Biochemical changes in dormant grapevine shoot tissues in response to chilling: Possible role in dormancy release

At leaf fall, one-year-old shoots of cv. Superior Seedless table grape were collected and cut into single-node sections. These cuttings were subjected to 0, 100, 200, 300, 400 or 500 h of chilling at 5 °C to simulate natural chilling accumulation. After each treatment, one group of cuttings was forced to break buds while a second group was used to study biochemical changes taking place in the bud and underlying internode tissues. Carbohydrates, free polyamines and proline concentrations were determined and amylolitic and invertase (EC 3.2.1.26) activities were estimated. Low temperature treatment caused a hydrolysis of starch concomitant with an accumulation of sucrose. There was also a rapid build-up of proline, putrescine (Put) and spermidine (Spd) which reached their maximum levels at 300 positive chill units (PCU). Afterwards, as buds approached chilling satisfaction (400 and 500 PCU), hexoses accumulated in the buds while sucrose concentration increased considerably in both structures. Proline and Put, however, decreased in both tissues. Spd level remained high, while spermine (Spm) increased slightly. Changes in starch concentration seem to be controlled by α-amylase (EC 3.2.1.1). Sucrolytic activity, consisting mainly in the acid invertase form, changed inversely to sucrose concentrations. Nevertheless, at chilling satisfaction both sucrose content and invertase activity remained high in the buds implying a possible import of sucrose into the bud which acted as a strong utilizing sink. Our data suggest that limited budbreak due to a lack of chilling may be due to low hexoses availability. However, as buds approached chilling satisfaction, a high acid invertase activity, high soluble sugars concentration and a decrease in Put to Spd plus Spm ratio appear to be correlated with bud dormancy release and improve budbreak. Furthermore, endodormancy can be divided into two phases: the first one (from 0 to 300 PCU) is an acclimation period; the second (from 300 to 500 PCU) is a beginning of growth resumption.     

Carbohydrate changes in flowers,leaves, shoots and spurs of ‘Cox’s Orange Pippin’ apple during flowering and fruit setting periods

Summary

Changes of carbohydrate concentrations in different parts of the flower and the surrounding tissues (leaves, spurs and shoots) were measured in apple (Malus pumila) in 1987 and 1988, during the periods of flowering and fruit setting, to investigate their importance for fruit setting. HPLC was used for soluble sugar and sorbitol analysis. Starch was hydrolysed to glucose enzymatically and glucose concentration was determined colorometrically to estimate starch concentrations. Soluble sugars plus sorbitol (the soluble pool) increased rapidly in all parts of the flower from bud burst until full bloom. In contrast, in the same period, starch concentrations decreased rapidly and reached about zero at full bloom in the storage organs (shoots and spurs), indicating starch conversion to sugars and their movement to the growing flowers. Sorbitol was the most abundant carbohydrate in all apple tissue measured, with the exception of sepals, in which glucose concentration was the highest from full bloom onwards. Sepals had much higher glucose and fructose concentrations than leaf laminae but much lower sorbitol concentrations. Although dry weight, soluble pool and starch concentrations and total soluble pool content increased in the receptacle after petal fall, sucrose concentrations and total sucrose content dramatically decreased. These results suggest a preferential mobilization and utilization of sucrose rather than sorbitol during the fruit setting period and probably an important role of sucrose metabolism in fruit setting.     

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.     

Effect of artificial chilling on the depth of endodormancy and vegetative and flower budbreak of peach and nectarine cultivars using excised shoots

Stem cuttings were obtained from 12 peach and nectarine cultivars during leaf fall, placed in plastic bags at 3.0 ± 0.1 °C to simulate 0–800 h of chilling and forced to budbreak at 20.0 ± 1.0 °C for a period of 6 weeks. Some cultivars showed high blooming and leafing without exposure to chilling; chilling enhances leafing and blooming but the percentage increment was higher in leaf buds. In general, maximum budbreak was reached with less chilling accumulation (<100–200 h) in flower buds compared with leaf buds; excessive chilling caused a reduction of the percentage budbreak in flower but not in leaf buds. Additionally, chilling modified the proportion of blooming that occurred before leafing. In non-chilled shoots, blooming occurred earlier than leafing, except in cv. ‘San Pedro 16–33’ but the proportion of blooming before leafing decreased significantly with chilling in most cases. By studying the mean time to budbreak, we conclude that the flower bud generally has a lower intensity of rest; the intensity of rest declines at a slower rate in flower than in leaf buds with chilling; flower buds had greater heat requirements than leaf buds when the chilling requirement had been covered, so that each peach cultivar had a point of critical chilling accumulation below which blooming tended to occur earlier, and above which leafing tends to occur first. Flower and leaf buds had different depths of endodormancy but similar chilling requirements in the majority of peach and nectarine cultivars studied. Finally, different varieties with similar chilling requirements showed different responses to chilling. Therefore, the cutting test measuring the response of vegetative and floral buds provides considerable information on the characterisation of the variety, compared with the sole and traditional data of chilling requirements.     

