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 Temperature Response of Whole-plant CO2 Exchange Rates of Three Magnolia Cultivars

1999 ◽  
Vol 124 (3) ◽  
pp. 277-282 ◽  
Author(s):  
Marc W. van Iersel ◽  
Orville M. Lindstrom
Keyword(s):  
Exchange Rates ◽  
Environmental Conditions ◽  
Dark Respiration ◽  
Temperature Response ◽  
Rapid Decline ◽  
Optimal Temperature ◽  
Response Curves ◽  
Gross Photosynthesis ◽  
Temperature Range ◽  
Increasing Temperature

Temperature-response curves for photosynthesis and respiration are useful in predicting the ability of plants to perform under different environmental conditions. Whole crop CO2 exchange rates of three magnolia (Magnolia grandiflora L.) cultivars (`MGTIG', `Little Gem', and `Claudia Wannamaker') were measured over a 25 °C temperature range. Plants were exposed to cool temperatures (13 °C day, 3 °C night) temperatures before the measurements. Net photosynthesis (Pnet) of all three cultivars increased from 3 to 15 °C and decreased again at higher temperatures. `MGTIG' had the highest and `Little Gem' the lowest Pnet, irrespective of temperature. The Q10 (relative increase in the rate of a process with a 10 °C increase in temperature) for Pnet of all three cultivars decreased over the entire temperature range. `MGTIG' had the lowest Q10 at low temperatures (1.4 at 8 °C), while `Little Gem' had the lowest Q10 for Pnet at temperatures >17 °C and a negative Q10 > 23 °C. This indicates a rapid decline in Pnet of `Little Gem' at high temperatures. The decrease in Pnet of all three cultivars at temperatures >15 °C was caused mainly by an exponential increase in dark respiration (Rdark) with increasing temperature. `Little Gem' had a lower Rdark (per unit fresh mass) than `MGTIG' or `Claudia Wannamaker', but all three cultivars had a similar Q10 (2.46). Gross photosynthesis (Pgross) was less sensitive to temperature than Pnet and Rdark. The optimal temperature for Pgross of `MGTIG' was lower (19 °C) than those of `Little Gem' (21 °C) and `Claudia Wannamaker' (22 °C). The Q10 for Pgross decreased with increasing temperature, and was lower for `MGTIG' than for `Little Gem' and `Claudia Wannamaker'. All three cultivars had the same optimal temperature (11 °C) for net assimilation rate (NAR), and NAR was not very sensitive to temperature changes from 3 to 17 °C. This indicates that the plants were well-adapted to their environmental conditions. The results suggest that respiration rate may limit magnolia growth when temperatures get high in winter time.

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

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.

Photosynthetic light and temperature responses of Eucalyptus cloeziana and Eucalyptus argophloia

2003 ◽  
Vol 51 (5) ◽  
pp. 573 ◽  
Author(s):  
Michael R. Ngugi ◽  
Mark A. Hunt ◽  
David Doley ◽  
Paul Ryan ◽  
Peter J. Dart
Keyword(s):  
Quantum Yield ◽  
Dark Respiration ◽  
Temperature Response ◽  
Net Photosynthesis ◽  
Photosynthetic Photon Flux Density ◽  
Photon Flux ◽  
Photon Flux Density ◽  
Response Curves ◽  
Growth Environment ◽  
Eucalyptus Cloeziana

Acclimation of gas exchange to temperature and light was determined in 18-month-old plants of humid coastal (Gympie) and dry inland (Hungry Hills) provenances of Eucalyptus cloeziana F.Muell., and in those of a dry inland provenance of Eucalyptus argophloia Blakely. Plants were acclimated at day/night temperatures of 18/13, 23/18, 28/23 and 33/28�C in controlled-temperature glasshouses for 4 months. Light and temperature response curves were measured at the beginning and end of the acclimation period. There were no significant differences in the shape and quantum-yield parameters among provenances at 23, 28 and 33�C day temperatures. Quantum yield [μmol CO2 μmol–1 photosynthetic photon flux density (PPFD)] ranged from 0.04 to 0.06 and the light response shape parameter ranged from 0.53 to 0.78. Similarly, no consistent trends in the rate of dark respiration for plants of each provenance were identified at the four growth temperatures. Average values of dark respiration for the plants of the three provenances ranged from 0.61 to 1.86 μmol m–2 s–1. The optimum temperatures for net photosynthesis increased from 23 to 32�C for the humid- and from 25 to 33�C for the dry-provenance E. cloeziana and from 21 to 33�C for E. argophloia as daytime temperature of the growth environment increased from 18 to 33�C. These results have implications in predicting survival and productivity of E. cloeziana and E. argophloia in areas outside their natural distribution.

