lengths were established by lengthening the natural day-lengths to 14 and 16 h with the use of night break photoperiodic lighting at 1.8–1.9 μmol m⁻² s⁻¹ in 400–700 nm. Photoperiodic lighting, in particular the 16-h day-length treatments, slightly (maximally 15 days) shortened days to flowering and increased plant height in all sowing times relative to natural photoperiods. There were no significant differences in stem and branch inflorescence diameters, in lengths of branch, in main and branch inflorescences in plants grown under natural photoperiod, and 16-h day-length treatments. The highest main inflorescence diameter, the number of branches per plant, and flower numbers on main and branch inflorescences were recorded in plants grown under natural photoperiods, whereas 14-h day-length treatments did not provide sufficient specimens to allow for the measurement of most of the characteristics studied. These findings were interpreted to indicate that L. varius behaves as a facultative long day plant. Additionally, there was a particular shortening of days to flower and growth, and flowering quality decreased linearly with delayed sowing dates under all photoperiodic treatments. The earliest and latest flowering dates were recorded for plants sown in September under 16-h day-length, and plants sown in November under natural photoperiods, respectively. Therefore, sowing in September under natural photoperiods or 16-h artificial day-length resulted in earlier flowering dates and a longer time from sowing to flowering and was consequently the best sowing time with respect to all of the characteristics considered in this study.     

The impact of photoperiod and irradiance on flowering of several herbaceous ornamentals

Forty-one herbaceous species were grown under short-days (8 h photoperiod, ambient irradiance averaged 12–13.2 and 6.4–8.3 mol m⁻² day⁻¹ for Experiments I and II, respectively) with or without supplemental high-pressure sodium lighting (+50, 100, or 150 μmol m⁻² s⁻¹); or under long-days delivered using natural day lengths and irradiance with night interruption lighting (2200–0200 h at 2 μmol m⁻² s⁻¹ from incandescent lamps) or under ambient daylight plus supplemental irradiance during the day and as a day extension to 18 h (0800–0200 h) with supplemental high pressure sodium lighting (+50, 100, or 150 μmol m⁻² s⁻¹) to identify the impact of photoperiod and irradiance on flowering of each species. Days to first open flower, leaf number below first flower, and mean dry weight gain per day (MDWG) were measured when the first flower opened. Twenty-seven species were photoperiodic with examples of five photoperiodic response groups represented: obligate short-day (2), facultative short-day (5), obligate long-day (16), facultative long-day (4); 13 were day neutral (no photoperiod response in flowering). One species, Salvia sclarea L., did not flower. A facultative irradiance response was observed with 10 species; 28 species were irradiance indifferent; 2 had delayed flowering as irradiance increased. Photoperiod affected MDWG of 30 species. Increasing irradiance affected MDWG with 14 species. Photoperiod interacted with irradiance to affect MDWG of 11 species. Cobaea scandens had the greatest MDWG (0.40 g day⁻¹) while Amaranthus hybridus had the least MDWG (0.01 g day⁻¹) across photoperiod and irradiance levels.     

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

Summary

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

Temperature and irradiance effects on Sandersonia aurantiaca flower shape and pedicel length

Sandersonia flowers can vary from being lantern- to tubular-shaped. Lantern-shaped flowers are considered to be most commercially desirable when the ratio of the widest to the narrowest diameters of a flower, termed the ratio of hips to waist, is 1.5 or greater. Pedicel length can also affect the overall appearance of a flower stem. Short pedicels are considered more desirable. The influences of temperature and irradiance on Sandersonia aurantiaca flower shape and pedicel length were examined in controlled environment (CE) growth rooms. The growing environments were at constant temperatures of 15, 18, 21, 24 or 27 °C; or day/night temperature differentials of −6, 0, +6, +12, or +18 °C, with a mean of 21 °C. Photosynthetic photon flux densities (PPFD) were 700, 460 or 210 μmol m⁻² s⁻¹. At harvest, measurements were made of the widest and narrowest diameters of the oldest flower on each stem and the ratio of these parts was calculated. The pedicel length of the oldest flower was also measured. Environments with constant temperatures below 23 °C and the least day/night temperature differentials (−6, 0 and +6 °C) produced flowers of the most desirable shape, defined as having a hips to waist ratio of 1.5 or greater. At these temperatures, irradiance had a variable effect on flower shape. Pedicel length was also highly dependent on temperature and PPFD. As mean temperatures increased or as the temperature differential changed towards a differential of 12 °C, and as PPFD decreased, pedicel length increased significantly. Hip diameter was more sensitive to environmental changes than waist diameter and thus had a greater effect on flower shape. This work indicates to growers that they can enhance Sandersonia flower quality by producing more desirably shaped flowers with short pedicels through maintaining relatively low (less than 23 °C) mean temperatures, minimising temperature differentials, and maintaining irradiance levels as high as possible.     

