Stomatal conductance, usually measured in mmol m−2 s−1 by a porometer, estimates the rate of gas exchange (i.e., carbon dioxide uptake) and transpiration (i.e., water loss as water vapor) through the leaf stomata as determined by the degree of stomatal aperture (and therefore the physical resistances to the movement of gases between the air and the interior of the leaf).[1]
The stomatal conductance, or its inverse, stomatal resistance, is under the direct biological control of the leaf through its guard cells, which surround the stomatal pore. The turgor pressure and osmotic potential of guard cells are directly related to the stomatal conductance.
Stomatal conductance is a function of stomatal density, stomatal aperture, and stomatal size. Stomatal conductance is integral to leaf level calculations of transpiration. Multiple studies have shown a direct correlation between the use of herbicides and changes in physiological and biochemical growth processes in plants, particularly non-target plants, resulting in a reduction in stomatal conductance and turgor pressure in leaves.
For mechanism, see: Stomatal opening and closingStomatal conductance is a function of the density, size and degree of opening of the stomata; with more open stomata allowing greater conductance, and consequently indicating that photosynthesis and transpiration rates are potentially higher. Therefore, stomatal opening and closing has a direct relationship to stomatal conductance.
Light-dependent stomatal opening occurs in many species and under many different conditions. Light is a major stimulus involved in stomatal conductance, and has two key elements that are involved in the process: 1) the stomatal response to blue light, and 2) photosynthesis in the chloroplast of the guard cell. In C3 and C4 plants, the stomata open when there is an increase in light, and they close when there is a decrease in light. In CAM plants, however, the stomata open when there is a decrease in light.
For more details about CAM plant stomatal conductance, see: CAM Plants
Stomatal opening occurs as a response to blue light. Blue light activates the blue light receptor on the guard cell membrane which induces the pumping of protons out of the guard cell. This efflux of protons creates an electrochemical gradient that causes free floating potassium (K+) and other ions to enter the guard cells via a channel. This increase in solutes within the guard cells leads to a decrease in the osmotic potential of the cells, resulting in a decrease in water potential. Then, because water flows from a system with higher water potential to a system with lower water potential, water floods into the guard cells, causing the guard cells to become enlarged and therefore causes the stomata to open.
Studies showed that stomata responded greatly to blue light, even when in a red-light background (see Figure 1). In one study, the experiment began once stomatal opening had reached its saturation in red-light. Then, when blue light was added, stomatal opening increased even further, showing that a different photoreceptor system, stimulated by blue light, mediates the additional increases in opening.
The second key element involved in light-dependent stomatal opening is photosynthesis in the chloroplast of the guard cell. In response to carbon dioxide (CO2) entering the chloroplasts, photosynthesis occurs. This increases the amount of solutes that are being produced by the chloroplast which are then released into the cytosol of the guard cell. This causes a decrease in osmotic potential, causing a decrease in the water potential inside the guard cells. Again, this decrease in water potential causes water to enter into the guard cells. The guard cells subsequently swell up with water and the stomata is opened.
Recent studies have looked at the stomatal conductance of fast growing tree species to identify the water use of various species. Through their research it was concluded that the predawn water potential of the leaf remained consistent throughout the months while the midday water potential of the leaf showed a variation due to the seasons. For example, canopy stomatal conductance had a higher water potential in July than in October. The studies conducted for this experiment determined that the stomatal conductance allowed for a constant water use per unit leaf area.
Another study also showed that stomatal opening is dependent on guard cell photosynthesis. This was carried out by isolating guard cells that were localized to the lower surface of the Adiantum leaves used in the study. It was thus hypothesized that if guard cell chloroplasts are responsible for stomatal opening, it would be expected that light applied to the lower leaf surface would be much more effective at increasing stomatal conductance than light applied to the upper surface. And indeed, when red light was applied to the lower surface, stomatal conductance increased at a light intensity of <5 μmol m−2 s−1 and continued to increase with increasing light intensity, reaching a maximum at about 20 μmol m−2 s−1.
