scholarly journals A Multiple Chamber, Semicontinuous, Crop Carbon Dioxide Exchange System: Design, Calibration, and Data Interpretation

2000 ◽  
Vol 125 (1) ◽  
pp. 86-92 ◽  
Author(s):  
M.W. van Iersel ◽  
B. Bugbee
Keyword(s):  
Environmental Control ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Data Interpretation ◽  
Crop Growth ◽  
Carbon Gain ◽  
Carbon Dioxide Exchange ◽  
Gross Photosynthesis ◽  
Carbon Use Efficiency ◽  
Use Efficiency

Long-term, whole-crop CO2 exchange measurements can be used to study factors affecting crop growth. These factors include daily carbon gain, cumulative carbon gain, and carbon use efficiency, which cannot be determined from short-term measurements. We describe a system that measures semicontinuously crop CO2 exchange in 10 chambers over a period of weeks or months. Exchange of CO2 in every chamber can be measured at 5 min intervals. The system was designed to be placed inside a growth chamber, with additional environmental control provided by the individual gas exchange chambers. The system was calibrated by generating CO2 from NaHCO3 inside the chambers, which indicated that accuracy of the measurements was good (102% and 98% recovery for two separate photosynthesis systems). Since the systems measure net photosynthesis (Pnet, positive) and dark respiration (Rdark, negative), the data can be used to estimate gross photosynthesis, daily carbon gain, cumulative carbon gain, and carbon use efficiency. Continuous whole-crop measurements are a valuable tool that complements leaf photosynthesis measurements. Multiple chambers allow for replication and comparison among several environmental or cultural treatments that may affect crop growth. Example data from a 2 week study with petunia (Petunia ×hybrida Hort. Vilm.-Andr.) are presented to illustrate some of the capabilities of this system.

scholarly journals Light Effects on Wax Begonia: Photosynthesis, Growth Respiration, Maintenance Respiration, and Carbon Use Efficiency

2004 ◽  
Vol 129 (3) ◽  
pp. 416-424 ◽  
Author(s):  
Krishna S. Nemali ◽  
M.W. van Iersel
Keyword(s):  
Growth Period ◽  
Dry Weight ◽  
Carbon Gain ◽  
Maintenance Respiration ◽  
Gross Photosynthesis ◽  
Carbon Use Efficiency ◽  
Whole Plant ◽  
Growth Respiration ◽  
Use Efficiency ◽  
Gas Exchange System

The effect of increasing daily light integral (DLI; 5.3, 9.5, 14.4, and 19.4 mol·m-2·d-1) on photosynthesis and respiration of wax begonia (Begonia semperflorens-cultorum Hort.) was examined by measuring CO2 exchange rates (CER) for a period of 25 d in a whole-plant gas exchange system. Although plant growth rate (GR, increase in dry weight per day) increased linearly with increasing DLI, plants grown at low DLI (5.3 or 9.5 mol·m-2·d-1) respired more carbohydrates than were fixed in photosynthesis during the early growth period (13 and 4 d, respectively), resulting in a negative daily carbon gain (DCG) and GR. Carbon use efficiency [CUE, the ratio of carbon incorporated into the plant to C fixed in gross photosynthesis (Pg)] of plants grown at low DLI was low, since these plants used most of the C fixed in Pg for maintenance respiration (Rm), leaving few, if any, C for growth and growth respiration (Rg). Maintenance respiration accounted for a smaller fraction of the total respiration with increasing DLI. In addition, the importance of Rm in the carbon balance of the plants decreased over time, resulting in an increase in CUE. At harvest, crop dry weight (DWCROP) increased linearly with increasing DLI, due to the increased photosynthesis and CUE at high PPF.

