This study was carried out to establish the reasonable level of nitrogen (N) fertilization based on soil nitrate nitrogen $(NO_3-N)$ content for cucumber (Cucumis sativus L.) under plastic film house. Cucumber plants were cultivated with standard and free N fertilization in eight soils which had various amount of $NO_3-N$ ranging from 67 to 343 mg/kg. The yield of cucumber was in the range of 1006 to 2369 g/plant depending on the nitrogen supplying capability of soils. The amount of $NO_3-N$ in the soil was negatively correlated with agronomic efficiency (AE) and N use efficiency (NUE). The critical level of soil $NO_3-N$ content for cucumber in N free fertilization was found to be about 260 mg/kg in Cate-Nelson analysis of variance between soil $NO_3-N$ and AE or NUE. Also the same critical soil $NO_3-N$ content was found in the yield and amount of N uptake of cucumber under N free fertilization. A standard N fertilization was required when soil $NO_3-N$ content was below 70 mg/kg. The optimal application rate of N fertilizer for cucumber in the soils containing $NO_3-N$ between 260-70 mg/kg could be recommended by the equation Y=-1.032X+269.2 (Y: N fertilization rate, kg/ha; X : soil $NO_3-N$ content mg/kg).
This experiment was conducted to find out the effect of nutrient solution composition on the growth of cucumber plants and the changes in macro-elements in nutrient solutions in recirculating hydroponic systems. Cucumber plants (Cucumis sativus L. cv. Joeun Baegdadagi) were grown in closed perlite cultivation systems supplied with different nutrient solutions developed by NHRS (National Horticultural Research Station in Japan), Yamasaki, PBG (Proefstation voor Bloemisterij en Glasgroente), and NIHHS (National Institute of Horticultural and Herbal Science in Korea). The concentrations of $NO_{3^-}N$, $Ca^{2+}$, $Mg^{2+}$, and $SO_{4^-}S$ in the recycled nutrient solutions increased but that of $NH_{4^-}N$ decreased gradually in all the treatments. The $PO_{4^-}P$ and $K^+$ concentrations were continuously reduced from the beginning of the harvest to the harvest peak period. There were no significant differences in the concentrations of $NO_{3^-}N$, $NH_{4^-}N$, and $Ca^{2+}$ in the recirculated nutrient solutions among four treatments, while the concentrations of $PO_{4^-}P$ and $K^+$ were lowest and those of $Mg^{2+}$ and $SO_{4^-}S$ were highest in the treatment of Yamasaki's nutrient solution. All growth-related parameters of cucumber plants except for leaf number were not significantly affected by the nutrient solution compositions. Due to its low concentrations of $PO_{4^-}P$ and $K^+$ in the recycled nutrient solution, however, the number and yield of cucumber fruits were lowest in the treatment of Yamasaki's nutrient solution.
Gross photosynthetic rats of leaves of hydroponically grown cucumber plants(Cucumis sativus L. cv. Guwoosalichungjang) were measured under various conditions of photosynthetic photon flux(PPF), ambient $CO_2$ concentration, air temperature and leaf nitrogen contents. Light compensation point of leaf photosynthesis appeared to be in the range of 10~20$\mu$mol.m$^{-2}$ .s$^{-1}$ and light saturation point be above 1000$\mu$mol.m$^{-2}$ .s$^{-1}$ . Gross photosynthetic rates increased persistently and asymptotically as air temperature rose from 12$^{\circ}C$ to 32$^{\circ}C$. However, there were only small differences in gross photosynthetic rates in the range of 24-32$^{\circ}C$, so that the range seemed to be optimal for photosynthesis of cucumber plants at the condition of $CO_2$ concentration of 400$\mu$mol.mol$^{-1}$ and PPF of around 400$\mu$mol.m$^{-2}$ .s$^{-1}$ . $CO_2$ compensation point of leaf photosynthesis appeared to be in the range of 20-40$\mu$mol.mol$^{-1}$ and $CO_2$ saturation point be above 1200$\mu$mol.mol$^{-1}$ . Gross photosynthetic rates increased sigmoidally as leaf nitrogen content increased. These environmental factors interacted synergistically to enhance gross photosynthetic rate, so that the rate increased multiplicatively s level of one factor increased progressively with higher levels of he other factors. Mathematical models wer developed to estimate the gross photosynthetic rate in accordance with the variations of these environmental factors. These modes can be used not only to explain he variation of growth or yield of cucumber plants under different environmental conditions but also as building blocks of plant growth model or expert system of cucumber plants.
