Search Results

You are looking at 31 - 40 of 919 items for :

  • "photosynthetic photon flux" x
  • Refine by Access: All x
Clear All
Free access

Richard P. Marini and Donald L. Sowers

`Redhaven' peach [Prunus persica (L.) Batsch] trees were shaded to five light levels [100%, 45%, 23%, 17%, and 9% photosynthetic photon flux (PPF)] for four different periods. Net photosynthesis (Pn), measured under the various shade levels, increased nonlinearly with increasing percent PPF. After 18 days of shading, specific leaf weight (SLW) was positively and linearly related to percent PPF. After shade removal, Pn and SLW returned to control levels in 26 and 4 days, respectively. Flower density was positively related to percent PPF when trees were shaded from 16 June to 4 July or 4-31 July, but not from 31 July to 30 Sept. of the previous year.

Free access

Ben Wherley, Ambika Chandra, Anthony Genovesi, Mason Kearns, Tim Pepper, and Jim Thomas

measured under moderate [32% photosynthetic photon flux ( PPF )] shade. z Table 3. St. augustinegrass parameters measured under heavy [15% photosynthetic photon flux ( PPF )] shade. z Final green cover. Scores for final green cover showed a similar range of

Free access

Marc W. van Iersel and David Gianino

treatments, the LED light was off when the PPF was above the threshold. Fig. 1. Diagram of the adapative lighting control system. A datalogger and control system uses a quantum sensor to measure the photosynthetic photon flux ( PPF ) underneath the LED

Free access

Richard P. Marini, Donald Sowers, and Michele Choma Marini

Abbreviations: DAFB, days after full bloom; DBH, days before harvest; IPPFD, incident photosynthetic photon flux density; PPFD, photosynthetic photon flux density. 1 Associate Professor. 2 Laboratory Technician. 3 Research Technician. The cost of

Free access

Usha Palaniswamy, Richard McAvoy, and Bernard Bible

Watercress (Nasturtium officinale R.Br.) plants were grown in growth chambers at 15 °C or 25 °C and either 8- or 12-h photoperiod (PP). The photosynthetic photon flux (PPF) was 265 μmol·m-2s-1 in all chambers, but beginning 1 week before harvest, half of the plants in each chamber were subjected to a higher PPF (435 μmol·m-2·s-1). At harvest, watercress leaves and stems were analyzed for phenethyl isothiocyanate (PEITC) concentration. Without supplemental PPF, watercress grown at 25 °C and 12-h PP produced higher PEITC concentration in leaves and stems than plants grown at 15 °C and 12-h PP, or plants grown at 8-h PP and either temperature. With one week of supplemental PPF before harvest, plants grown at 15 or 25 °C and the 8-h PP produced PEITC concentrations as high as plants exposed to 12-h PP and similar temperatures. However, a week of supplemental PPF did not alter PEITC concentrations in plants grown at the 12-h PP, regardless of temperature. At 25 °C, plants grown under the low PPF and the 12-h PP produced 62% greater dry mass than plants exposed to a week of high PPF and the 8-h PP, but did not differ in PEITC content. Thus, the effect of one week of high PPF on PEITC concentration depended on photoperiod.

Free access

Kara Senger Lewallen and Richard P. Marini

The influence of photosynthetic photon flux (PPF) on peach [Prunus persica (L.) Batsch] fruit quality and the relationship between ground color and flesh firmness was studied by performing three experiments. Fruit with varying ground colors were sampled from different canopy positions with varying PPF. Fruit skin color was measured with a tristimulus colorimeter and values for L* (lightness), chroma (brightness), and hue angle (numerical values for color) were calculated for each fruit. Fruit from the canopy exterior generally were larger, had more surface area colored red, had higher soluble solids concentrations, and were darker, duller, and redder than fruit harvested from interior positions. In all three experiments, the relationship between hue angle and fruit firmness was affected by PPF, but the nature of the relationship (linear vs. curvilinear) and the influence of position was not consistent. When fruit were covered with aluminum foil or a section of the fruit surface was covered with duct tape to prevent light-induced red coloration of the skin, the relationship between hue angle and fruit firmness was similar for different canopy positions. Therefore, the relationship between ground color and fruit firmness is influenced by the light environment in which a fruit develops, and not by canopy position. Ground color does not seem to be a good indicator of fruit firmness because fruit with the same hue angle had greatly differing firmnesses.

