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Connecting Biochemical Photosynthesis Models with Crop Models to Support Crop ImprovementAcclimation of Biochemical and Diffusive Components of Photosynthesis in Rice, Wheat, and Maize to Heat and Water Deficit: Implications for Modeling Photosynthesis.Increasing water use efficiency along the C3 to C4 evolutionary pathway: a stomatal optimization perspectiveCarbon isotope discrimination as a diagnostic tool for C4 photosynthesis in C3-C4 intermediate species.Root-Zone Warming Differently Benefits Mature and Newly Unfolded Leaves of Cucumis sativus L. Seedlings under Sub-Optimal Temperature Stress.Inside out: efflux of carbon dioxide from leaves represents more than leaf metabolism.Kranz and single-cell forms of C4 plants in the subfamily Suaedoideae show kinetic C4 convergence for PEPC and Rubisco with divergent amino acid substitutions.Why small fluxes matter: the case and approaches for improving measurements of photosynthesis and (photo)respiration.The influence of leaf anatomy on the internal light environment and photosynthetic electron transport rate: exploration with a new leaf ray tracing model.Do the rich always become richer? Characterizing the leaf physiological response of the high-yielding rice cultivar Takanari to free-air CO2 enrichment.An Excel tool for deriving key photosynthetic parameters from combined gas exchange and chlorophyll fluorescence: theory and practice.The rapid A-Ci response: photosynthesis in the phenomic era.Rubisco Catalytic Properties and Temperature Response in Crops.Can increased leaf photosynthesis be converted into higher crop mass production? A simulation study for rice using the crop model GECROS.Implications of the mesophyll conductance to CO2 for photosynthesis and water-use efficiency during long-term water stress and recovery in two contrasting Eucalyptus species.A generalized stoichiometric model of C3, C2, C2+C4, and C4 photosynthetic metabolism.An improved approach for measuring the impact of multiple CO2 conductances on the apparent photorespiratory CO2 compensation point through slope-intercept regression.The harsh life of an urban tree: the effect of a single pulse of ozone in salt-stressed Quercus ilex saplings.Temperature response of bundle-sheath conductance in maize leavesModelling water use efficiency in a dynamic environment: An example using Arabidopsis thaliana.Localization of (photo)respiration and CO2 re-assimilation in tomato leaves investigated with a reaction-diffusion model.A high throughput gas exchange screen for determining rates of photorespiration or regulation of C4 activity.Simple generalisation of a mesophyll resistance model for various intracellular arrangements of chloroplasts and mitochondria in C3 leaves.What is the most prominent factor limiting photosynthesis in different layers of a greenhouse cucumber canopy?Acclimation of C4 metabolism to low light in mature maize leaves could limit energetic losses during progressive shading in a crop canopy.Quantification of the effects of architectural traits on dry mass production and light interception of tomato canopy under different temperature regimes using a dynamic functional-structural plant model.Informing the improvement and biodesign of crassulacean acid metabolism via system dynamics modelling.Temperature Responses of C4 Photosynthesis: Biochemical Analysis of Rubisco, Phosphoenolpyruvate Carboxylase, and Carbonic Anhydrase in Setaria viridis.Improved method for measuring the apparent CO2 photocompensation point resolves the impact of multiple internal conductances to CO2 to net gas exchange.Phosphorus recycling in photorespiration maintains high photosynthetic capacity in woody species.Expanding knowledge of the Rubisco kinetics variability in plant species: environmental and evolutionary trends.Mesophyll cells of C4 plants have fewer chloroplasts than those of closely related C3 plants.Cell density and airspace patterning in the leaf can be manipulated to increase leaf photosynthetic capacity.Size matters for single-cell C4 photosynthesis in Bienertia.Dynamic modelling of limitations on improving leaf CO2 assimilation under fluctuating irradiance.Pyrenoid loss in Chlamydomonas reinhardtii causes limitations in CO2 supply, but not thylakoid operating efficiency.The influence of photosynthetic acclimation to rising CO2and warmer temperatures on leaf and canopy photosynthesis models
P2860
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P2860
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Steady-state models of photosynthesis.
@en
Steady-state models of photosynthesis.
@nl
type
label
Steady-state models of photosynthesis.
@en
Steady-state models of photosynthesis.
@nl
prefLabel
Steady-state models of photosynthesis.
@en
Steady-state models of photosynthesis.
@nl
P2860
P356
P1476
Steady-state models of photosynthesis.
@en
P2860
P304
P356
10.1111/PCE.12098
P577
2013-04-22T00:00:00Z