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.     

Vernalization promotes flowering of a heat tolerant Calandrinia while long days replace vernalization for early flowering of Brunonia

The flowering responses of Brunonia australis (blue pincushion) and Calandrinia sp. to vernalization, photoperiod, temperature and plant age were investigated to provide a foundation for manipulating flowering in these potential potted plants. Plants were vernalized at 4.8 °C for 0, 3 or 6 weeks at the plant age of 1–4 or 8–14 leaves. Following vernalization, plants were grown at 25/10 or 35/20 °C (day/night) under short days (11 h, ambient daylight averaged 380 ± 44 μmol m⁻² s⁻¹) or long days (16 h) provided by an additional 5 h night break (21:00–2:00 h at <4.5 μmol m⁻² s⁻¹ from incandescent lamps), for 85 days. This is the first work to investigate flowering of these ornamental species. Both species showed enhanced flowering following vernalization and a quantitative requirement for long days. The reduction of the time until the first visible inflorescence (Brunonia) or flower (Calandrinia) buds by 8–13 days was affected by vernalization for 3 or 6 weeks, respectively. Long days were effective for reducing the time to first visible floral bud and increasing the number of inflorescence or flowers per plant for both species. For Brunonia, LDs replaced vernalization when applied to plants with 1–4 leaves. Raising temperature from 25/10 to 35/20 °C increased the number of flowers per plant of Calandrinia by 2–2.5-fold for plants with 1–4 or 8–14 leaves respectively.     

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.     

Effect of photoperiod and temperature on inflorescence appearance and subsequent development towards flowering in onion raised from sets

The plants of two onion cultivars Sturon and Stuttgarter were raised from sets and placed in a growth room at 12 °C, a light flux density of 120 μmol m⁻² s⁻¹ and a 16 h photoperiod. Cultivar Stuttgarter took 195 days to initiate, whereas time for initiation in cv. Sturon was 201 days. After initiation the plants were transferred to wide range of photo-thermal regimes consisting of six set point temperatures (6, 10, 14, 18, 22 and 26 °C) and four photoperiods (8, 11, 14 and 17 h day⁻¹). An overall mean temperature for all developmental stages under each photo thermal combination was 12.2, 12.4, 15.9, 17.8, 23 and 24.4 °C. Time to inflorescence appearance, spathe opening and floret opening decreased linearly as temperature and photoperiod increased. At low to mild temperatures (12.2–17.8 °C), longer photoperiod enhanced florets per umbel, whereas at higher temperatures (23–24.4 °C), the floret number declined with lengthening photoperiods. As the photoperiod extension in each temperature advanced inflorescence appearance, spathe opening and floret opening and this would be beneficial in a programme to accelerate seed production in onion.     

A time-course study of flavonoids in the sprouts of tartary (Fagopyrum tataricum Gaertn.) buckwheats

The evolution, from 1 to 10 days after germination, of flavonoid content in sprouts of tartary buckwheat (Fagopyrum tataricum Gaertn.), grown in a greenhouse under low light conditions (16 μmol m⁻² s⁻¹), was investigated. Chlorogenic acid and flavonoids including C-glycosylflavones (orientin, isoorientin, vitexin, isovitexin), rutin and quercetin were separated from the sprouts by HPLC and quantified with their commercial standards. Rutin content in the edible portion of the sprouts (mean 20 and 37 mg g⁻¹ DW in ‘Hokkai T 8’ and ‘Hokkai T 10’, respectively) was 3- to 31-fold greater than that in the roots or pericarp. The free radical scavenging activity of seed sprouts was assessed through the 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay. From 6 to 10 days after sowing, the free radical scavenging activity in the edible portions rose significantly from 1.52 to 2.33 μmol Trolox equiv. g⁻¹ DW in ‘Hokkai T 8’ and from 1.46 to 2.09 μmol Trolox equiv. g⁻¹ DW in ‘Hokkai T 10’, but differences between ‘Hokkai T 8’ and ‘Hokkai T 10’ were not significant. As the results, the sprouts of tartary buckwheat, particularly those of ‘Hokkai T 10’ are strongly recommended as new high rutin food.     