Flowering control in Watsonia: Effects of corm size,temperature, photoperiod and irradiance

The role of corm size, light and temperature in flowering of Watsonia species was evaluated to facilitate their commercial production. In addition to exhibiting desirable ornamental attributes, the species selected represented the major climatic regions in South Africa. A day/night temperature regime of 12/7 °C released vegetative dormancy in all species and thereafter elicited vernalization in Watsonia pillansii – highlighting an obligate cold requirement for this species. Flowering of Watsonia borbonica and Watsonia tabularis was not enhanced by additional chilling, but rather by long (16 h) or day-neutral (12 h) photoperiods. Microscopic examination of the shoot apical meristem revealed that extension of the 2nd leaf was a critical stage developmentally, and signified the anatomical transition to flowering. Late-development temperatures to a maximum of 25 °C ensured healthy vegetative growth and supported the maturation of the inflorescence and the opening of floret buds. Irradiance did not affect flower induction, but a minimum light intensity of 150 μmol m⁻² s⁻¹ proved essential in sustaining the energetic demands of the competitive growth and reproductive processes. Excessively high irradiance (950 μmol m⁻² s⁻¹) impacted negatively on attractiveness through increased bud blasting. Flowering success was not correlated to corm mass, but rather to the environment under which the corm was stored, or the conditions under which the plant was grown. Understanding the phenology of these species in situ and the link between flowering and season provide a useful tool for predicting the artificial requirements necessary to elicit optimal flowering under industry conditions.     

High temperatures and time to budbreak in low chill apricot ‘Palsteyn’. Towards a better understanding of chill and heat requirements fulfilment

The efficiency of different temperature cycles in inducing budburst of one-year-old shoots of the apricot cultivar ‘Palsteyn’ from dormancy was evaluated. Three replications of shoots were collected during two consecutive years from adult trees, following the accumulation of different amounts of chilling in the field. Thereafter, shoots were exposed to different temperature cycles in growth chambers, for 60 days. The temperature treatments included a continuous temperature of 5 °C; daily temperature cycles of 19/5 h at 5/15 °C, at 5/20 °C, and at 5/25 °C; and the same temperature cycles for the remainder of the 60-day period, after pretreatment at 5 °C for 30 or 45 days. After the temperature treatments, shoots were forced at 25 °C until budburst. The mean time to budburst (MTB) (in days) of lateral vegetative, terminal vegetative and reproductive buds was evaluated. The efficiency of the different treatments was greatly influenced by the date on which shoots were cut. High temperatures had a more positive effect on the reduction of MTB when chilling accumulation had occurred in the field instead of the growth chamber. After partial chilling accumulation in the field, high temperatures (25 °C) combined with low temperatures are more efficient than cycles of moderate temperatures (15 or 20 °C) to induce an earlier budburst. In view of these results, a parallel accumulation of both chilling and heat requirements after partial chilling accumulation is suggested. The application of these results could assist in the development of more accurate models for the prediction of the overcoming of dormancy and blooming.     

Nitrogen content determines adventitious rooting in Euphorbia pulcherrima under adequate light independently of pre-rooting carbohydrate depletion of cuttings