Free access

James E. Faust and Royal D. Heins

The effects of temperature and daily-integrated photosynthetic photon flux (PPFDI) on African violet (Saintpaulia ionantha Wendl.) flower initiation and development were quantified to provide the basis for an inflorescence development model. The percentage of leaf axils in which an inflorescence initiated and continued development increased as the PPFDI increased from 1 to 4 mol·m-2·day-1, while the rate of inflorescence development was a function of the average daily temperature (ADT). The appearance of a visible flower bud (VB) in a leaf axil was related to the growth of the subtending leaf blade. A polynomial model based on ADT and PPFDI was used to describe leaf blade length at visible bud (LBLVB). A nonlinear model was used to describe the influence of ADT on leaf expansion rate (LER). Inflorescence appearance in the leaf axil was predicted by measuring LBL and estimating the time for the leaf blade to develop to the length required for VB. A phasic-development scale was developed to quantify inflorescence development. Days required for an inflorescence to develop from VB to first open flower was described as a function of ADT and either inflorescence height or inflorescence development stage (IDS). Days from leaf emergence to first open flower for the inflorescence initiated in that leaf axil decreased from 86 to 55 as ADT increased from 18 to 26C.

Open access

M.G. Karlsson and R.D. Heins

Abstract

Chrysanthemum morifolium Ramat. ‘Bright Golden Anne’ plants were grown under 15 combinations of photosynthetic photon flux (PPF), day temperature, and night temperature in a central composite design. Time to flower was a function of both irradiance and the interaction between day and night temperature. The surface response to temperature was bowl shaped with delayed development as temperatures were either increased or decreased from the optimum combinations. High temperature delay was compensated for in part by increased PPF. Shoot length increased linearly as day temperature increased; final shoot length first decreased, then increased with increasing night temperature. The response surface appeared as a rising valley with the longest shoot lengths at high day temperatures. Total flower area per plant increased as PPF increased or as night temperature decreased. For any PPF and night temperature, maximum flower area occurred near 20°C. At a constant PPF, the response surface appeared as a rising ridge with maximum flower area at low night temperature.

Free access

D.G. Mortley, P.A. Loretan, W.A. Hill, C.K. Bonsi, and C.E. Morris

Two sweetpotato [Ipomoea batatas (L.) Lam] genotypes (`Georgia Jet' and the breeding clone TI-155) were grown at 12-, 15-, 18-, and 21-h light/12-, 9-, 6-, 3-h dark cycles, respectively, to evaluate their growth and elemental concentration responses to duration and amount of daily lighting. Vine cuttings (15 cm long) of both genotypes were grown in rectangular nutrient film technique channels for 120 days. Conditions were as follows: photosynthetic photon flux (PPF) mean 427 μmol·m–2·s–1, 28C day/22C night air cycle, and 70% ± 5% relative humidity. The nutrient solution used was a modified half-strength Hoagland's solution. Storage root count per plant and per unit area, yield (in grams per square meters per day), and harvest index increased, while production efficiency (in grams per mole) decreased with increased daily PPF. Stomatal conductance for both genotypes declined with increased daily PPF. Leaves were smallest for both genotypes at the 21-h light period, while storage root yield declined as leaf area index increased. Except for a linear decrease in leaf N and K with increased light period, elemental concentration was not significantly influenced.

Free access

David L. Bubenheim, Raman Sargis, and David Wilson

Electronic dimming of high-intensity discharge lamps offers control of photosynthetic photon flux (PPF) but is often characterized as causing significant spectral changes. Growth chambers with 400-W metal halide (MH) and high-pressure sodium (HPS) lamps were equipped with a dimmer system using silicon-controlled rectifiers (SCR) as high-speed switches. Phase control operation turned the line power off for some period of the alternating current cycle. At full power, the electrical input to HPS and MH lamps was 480 W (root mean squared) and could be decreased to 267 W and 428 W, respectively, before the arc was extinguished. Concomitant with this decrease in input power, PPF decreased by 60% in HPS and 50% in MH. The HPS lamp has characteristic spectral peaks at 589 and 595 nm. As power to the HPS lamps was decreased, the 589-nm peak remained constant while the 595-nm peak decreased, equaling the 589-nm peak at 345-W input, and the 589-nm peak was almost absent at 270-W input. The MH lamp has a broader spectral output but also has a peak at 589 nm and another smaller peak at 545 nm. As input power to the MH lamps decreased, the peak at 589 diminished to equal the 545-nm peak. As input power approached 428 W, the 589-nm peak shifted to 570 nm. While the spectrum changed as input power was decreased in the MH and HPS lamps, the phytochrome equilibrium ratio (Pfr: Ptot) remains unchanged for both lamp types.