Two physiological races of Tsuga canadensis in Wisconsin

1975 ◽  
Vol 53 (9) ◽  
pp. 940-951 ◽  
Author(s):  
William Eickmeier ◽  
Michael Adams ◽  
Donald Lester
Keyword(s):  
Dark Respiration ◽  
Net Photosynthesis ◽  
Tsuga Canadensis ◽  
Seedling Morphology ◽  
Seed Sources ◽  
Temperature Regimes ◽  
Disjunct Populations ◽  
Use Efficiency ◽  
Osmotic Potentials ◽  
Carbon Dioxide Balance

Population differentiation in Tsuga canadensis (L.) Carr. from Wisconsin was tested by comparing seedlings grown from seed collected within the present range in the northeast and from seed collected in disjunct populations southwest of the present range. The seedlings, established in hydroponic culture, were subjected to two preconditioning temperature regimes and two water stress simulations. Net photosynthesis, dark respiration, and transpiration capacities were measured and internal leaf resistances were calculated.The southwestern Wisconsin population had a more favorable carbon dioxide balance at warmer tissue temperatures, particularly at low irradiance levels, and at higher osmotic potentials, than did the northeastern population, which was better adapted to lower tissue temperatures and lower osmotic potentials. Additional differences between seed sources in seedling morphology, transpiration rate, and water-use efficiency were found. These differences in morphology and physiological responses corresponded to the macroclimates in which these populations were found, southwestern Wisconsin being warmer and drier than the northeastern part of the state.

scholarly journals Growth Respiration, Maintenance Respiration, and Carbon Fixation of Vinca: A Time Series Analysis

2000 ◽  
Vol 125 (6) ◽  
pp. 702-706 ◽  
Author(s):  
Marc W. van Iersel ◽  
Lynne Seymour
Keyword(s):  
Carbon Balance ◽  
Carbon Fixation ◽  
Plant Size ◽  
Carbon Gain ◽  
Maintenance Respiration ◽  
Carbon Use Efficiency ◽  
Size Growth ◽  
Growth Respiration ◽  
Use Efficiency ◽  
Traditional Approaches

Respiration is important in the overall carbon balance of plants, and can be separated into growth (Rg) and maintenance respiration (Rm). Estimation of Rg and Rm throughout plant development is difficult with traditional approaches. Here, we describe a new method to determine ontogenic changes in Rg and Rm. The CO2 exchange rate of groups of 28 `Cooler Peppermint' vinca plants [Catharanthus roseus (L.) G. Don.] was measured at 20 min intervals for 2 weeks. These data were used to calculate daily carbon gain (DCG, a measure of growth rate) and cumulative carbon gain (CCG, a measure of plant size). Growth and maintenance respiration were estimated based on the assumption that they are functions of DCG and CCG, respectively. Results suggested a linear relationship between DCG and Rg. Initially, Rm was three times larger than Rg, but they were similar at the end of the experiment. The decrease in the fraction of total available carbohydrates that was used for Rm resulted in an increase in carbon use efficiency from 0.51 to 0.67 mol·mol-1 during the 2-week period. The glucose requirement of the plants was determined from Rg, DCG, and the carbon fraction of the plant material and estimated to be 1.39 g·g-1, while the maintenance coefficient was estimated to be 0.031 g·g-1·d-1 at the end of the experiment. These results are similar to values reported previously for other species. This suggests that the use of semicontinuous CO2 exchange measurements for estimating Rg and Rm yields reasonable results.

scholarly journals PHOTOSYNTHESIS, RESPIRATION, AND CARBON COST OF DEVELOPING RABBITEYE BLUEBERRY FRUIT

HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1165g-1166
Author(s):  
Keith Birkhold ◽  
Rebecca Darnell ◽  
Karen Koch
Keyword(s):  
Weight Gain ◽  
Fruit Development ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Dry Weight ◽  
Total Carbon ◽  
Vaccinium Ashei ◽  
Gross Photosynthesis ◽  
Carbon Cost ◽  
Fruit Photosynthesis

Carbon exchange and content of blueberry (Vaccinium ashei) fruit were measured from anthesis through fruit ripening in order to determine the amount of imported carbon required for fruit development. Net photosynthesis occurred in blueberry fruit from petal fall through color break. During this time, gross photosynthesis of fruit decreased from 30.1 μmol CO2·g fw-1·hr-1 to 4.8 μmol CO2·g fw-1·hr-1, and dark respiration decreased from 14.3 μmol CO2·g fw-1·hr-1 to 4.6 μmol CO2·g fw-1·hr-1. After color break, the photosynthetic rate fell to zero, and the respiration rate increased to 8.0 μmol CO2·g fw-1·hr-1, before decreasing. Preliminary data suggest that fruit photosynthesis contributes 11% of the total carbon required (dry weight gain + respiratory loss) during fruit development however, it supplies 50% of the total carbon required during the first 5 days after petal fall. This contribution of carbon from fruit photosynthesis may be critical in initial fruit development since the current season's vegetative growth is not yet providing carbohydrates.