This study was carried out to investigate the optimum ionic strength of nutrient solution were treated with a quarter, a half, three quarters, standard, one and half, and double ionic strength of balanced nutrient solution of Yamazaki solution recommended for cucumber plants. Plant height and number of loaves of growing period were rapidly increased in 1/2 ionic strength of nutrient solution. Growth characteristics of cucumber plant as affected by the different ionic strength of nutrient solution were not significant differences, however, in the growing period, plant height, stem length and leaf area were highest in 1/2 ionic strength of nutrient solution. Fruit yield of cucumber plant as affected by the different ionic strength of nutrient solution was not significant differences, however, fruit yield was highest in 1/2 ionic strength of the lowering ionic strength of nutrient solution. Nitrogen concentration was not significant differences, however, it was high corcentration in 1/2 ionic strength of nutrient solution. Growth and yield characteristic of cucumber as affected by 1/2 ionic strength of nutrient solution at 36 days transplanting analyzed correlation cofficient. Plant height showed positive correlated with number of plant and positive correlated with yield.
To investigate the effects of different UV-B levels on growth and biochemical defense response in plants, cucumber plants were subjected to three levels of biologically effective ultraviolet-B $(UV-B_{BE})$ radiation [daily dose: 0.03 (No), 6.40 (Low) and $11.30\;(High)\;kJ{\cdot}m^{-2}$, $UV-B_{BE}$] in the growth chambers for 3 weeks during the early growth period. Enhanced UV-B radiation drastically decreased both dry weight and leaf area of cucumber. With increasing UV-B intensity, chlorophyll content was decreased, however the level of malondialdehyde was highly increased linearly. Total contents of ascorbic acid and glutathione were tended to increase by UV-B, while the ratios of dehydroascorbate/ascorbate and oxidized glutathione/reduced glutathione were significantly increased with increasing UV-B intensity in cucumber. All the enzyme activities investigated (superoxide dismutase, ascorbate peroxidase, dehydroascorbate reductase, guaiacol peroxidase etc.) in cucumber were increased by the UV-B enhancement. These results suggested that enhanced UV-B irradiation caused photooxidative stress in cucumber plant and resulted in significant reduction in plant growth. Biochemical protection responses might be activated to prevent the leaves from damaging effects of oxidative stress generated by UV-B irradiation.
A prototype of closed-type transplant production system(CTTPS) with fully environmental control was developed to produce massively quality transplants. Four photosynthetic photon flux(PPF) levels of 200,300,400 and 500$\mu$mol . m$^{-2}$ .s$^{-1}$ , four photoperiod levels of 1816 h,12/12h, 9/15 h and 6/18 h were provided to analyze the growth and development of cucumber plug seedlings(Cucumis sativus L., cv. Kyuewosalichungiang) as affected by PPF and photoperiod in a CTTPS. Effect of photoperiod on the growth and development of cucumber plug seedlings produced in a CTTPS was higher than PPF, Stem diameters dry weight of shoot and roots number of leaves, leaf with and length, and SPAD value of cucumber plug seedlings produced in a CTTPS were significantly high as compared to the control. But stem length of plug seedlings produced in a CTTPS was shorter than those of the control. Growth characteristics of cucumber plug seedlings raised at photoperiod of 6/18 h and PPF of 200$\mu$mol . m$^{-2}$ .s$^{-1}$ were similar to the those of the control. These results suggest that cucumber quality transplant can be produced at relatively short photoperiod and low PPF, It means that the electric energy consumed for the production of cucumber plug seedlings in a CTTPS can be saved.
This studies were carried out in summer season to increase high temperature tolerance using hydrogen peroxide treatments on cucumber in greenhouse. The water stress of cucumber in greenhouse by the hydrogen peroxide treatments showed as control>250 mM>500 mM treatments in order. The photosynthesis rate of cucumber at $30^{\circ}C$ did not show difference with each hydrogen peroxide treatment in temperature controlled greenhouse. However, the photosynthesis rate of cucumber in the control and hydrogen peroxide treatments at $40^{\circ}C$ was significantly different. The photosynthesis rate of cucumber in combined treatment with 1,000 $mg{\cdot}L^{-1}\;CO_2$ supply and hydrogen peroxide was also higher than control, however, there was no different of photosynthesis in 250 mM and 500 mM treatment. The value of $F_v/F_m$ and $F_m/F_o$ of chlorophyll fluorescent in 500 mM hydrogen peroxide treatment at $40^{\circ}C$ was highest. Also the activity of POD, the antioxidant enzyme, was higher with high hydrogen peroxide concentration than the other treatments. The high temperature limits for growth were $43^{\circ}C$ in the control, $44^{\circ}C$ in the 250 mM and $46^{\circ}C$ in the 500 mM according to analyze chlorophyll fluorescent $F_o$. The high temperature tolerance in cucumber increased approximately $3^{\circ}C$ by the hydrogen peroxide treatments under this experiment conditions.
