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.     

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.     

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.     

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.     

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.     

Analysis and modeling of gas exchange processes in Scaevola aemula

Scaevola aemula is a popular ornamental crop cultivated as a bedding plant or for hanging baskets. We characterized gas exchange properties of S. aemula ‘New Wonder’ in response to photosynthetically active radiation (PAR), carbon dioxide concentration, and leaf temperature. Net CO₂ assimilation rate (A) was responsive to CO₂, exhibiting a saturation when intercellular CO₂ concentration (C_i) was greater than 600 μmol mol⁻¹. Net CO₂ assimilation rate and dark respiration rate (R_d) were 23.1 and 2.3 μmol m⁻² s⁻¹, respectively, at 25 °C and PAR = 1500 μmol m⁻² s⁻¹. Net CO₂ assimilation rates were similar at leaf temperatures between 20 and 30 °C but significantly reduced at 15 °C. These gas exchange results were used to test the extendibility of a coupled gas exchange model previously developed for cut-roses. Utilizing the gas exchange data measured at 25 °C leaf temperature, several model parameters were independently determined for S. aemula. Model predictions were then compared with observations at different leaf temperatures. The model predicted the rates of net CO₂ assimilation and transpiration of S. aemula reasonably well. Without additional calibration, the model was capable of predicting the temperature dependence of net CO₂ assimilation and transpiration rates. Applying the model to predict the effects of supplemental lighting and CO₂ enrichment on canopy photosynthesis and transpiration rates, we show that this model could be a useful tool for examining environmental control options for S. aemula production in the greenhouse.     

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.     

Plant regeneration of Carica papaya L. through somatic embryogenesis in response to light quality,gelling agent and phloridzin

Difficulties to develop an easy and reproducible protocol to get healthy and well formed plants from somatic embryos of papaya (Carica papaya L.) had included low germination, callus production at the base of the embryo radicle and the occurrence of hyperhydric plantlets among others, and by consequence unsuccessful transfer to the field. With the aim of improving a propagation method, the effects of light quality, gelling agent and phloridzin concentration on the germination of somatic embryos of hermaphrodite C. papaya L. var. Maradol were studied. Somatic embryos were grown on half strength MS medium, with the addition of Chen vitamins [Chen, M.H., Wang, P.J., Maeda, E., 1987. Somatic embryogenesis and plant regeneration in Carica papaya L. tissue culture derived from root explants. Plant Cell Rep. 6, 348–351], solidified with three distinct gelling agents: Sigma^® Agar–Agar, Difco^® Bacto agar and Phytagel^®; supplemented with phloridzin and exposed to different light qualities: blue (54 μmol m⁻² s⁻¹), red (65 μmol m⁻² s⁻¹), gro-lux (68 μmol m⁻² s⁻¹), red + blue, white (32 μmol m⁻² s⁻¹) and wide spectrum (49 μmol m⁻² s⁻¹) during a period of 4 weeks. Results show that light quality and gelling agent had important effects on germination and plant growth, while 3.0 mg L⁻¹ phloridzin had an important role on germination as well as in root development. Somatic embryos exposed to white light, culture medium solidified with 3.0 mg L⁻¹ phytagel and 3.0 mg L⁻¹ phloridzin showed longer roots. Meanwhile, germination and plant length were promoted on an improved culture medium solidified with 7.5 g L⁻¹ Difco^® Bacto agar, 3.0 mg L⁻¹ phloridzin and exposed to gro-lux lamps. Under these conditions, 70% of somatic embryos germinated and developed normal roots without hyperhydricity. The regenerated plantlets with well developed roots and shoots were successfully transferred to a greenhouse with a survival rate of 95%.     

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.     