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.

Maximum growth potential in loblolly pine: results from a 47-year-old spacing study in Hawaii

2010 ◽  
Vol 40 (10) ◽  
pp. 1914-1929 ◽  
Author(s):  
Lisa J. Samuelson ◽  
Thomas L. Eberhardt ◽  
John R. Butnor ◽  
Tom A. Stokes ◽  
Kurt H. Johnsen
Keyword(s):  
Loblolly Pine ◽  
Dark Respiration ◽  
Basal Area ◽  
Net Photosynthesis ◽  
Maximum Growth ◽  
Growth Potential ◽  
Carbon Gain ◽  
Native Range ◽  
Woody Root ◽  
Area And Volume

Growth, allocation to woody root biomass, wood properties, leaf physiology, and shoot morphology were examined in a 47-year-old loblolly pine ( Pinus taeda L.) density trial located in Maui, Hawaii, to determine if stands continued to carry the high density, basal area, and volume reported at younger ages and to identify potential factors controlling expression of maximum growth potential. Basal area and volume were similar among spacings (square: 1.8, 2.4, 3.0, and 3.7 m) and averaged 93 m2·ha–1 and 1076 m3·ha–1, respectively, and were double the maxima reported for loblolly pine in its native range. Spacing had a significant influence on density, quadratic mean diameter, and height. Ring-specific gravity and percent latewood were similar among spacing treatments but values were high compared to mainland stands. Leaf light-saturated net photosynthesis, dark respiration, stomatal conductance, and quantum yield were comparable with values reported for loblolly pine in its native range. Foliar calcium concentrations, specific leaf area, and flush number were high in the Hawaii study. Higher carrying capacity in Hawaii may be related to a more favorable climate conducive to year-round leaf carbon gain, high nutrient availability, increased flushing, and less allocation to belowground mass.

scholarly journals Acclimation of Plant Populations to Shade: Photosynthesis, Respiration, and Carbon Use Efficiency

2005 ◽  
Vol 130 (6) ◽  
pp. 918-927 ◽  
Author(s):  
Jonathan M. Frantz ◽  
Bruce Bugbee
Keyword(s):  
Growth Models ◽  
Photon Flux ◽  
Carbon Gain ◽  
Low Light ◽  
Carbon Use Efficiency ◽  
Grand Rapids ◽  
Use Efficiency ◽  
Gas Exchange System ◽  
Photosynthesis And Respiration

Cloudy days cause an abrupt reduction in daily photosynthetic photon flux (PPF), but we have a poor understanding of how plants acclimate to this change. We used a unique 10-chamber, steady-state, gas-exchange system to continuously measure daily photosynthesis and night respiration of populations of a starch accumulator [tomato (Lycopersicon esculentum Mill. cv. Micro-Tina)] and a sucrose accumulator [lettuce (Lactuca sativa L. cv. Grand Rapids)] over 42 days. All measurements were done at elevated CO2 (1200 μmol·mol-1) to avoid any CO2 limitations and included both shoots and roots. We integrated photosynthesis and respiration measurements separately to determine daily net carbon gain and carbon use efficiency (CUE) as the ratio of daily net C gain to total day-time C fixed over the 42-day period. After 16 to 20 days of growth in constant PPF, plants in some chambers were subjected to an abrupt PPF reduction to simulate shade or a series of cloudy days. The immediate effect and the long term acclimation rate were assessed from canopy quantum yield and carbon use efficiency. The effect of shade on carbon use efficiency and acclimation was much slower than predicted by widely used growth models. It took 12 days for tomato populations to recover their original CUE and lettuce CUE never completely acclimated. Tomatoes, the starch accumulator, acclimated to low light more rapidly than lettuce, the sucrose accumulator. Plant growth models should be modified to include the photosynthesis/respiration imbalance and resulting inefficiency of carbon gain associated with changing PPF conditions on cloudy days.