Plant regeneration of pansy (Viola wittrockiana) ‘Caidie’ via petiole-derived callus

An in vitro plant regeneration protocol for pansy (Viola wittrockiana) cultivar ‘Caidie’ from petioles was established as following: callus induction on a half-strength MS medium supplemented with 0.45 μmol l⁻¹ 2,4-d plus 8.9 μmol l⁻¹ BA, callus subculture on medium F (1/2MS with 4.5 μmol l⁻¹ 2,4-d, 2.7 μmol l⁻¹ NAA and 0.44 μmol l⁻¹ BA) and then on medium T (1/2MS with 4.5 μmol l⁻¹ 2,4-d, 2.7 μmol l⁻¹ NAA and 2.2 μmol l⁻¹ BA), shoot regeneration on medium D3 (MS media supplemented with 2.9 μmol l⁻¹GA₃, 23.6 μmol l⁻¹ AgNO₃, 0.02% active charcoal and 4.5 μmol l⁻¹ TDZ), shoot multiplication on medium M (half-strength MS medium containing NAA 1.1 μmol l⁻¹, TDZ 9.1 μmol l⁻¹ and GA₃ 8.7 μmol l⁻¹), and then shoot elongation and rooting on medium R (MS medium supplemented with 1.1 μmol l⁻¹ NAA and 1.1 μmol l⁻¹ BA). Subculture on appropriate medium was found to be important for successful shoot regeneration.     

Modeling plant morphology and development of petunia in response to temperature and photosynthetic daily light integral

The effects of mean daily temperature (MDT) and mean photosynthetic daily light integral (MDLI) on flowering during the finish stage of two petunia (Petunia × hybrida) cultivars were quantified. Petunia ‘Easy Wave Coral Reef’ and ‘Wave Purple’ were grown in glass-glazed greenhouses at 14–23 °C or 14–26 °C and under 4–19 mol m⁻² d⁻¹ with a 16-h photoperiod. The flower developmental rate was predicted using a model that included a linear MDT function with a base temperature multiplied by an exponential MDLI saturation function. The flower developmental rate increased and time to flower decreased as MDT increased within the temperature range studied. For example, under a MDLI of 12 mol m⁻² d⁻¹, as MDT increased from 14 to 23 °C, time to flower of ‘Easy Wave Coral Reef’ and ‘Wave Purple’ decreased from 51 to 22 d and 62 to 30 d, respectively. Flower developmental rate increased as MDLI increased until saturation at 14.1–14.4 mol m⁻² d⁻¹. Nonlinear models were generated for effects of MDT and MDLI on flower bud number and plant height at flowering. The number of flower buds at flowering increased as MDT decreased and MDLI increased. For example, at an MDT of 14 °C with 18 mol m⁻² d⁻¹, plants had 2.5–2.9 times more flower buds than those grown at 23 °C and 4 mol m⁻² d⁻¹. Models were validated with an independent data set, and the predicted time to flower, flower bud number, and plant height were within ±7 d, ±20 flowers, and ±4 cm, respectively, for 96–100%, 62–87%, and 93–100% of the observations, respectively. The models could be used during greenhouse crop production to improve scheduling and predict plant quality of these petunia cultivars.     