Root regeneration in shoot tip cuttings responds to graduated nitrogen (N) fertilization of stock plants. In pelargonium cuttings, reduced carbohydrate reserves caused by high N absorption by the donor plants and post-harvest storage of cuttings limit adventitious root formation, especially in low-light environments. In contrast, in chrysanthemum, similar carbohydrate reserves do not have this dominant effect on rooting capacity. The positive correlation between rooting capacity and internal N status is stable across a wide range of environments and is genotypically consistent for this species. However, the influence of N and carbohydrates on adventitious rooting of Euphorbia pulcherrima is unknown. We investigated the consequences of different N fertilization regimens applied to E. pulcherrima stock plants and cold and dark storage of the cuttings on N absorption, carbohydrate distribution, and rooting capacity of cuttings. Increasing time of stock plant cultivation with graduated N nutrition produced cuttings with N contents, ranging from 19 to 51 mg N g⁻¹ dry mass (DM). High N absorption resulted in low carbohydrate concentrations in cuttings, and subsequent storage decreased carbohydrate concentrations further, particularly in stems. Lower sucrose contents in leaves were correlated with reduced rooting of stored cuttings at a particular harvest date. However, despite the lower carbohydrate levels, root numbers and lengths correlated positively with internal N concentrations. These relationships remained stable in unstored and stored cuttings, even when overall rooting intensity was reduced under lower natural light during autumn. Multivariate regressions accounting for nitrogen content, sucrose content and daily light integral during rooting highlighted these relationships and explained up to 79% of rooting variances. We conclude N nutrition of stock plants and N absorption by cuttings are the dominant factors determining the rooting capacity of poinsettia when rooting occurs under sufficient light, as is commonly available during propagation. To maximize rooting capacity of poinsettia cuttings their nitrogen content should exceed a threshold of 40 mg N g⁻¹ DM.     

Carbohydrate profiles in the graft union of young sweet cherry trees grown on dwarfing and vigorous rootstocks

In composite (scion–rootstock) dwarfing fruit trees, an overgrowth at the graft union is often observed, the severity of which is correlated with degree of dwarfing. The graft union of dwarfing sweet cherry (Prunus avium L.) rootstocks may limit soluble sugar transport or starch mobilization, leading to localized accumulation. Soluble sugars and starch were measured in the tissues surrounding the graft union of young ‘Rainier’ (2002) and ‘Lapins’ (2003) sweet cherry trees on ‘Gisela 5’ (‘Gi 5’; dwarfing) and ‘Colt’ (vigorous) rootstocks. Separate rootstock shank, rootstock, graft union, and scion tissues were analyzed for both starch and soluble sugar content throughout the growing season in both years. Starch concentrations did not vary among locations within the graft union for ‘Rainier’ on either the dwarfing or vigorous rootstock, or for ‘Lapins’ on the dwarfing stock. However, for ‘Lapins’ on ‘Colt’, starch was highest in the rootstock shank and declined vertically (rootstock shank ? rootstock > union > scion). Soluble sugar concentrations were generally similar to or higher in scions on ‘Gi 5’ than on ‘Colt’, and were similar to or lower in the rootstock and rootstock shank on ‘Gi 5’ than on ‘Colt’. Results suggest that rootstock has a significant effect of localized accumulations of carbohydrates above and within the graft union of ‘Gi 5’ and below the graft union of ‘Colt’.     

Status of nitrogenous and carbohydrate compounds as affected by nitrogen fertigation rates in young persimmon trees

The effects of nitrogen (N) fertigation rates on levels of nitrogenous and carbohydrate compounds were determined in young ‘Fuyu’ persimmon trees. Total N amounts of 0 g, 10 g, 20 g, 30 g, and 40 g were distributed, respectively, to a 50-L pot by fertigation as different volumes of 1% (w/v) urea solution every week from May 15 to September 25. Fruits were sampled on November 2, and shoots and roots on November 17. High N fertigation rates significantly increased the N and amino acids in all the tree parts and protein in fruits and shoots. In contrast, the concentration of soluble sugars significantly decreased in the fruits and perennial parts as the N rate increased from 10 g to 40 g. A notable reduction of starch was also found in the shoots and roots of trees with high N fertigation rates. The percentage of shoots died due to cold injury during the winter was the highest at the 0 g N rate; however, it was 2.3-fold greater at the 40 g N rate as compared to the 10 g N rate. We concluded that high N fertigation could interfere not only with sugar accumulation of fruits through increased N metabolism, but also reserve carbohydrates of perennial organs.     

Callus induction and plant regeneration in Cardiospermum halicacabum Linn. an important medicinal plant