Cost-efficient light control for production of two campanula species

A cost-efficient light control system based on weather forecasts, electricity prices and daily photosynthesis integral (DPI) was evaluated for application in the commercial production of the long-day (LD) plant Campanula portenschlagiana ‘Blue Get Mee’ and C. cochlearifolia ‘Blue Wonder’. Experiments were conducted under both autumn and spring conditions and included four treatments. Three treatments were controlled by the software system DynaLight Desktop which automatically defined the most cost-efficient use of supplemental light, -based on a predefined set point of DPI, forecasted solar irradiance and the market price on electricity. The set points of DPI in the three treatments were 300, 450 and 600 mmol CO₂ m⁻² leaf d⁻¹ and the treatments were compared with a traditional LD 19-h treatment. The DPI-based light control strategy resulted in very irregular light patterns including daily periods of solar irradiance combined with supplemental light in low light periods and a night period interrupted by irregular light breaks (NB-lighting). Both campanula species flowered in the DPI-based treatments during spring, but the flowering percentage was low and non-uniform during autumn. This was caused by a combination of the irregular light, low natural light intensities and a decrease in daily light integral (DLI), and could be restored by maintaining a continuous 19 h photoperiod with incandescent lamps (<5 μmol m⁻² s⁻¹), illustrating that photoperiod was an important factor for flowering in LD species grown under low light intensities. Growth in terms of carbon gain was marginally affected by the irregular light and a 25% reduction in electricity costs was achieved without major reductions in plant quality in spring. Our results illustrate that plant production of LD species can be maintained in a cost-efficient light control system where the use of supplemental light is based on weather forecasts and electricity prices.     

Involvement of phytochrome B in DIF mediated growth in cucumber

This study aimed to compare the interaction between light quality and alternating day (DT) and night temperature (NT) under two different daily light integrals (DLI) on morphology of a wild type (wt) and a phytochrome B deficient mutant (lh) of cucumber (Cucumis sativus L.). Different light qualities were established by light quality selective plastic films. Plants were grown for 18 days (lh) or 19 days (wt) under DT/NT regimes of 25/19 °C (positive DIF), 22/22 °C and 19/25 °C (negative DIF) (12-h thermoperiod) in combination with plastic films establishing a low (0.75, LRFR) and high red (R)/far-red (FR) ratio (1.62, HRFR) and a control (R/FR of 1.11). Stem, hypocotyl and internode elongation in the wt were more affected by DIF under LRFR than HRFR. In general, length was reduced 45–50% under HRFR compared to the control, while the reduction by negative DIF was 38% on average. Hypocotyl length of the lh mutant was neither affected by temperature regime nor light quality, while negative DIF reduced stem length with 15–20% compared to positive DIF due to a delayed internode elongation. The general response pattern in both genotypes was not affected by an additional reduction in DLI of 50%. In conclusion, the strongest effect of DIF was found under a LRFR which is the opposite of findings in earlier studies with day extentions with different light qualities. In general, HRFR reduced stem elongation of cucumber more than negative DIF. The results indicate a crosstalk between light phytochrome responses and thermoperidism.     

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.     

Effects of leaf aging and light duration on photosynthetic characteristics in a cucumber canopy

Photosynthetic characteristics, chlorophyll index and leaf area were examined in selected leaves of cucumber (Cucumis sativus L. cv. Euphorbia). In the first experiment, plants of cucumber were grown horizontally at a lighting period of 20 h day⁻¹. Photosynthetic measurements in horizontally growing cucumbers showed that there was no decline in photosynthetic capacity when cucumber leaves are developing under good light conditions. In a second experiment, plants were grown in a traditional high-wire cultivation system under 20 h day⁻¹ lighting period until they reached final height and then exposed to different lighting periods (20 and 24 h day⁻¹) for 3 weeks. In stands of cucumber plants photosynthetic measurements showed that the lower leaves have a significant reduction in photosynthetic capacity due to reduced light conditions. Three weeks exposure to 24 h day⁻¹ lighting period reduced leaf area by 20%. Plant grown under continuous light had also lower chlorophyll index compared to plants grown under 20 h day⁻¹ lighting period.     

