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Canopy-scale relationships between stomatal conductance and photosynthesis in irrigated rice

Modeling stomatal behavior is critical in research on land–atmosphere interactions and climate change. The most common model uses an existing relationship between photosynthesis and stomatal conductance. However, its parameters have been determined using infrequent and leaf‐scale gas‐exchange measur...

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Published in:Global change biology 2013-07, Vol.19 (7), p.2209-2220
Main Authors: Ono, Keisuke, Maruyama, Atsushi, Kuwagata, Tsuneo, Mano, Masayoshi, Takimoto, Takahiro, Hayashi, Kentaro, Hasegawa, Toshihiro, Miyata, Akira
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description Modeling stomatal behavior is critical in research on land–atmosphere interactions and climate change. The most common model uses an existing relationship between photosynthesis and stomatal conductance. However, its parameters have been determined using infrequent and leaf‐scale gas‐exchange measurements and may not be representative of the whole canopy in time and space. In this study, we used a top‐down approach based on a double‐source canopy model and eddy flux measurements throughout the growing season. Using this approach, we quantified the canopy‐scale relationship between gross photosynthesis and stomatal conductance for 3 years and their relationships with leaf nitrogen content throughout each growing season above a paddy rice canopy in Japan. The canopy‐averaged stomatal conductance (gsc) increased with increasing gross photosynthesis per unit green leaf area (Ag), as was the case with leaf‐scale measurements, and 41–90% of its variation was explained by variations in Ag adjusted to account for the leaf‐to‐air vapor‐pressure deficit and CO2 concentration using the Leuning model. The slope (m) in this model (gsc versus the adjusted Ag) was almost constant within a 15‐day period, but changed seasonally. The m values determined using an ensemble dataset for two mid‐growing‐season 15‐day periods were 30.8 (SE = 0.5), 29.9 (SE = 0.7), and 29.9 (SE = 0.6) in 2004, 2005, and 2006, respectively; the overall mid‐season value was 30.3 and did not greatly differ among the 3 years. However, m appeared to be higher during the early and late growing seasons. The ontogenic changes in leaf nitrogen content strongly affected Ag and thus gsc. In addition, we have discussed the agronomic impacts of the interactions between leaf nitrogen content and gsc. Despite limitations in the observations and modeling, our canopy‐scale results emphasize the importance of continuous, season‐long estimates of stomatal model parameters for crops using top‐down approaches.
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The canopy‐averaged stomatal conductance (gsc) increased with increasing gross photosynthesis per unit green leaf area (Ag), as was the case with leaf‐scale measurements, and 41–90% of its variation was explained by variations in Ag adjusted to account for the leaf‐to‐air vapor‐pressure deficit and CO2 concentration using the Leuning model. The slope (m) in this model (gsc versus the adjusted Ag) was almost constant within a 15‐day period, but changed seasonally. The m values determined using an ensemble dataset for two mid‐growing‐season 15‐day periods were 30.8 (SE = 0.5), 29.9 (SE = 0.7), and 29.9 (SE = 0.6) in 2004, 2005, and 2006, respectively; the overall mid‐season value was 30.3 and did not greatly differ among the 3 years. However, m appeared to be higher during the early and late growing seasons. The ontogenic changes in leaf nitrogen content strongly affected Ag and thus gsc. 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The canopy‐averaged stomatal conductance (gsc) increased with increasing gross photosynthesis per unit green leaf area (Ag), as was the case with leaf‐scale measurements, and 41–90% of its variation was explained by variations in Ag adjusted to account for the leaf‐to‐air vapor‐pressure deficit and CO2 concentration using the Leuning model. The slope (m) in this model (gsc versus the adjusted Ag) was almost constant within a 15‐day period, but changed seasonally. The m values determined using an ensemble dataset for two mid‐growing‐season 15‐day periods were 30.8 (SE = 0.5), 29.9 (SE = 0.7), and 29.9 (SE = 0.6) in 2004, 2005, and 2006, respectively; the overall mid‐season value was 30.3 and did not greatly differ among the 3 years. However, m appeared to be higher during the early and late growing seasons. The ontogenic changes in leaf nitrogen content strongly affected Ag and thus gsc. In addition, we have discussed the agronomic impacts of the interactions between leaf nitrogen content and gsc. Despite limitations in the observations and modeling, our canopy‐scale results emphasize the importance of continuous, season‐long estimates of stomatal model parameters for crops using top‐down approaches.</abstract><cop>Oxford</cop><pub>Blackwell Publishing Ltd</pub><pmid>23504912</pmid><doi>10.1111/gcb.12188</doi><tpages>12</tpages></addata></record>
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subjects Agricultural Irrigation
agroecosystems
Agronomy. Soil science and plant productions
Animal and plant ecology
Animal, plant and microbial ecology
Biological and medical sciences
canopy micrometeorology
China
Climate change
CO2 flux
crop physiology
eddy covariance
evapotranspiration
Fundamental and applied biological sciences. Psychology
General agroecology
General agroecology. Agricultural and farming systems. Agricultural development. Rural area planning. Landscaping
General agronomy. Plant production
General aspects
Generalities. Agricultural and farming systems. Agricultural development
Irrigation
leaf nitrogen
Models, Biological
net ecosystem exchange
Oryza - growth & development
Oryza - physiology
Oryza sativa
Photosynthesis
Photosynthesis - physiology
Plant biology
Plant Stomata - growth & development
Plant Stomata - physiology
Rice
Seasons
surface energy balance
Synecology
Time Factors
water-use efficiency
Weather
title Canopy-scale relationships between stomatal conductance and photosynthesis in irrigated rice
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