Cardiospermum halicacabum Linn. is an important medicinal twining herb belonging to the family sapindaceae. A method for rapid micropropagation of C. helicacabum through plant regeneration from leaf and nodal explant derived calli has been developed. The nodal and leaf segments were cultured on Murashige and Skoog (MS) medium supplemented with 2,4-dichlorophenoxy acetic acid (2,4-D; 0.5–9 μM) for callus induction. Callus production was highest at 5 μM 2,4-D where 96 and 90% of cultured leaf and nodal cuttings produced callus, respectively. The viable calli were maintained at reduced concentration of 2,4-D (2 μM). These calli were transferred to MS medium supplemented with various concentrations of 6-benzyladenine (BA; 2–10 μM) or kinetin (2–10 μM) alone or in combination with indole 3-acetic acid (IAA; 0.2–1.0 μM) for shoot regeneration. The addition of low concentrations of IAA into BA or kinetin containing medium significantly increased the frequency of shoot regeneration in both nodal cuttings and leaf-derived calli. The highest number of adventitious shoots (28 per callus) formed at 8 μM Kin and 0.5 μM IAA. For rooting of the shoots, half-strength MS medium supplemented with different concentrations of indole 3-acetic acid, indole 3-butyric acid (IBA) and (alpha)-naphthalene acetic acid (NAA) 1–5 μM was tried. The optimal result was observed on half-strength MS medium supplemented with 2.5 μM IBA, on which 91% of the regenerated shoots developed roots with an average of 4.2 roots per shoot within 45 days. The in vitro raised plantlets were acclimatized and transferred to soil with 90% success. This in vitro propagation protocol should be useful for conservation as well as mass propagation of this medicinal plant.     

Direct and callus-mediated regeneration of Curcuma soloensis Valeton (Zingiberaceae) and ex vitro performance of regenerated plants

Protocols are outlined for the regeneration of Curcuma soloensis, an attractive tropical ornamental plant, from young vegetative bud explants. We used both direct and callus-mediated regeneration techniques to produce material suitable for mass propagation and the development of transgenic plants. During direct plantlet propagation, the presence of thidiazuron (TDZ) in the growing medium induced more than three times as many shoots as 6-benzylaminopurine (BA), with a mean of 18.7 shoots per explant on MS medium containing 2.5 μM TDZ compared to 5.0 shoots with 40 μM BA. Subsequently, the shoots rooted readily on MS basal medium that was free of plant growth regulators. During indirect plantlet regeneration, TDZ combined with BA and 2,4-dichlorophenoxyacetic acid (2,4-D) had significant effects on embryogenic callus induction and multiplication. The frequency of callus formation was 91.1% for explants cultured on MS basal medium supplemented with 2.5 μM TDZ, 2.0 μM BA and 1.2 μM 2,4-D. On average 7.1 shoots were produced per callus mass cultured on MS medium supplemented with 2.5 μM TDZ, 9.0 μM BA and 1.2 μM naphthaleneacetic acid (NAA). Regenerated shoots were transferred to MS medium supplemented with 2.5 μM TDZ, to produce multiple shoots. In vitro cultured plantlets readily acclimatized to greenhouse conditions, showing 100% survival rates in a sphagnum, perlite and sand (1:1:1) medium. These plants were transplanted into pots or planted in the field. The ex vitro acclimated plants grew vigorously and produced showy inflorescences 5–6 months after planting. The high-frequency of shoot multiplication and rapid flowering of tissue-cultured plants indicate that C. soloensis has great potential in the floricultural market.     

Effects of fruit load on flower bud initiation and development in peach

Summary

This study aims to quantify the effects of fruit crop-load on flowering and to determine the relationships between flowering and phloem sap carbohydrate and nitrogen content fractions from budding to dormancy in ‘Zincal 5’ nectarine. Fruit load significantly reduced the number of flowers per tree both indirectly, by reducing the number of shoots per tree and the number of nodes per shoot, and directly, by reducing the number of floral buds per node. The intensity of the response depended on the number of fruits developed per tree. Trees that kept all fruits up to senescence flowered 35% less than trees thinned by hand to 40% of fruits at pit hardening, and 55% less than trees completely thinned in bloom by hand. Trees that kept all fruits had significantly lower glucose and sorbitol contents in the phloem sap of mixed branches up to harvest date and full vegetative growth, respectively, but no significant relationships were found between the concentrations of these carbohydrates and flowering intensity in the following Spring. Sucrose and fructose did not show any significant difference in regard to crop-load. In fibrous roots, starch content was not related to fruit load up to dormancy, indicating that starch content is not associated with flower bud induction and differentiation. The nitrate-nitrogen fraction was significantly higher, and the ammonium-nitrogen fraction was significantly lower, in trees that tended to flower less, suggesting some disturbance in nitrate reduction in these trees.     