Growth and photosynthetic characteristics of blueberry (Vaccinium corymbosum cv. Bluecrop) under various shade levels

Blueberry can readily be shaded as a bush type plant, maybe affecting its growth and photosynthesis. Growth and photosynthetic characteristics of ‘Bluecrop’ blueberry grown under various shade levels were investigated to understand acclimation under shade conditions and to determine the optimal light conditions for agricultural purpose. Shade decreased the number of shoots per shrub, but increased shoot length. However, shade did not affect the number of leaves on the main axis. With increasing shade level, leaf length, width and area increased, but leaf thickness decreased. However, there was no obvious tendency in leaf length/width ratio with increasing shade level. Shade leaves had less dense stomata than sun leaves, but stoma was bigger in shade leaves than in sun leaves. With increasing shade level, non-photochemical quenching in blueberry leaves increased and the values were higher at low photosynthetic photon flux densities (PPFDs) in shade leaves than in sun leaves, resulting in the decreases in quantum yield, electron transport rate and net CO₂ assimilation rate (A_n). The maximum A_n at 31, 60, 73 and 83% shade levels was 11.8, 11.0, 8.4 and 7.5 μmol m⁻² s⁻¹, respectively. Following the slight decrease up to 100 μmol m⁻² s⁻¹ PPFD, stomatal conductance (g_s) linearly increased up to 600 μmol m⁻² s⁻¹ PPFD and became saturated at all shade levels. The leaves of the shrubs grown under the 83% shade level had a significantly lower g_s as compared to the leaves of the shrubs grown under the 31, 60 and 73% shade levels. Transpiration rate (E) linearly increased up to 600 μmol m⁻² s⁻¹ PPFD and was saturated at the 73 and 83% shade levels. However, E increased linearly at both 31 and 60% shade levels with increasing PPFD. The reproductive growth characteristics such as number of flowers, fruit set rate per flower bud and fruit yield also significantly decreased with increasing shade level. For agricultural purpose, therefore, shade level above approximately 60% of full sunlight must be avoided for optimal photosynthesis and growth of the ‘Bluecrop’ blueberry.     

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.     

Effects of plant density in broccoli on yield and radiation use efficiency

The effects of plant density on broccoli (Brassica oleracea L. var. italica Plenck) commercial characteristics are well determined. However, it is not completely clear how the broccoli plant respond to changes in plant shading as a result of different plant densities. The objective of this experiment was to determine the effect of plant density on intercepted photosynthetically active radiation (PAR), plant architecture, and plant growth and production. “Legacy” broccoli plants were grown in pots in a greenhouse in the seasons of 2002 and 2003 at 2, 4, 6 or 8 plants m⁻² (temperatures: between 10.0 and 16.1 °C, average incident PAR: 12 mol m⁻² day⁻¹). Plant density affected the intercepted and accumulated PAR. There were not effects on the length of the vegetative and reproductive periods, the total and final number of leaves, and the spear diameter and fresh weight. The magnitude and evolution of leaf area (LA) was independent of plant density up to 70 days after transplant (dat). Since then on, LA increased linearly with plant density. The highest intercepted PAR was 70–72% with 6–8 plants m⁻². With the increase in plant density: the erectness of the upper leaves and stem length increased, the extinction coefficient decreased and commercial spear (inflorescence plus a portion of stem 10 cm long) weight decreased (but it was due to the stem portion of the spear and not to the edible portion). On an area basis, the decrease in commercial spear weight with plant density was more than compensated by the higher number of plants. The radiation use efficiency (RUE) increased proportionally with the leaf area index (LAI) up to a LAI of about 3, and then stabilized. The only effect of plant density on dry weight partitioning was to decrease the dry weight allocated to the stem portion of the spear. As plant density increased, and consequently the degree of shading increased, the net assimilation rate (NAR) decreased and the leaf area ratio (LAR) increased. This compensatory change between NAR and LAR, kept the relative growth rate (RGR) for individual plants almost constant.     