Positive effect of salicylates on the flowering of African violet

Aqueous solutions of 1.0 μM to 0.1 nM concentrations of salicylic acid (SA) were sprayed on African violet grown under greenhouse conditions to estimate its effect on the flower expression of the plant. These solutions were sprayed on the shoots of the plant on three occasions, 21, 28 and 35 days after being potted. Salicyliclate at 0.1 nM increased the number of leaves from 16 to 19, the number of flower primordia from 8 to 14, the rosette diameter from 130 to 177 mm in comparison with the control. The same concentration induce flowering at 74 days of plant age whilest the control plants last 89 days to flower.     

Effect of photoperiod on flower bud initiation and development in myoga (Zingiber mioga Roscoe)

Selection of suitable production locations in Australia and New Zealand for production of myoga (Zingiber mioga Roscoe) has been limited by lack of information on climatic influences on flowering. This study focused on photoperiod as potential production sites within Australia differ considerably in daylength due to the geographical range. The two cultivars available in Australia (Inferior and Superior) were examined in this trial due to previously observed differences in vegetative and reproductive development.Plants grown under long-day conditions (16 h) and short-day conditions (8 h) with a night break produced flower buds, while those under short-day conditions (8 h) did not. The failure of plants under short-day conditions to produce flower buds was due to abortion of developing floral primordia rather than a failure to initiate inflorescences. It was concluded that for flower development in myoga a qualitative long-day requirement must be satisfied, but that flower initiation was day-neutral.Short-day conditions resulted in abortion of flower primordia, premature senescence of foliage and reduced foliage dry weight in both cultivars. Early senescence and low flower bud yield of the Inferior cultivar, but not the Superior cultivar have been observed in crop evaluation trials in Southern Australia and New Zealand. Differences in critical photoperiod between the two cultivars may explain this observation and therefore photoperiodic requirements may be an important consideration in site and planting date selection for different cultivars.     

The influence of increasing tree cover on mean radiant temperature across a mixed development suburb in Adelaide,Australia

The implementation of trees in urban environments can mitigate outdoor thermal stress. Growing global urban population and the risk of heatwaves, compounded by development driven urban warmth (the urban heat island), means more people are at risk of heat stress in our cities. Effective planning of urban environments must minimise heat-health risks through a variety of active and passive design measures at an affordable cost. Using the Solar and Longwave Environmental Irradiance Geometry (SOLWEIG) model and working within the bounds of current urban design, this study aimed to quantify changes in mean radiant temperature (T_mrt) from increased tree cover at five different 200 × 200 m urban forms (including compact mid-rise development, residential and open grassy areas) within a suburb of Adelaide, Australia during summer. Following a successful validation of SOLWEIG, street trees were strategically distributed throughout each of the five urban forms and the model run over five warm sunny days (13–17 February 2011). Results showed spatially averaged daytime (7:30–20:00) T_mrt reduced by between 1.7 °C and 5.1 °C at each site, while under peak heating conditions (16 February, 14:00) T_mrt reduced by between 2.0 °C and 7.1 °C. The largest reduction in T_mrt under peak warming conditions was at the residential site, despite having the fewest number of trees added. Directly below clusters of trees, T_mrt could be reduced by between 14.1 °C and 18.7 °C. SOLWEIG also highlighted that more built-up sites showed higher T_mrt under peak warming conditions due to increased radiation loading from 3D urban surfaces, but over the course of the day, open sites were exposed to greater and more uniform T_mrt. This study clearly demonstrates the capacity of street trees to mitigate outdoor thermal stress and provides guidance for urban planners on strategic street tree implementation.     

