Optimizing aerial environments for greenhouse rose production utilizing whole-plant net CO2 exchange data

1991 ◽  
Vol 71 (1) ◽  
pp. 253-261 ◽  
Author(s):  
J. Jiao ◽  
M. J. Tsujita ◽  
B. Grodzinski
Keyword(s):  
Dark Respiration ◽  
Net Photosynthesis ◽  
Co2 Exchange ◽  
Day Length ◽  
Daily Growth ◽  
Relative Contribution ◽  
Whole Plant ◽  
Nondestructive Measurements ◽  
Environment Modelling ◽  
Exchange Data

A daily growth model was developed for Samantha roses based on nondestructive measurements of whole-plant net CO2 exchange rate (NCER) under various aerial environmental conditions. Irradiance, CO2 concentration, and temperature accounted for 70, 20, and 5%, respectively, of the variance in whole-plant net photosynthesis explainable by a second-order polynomial model (R2 = 0.86). The predicted optimal temperatures for whole-plant net photosynthesis increased from 19 to 24 °C with increasing irradiance from 100 to 1200 μmol m−2 s−1 and CO2 concentration from 350 to 1500 μL L−1. Dark respiration rate increased exponentially with temperature and could be predicted by the Arrhenius equation. Even though respiratory carbon (C) loss at night increased linearly with daytime C gain, daily C gain (AC) was still proportional to daytime net photosynthesis. The relative contribution of irradiance (100–1200 μmol m−2s−1), day length (8–16 h), CO2 concentration (350–1500 μL L−1), day temperature (15–30 °C), and night temperature (15–25 °C) to plant daily growth was 64, 31, 4, 0.3, and 0.7%, respectively. Key words: Carbon balance, environment, modelling, photosynthesis, respiration, Rosa hybrida

Influence of temperature on net CO2 exchange in roses

1991 ◽  
Vol 71 (1) ◽  
pp. 235-243 ◽  
Author(s):  
J. Jiao ◽  
M. J. Tsujita ◽  
B. Grodzinski
Keyword(s):  
Dark Respiration ◽  
Net Photosynthesis ◽  
Co2 Exchange ◽  
Effect Of Temperature ◽  
Flower Bud ◽  
Temperature Range ◽  
Whole Plant ◽  
Optimal Temperature Range ◽  
Influence Of Temperature On ◽  
Whole Plants

The effect of temperature on net CO2 exchange of source and sink tissues of the flowering shoots and of whole plants was examined using single-stemmed Samantha roses. At all stages of shoot development, the optimal temperature range for whole-plant carbon (C) gain at saturating irradiance and ambient CO2 level was between 20° and 25 °C, narrower than the temperature range for optimal leaf net photosynthesis. Dark respiration increased more dramatically than photosynthesis with temperatures between 15 and 35 °C. At 25 °C, C loss due to respiration from the flower bud at colour bud stage accounted for 45% of the C loss of the flowering shoot. At low irradiance levels (e.g. 200 μmol m−2 s−1) whole-plant net photosynthesis was greater at 16° than at 22 °C because of a greater reduction in respiration. Lowering the night temperature from 27 to 17 °C also increased daily C gain due to a reduction in the C lost at night. Whole-plant net photosynthesis of plants grown and measured at enriched (1000 ± 100 μL L−1) CO2 was greater than that of plants grown and measured at ambient (350 ± 50 μL L−1) level at temperatures between 15° and 35 °C. Furthermore, the optimal temperatures for whole-plant net photosynthesis in CO2 enrichment was higher than at ambient CO2 level. Key words: Dark respiration, net photosynthesis, Rosa hybrida, temperature

Temperature Response of Whole-plant CO2 Exchange Rates of Magnolia (Magnolia grandiflora L.)

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 511d-511
Author(s):  
Marc W. van Iersel ◽  
Orville M. Lindstrom
Keyword(s):  
Dark Respiration ◽  
Temperature Response ◽  
Net Photosynthesis ◽  
Co2 Exchange ◽  
Limiting Factor ◽  
Response Curves ◽  
Gross Photosynthesis ◽  
Temperature Range ◽  
Whole Plant ◽  
Increasing Temperature

Photosynthesis and respiration temperature-response curves are useful in predicting the ability of plants to perform under different environmental conditions. Whole crop CO2 exchange of two groups of magnolia `Greenback' plants was measured over a 26 °C temperature range. Net photosynthesis (Pnet) increased from 2 to 17% C and decreased again at higher temperatures. The Q10 for Pnet decreased from ≈4 at 6 °C to 0.5 at 24 °C. The decrease in Pnet at temperatures over 17 °C was caused by a rapid increase in dark respiration (Rdark) with increasing temperature. The Q10 for Rdark was estimated by fitting an exponential curve to data, resulting in a temperature-independent Q10 of 2.8. Gross photosynthesis (Pgross), estimated as the sum of Rdark and Pnet, increased over the entire temperature range (up to 25 °C). The Q10 for Pgross decreased with increasing temperature, but remained higher than 1. The data suggest that high respiration rates may be the limiting factor for growth of magnolia exposed to high temperatures, since it may result in a net carbon loss from the plants. At temperatures below 5 °C, both Pnet and Rdark become low and the net CO2 exchange of the plants would be expected to be minimal.