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 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.

Photosynthesis and Respiration of Developing Soybean Pods

1977 ◽  
Vol 4 (5) ◽  
pp. 713 ◽  
Author(s):  
EY Sambo ◽  
J Moorby ◽  
FL Milthorpe
Keyword(s):  
Dark Respiration ◽  
Photochemical Efficiency ◽  
Net Photosynthesis ◽  
Dry Weight ◽  
Daily Basis ◽  
Co2 Uptake ◽  
Response Curves ◽  
Total Import ◽  
Co2 Response ◽  
Gross Photosynthesis

Net CO2 uptake by soybean pods in the light was much less and output in darkness much greater than from equal areas of leaves. The net photosynthesis decreased, becoming negative, and dark respiration increased as seed filling progressed. The photochemical efficiency was the same but the diffusive resistance of pods was about twice and the internal resistance two to three times those of leaves. Fluxes into open deseeded pods were initially much greater than into intact pods but drying out of the tissue soon led to fluxes only about three times greater. From these measurements and light- and CO2-response curves of intact pods, estimates of gross photosynthesis, photorespiration and dark respiration of seeds and hulls were made. These indicated that seed reassimilated slightly more CO2 than they respired when young and about two-thirds thereof at a later stage. Hulls fixed about similar amounts but these were insufficient to prevent net effluxes from pods during the later stages of their development, even at irradiances of 190 W m-2. On a daily basis, direct uptake of CO2 made a negligible contribution to the total import of dry weight by the pod; nevertheless, photosynthesis in the seeds and hulls refixed some 50-70% of the CO2 respired by these tissues.

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.

scholarly journals Short-term Temperature Change Affects the Carbon Exchange Characteristics and Growth of Four Bedding Plant Species

2003 ◽  
Vol 128 (1) ◽  
pp. 100-106 ◽  
Author(s):  
Marc W. van Iersel
Keyword(s):  
Growth Rate ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Tagetes Patula ◽  
Short Term ◽  
Response Curves ◽  
Gross Photosynthesis ◽  
Bedding Plants ◽  
Bedding Plant ◽  
Wide Range

Bedding plants are exposed to a wide range of environmental conditions, both during production and in the landscape. This research compared the effect of short-term temperature changes on the CO2 exchange rates of four popular bedding plants species. Net photosynthesis (Pnet) and dark respiration (Rdark) of geranium (Pelargonium ×hortorum L.H. Bail.), marigold (Tagetes patula L.), pansy (Viola ×wittrockiana Gams.), and petunia (Petunia ×hybrida Hort. Vilm.-Andr.) were measured at temperatures ranging from 8 to 38 °C (for Pnet) and 6 to 36 °C (for Rdark). Net photosynthesis of all species was maximal at 14 to 15 °C, while Rdark of all four species increased exponentially with increasing temperature. Gross photosynthesis (Pgross) was estimated as the sum of Pnet and Rdark, and was greater for petunia than for the other three species. Gross photosynthesis was less sensitive to temperature than either Pnet or Rdark, suggesting that temperature effects on Pnet were caused mainly by increased respiration at higher temperatures. Gas exchange-temperature response curves were not useful in determining the heat tolerance of these species. There were significant differences among species in the estimated Rdark at 0 °C and the Q10 for Rdark. Differences in the Q10 for Rdark were related to growth rate and plant size. Large plants had a greater Q10 for Rdark, apparently because these plants had a higher ratio of maintenance to growth respiration than small plants. The Q10 of the maintenance respiration coefficient was estimated from the correlation between the Q10 and relative growth rate, and was found to be 2.5 to 2.6.

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

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