Physiological control of stomatal conductance (Gs) permits plants to balance CO2-uptake for photosynthesis (PN) against water-loss, so optimizing water use efficiency (WUE). An increase in the atmospheric concentration of carbon dioxide ([CO2]) will result in a stimulation of PN and reduction of Gs in many plants, enhancing carbon gain while reducing water-loss. It has also been hypothesized th...

Acclimation to CO2 enrichment was studied in maize plants grown to maturity in either 350 or 700 microl l-1 CO2. Plants grown with CO2 enrichment were significantly taller than those grown at 350 microl l-1 CO2 but they had the same number of leaves. High CO2 concentration led to a marked decrease in whole leaf chlorophyll and protein. The ratio of stomata on the adaxial and abaxial leaf surfac...

The short and long-term responses of flag leaf stomatal conductance (gs) and rate of photosynthesis (An) to elevated CO2 (757 μmol mol), 4 oC warmer temperatures and N supply were investigated in spring wheat (Triticum aestivum L. cv. Alcalá) crops grown in two seasons in field conditions under temperature gradient tunnels, in a Mediterranean environment. Plants grown at elevated CO2 had lower ...

Elevated carbon dioxide (CO2) in leaves closes stomatal apertures. Research has shown key functions of the β-carbonic anhydrases (βCA1 and βCA4) in rapid CO2-induced stomatal movements by catalytic transmission of the CO2 signal in guard cells. However, the underlying mechanisms remain unclear, because initial studies indicate that these Arabidopsis (Arabidopsis thaliana) βCAs are targeted to d...

Angiosperm and conifer tree species respond differently when exposed to elevated CO2, with angiosperms found to dynamically reduce water loss while conifers appear insensitive. Such distinct responses are likely to affect competition between these tree groups as atmospheric CO2 concentration rises. Seeking the mechanism behind this globally important phenomenon we targeted the Ca(2+)-dependent ...

In general, stomatal density (SD) decreases when plants are grown at high CO2 concentrations. Recent studies suggest that signals produced from mature leaves regulate the SD of expanding leaves. To determine the underlying driver of these signals in poplar (Populus trichocarpaxP. deltoides) saplings, a cuvette system was used whereby the environment around mature (lower) leaves could be control...

[1] Previous work suggests that the relationship between the carbon isotope composition of air (dCa) and plant leaf tissue (dCp) can be used to track changes in the carbon isotope composition of paleo-atmospheric CO2. Here we test this assertion in a series of experiments using the model plant Arabidopsis thaliana grown under a range of atmospheric CO2 concentrations relevant to geologic time (...