Embryo induction via anther culture in papaya and sex analysis of the derived plantlets

We investigated the embryo induction of papaya by anther culture, and identified the sex of plantlets derived from embryos using a sex-diagnostic PCR. Anthers, containing approximately 80% uninucleate pollen, were collected from 10 to 14 mm long male flower buds. They were pre-treated on agar (0.8%) or in liquid medium for 1–5 days at 25 or 35 °C, then transferred to agar medium with 0.1 mg l⁻¹ BA and 0.1 mg l⁻¹ NAA. Agar and liquid media used for the pre-treatment contained water only or MS nutrients with or without sucrose (2.0%). On the agar medium, no embryos were induced at any pre-treatment temperature. In the liquid medium at 25 °C, embryos were induced at about 1.0% (rate of anthers forming embryos) in MS medium with sucrose for 3 or 5 days. At 35 °C, embryo induction rate tended to increase up to about 4.0% when anthers were treated in water for 1 day or MS medium with sucrose for 3 or 5 days. The sex of plantlets established through anther culture was analyzed using a sex-diagnostic PCR. All plantlets were determined as female. From these results, we suggest that all plantlets established through anther culture were of microspore origin, and that the anther culture technique is useful for the breeding of female papaya.     

Reduction of chilling injury in ‘Tommy Atkins’ mangoes during ripening

Studies were conducted to investigate how harvest maturity influence fruit ripening processes to alleviate chilling injury (CI) in mangoes (cv. Tommy Atkins). Fruit at three stages of maturity, immature (M1), half-mature (M2) and mature (M3) were stored for 18 days at 5 °C and then at 1 or 3 days at 20 °C. M1 fruit succumbed to CI after 18 days at 5 °C, with symptoms increasing in severity upon warming. Low C₂H₄ production, poor colour development, minor changes to fruit composition, insipid flavour and poor aroma revealed that fruit ripening was insufficient to reduce CI compared to M2 and M3 fruits. M2 and M3 fruits had higher C₂H₄ production rates than M1 fruit and ripened normally with acceptable flavour and aroma after 18 days at 5 °C and 3 days at 20 °C. While M3 fruit had no CI symptoms, they were overripe and fruit decay incidence was 26.6%, compared to M2 fruit which had no decay, a trace of CI symptoms and possessed the best overall quality.     

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.     

Effects of pre-blossom temperatures on flower development and fruit set in apricot

The influence of pre-blossom temperatures on flower development and fruit set is ascertained in apricot (Prunus armeniaca L.), a species without previous records on the effect of pre-blossom temperature on fruit set, but that is particularly prone to erratic fruit set. A polyethylene cage was used during pre-blossom development of flower buds to increase maximum temperatures by 6–7 °C and mean temperatures by 3 °C in orchard conditions. This increase in temperature accelerated flower bud development, caused a hastening in flowering time and following hand-pollination, reduced fruit set. At anthesis, flowers that had developed in warmer conditions weighed less and showed less development of the pistil than control flowers. Pistil growth of flowers under warm conditions did not differ from that of the control flowers when both the populations were compared on a real time scale in spite of the fact that warmed buds were at an advanced external phenological stage. Thus, hastening of external floral development by warm pre-blossom temperatures was not accompanied by advance in pistil development. This lack of synchrony resulted in premature flowering of flowers with underdeveloped pistils that had a reduced capability to set fruit. The results are discussed in terms of flower quality and its implications in fruit set and subsequent crop load.     

