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- Author or Editor: W. C. Kelly x
Transpiration rates of chrysanthemum [Dendranthema ×grandiflorum (Ramat.) Kitamura] plants grown under spectral filters were evaluated as part of an investigation on using light quality to regulate plant growth. The 6% CuSO4·5H2O spectral filter reduced photosynthetic photon flux density in red (R) and far red (FR) wavelengths and increased the R: FR and blue (B): R ratios (B = 400 to 500 nm; R = 600 to 700 nm; FR = 700 to 800 nm) of transmitted light relative to the water (control) filter. After 28 days, cumulative water use of plants grown under CuSO4 filters was ≈37% less than that of control plants. Transpiration rates were similar among plants grown under CuSO4 and control filters when expressed as leaf area, a result suggesting that the reduced cumulative water loss was a result of smaller plant size. Plants grown under CuSO4 filters had slightly lower (10%) stomatal density than control plants. Light transmitted through CuSO4 filters did not alter the size of individual stomata; however, total number of stomata and total stomatal pore area per plant was ≈50% less in plants grown under CuSO4 filters than in those grown under control filters due to less leaf area. The results suggest that altering light quality may help reduce water use and fertilizer demands while controlling growth during greenhouse production.
The interaction of light quality and growing season on growth and carbohydrate metabolism of chrysanthemum was evaluated using 6% CuSO4 and water as spectral filters. Light transmitted through the CuSO4 filter significantly reduced plant height and internode length compared to control plants regardless of the season. Light transmitted through CuSO4 filters delayed flowering. Total number of flowers was not affected but plants grown under CuSO4 filter had smaller flowers than those grown under the control filter. Light transmitted through CuSO4 filter reduced leaf and stem soluble sugar and starch concentrations regardless of the growing season. However, me magnitude of reduction was greater in spring than in fall-grown plants. Stems of fall-grown plants had mom starch deposition than spring-grown plants under both filters. The reduction of leaf and stem carbohydrate content (per organ basis) was greater than that of concentrations due to reduced stem elongation and total dry matter accumulation. Filters with specific spectral characteristics can be used as alternative means of controlling height and producing compact plants in the greenhouses regardless of the growing season. However, flowering should be evaluated with individual flower crops as flowering response may interact with the quality of light and growing season.
The response of chrysanthemum plants to varying R:FR ratios and phytochrome photoequilibrium values (Ø = Pfr/Ptot) was evaluated by growing plants under 6%, or 40% CuSO4 and water spectral filters. Using a narrow band-width (R = 655-665 and FR = 725-735 nm) and a broad bandwidth (R = 600-700 and FR = 700-800 nm) for R:FR calculation, 6% CUSO4 filter transmitted light with greater R:FR (3.9) and grater Ø (0.81) than 40% CuSO4 or water filters. Light transmitted through 40% CuSO4 and water filters had a similar narrow band R:FR ratio (1.2), but the broad band R:FR ratio (2.1) of 40% CuSO4 filter was higher than water filter. Estimated Ø value was similar for both water and 40% CuSO4 filters. Final height of plants grown in CuSO4 chambers was about 30% less than the plants in control chambers. The results suggest that broad band R:FR ratio correlated more closely to plant response than the narrow band R:FR ratio.
The use of light quality as an alternate method for controlling ornamental plant growth was evaluated using copper sulfate solutions as optical filters, The light passed through CuSO4 solutions had high red/far-red (R/FR) ratio. Plant height and average internode length were significantly reduced by high R/FR light. Plants grown under high R/FR light had smaller leaves and a lower total leaf area but had thicker leaves, as indicated by specific leaf weight, than the control plants. Fresh and dry weights of leaves, stems and roots were reduced by high R/FR light. Dry matter accumulation in leaves was increased by high R/FR light while it was reduced in stems. Exogenous gibberellic acid (GA) application partially overcame the height reduction under high R/FR light indicating that GA biosynthesis maybe affected by light treatment. Results suggests alteration of light quality could be used in controlling ornamental plant growth as an alternate method to conventional chemical growth regulator applications.
The interactions of light quality and growing season on growth and carbohydrate content of chrysanthemum [Dendranthema × grandiflorum (Ramat.) Kitamura] plants were evaluated using 6% CuSO4 and water (control) as spectral filters. Light transmitted through the CuSO4 filter significantly reduced plant height and internode length compared to control plants regardless of the season. However, the degree of response varied with growing season. Light transmitted through CuSO4 filters delayed flowering. Total number of flowers was not affected by spectral filter, but plants grown under CuSO4 filter had smaller flowers than those grown under the control filter. Light transmitted through CuSO4 filter resulted in reduced leaf and stem soluble sugar (sucrose, glucose, and fructose) and starch concentrations regardless of the growing season. However, the magnitude of reduction was greater in spring- than in fall-grown plants. Stems of fall-grown plants had more starch deposition than spring-grown plants under both filters. Filters with specific spectral characteristics can be used as alternative means of producing compact plants in the greenhouses, however, the delay in flowering and smaller flowers could limit their use for growth control of plants intended for flower production.