Effects of low temperature storage on growth and transplant quality of non-grafted and grafted cantaloupe-type muskmelon seedlings

Grafting is a unique horticultural technology that allows the grower to select an alternate, compatible root system with natural disease resistance for their desired crop. Short-term storage of grafted seedlings under low temperature may extend the production window of grafted seedlings, reduce the labor input and increase production of grafted seedlings with a small propagation capacity. To evaluate the low temperature storage conditions, Cucumis melo ‘Olympic Gold’ seedlings were grafted onto Cucurbita maxima x Cucurbita moschata ‘Tetsukabuto’ rootstock and stored for a period of 2 or 4 weeks at 9, 12, or 15 °C under 12 μmol m⁻² s⁻¹ photosynthetic photon flux (PPF). The study demonstrated that grafted seedlings could be stored at 12 °C for 4 weeks without significant dry mass accumulation or effects on post-storage growth and development. Grafted seedlings stored at 15 °C for 4 weeks had a significant increase in dry mass and stem elongation; this was not observed for the non-grafted seedlings stored under the same conditions, suggesting that the rootstock enhanced the scion growth at lower temperatures than optimal for muskmelon. Storing muskmelon seedlings at 9 °C caused chilling damage but the damage was pronounced for non-grafted seedlings than grafted seedlings. ‘Tetsukabuto’ rootstock, an interspecific squash, presumably has a chilling tolerance and increased the storability of muskmelon seedlings. Further optimization is needed but there is potential for using this technique as a tool for mass production of grafted muskmelon seedlings.     

CO2 and air circulation effects on photosynthesis and transpiration of tomato seedlings

In the daytime, a CO₂ depletion of 10–15% and air circulation of less than 0.5 m s⁻¹ often occur in a naturally ventilated greenhouse during a sunny day with high wind speed (3–5 m s⁻¹). We, therefore, investigated the effects of moderate increase of the CO₂ concentration above the atmospheric level (500–600 μmol mol⁻¹) and air circulation up to 1.0 m s⁻¹ in a growth chamber on the net photosynthetic and transpiration rates of tomato seedlings as the first step. The average net photosynthetic rates were 2.1, 1.8, and 1.6 times higher in the growth chambers with increased CO₂ concentration (500–600 μmol mol⁻¹) and air circulation (1.0 m s⁻¹), increased CO₂ concentration, and increased air circulation, respectively, compared with those in the control (no increase in CO₂ concentration (200–300 μmol mol⁻¹) or air circulation (0.3 m s⁻¹). The transpiration rate increased with increased air circulation, while it decreased with increased CO₂ concentration regardless of air circulation. From the results, we consider that increasing the CO₂ concentration and/or air circulation in ventilated greenhouses up to the outside concentration (350–450 μmol mol⁻¹) and 1.0 m s⁻¹, respectively, can significantly increase the net photosynthetic rate of greenhouse plants.     

Quantifying the thermal flowering rates of eighteen species of annual bedding plants

The effect of mean daily air temperature (MDT) on flowering rate (the reciprocal of days to flower) was quantified for 18 species of annual bedding plants. Plants were grown in environmental growth chambers at constant air temperature set points of 5, 7.5, 10, 15, 25, or 30 °C and under an irradiance of 160–180 μmol m^–2 s^–1, with a 16-h photoperiod. Nonlinear mathematical equations were developed to predict the effect of MDT on flowering rate and to estimate the base, optimum, and maximum temperatures (T_min, T_opt, and T_max), which are the temperatures at which flowering rates are zero (low temperature), maximal, and zero once again (high temperature), respectively. The estimated T_min varied among species and ranged from 1.1 °C in French marigold (Tagetes patula L.) to 9.9 °C in angelonia (Angelonia angustifolia Benth.). T_opt and T_max were only observed for 8–10 species with the temperature range tested. T_opt ranged from 19.1 °C in dahlia (Dahlia × hybrida Cav.) to 28.0 °C in blue salvia (Salvia farinacea Benth.), whereas T_max ranged from 30.3 °C in snapdragon (Antirrhinum majus L.) to 31.7 °C in moss rose (Portulaca grandiflora Hook.). Angelonia, browallia (Browallia speciosa Hook.), cosmos (Cosmos sulphureus Cav.), dahlia, and snapdragon grown at 25 or 30 °C developed a mean of two to seven more nodes before flowering compared with plants grown at ≤15 °C. The results indicate that in many species, flowering rate in response to MDT is asymmetrical around T_opt and the temperature range between T_min and T_opt is wider than that between T_opt and T_max. This information could be used to improve the predictability of flowering time of these ornamental crops and to assist growers in determining energy-efficient production temperatures.     