scholarly journals Auxin Applications Affect Posttransplant CO2 Exchange Rate and Growth of Bare-rooted Vinca [Catharanthus roseus (L.) G. Don] Seedlings

1999 ◽  
Vol 124 (3) ◽  
pp. 234-238 ◽  
Author(s):  
Marc van Iersel
Keyword(s):  
Exchange Rate ◽  
Catharanthus Roseus ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Dry Mass ◽  
Co2 Exchange ◽  
Naphthaleneacetic Acid ◽  
Negative Effects ◽  
Transplant Shock ◽  
Whole Plant

Uprooting and transplanting seedlings can cause root damage, which may reduce water and nutrient uptake. Initiation of new roots and rapid elongation of existing roots may help minimize the negative effects of transplant shock. In this study, seedlings with four true leaves were transplanted into diatomaceous earth and the plants were transferred to a growth chamber, where they were treated with NAA (0, 0.025, 0.25, and 2.5 mg·L-1; 36 mL/plant). The effects of drenches with various amounts of 1-naphthaleneacetic acid (NAA) on the posttransplant CO2 exchange rate of vinca [Catharanthus roseus (L.) G. Don] were quantified. Whole-plant CO2 exchange rate of the plants was measured once every 20 minutes for a 28 day period. Seedlings treated with 0.025 or 0.25 mg·L-1 recovered from transplant shock more quickly than plants in the 0 and 2.5 mg·L-1 treatments. Naphthaleneacetic acid drenches containing 0.025 or 0.25 mg·L-1 increased whole-plant net photosynthesis (Pnet) from 10 days, dark respiration (Rdark) from 12 days, and carbon use efficiency (CUE) from 11 days after transplanting until the end of the experiment. The increase in CUE seems to have been the result of the larger size of the plants in these two treatments, and thus an indirect effect of the NAA applications. These differences in CO2 metabolism among the treatments resulted in a 46% dry mass increase in the 0.025 mg·L-1 treatment compared to the control, but shoot-root ratio was not affected. The highest rate of NAA (2.5 mg·L-1) was slightly phytotoxic and reduced the growth rate of the plants.

scholarly journals 155 Fertilizer Concentration Affects Whole Plant CO2 Exchange and Growth of Subirrigated Pansies

HortScience ◽  
2000 ◽  
Vol 35 (3) ◽  
pp. 416D-416
Author(s):  
Marc van Iersel ◽  
Jong-Goo Kang
Keyword(s):  
Root System ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Co2 Exchange ◽  
Bedding Plants ◽  
Whole Plant ◽  
Growing Medium ◽  
Wide Range ◽  
K Deficiency ◽  
Plant Photosynthesis

Subirrigation is an economically attractive irrigation method for producing bedding plants. Because excess fertilizer salts are not leached from the growing medium, salts can accumulate in the growing medium. Fertilizer guidelines developed for overhead irrigation may not be appropriate for subirrigation systems. Our objective was to quantify the effect of the fertilizer concentration (N at 0, 135, 285, and 440 mg·L–1) on whole-plant CO2 exchange and growth of subirrigated pansies. Whole plant CO2 exchange rate (net photosynthesis and dark respiration) was measured once every 10 min for 31 days. Whole-plant photosynthesis, dark respiration, and carbon use efficiency increased during the experiment. Fertilizer concentration started to affect the growth rate of the plants after approximately 7 days. Maximum photosynthesis and growth were achieved with N at about 280 mg·L–1 in the fertilizer solution [electrical conductivity = 2 dS·m–1]. Growth was reduced by ≈10% when the plants were fertilized with N at 135 and 440 mg·L–1 compared to 280 mg·L–1. Growth of plants watered without any fertilizer was greatly reduced, and plants showed symptoms of N and K deficiency. The size of the root system decreased and the shoot: root ratio increased with increasing fertilizer concentration, but the size of the root system was adequate in all treatments. These results indicate that subirrigated pansies can tolerate a wide range of fertilizer concentrations with relatively little effect on plant growth.