Several physiological responses were investigated in plants treated with TOPE as a preliminary step to know its action site. Unlike photo-dependent diphenylethers, herbicidal activity of TOPE appeared slowly and its typical symptoms were both burning of leaf blades and abnormal division of meristem in grasses, Similarly, both leakage of cell electrolytes and the curling of cotyledon margin were also shown in cucumber(Cucumis sativus L.). Biosynthesis of chlorophyll in etiolated cucumber cotyledon was not inhibited directly by treatment of TOPE at low light intensity(5.5${\mu}$ mol $m^{-2}s^{-1}$ PAR) and protoporphyrin IX was not also accumulated. The contents of phytoene, phytofluene and ${\beta}$-carotene were abnormaly increased. Photosynthesis was inhibited only at high concentration. Mitochondrial respiration was inhibited at high concentration but rather increased significantly at 10${\mu}$M of TOPE. However, respiration inhibitors did not alleviate the two symptoms of TOPE in cucumber cotyledon. In the same experiments, using inhibitors of protein or nucleic acid biosynthesis, only one of the two symptoms was alleviated by chloramphenicol and cycloheximide. In contrast, both symptoms were alleviated by actinomycin-D and hydroxyurea, suggesting that nucleic acid metabolism might be preferentially related to the mode of action of TOPE. DNA, RNA and protein contents were accumulated in both cucumber cotyledon and rice (Oryza sativa L.) routs treated with TOPE, and the DNA of them was increased at first. Thus, it is conjectured that TOPE increase nucleic acid metabolism directly or indirectly, and then disturb various metabolic pathways causing abnormal physiological and morphological effects followed by final death.
To investigate the cucumber regeneration from embryogenic calli, shoot tips of aseptically-grown cucumber seedlings were used as explants for establishing tissue cultures. Growth and differentiation of callus were studied by using Murashige and Skoog's (MS) medium containing 0.5 to 2 mg/L 2,4-D. Plantlets were induced from shoot tip culture on the plant growth regulators-free MS medium. Non-embryogenic calli and viscous calli were induced on the medium supplemented with 0.5 to 2 mg/L 2,4-D, but embryogenic callus was not induced on the same medium. Segments (ca. 5∼10 mm) of aseptically-grown hypocotyl from five to seven days old seedlings after germination were placed on MS medium supplemented with 1 mg/L 2,4-D for 50 days. Embryogenic calli and embryoids were induced only from the seedlings grown in dark condition, and hypocotyl was placed on the media explanted in light condition. Foully-five point one percent of white fragile calli and 0.6% yellowish compact calli formed roots. Yellowish callus lines were investigated to have a considerably higher concentration of crude proteins than white callus lines. Plantlets derived from embryogenic calli or embryoids have been transferred to pots containing sterile vermiculite and perlite. Normal fruits were harvested from nutrient culture on aggregated hydroponics in the F-clean house.
When cucumber (Cucumis sativus L.) cotyledon discs were floated on $\delta$-aminolevulinic acid, oxyfluorfen, or rose bengal solution under light condition following 20 h dark incubation, rapid electrolyte leakage from the tissues occurred. The electrolyte leakage from the tissues was dependent on the compounds treated, their concentrations, and the duration of light exposure to the tissues. Dark incubation before exposure to continuous white light enhanced electrolyte leakage from the tissues treated with the compounds and reduced lag period for the activity of the compounds. Electrolyte leakage from the treated tissues was greatly influenced by the light intensity to which they were exposed. Higher light intensities stimulated electrolyte leakage and reduced lag period. Porphyrin biosynthesis inhibitors, gabaculine and 4,6-dioxoheptanoic acid, completely inhibited electrolyte leakage from the oxyfluorfen-treated tissues. Protection against the activity of $\delta$-aminolevulinic acid from electrolyte leakage was complete with 4,6-dioxoheptanoic acid, but not with gabaculine. However, gabaculine and 4,6-dioxoheptanoic acid gave no such protection against rose bengal activity. In summary, our results indicate that $\delta$--aminolevulinic acid, oxyfluorfen, and rose bengal exert their effects by causing electrolyte leakage from the treated tissues in a similar manner, except that oxyfluorfen has an apparent lag period for its action on electrolyte leakage increase. All above compounds require preincubation of treated tissues in darkness and subsequent light exposure with a high intensity for their maximal activities. Our results also support that in the presence of light, $\delta$-aminolevulinic acid and oxyfluorfen cause cellular damage through the indirect generation of singlet oxygen from accumulated tetrapyrroles of porphyrin pathway, whereas rose bengal causes cellular damage through the direct generation of singlet oxygen.
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