Influence of temperature and bark injuries on the development of Phytophthora cactorum and P. Citrophthora on peach trees

The effect of temperature and bark injuries on the occurrence of crown rot of peach trees caused by P. cactorum and P. citrophthora were examined in field and laboratory. Lesions developed at 35 °C (the complete range of temperatures tested) but maximum development occurred at 20–25 °C. Greatest growth of these fungi on cornmeal agar (CMA) also occurred between 15 and 30 °C. Both pathogens could infect injured trees up to 20 days after wounding, but could not infect uninjured plants or plants wounded 40 and 30 days before inoculation, respectively. This study showed that temperature is a critical factor for the development of Phytophthora crown rot of peach trees. In addition, crown rot developed from recent wounds inoculated with agar plugs of Phytophthora.     

Prohexadione-calcium affects growth and flowering of petunia and impatiens grown under photoselective films

The response of petunia (Petunia x hybrida Vilm.-Andr. ‘Countdown Burgundy’) and impatiens (Impatiens wallerana Hook ‘Accent Orange Tempo’) to Prohexadione-calcium was evaluated under a clear and a far-red light absorbing greenhouse (A_FR) film to investigate the dosage effect of Prohexadione-Ca and to determine if it can overcome the flowering delay under FR deficient greenhouse environments. Prohexadione-Ca reduced stem elongation of petunia and impatiens under A_FR and clear films when applied 3 weeks after germination. Late applications were less effective. In both crops, main stem length decreased in a quadratic pattern as the concentration of Prohexadione-Ca increased. Under both films, 50–100 mg l⁻¹ Prohexadione-Ca resulted in ≈30% shorter petunia plants. Greater concentrations (500 and 1000 mg l⁻¹) resulted in excessively short plants (over 70%). Prohexadione-Ca at 100 mg l⁻¹ delayed anthesis of petunia by 8 and 3 days under the clear film and the A_FR film, respectively during less inductive photoperiods but had no effect during inductive photoperiods. In impatiens, Prohexadione-Ca at 100 mg l⁻¹ delayed anthesis over 10 days under clear or A_FR film. Greater concentrations (200 and 300 mg l⁻¹) inhibited flowering of impatiens. Prohexadione-Ca treatments significantly affected flower color development. Untreated petunia plants had dark burgundy flowers. Prohexadione-Ca treatment increased L*, a*, and C* values and decreased hue angle indicating that the flowers were faded. Flowers of untreated impatiens plants were bright orange color. Prohexadione-Ca at 100 mg l⁻¹ increased L* value and decreased a*, b*, and C* values indicating that significant petal fading had occurred. Flowers of treated plants were nearly white under both films. Although effective in height control, loss of color would be a major limitation to the use of Prohexadione-Ca on flowering crops.     

In vitro production of Prunus necrotic ringspot virus-free begonias through chemo- and thermotherapy

Prunus necrotic ringspot virus (PNRSV)-free Begonia spp. plants were raised from petioles of virus-infected plants using in vitro techniques. The petioles were grown on MS medium supplemented with 0.2 mg/l NAA and 0.2 mg/l BAP (pH 5.8). For rooting, half-strength MS medium without any plant growth regulators was used. On rooting medium, shoots were subjected to chemotherapy (virazole, 2-thiouracil or 6-azauracil) and thermotherapy (38 °C for 16 h light period and 22 °C for 8 h dark period) separately or in combination. Regenerated plants (treated with chemo- and thermotherapy) were indexed for PNRSV by DAS-ELISA and RT-PCR. An amplified product of 785 bp was obtained by RT-PCR in PNRSV-infected plants. Virazole at a concentration of 20 mg/l was found to be more effective (30 and 20% of PNRSV-free plants as indexed by ELISA and RT-PCR, respectively) in comparison to the other chemicals. Thermotherapy for 25 days gave 35 and 25% PNRSV-free plants as indexed by DAS-ELISA and RT-PCR, respectively. A combination of both treatments gave a good number of PNRSV-free plants (67.5 and 57.5% as indexed by DAS-ELISA and RT-PCR, respectively). At higher concentrations all three chemicals were found to be toxic. Thermotherapy for more than 25 days caused browning of leaves and shoots died.