Amelioration of chilling stress by paclobutrazol in watermelon seedlings

Paclobutrazol (PBZ) is a member of the triazole plant-growth inhibitor group that is responsible for inducing tolerance to number of biotic and abiotic stresses. An experiment was, therefore, conducted to test whether PBZ application at various concentrations (0, 25, 50 and 75 mg L⁻¹) through seed soaking or foliar spray would protect watermelon (Citrullus lanatus) seedlings, subjected to chilling stress. Thirty-five-day old plants were exposed to chilling 5 h/day at 4 °C for 5 days. PBZ improved growth rate of watermelon seedling subjected to chilling stress and increased relative leaf chlorophyll content (RLCC) and chlorophyll fluorescence ratio (Fv/Fm) compared with the control at the end of chilling stress. PBZ ameliorated the injury caused by chilling stress by inhibiting increases in proline and leaf electrolyte leakage, which suggested that PBZ ameliorated the negative effect of chilling stress. PBZ was most effective in increased chilling tolerance of watermelon seedling when applied using the seed soak method than as a foliar spray. The best protection appeared to be obtained from seedlings seed soaked with PBZ at 50 and 75 mg L⁻¹.     

Interacting effects of temperature integration and light intensity on growth and development of single-stemmed cut rose plants

Energy conservation in horticulture can be achieved by allowing temperatures to fluctuate within predefined bandwidths instead of using rigid set points for heating and ventilation. In temperature integration, plants are supposed to compensate effects of temporarily deviations of the average temperature some time later by deviations in the opposite direction. However, little is still known on the effects of integration periods exceeding 1 day. In this study, effects of temperature integration on growth and development of single-stemmed cut rose plants were determined. Pruned rose shoots were placed in climate chambers in which light levels switched daily (2 days integration period) or weekly (14 days integration period) from high light intensity (300 μmol m⁻² s⁻¹) to low light (150 μmol m⁻² s⁻¹). Temperatures were kept continuously at 20 °C (control) or changed with the light intensity (phase, high temperature at high light intensity, low temperature at low light intensity) or changed opposite to the light intensity (counter phase). Bandwidths of temperature integration were 0, 6 or 10 °C. Under these conditions, buds grew out to harvestable shoots in approximately 45 days. At both integration periods, shoot length was significantly reduced with increasing bandwidths of temperature integration. Shoot dry weights were reduced when a bandwidth of 10 °C was applied. At both integration periods, rates of photosynthesis were primarily determined by light intensity. However, in the counter phase treatments, photosynthesis rate at high light and low temperature was reduced compared to the high light condition of the control. Under these conditions, starch content increased to approximately 10%, suggesting a feedback inhibition of the rate of photosynthesis. However, this did not (yet) affect plant growth or development.     

Effects of defoliation on fruit growth,carbohydrate reserves and subsequent flowering of ‘Hayward’ kiwifruit vines

A partial defoliation study was carried out on ‘Hayward’ kiwifruit vines with the aim of evaluating effects on fruit yield, changes in concentration of carbohydrates, and return bloom. At full bloom, ‘Hayward’ kiwifruit vines trained to the pergola system were submitted to 0% (control), 50% and 75% defoliation in the 2.0 m wide central horizontal area of the canopy. This area represents the vine ‘replacement cane zone’ (RCZ), whereas the remaining external area represents the ‘fruiting zone’ (FZ). Removing 50% of the leaves resulted in a small (−9 g in the RCZ and −3.3 g in the FZ), but significant, reduction in fruit weight compared to the control vines. More severe defoliation (75%) reduced fruit weight by 13 g in the RCZ and 7 g in the FZ. The defoliation treatment reduced the concentrations of starch and total soluble carbohydrates (glucose + fructose + sucrose) in the shoots and starch in trunk bark compared to those in control vines. The treatments caused a large reduction in return bloom, expressed as number of flowers per winter bud, by about 25% and 53% in vines with 50% and 75% defoliation, respectively.     

Gibberellic acid and flower bud development in loquat (Eriobotrya japonica Lindl.)

The application of gibberellic acid (GA₃) to the whole loquat tree from mid-May to early June and from early August to the onset of flowering, significantly reduced the number of premature flowering shoots per current shoot and per m³ of canopy, and so reduced the total number of panicles per m³ of canopy. The number of vegetative shoots per m³ of canopy was also significantly reduced by applying GA₃. The response depended on the concentration applied and produced optimal results at 50 mg l⁻¹. Differences in the number of flowers per panicle and leaves per shoot were not significantly modified by the treatment. Nevertheless, GA₃ applied directly to the developing apex near to flower differentiation reduced the number of flowers per panicle by 25–35% and without modifying the morphological characteristics of the panicle. Results suggest that less sprouting of lateral buds was largely responsible for the reduction in flowering intensity caused by GA₃. Best treatments reduced thinning costs (60%, approximately) of premature flowering shoots, slightly increased fruit diameter and significantly improved fruit colour and juice quality, thus advancing harvest date.     