Closed cycle subirrigation with low concentration nutrient solution can be used for soilless tomato production in saline conditions

Closed cycle soilless techniques can be adopted to minimize water and fertilizer losses in greenhouse cultivation. There is a general lack of information regarding the soilless cultivation of vegetables with closed cycle subirrigation techniques, specifically when using saline water. In this study, a trough bench subirrigation system (SUB), with two fertilizer concentrations (“100%”, containing 9.8 mol m⁻³ N-NO₃, 1.6 mol m⁻³ P-H₂PO₄, 8.7 mol m⁻³ K⁺, 2.8 mol m⁻³ Ca⁺, 1.8 mol m⁻³ Mg⁺, 4 mol m⁻³ S-SO₄, and “70%”, containing 70% of the macronutrient concentration) in the nutrient solution (NS), was compared with open cycle drip-irrigation (DRIP with “100%” NS). For all the three treatments, NS was prepared using rain water (0.05 dS m⁻¹) and adding NaCl (1 g L⁻¹), in order to simulate moderate saline irrigation water. The effect of the treatments on tomato (Solanum lycopersicum L.) plant growth, yield, fruit quality, water use efficiency (WUE) and fertilizer consumption was evaluated. Substrate and recirculating NS composition were also studied. Subirrigation, regardless of NS concentration, reduced plant height (by 30 cm), leaf area (by 1411 cm²), total fresh and dry weight (by 429 and 48.5 g plant⁻¹, respectively) but not dry matter percentage of the whole plant, with respect to DRIP. Yield was reduced when plants were subirrigated with the higher concentrated NS, but no differences with open cycle DRIP were recorded when the lower NS concentration was used in SUB. Fruit quality was not affected by irrigation system or NS concentration. The higher WUE was obtained with subirrigation. NaCl accumulated similarly over the crop cycle in recirculating NS of both SUB treatments and in growing substrates of all the three treatments. Higher salt concentration was found in subirrigated substrates, in particular in the upper part of the substrate profile. Fertilizers accumulated in the subirrigated substrates when the higher NS concentration was used, but not when the NS concentration was reduced by 30%. The results of this study indicate that tomato can be grown successfully in a closed cycle subirrigation system, using saline water, by reducing the fertilizer NS concentration normally used with traditional open cycle systems.     

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.     

The response of plant growth and leaf gas exchange to the speed of lamp movement in a greenhouse

High-pressure sodium (HPS) light supplementation during the low-light months has become quite common for high-light requiring crops at latitudes above 45°. Most common systems have fixed installations, while movable systems have been tried with various results in greenhouses. The concept is that fewer lamps are used on a track system, and that light intensity varies over time. In two trials, we determined whether the speed of the HPS lamp movement had any effect on leaf CO₂ exchange rate, growth and developments of various plants species. Plants (chrysanthemum, petunia, rose and tomato) were grown in a greenhouse supplemented with HPS lamps which moved at various speeds (0, 2, 8 and 20 mm s⁻¹) between 06:00 and 24:00 h daily for about 6–7 weeks. One trial started at the end of November and one started at the end of January. The light sum from the lamps were 0.212 ± 0.004 mol m⁻² h⁻¹ at bench level, and the supplemental lighting represented 55 and 35% of the total light received by the plants for the two trial dates, respectively. The growth (dry matter) was reduced for tomato only when grown under moving lights compared to those grown under the stationary system, while plant height was not affected. Light saturated CO₂ exchange rate on the youngest fully developed leaves increased with lamp speed for petunia and tomato, but not for chrysanthemums, while apparent quantum yield was not affected by lamp speed for any species. In situ measurements of net CO₂ exchange rate (NCER) with supplemental lighting only, showed that NCER decreased exponentially when lamp speed increased from 0 to 20 mm s⁻¹.