Nocturnal stomatal conductance (gn) across both C3 and C4 plants remains a highly researched topic, as the biological function of this phenomenon is ambiguous. Since photosynthesis does not occur at night, gn contributes to significant water loss at night without fixing any carbon in both C3 and C4 plants. Recent studies have compiled extensive literature/data sets that reveal relative growth rate is positively correlated with nocturnal stomatal conductance. However, gn does not directly correlate with positive growth; in fact, the direct effects of nocturnal stomatal conductance lead to higher transpiration rate, which decreases turgor pressure and consequently growth. Thus, it is likely that the indirect effects of gn are what lead to a positive growth rate, as predawn stomatal priming reduces the time it takes to reach complete stomatal responses to illumination. Further studies are needed to see how nocturnal stomatal conductance shortens the time to reach operating daytime stomatal conductance, and whether faster stomatal responses upon illumination correlate to an increase in carbon assimilation that lead to a significant contribution to the growth of the plant.[2]
Studies have shown that nocturnal conductance is not the result of stomatal leakiness. As there is extensive genetic variation across a variety of C3 and C4 plants, gn has most likely been selected for during evolution of said plants. Additionally, experiments have revealed that nocturnal stomatal conductance is regulated in an active manner, as there is a temporal change witnessed due to the presence of a circadian clock. Finally, it has been witnessed that gn declines during drought, demonstrating an active response to drought. These reasons disprove the theory that stomatal leakiness causing nocturnal stomatal conductance.
Lastly, there is not consistent evidence across various plant species that the main functions of gn are: to get rid of surplus CO2 (could limit growth), improve oxygen delivery, or aid in nutrient supply.
Regulating stomatal conductance is critical to controlling to the amount of transpiration, or water loss from the plant. Since over 95% of water loss comes directly from the stomatal pore, changes in stomatal resistance are critical to regulating water loss. Stomatal conductance also assists in the regulation of CO2 uptake from the atmosphere. Regulation of stomatal transcription is especially important when transcription rates are high. High transcription rates can lead to cavitation events, or when the tension in the xylem increases to the point where air bubbles begin to fill the xylem vessels. This is harmful to the plant because these air bubbles can block the flow of water up the xylem to the aerial parts of the plant. Recent studies have investigated the relationship between stomatal conductance, cavitation, and water potential. Cavitation events have been shown to decrease stomatal conductance while maintaining a stable water potential. In other words, cavitation events cause stomata to close to different extents. This limits transpiration and allows the plant to begin to repair the damaged, cavitated xylem.[3]
Similarly, some studies have explored the relationship between drought stress and stomatal conductance. Recent studies have found that drought resistant plants regulate their transpiration rate via stomatal conductance. The hormone ABA is triggered by drought conditions and can assist in closing the stomata. This minimizes water loss and allows the plant to survive under low water conditions. However, closing the stomates can also lead to low photosynthetic rates because of limited CO2 uptake from the atmosphere.[4]
Stomatal conductance can be measured in several ways:Steady-state porometers:A steady state porometer measures stomatal conductance using a sensor head with a fixed diffusion path to the leaf. It measures the vapor concentration at two different locations in the diffusion path. It computes vapor flux from the vapor concentration measurements and the known conductance of the diffusion path using the following equation:
| CvL-Cv1 | = | |
| Rvs+R1 |
| Cv1-Cv2 | |
| R2 |
CvL
Cv1
Cv2
Rvs
R1
R2
Rvs=
| 1-h1 | |
| h2-h1 |
R2-R1
Stomatal conductance is the reciprocal of resistance, therefore
gvs=
| 1 | |
| Rvs |
A dynamic porometer measures how long it takes for the humidity to rise from one specified value to another in an enclosed chamber clamped to a leaf. The resistance
R
\Deltat=
| \left(R+A\right)l\Deltah | |
| 1-h |
where ∆
t
h
h
l
A
Null balance porometers maintain a constant humidity in an enclosed chamber by regulating the flow of dry air through the chamber and find stomatal resistance from the following equation:
Rvs=
| A | \left( | |
| f |
| 1 | |
| h |
-1\right)-Rva
where
Rvs
Rva
A
f
h
The resistance values found by these equations are typically converted to conductance values.
A number of models of stomatal conductance exist.
The Ball-Berry-Leuning model was formulated by Ball, Woodrow and Berry in 1987, and improved by Leuning in the early 90s.[5] The model formulates stomatal conductance,
g
g=g0+
| a1An | |||||||||
|
where
g
g0
g
An
Ds
cs
\Gamma
a1
D0