Stoloniferous shoot protoplast,an efficient cell system in potato for somatic cell genetic manipulations

The present study reports that protoplasts isolated from stoloniferous shoots (SS) of potato represent an efficient system for somatic cell genetic manipulations. SS were established from single-node cuttings on MS medium supplemented with either 0.1 or 0.2 M sucrose (Suc), and protoplasts were isolated and cultured within the alginate strip, following an improved method. SS induced by 0.1 M Suc yielded 8–22 × 10⁵ protoplasts g⁻¹ fresh mass, with a high morphogenic competence. However, 0.2 M Suc-induced SS yielded protoplasts that contained large amounts of starch grains, resulting in their high degree of fragility, delayed cell division and poor morphogenic competence. For symmetric somatic hybridization (electrofusion) between Solanum tuberosum Gp. Tuberosum androgenic (di)haploid (2n = 2x = 24) ‘C-13’ and diploid (2n = 2x = 24) wild species S. pinnatisectum, protoplasts isolated from 0.1 M Suc-induced SS were also found to be most responsive. Out of several putative somatic hybrids, there were two tetraploids and five diploids, with 48 and 24 chromosomes, respectively at all the three shoot layers (L₁–L₃). This precluded the occurrence of mixoploidy vis-à-vis chimaerism in regenerants, as common in somatic fusion involving mesophyll protoplasts of S. pinnatisectum. Nuclear microsatellite analyses based on the two single-locus nSSR loci (STM0037 and STM2030) confirmed that one of the tetraploids was a true nuclear hybrid (heterokaryon), while the other a homokaryon of the Tuberosum parent ‘C-13’. The use of 0.2 M Suc-induced SS protoplasts for fundamental studies on tissue- and/or cell type-specific transient gene expression underlying tuberization has been discussed.     

Effects of auxins on soluble carbohydrates,starch and soluble protein content in Aechmea blanchetiana (Bromeliaceae) cultured in vitro

We investigated the content of soluble carbohydrates, starch and soluble proteins after treatment with auxins indole-3-butylic acid (IBA) and 1-naphthaleneacetic acid (NAA) during the development of Aechmea blanchetiana (Bromeliaceae) plantlets cultured in vitro, to determine the contribution of these compounds in plant propagation. Fresh and dry mass of roots increased more than fivefold with NAA (5.37 and 16.11 μM) compared to those with the auxin-free control. After 70 days of culture concentration of soluble protein concentration content was higher in the roots and leaves of plantlets treated with IBA and similar to auxin-free control, while a maximum accumulation of sugars was observed at 90 days in the roots of plantlets treated with NAA (0.54 μM) or IBA (0.49 and 4.9 μM). The major carbon reserves in the roots were soluble carbohydrates, suggesting that they play an important role in the growth of in vitro-cultured epiphytic bromeliads.     

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     

Night interruption promotes vegetative growth and flowering of Cymbidium

The effects of night interruption (NI) were examined on the vegetative growth and flowering of Cymbidium ‘Red Fire’ and ‘Yokihi’. Plants were grown under 9/15 h ambient light/dark (control), 9 h ambient light plus night interruption (22:00–02:00 h) with low light intensity at 3–7 μmol m⁻² s⁻¹ (LNI) and 9 h ambient light plus NI with high light intensity at 120 μmol m⁻² s⁻¹ (HNI) conditions. The number of leaves, leaf length, number of pseudobulbs and pseudobulb diameter increased in both LNI and HNI compared to controls for both cultivars. While none of the control plants flowered within 2 years, 100% of the ‘Yokihi’ and 80% of the ‘Red Fire’ plants grown under HNI condition flowered. In the LNI group, 60% of the plants flowered in both cultivars. Plants in the HNI group showed a decreased time to visible inflorescence and flowering than those in the LNI group. The number of inflorescences and florets were greater in the plants grown under HNI than those in the LNI group. The tallest plants at flowering were in the HNI group in both cultivars. NI with low light intensity can be used effectively to promote flower induction with increased growth rate during the juvenile stage in Cymbidium. To obtain high quality plants, however, NI with high light intensity strategies should be considered.