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.     

Screening Capsicum species of different origins for high temperature tolerance by in vitro pollen germination and pollen tube length

Successful fruit set depends on several reproductive processes including pollen germination and tube growth processes. An experiment was conducted to determine the effects of temperature on pollen germination characteristics and to identify species/genotypic differences in Capsicum using the cumulative temperature response index (CTRI) concept. Pollen was collected from plants of seven genotypes from five Capsicum species, adapted to various parts of the world and grown outdoors in large pots. The pollen was subjected to in vitro temperatures ranging from 15 to 50 °C at 5 °C intervals. Pollen germination and tube lengths were recorded for all species after 24 h of incubation at the respective treatments. Species/genotypes differed significantly for in vitro pollen germination percentage and pollen tube length with mean values of 78% and 734 μm, respectively. The mean cardinal temperatures (T_min, T_opt, and T_max) averaged over genotypes, were 15.2, 30.7, and 41.8 °C for pollen germination and 12.2, 31.2, and 40.4 °C for pollen tube growth. The CTRI of each species/genotype calculated as the sum of eight relative individual stress response values, such as maximum pollen germination, maximum pollen tube length; T_min, T_opt, and T_max temperatures of pollen germination, and pollen tube lengths, identified species tolerance to high temperatures. Capsicum annum cv. Mex Serrano from Mexico was identified as tolerant, C. chacoense cv. 1312 and C. spp. cv. Cobanero from Argentina and Guatemala, respectively as intermediate and C. frutescens cv. Early Spring Giant from China, C. annum cv. Long Green from South Korea, C. spp. cv. NM89C130 and C. pubescens cv. 90002 from Guatemala as sensitive to high temperatures. The tolerant species/genotypes can be used in breeding programs to develop new genotypes that can withstand high temperature conditions both in the present climate and particularly in a future warmer climate.     

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.     

Effect of high temperature stress on the reproductive growth of strawberry cvs. ‘Nyoho’ and ‘Toyonoka’

High temperatures are known to reduce fruit size and fruit weight in strawberry, but cultivar differences in the response to high temperature stress during the reproductive stage up to the second inflorescence have not been sufficiently reported. We examined the effect of two day/night temperature regimes on fruit set and fruit growth in two cultivars, ‘Nyoho’ and ‘Toyonoka’. A high day/night temperature of 30/25 °C reduced the number of inflorescences, flowers, and fruits in both cultivars compared with plants grown at 23/18 °C. The percentage of fruit set in ‘Nyoho’ was not significantly different between the two temperature treatments, while that in ‘Toyonoka’ was much lower at 30/25 °C than at 23/18 °C. Days to ripening was shorter at 30/25 °C than at 23/18 °C, and no cultivar differences were observed. Fresh weight of primary, secondary, and tertiary fruits was greater at 23/18 °C than at 30/25 °C in both cultivars, and no cultivar differences were observed, except in tertiary fruits. The diameter of fruits from all positions was also reduced at 30/25 °C in both cultivars. Relative growth rates of fruits showed two peaks in both cultivars and in both temperature treatments. Both peaks appeared earlier at 30/25 °C than at 23/18 °C. Percentage of fruit set at 30/25 °C in the second inflorescence was also significantly lower in ‘Toyonoka’ than in ‘Nyoho’. These results indicate that high temperature stress negatively affects the reproductive process in strawberry and that plant response to high temperature stress is cultivar-related in such responses.     

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.     