The role of light quality and quantity in regulating growth of vegetative Dendranthema × grandiflorum (Ramat.) Kitamura was evaluated using CuSO4 solutions and water (control) as spectral filters. Copper sulfate filters increased the red (R): far-red (FR) and the blue (B): R ratios (R = 600 to 700 nm; FR = 700 to 800 nm; B = 400 to 500 urn) of transmitted light. Photosynthetic photon flux (PPF) under 4%, 8% and 16% CuSO4 filters was reduced 26%, 36%, and 47%, respectively, from natural irradiance in the greenhouse, which averaged ≈ 950 μmol·m-2·s-1. Control treatments were shaded with Saran plastic film to ensure equal PPF as the corresponding C uSO4 chamber. Average daily maxima and minima were 26 ± 3C and 16 ± 2C. At the end of the 4-week experimental period, average height and internode length of plants grown under CuSO4 filters were ≈ 40% and 34% shorter than those of plants grown under control filter. Reduction in plant height and internode length was apparent within 1 week after the beginning of treatment. Total leaf area (LA) was reduced by 32% and leaf size (LS) was reduced by 24% under CuSO4 filters. Specific leaf weight (SLW) was higher under CuSO4 filters than for the controls. Irradiance transmitted through CuSO4 filters reduced fresh and dry leaf weights by 30%. Fresh and dry stem weights of plants grown under CuSO4 filters were 60% lower than those of controls. Relative dry matter accumulation into leaves was increased in plants grown under CuSO4 filters while it was reduced in stems. A single application of GA3 before irradiation partially overcame the height reduction under CuSO4 filters, suggesting GA biosynthesis/action may be affected by light quality. Our results imply that alteration of light quality could be used to control chrysanthemum growth as an alternative method to conventional control by chemical growth regulators. Chemical names used: gibberellic acid (GA)
The root defect of carrot (Daucus carota L.) called cavity spot is injury due to feeding of the fungus gnat larvae, Bradysia impatiens (Joh.). In sand cultures and in the field, carrots treated with the systemic insecticide, aldicarb (2-methyl-2(methylthio) propionaldehyde 0-(methylcarbamoyl) oxime) were free of the defect. The symptoms of cavity spot on carrot roots grown in sand culture were the same as those on field-grown roots. Eliminating Ca from the nutrient solution reduced the Ca content of roots and leaves but had no effect on the incidence of cavity spot. Plants with Ca-deficiency symptoms on the foliage produced roots that, except for size, were indistinguishable from roots of plants receiving the complete nutrient solution.
Seedstalk height of carrot (Daucus carota L.) was reduced as the post-vernalization temperature increased from 15/21° to 27/32°C (night/day) with no significant effect on flowering and seed formation. Seedstalks of ‘Royal Chantenay ’ carrot were most affected by the high temperatures and ‘Scarlet Nantes’ were the least affected while ‘Danvers 126’ was intermediate. Few plants had macroscopic seedstalk development 6 weeks after vernalization although the temperature during this period had a permanent influence on ultimate seedstalk height. Carrots grown at 27/32° during the initial 6 weeks following vernalization and then transferred to the optimum 15/21° grew no taller than plants held at 27/32°. Vernalization temperatures of 0°, 5°, and 10° for 10 weeks did not affect the percentage of plants flowered, time of bolting, or rate of seedstalk elongation. Ultimate seedstalk height was reduced only in ‘Royal Chantenay’ vernalized at 10°. Flowering was decreased by post-vernalization temperatures of 27/32° and 2l/27°C when carrots were stored only 5 weeks at 5° but not, after storage for 10 weeks or more. Increasing the vernalization time to 10 weeks hastened the rate of bolting in all three cultivars and increased ultimate seedstalk height in only ‘Royal Chantenay’ and ‘Danvers 126.’ Temperature during the first year of root growth, foliage removal from mature roots prior to storage, and photoperiod following vernalization did not affect seedstalk elongation or flowering.
Orange end Red Sunblaze miniature rose plants were forced. to flower in a glasshouse in 10 cm pots. At harvest, flower stage (FST) 1 (tight bud), 2 (reflexed calyx), and 3 (petals starting to reflex) flowers were designated and tagged. The plants were then stored at 4, 16 or 28°C for 2, 4, or 6 days. Subsequent to the simulated shipping treatments, plants were evaluated in a simulated home interior environment (21° with 30 μmoles M-2 sec-1 cool-white fluorescent light). After summer forcing, flowers of both cultivars developed at least 1 FST during simulated shipping. Flower development increased as storage duration increased for FST 1 and 2, but storage duration did not affect development of FST 3 flowers. The higher the temperature the faster flowers developed, but development was less than 1 FST at 4°. After winter forcing, flowers developed less than 1 FST during simulated shipping. Flower development increased with increasing temperature. In summer, plants with FST 2 flowers could be shipped at up to 16°, but plants with FST 3 flowers should be shipped at 4°. In winter, plants can be shipped at up to 16° with FST 3 flowers.