The ecology of Ramalina menziesii. VI. Laboratory responses of net CO2 exchange to moisture, temperature, and light

1987 ◽  
Vol 65 (1) ◽  
pp. 182-191 ◽  
Author(s):  
U. Matthes-Sears ◽  
T. H. Nash III ◽  
D. W. Larson
Keyword(s):  
Dark Respiration ◽  
Net Photosynthesis ◽  
Co2 Exchange ◽  
Response Curves ◽  
Central California ◽  
Photosynthetic Rates ◽  
Chlorophyll Contents ◽  
The Mean ◽  
The Difference ◽  
Thallus Water Content

The response of net CO2 exchange to thallus water content, thallus temperature, and photosynthetically active radiation was measured in the laboratory for two morphologically different forms of Ramalina menziesii collected from a coastal and an inland habitat in central California. Equations describing the response curves are fitted to the data and compared statistically for the two sites during two seasons. Significant differences were present for all responses both in summer and winter but were more pronounced for net photosynthesis than for dark respiration. The main differences between the two forms were in the absolute rates of net photosynthesis; a maximum of 6.2 was measured for the inland form but only 3.6 mg∙g−1∙h−1 for the coastal form. Chlorophyll contents were also different between the two forms, indicating that chlorophyll is the likely cause for the difference in net photosynthetic rates. Net photosynthetic rates were higher at low temperatures during winter than during summer, but otherwise seasonal variations in the gas exchange responses were relatively minor. Both forms of the lichen are light saturated at quantum fluxes greater than 200 μE∙m−2∙s−1. Both show an optimum temperature for maximum CO2 exchange at 25 °C, well above the mean operating temperature of R. menziesii in the field.

scholarly journals Nutrient Solution Concentration Affects Whole-plant CO2 Exchange and Growth of Subirrigated Pansy

2002 ◽  
Vol 127 (3) ◽  
pp. 423-429 ◽  
Author(s):  
Marc W. van Iersel ◽  
Jong-Goo Kang
Keyword(s):  
Plant Growth ◽  
Exchange Rates ◽  
Leaf Area ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Gross Photosynthesis ◽  
Whole Plant ◽  
Wide Range ◽  
Shoot To Root Ratio ◽  
Fertilizer Solution

To determine the effect of fertilizer concentration on plant growth and physiology, whole-plant C exchange rates of pansies (Viola ×wittrockiana Gams.) subirrigated with one of four fertilizer concentrations were measured over 30 days. Plants were watered with fertilizer solutions with an electrical conductivity (EC) of 0.15, 1.0, 2.0, or 3.0 dS·m-1 (N at 0, 135, 290, or 440 mg·L-1, respectively). Plants watered with a fertilizer solution with an EC of 2 dS·m-1 had the highest shoot dry weight (DW), shoot to root ratio, leaf area, leaf area ratio (LAR), and cumulative C gain at the end of the experiment compared to those watered with a solution with a higher or lower EC. Shoot tissue concentrations of N, P, K, S, Ca, Fe, Na, and Zn increased linearly with increasing fertilizer concentration. A close correlation between final DW of the plants and the measured cumulative C gain (CCG) (r2 = 0.98) indicated that the C exchange rates were good indicators of plant growth. There were quadratic relationships between fertilizer EC and gross photosynthesis, net photosynthesis, and dark respiration, starting at 13, 12, and 6 days after transplanting, respectively. Although plants fertilized with a fertilizer solution with an EC of 2 dS·m-1 had the highest C exchange rates, the final differences in shoot DW and CCG among ECs of 1.0, 2.0, and 3.0 dS·m-1 were small and it appears that pansies can be grown successfully with a wide range of fertilizer concentrations. Plants with a high LAR also had higher DW, suggesting that increased growth was caused largely by increased light interception. A detrimental effect of high fertilizer concentrations was that it resulted in a decrease in root DW and a large increase in shoot to root ratio.

scholarly journals Medium-incorporated PEG-8000 Reduces Elongation, Growth, and Whole-canopy Carbon Dioxide Exchange of Marigold

HortScience ◽  
2006 ◽  
Vol 41 (1) ◽  
pp. 124-130 ◽  
Author(s):  
Stephanie E. Burnett ◽  
Marc W. van Iersel ◽  
Paul A. Thomas
Keyword(s):  
Carbon Dioxide ◽  
Polyethylene Glycol ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Carbon Dioxide Exchange ◽  
Seedling Height ◽  
Tagetes Patula ◽  
Whole Plant ◽  
Growing Medium ◽  
Peg 8000

