(A) Net CO2 assimilation of A. thaliana plants at 100 ppm CO2 and 20 μE light intensity, respectively. (B) Correlation in log2 changes in metabolite concentrations between plants shifted to either low light or to low CO2 concentrations. (C) Reduction of the glucose concentration in response to both low light- and low CO2-shift. (D) Log2 changes of selected amino acids 24 h after the shifts. Data are the mean of three (light-shift) or five (CO2-shift) biological replicates ± SD. The whole data set is given in S1 File.</p
This work investigates how the photoacclimated state at the onset of nitrogen starvation and the lig...
The atmospheric concentration of CO{sub 2}, a radiatively-active ({open_quotes}green-house{close_quo...
The exchange of CO2 in light was studied in plants of six divisions. The rates of CO2 uptake in ligh...
Experimental studies on CO(2) assimilation of mesophytic C3 plants in relation to relative water con...
Ornithine (A, B) accumulates exclusively in response to low CO2concentrations, arginine (C, D) accum...
International audiencePlants alternate between a net surplus of carbon in the light and a net defici...
The non-proteinogenic amino acid ornithine links several stress response pathways. From a previous s...
Measurement of the changes in CO2 uptake by single leaves following the abrupt onset of darkness wer...
The hypothesis for the present work was that photosynthetic acclimation to increased atmospheric CO2...
The responses of higher plants to rising carbon dioxide concentration in the atmosphere are strongly...
The non-proteinogenic amino acid ornithine links several stress response pathways. From a previous s...
The atmospheric CO2 concentration ([CO2]) is rapidly increasing and this may have substantial impact...
An analysis of elevated CO2 effects (2-4 times ambient) on dark respiration rate and carbon content ...
The extent to which Crassulacean acid metabolism (CAM) plant δ13C values provide an index of the pro...
The responses of long-term growth of plants under elevated CO2 have been studied extensively. Compar...
This work investigates how the photoacclimated state at the onset of nitrogen starvation and the lig...
The atmospheric concentration of CO{sub 2}, a radiatively-active ({open_quotes}green-house{close_quo...
The exchange of CO2 in light was studied in plants of six divisions. The rates of CO2 uptake in ligh...
Experimental studies on CO(2) assimilation of mesophytic C3 plants in relation to relative water con...
Ornithine (A, B) accumulates exclusively in response to low CO2concentrations, arginine (C, D) accum...
International audiencePlants alternate between a net surplus of carbon in the light and a net defici...
The non-proteinogenic amino acid ornithine links several stress response pathways. From a previous s...
Measurement of the changes in CO2 uptake by single leaves following the abrupt onset of darkness wer...
The hypothesis for the present work was that photosynthetic acclimation to increased atmospheric CO2...
The responses of higher plants to rising carbon dioxide concentration in the atmosphere are strongly...
The non-proteinogenic amino acid ornithine links several stress response pathways. From a previous s...
The atmospheric CO2 concentration ([CO2]) is rapidly increasing and this may have substantial impact...
An analysis of elevated CO2 effects (2-4 times ambient) on dark respiration rate and carbon content ...
The extent to which Crassulacean acid metabolism (CAM) plant δ13C values provide an index of the pro...
The responses of long-term growth of plants under elevated CO2 have been studied extensively. Compar...
This work investigates how the photoacclimated state at the onset of nitrogen starvation and the lig...
The atmospheric concentration of CO{sub 2}, a radiatively-active ({open_quotes}green-house{close_quo...
The exchange of CO2 in light was studied in plants of six divisions. The rates of CO2 uptake in ligh...