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 Canopy Photosynthesis and Time-of-day Application of Supplemental Light

HortScience ◽  
2009 ◽  
Vol 44 (5) ◽  
pp. 1284-1290 ◽  
Author(s):  
Jakob Markvart ◽  
Eva Rosenqvist ◽  
Helle Sørensen ◽  
Carl-Otto Ottosen ◽  
Jesper M. Aaslyng
Keyword(s):  
Dark Respiration ◽  
High Growth ◽  
Net Photosynthesis ◽  
Time Of Day ◽  
Photon Flux ◽  
Carbon Gain ◽  
Climate Control ◽  
Low Light ◽  
Light Intensities ◽  
Supplemental Lighting

There is increasing use of electricity for supplemental lighting in the northern European greenhouse industry. One reason for this may be to secure a high growth rate during low-light periods by an attempt to increase net photosynthesis. We wanted to clarify which period of the day resulted in the best use of a 5-h supplemental light period for photosynthesis and growth. The periods tested were supplemental light during the night, day, morning, and evening. The experiments were carried out in daylight climate chambers measuring canopy gas exchange. The air temperature was 25 °C and the CO2 level ≈900 ppm. Vegetative chrysanthemum was used, because this species responds quickly to change in light level. The leaf areas of the plant canopies were nondestructively measured each week during the 4-week experimental period. The fact that the quantum yield of photosynthesis is greater at low than at high light intensities favors the use of supplemental light during the dark period, but growth measured as dry weight of the treated plants at the end of the experiments was not significantly different given identical light integrals of the treatments. However, one experiment indicated that increased time with dark hours during day and night (24 h) might decrease net photosynthesis. The assimilation per unit leaf area was approximately the same during times of sunlight through a diffusing screen at 100 μmol·m−2·s−1 of photosynthetic photon flux (PPF) as during times of supplemental (direct) light application at PPF of 200 μmol·m−2·s−1 by high-pressure sodium lamps. We conclude that during the winter and periods of low light intensities, the daily carbon gain does not depend on the time of supplemental light application, but is linked to the total light integral. However, extended time with dark hours during day and night (24 h) might be a disadvantage because of longer periods with dark respiration and subsequent loss of carbon. Our results indicate that during times of low light conditions, it is not necessary to include factors such as the timing of supplemental lighting application to achieve higher net photosynthesis in climate control strategies.

scholarly journals Photosynthesis in Leaves, Fruits, Stem, and Petioles of Tomato Plants Grown in Peat Bags with Different Fertigation Management

HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 865A-865
Author(s):  
Hui-lian Xu ◽  
Laurent Gauthier ◽  
André Gosselin
Keyword(s):  
Nutrient Solution ◽  
Photosynthetic Capacity ◽  
Potential Evapotranspiration ◽  
Dark Respiration ◽  
Physiological Activity ◽  
Leaf Age ◽  
Net Photosynthesis ◽  
Tomato Plants ◽  
Use Efficiency ◽  
Leaf P

Tomato plants were grown in peat bags in greenhouse to examine the effects of variation of the nutrient solution electrical conductivity (EC) and substrate water potential (Ψsub) on photosynthesis in leaves, fruits, stem, and petioles. EC of the nutrient solution delivered to peat bags varied between 1 to 4 dS·m–1 with Ψsub of either –5 kPa or –9 kPa as the setpoint for starting the irrigation. The EC variation was adjusted by a computer system according to potential evapotranspiration. Gross photosynthetic capacity (PC) decreased as the leaf age developed. PC in the 10th, 15th and 18th leaves from the top was only 76%, 37%, and 18% of PC in the 5th leaf, respectively. However, low quantum use efficiency (QUE) was only observed in the 18th leaf and low dark respiration (RD) was only in 15th and 18th leaves. Net photosynthesis (PN) was only observed in young fruits (≈10 g FW) or young petioles and no PN was observed in large fruits (50 g or more FW) and stems. Both PC and RD were lower in older fruits and petioles or in the lower part of the stem compared to the younger ones or upper parts. EC variation increased PC, QUE, and RD in most parts. Low Ψsub increased RD in most parts and decreased PC in fruits, stem, and petioles. It is suggested that EC variation increased plant physiological activity of tomato and low Ψsub increased carbon consumption, although it was not severe enough to depress leaf PC.

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