French marigold (Tagetes patula L. `Boy Orange') was grown in a peat-based growing medium containing different rates (0, 15, 20, 30, 42, or 50 g·L–1) of polyethylene glycol 8000 (PEG-8000) to determine if PEG-8000 would reduce seedling height. Only 28% to 55% of seedlings treated with 62, 72, or 83 g·L–1 of PEG-8000 survived, and these treatments would be commercially unacceptable. Marigolds treated with the remaining concentrations of PEG-8000 had shorter hypocotyls, and were up to 38% shorter than nontreated controls at harvest. Marigold cotyledon water (ψw), osmotic (ψs), and turgor (ψp) potentials were significantly reduced by PEG-8000, and ψp was close to zero for all PEG-treated seedlings 18 days after seeding. Whole-plant net photosynthesis, whole-plant dark respiration, and net photosynthesis/leaf area ratios were reduced by PEG-8000, while specific respiration of seedlings treated with PEG-8000 increased. Marigolds treated with concentrations greater than 30 g·L–1 of PEG-8000 had net photosynthesis rates that were close to zero. Fourteen days after transplanting, PEG-treated marigolds were still shorter than nontreated seedlings and they flowered up to 5 days later. Concentrations of PEG from 15 to 30 g·L–1 reduced elongation of marigold seedlings without negatively affecting germination, survival, or plant quality. It appears that marigold seedlings were shorter because of reduced leaf ψp and reductions in net photosynthesis.

scholarly journals A COMPARISON OF LEAF AND WHOLE PLANT NET PHOTOSYNTHESIS IN ALSTROEMERIA

HortScience ◽  
1992 ◽  
Vol 27 (6) ◽  
pp. 576c-576
Author(s):  
E.D. Leonardos ◽  
M.J. Tsujita ◽  
B. Grodzinski ◽  
T.J. Blom
Keyword(s):  
Dark Respiration ◽  
Net Photosynthesis ◽  
Stomatal Resistance ◽  
Gas Analysis ◽  
Whole Plant ◽  
Plant Photosynthesis ◽  
Mutual Shading ◽  
Photosynthetic Responses ◽  
Analysis System ◽  
Two Stages

Gas exchange (net photosynthesis Pn, dark respiration, transpiration, and stomatal resistance) of `Jaqueline' Alstroemeria, grown in pots in a greenhouse, were measured. Measurements were made under laboratory conditions using an open-flow infrared gas analysis system for leaf studies, and a semi-closed computer controlled whole plant photosynthesis system for whole plant studies. Apical fully expanded leaves on non-flowering and flowering (at two stages) shoots had similar photosynthetic responses in respect to photosynthetically active radiation (PAR) and to CO2 concentration. Light saturation occurred at 600 umol/m2/s PAR with maximum leaf Pn rates ranging from 9 to 11 umol CO2/m2/s. CO2 saturation was estimated at approximately 1100 to 1200 ppm with maximum leaf Pn rates from 17 to 22 umol CO2/m2/s. Whole plant Pn rates increased with increased PAR. Maximum rates 4 to 5 umol CO2/m2/s (half that of individual leaves) occurred at approximately 1000 to 1100 umol/m2/s PAR. CO2 saturation was estimated at 1100 to 1200 ppm, with maximum whole plant Pn rates ranging from 7 to 8 umol CO2/m2/s. These data will be discussed in relation to respiration and mutual shading at the leaf canopy.

scholarly journals Net Carbon Dioxide Exchange Rates and Predicted Growth Patterns in Alstroemeria `Jacqueline' at Varying Irradiances, Carbon Dioxide Concentrations, and Air Temperatures

1994 ◽  
Vol 119 (6) ◽  
pp. 1265-1275 ◽  
Author(s):  
E.D. Leonardos ◽  
M.J. Tsujita ◽  
B. Grodzinski
Keyword(s):  
Carbon Dioxide ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Growth Patterns ◽  
High Yield ◽  
Carbon Dioxide Exchange ◽  
Air Temperatures ◽  
Temperature Regimes ◽  
Whole Plant ◽  
Whole Plants

The influence of irradiance, CO2 concentration, and air temperature on leaf and whole-plant net C exchange rate (NCER) of Alstroemeria `Jacqueline' was studied. At ambient CO2, leaf net photosynthesis was maximum at irradiances above 600 μmol·m-2·s-1 photosynthetically active radiation (PAR), while whole-plant NCER required 1200 μmol·m-2·s-1 PAR to be saturated. Leaf and whole-plant NCERs were doubled under CO2 enrichment of 1500 to 2000 μl CO2/liter. Leaf and whole-plant NCERs declined as temperature increased from 20 to 35C. Whereas the optimum temperature range for leaf net photosynthesis was 17 to 23C, whole-plant NCER, even at high light and high CO2, declined above 12C. Dark respiration of leaves and whole plants increased with a Q10 of ≈2 at 15 to 35C. In an analysis of day effects, irradiance, CO2 concentration, and temperature contributed 58%, 23%, and 14%, respectively, to the total variation in NCER explained by a second-order polynomial model (R2 = 0.85). Interactions among the factors accounted for 4% of the variation in day C assimilation. The potential whole-plant growth rates during varying greenhouse day and night temperature regimes were predicted for short- and long-day scenarios. The data are discussed with the view of designing experiments to test the importance of C gain in supporting flowering and high yield during routine harvest of Alstroemeria plants under commercial greenhouse conditions.

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