Temperature and photoperiod control of morphology and flowering time in two greenhouse grown Hydrangea macrophylla cultivars

Knowledge of the factors involved, and tools to control morphology and flowering are important in intensive and cost-efficient greenhouse production. Hydrangea macrophylla is an important flowering pot plant in Norway and is produced year-around in greenhouses. Due to problems in scheduling, a study was conducted to compare floral transition and morphology of two commercially important cultivars of Hydrangea (‘Early Blue’ and ‘Schneeball’) under different flower initiating treatments in growth chambers. Plants were grown with high pressure sodium lamps (HPS) at moderate temperature (17 °C) (MT) and high (24 °C) temperature. At high temperature, the effect of (1) irradiance under long day conditions (16 h lighting with 70 or 200 μmol m⁻² s⁻¹), and (2) short day (8 h lighting) was investigated. The short day treatment had similar light integral as the low irradiance long day treatment (SD: 8 h × 140 μmol m⁻² s⁻¹ and LD: 16 h × 70 μmol m⁻² s⁻¹ = 4.0 mol m⁻² d⁻¹). The intention was to test the effect of irradiance and SD on flower transition and morphology under high temperatures. The results clearly showed that MT is the strongest signal for floral transition. MT resulted in a rapid floral transition of the terminal buds and lateral flower buds. A short forcing period was required and the plants became short and compact without any use of chemical growth retardants. At high temperatures only SD had a promotive effect on flower transition and the response was found to be stronger in ‘Schneeball’ than ‘Early Blue’. In general, all the treatments under high temperatures required a long forcing time and the plants tended to be very tall with a low number of lateral flower buds.     

Effects of low temperatures on sexual reproduction of ‘Tainong 1’ mango (Mangifera indica)

Prevailing ambient temperature during the reproductive phase is one of important factors for seed and fruit set in different plant species. In mango (Mangifera indica L.), natural low temperatures during flowering induced seedless fruits. Here the sexual reproduction process of ‘Tainong 1’ mango at low temperatures (diurnal maximum temperature < 20 °C) was studied. For comparison, we also examined this process at “normal” temperatures (diurnal maximum ranging from 25 to 30 °C, diurnal average temperature > 20 °C). Results showed: natural low temperatures significantly affected pistil and male gametophyte development, resulting in pollen grains with low viability. Meiotic chromosomal irregularities, including univalents, multivalents, laggards, bridges and micronuclei were detected at higher incidences and significantly greater proportions of nucleolus fragmentation and dissolution were detected when temperatures were low. Pollen tube growth was retarded under low temperature stress, either in vivo or in vitro. The virtual absence of sexual reproduction of ‘Tainong 1’ mango at low temperatures appears to be due largely to slow growth of pollen tube in vivo and to a low rate of successful fertilization.     

Behavior of arazá (Eugenia stipitata Mc Vaugh) fruit quality traits during growth,development and ripening

The period between fruit set and full ripening of arazá fruit grown in the Colombian Amazonia was 55 ± 5 days. Three stages of a sigmoidal growth were identified and longitudinal and equatorial traits fitted a logistic model better than three-degree polynomial models. Fruit growth clearly exhibited three different physiological stages, identified as follows: S1, involving cellular division during the first 14 days; S2, maximum fruit growth, during which cellular expansion took place (up to day 50), and a final S3 state of 5 days to reach physiological maturity. After this time, the fruit can be harvested with a dull green coloration. Parenchyma was the principal fruit tissue, and no support tissues (sclerenchyma or collenchyma) were evident. The respiratory pattern of arazá fruit was climacteric, with maximum respiration rates of around 200 mg CO₂ kg⁻¹ h⁻¹, preceded by a peak of ethylene production (20 μL C₄H₄ kg⁻¹ h⁻¹), a change in skin color from green to yellow, a total soluble solids value of 5°Brix, an increase in the sucrose and fructose content up to 2.8 μmol g⁻¹, a pH which increased to 3 units, and a decrease in titratable acidity to 400 mmol H⁺ L¹⁻. Malic acid was the main organic acid in the edible pulp and ascorbic acid was present in a concentration of 17.8 μmol g⁻¹. Skin color (as measured by hue angle) combined with titratable acidity and fruit firmness can be recommended as harvest indices for arazá fruit.     

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.