Measured profiles of photosynthetic capacity in plant crowns typically do not match those of average irradiance: the ratio of capacity to irradiance decreases as irradiance increases. This differs from optimal profiles inferred from simple models. To det
Light absorption and use efficiency (LAUE mol mol−1, daily gross photosynthesis per daily incident l...
Aims This paper reviews the way optimization theory has been used in canopy models to analyse the ad...
Plants respond to nitrogen availability by changing their root : shoot ratios. One hypothesis used t...
Measured profiles of photosynthetic capacity in plant crowns typically do not match those of average...
Optimization theory in combination with canopy modeling is potentially a powerful tool for evaluatin...
A long-established theoretical result states that, for a given total canopy nitrogen (N) content, ca...
Optimization models of stomatal conductance (g(s)) attempt to explain observed stomatal behaviour in...
From photosynthetic studies on a range of monocotyledonous (C-3 and C-4) and dicotyledonous (C-3) pl...
1. The significance for whole-plant carbon gain of plasticity in between-leaf and within-leaf partit...
Earth system models (ESMs) use photosynthetic capacity, indexed by the maximum Rubisco carboxylation...
Earth system models (ESMs) use photosynthetic capacity, indexed by the maximum Rubisco carboxylation...
There is a strong natural light gradient from the top to the bottom in plant canopies and along gap-...
<p>The squared difference between measured <i>N</i><sub>a</sub> and predicted <i>N</i><sub>ac</sub> ...
Maximum quantum yield for leaf CO2 assimilation under limiting light conditions (UCO2LL) is commonly...
The primary function of stomata is to minimise plant water loss while maintaining CO2 assimilation. ...
Light absorption and use efficiency (LAUE mol mol−1, daily gross photosynthesis per daily incident l...
Aims This paper reviews the way optimization theory has been used in canopy models to analyse the ad...
Plants respond to nitrogen availability by changing their root : shoot ratios. One hypothesis used t...
Measured profiles of photosynthetic capacity in plant crowns typically do not match those of average...
Optimization theory in combination with canopy modeling is potentially a powerful tool for evaluatin...
A long-established theoretical result states that, for a given total canopy nitrogen (N) content, ca...
Optimization models of stomatal conductance (g(s)) attempt to explain observed stomatal behaviour in...
From photosynthetic studies on a range of monocotyledonous (C-3 and C-4) and dicotyledonous (C-3) pl...
1. The significance for whole-plant carbon gain of plasticity in between-leaf and within-leaf partit...
Earth system models (ESMs) use photosynthetic capacity, indexed by the maximum Rubisco carboxylation...
Earth system models (ESMs) use photosynthetic capacity, indexed by the maximum Rubisco carboxylation...
There is a strong natural light gradient from the top to the bottom in plant canopies and along gap-...
<p>The squared difference between measured <i>N</i><sub>a</sub> and predicted <i>N</i><sub>ac</sub> ...
Maximum quantum yield for leaf CO2 assimilation under limiting light conditions (UCO2LL) is commonly...
The primary function of stomata is to minimise plant water loss while maintaining CO2 assimilation. ...
Light absorption and use efficiency (LAUE mol mol−1, daily gross photosynthesis per daily incident l...
Aims This paper reviews the way optimization theory has been used in canopy models to analyse the ad...
Plants respond to nitrogen availability by changing their root : shoot ratios. One hypothesis used t...
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