This paper describes the influence of the microclimate of a leaf and the stomatal exchange velocity (
Ds) on the sharing of net radiation between sensible and latent heat. Providing that a change in heat storage in the leaf and the energy fixed in photosynthesis are both nil, foliage Bowen ratio (β
f) is expressed as follows:
β
f1=(1+D
f/D
s)(φ
a+d/ΔT
f1)
-1, case 1
and β
f2=0.5(1+D
f/D
s)(φ
a+d/ΔT
f2)
-1, case 2
where
Df is the foliage exchange velocity (or leaf-air transfer coefficient) between the leaf surface and the surrounding air, φ
a the slope (mmHg/°C) at air temperature of the saturation vapour pressure vs. temperature curve,
d the saturation deficit (mmHg) and Δ
Tf the difference in temperature between leaf and air.
From the above equations, it is seen that for daytime conditions (larger positive Δ
Tf), increasing
Df and decreasing
Ds lead to increasing the foliage Bowen ratio. The above relations indicate also that the value of Bowen ratio for the leaf of case 1 is twice as much as that for the leaf of case 2. A hyperbolic relation between stomatal exchange velocity and radiation flux was used in model computations. As can be seen in Fig. 1, the value of foliage Bowen ratio increases or decreases with (1+D
f/D
s), depending on the sign of the temperature difference.
Fig. 2 shows that the dependence of the total latent heat transfer from the leaf on net radiation (
Sf) is largely affected by relative humidity in the air. In a relatively dry air, the percentage of the latent heat flux to net radiation decreases gradually with increasing net radiation. This result was found to be in good agreement with results obtained in a corn field (UCHIJIMA, UDAGAWA et al. 1969). The percentage decreases with increasing relative humidity in the air and becomes independent of net radiation in a saturated air. Fig. 3 indicates the increase in foliage Bowen ration with relative humidity in the air. This fact is due to the suppression of transpiration by increase in humidity.
The following equation is derived to relate the relative humidity at the leaf surface (foliage relative humidity
Rf) to the microclimate of the leaf and the stomatal exchange velocity.
R
f=D
s/D
f+D
s[1+D
f/D
sR
a{1+φ
aΔT
f/e(T
a)}
-1],
where
Ra is the relative humidity in the air and
e(Ta) the saturation vapour pressure (mmHg) at the air temperature. Curves in Fig. 4 were calculated for leaves of case 2 in a canopy where the air temperature was assumed to be 25°C and the foliage exhange velocity 0.5 and 1.0cm/sec, respectively. The decrease of the foliage relative humidity in a range of net radiation less than 0.15ly/min is thought to be caused by the closure of stomata due to low radiation intensity. In a range of net radiation higher than about 0.15ly/min, the foliage relative humidity decreases monotonically with increasing net radiation. In a sufficiently moist air (
Ra=90-100%), the foliage relative humidity is 65 to 95 per cent, always less than that in the surrounding air. The foliage relative humidity of the leaf is 55 to 70 per cent, in relatively dry air (
Ra=50%) showing that the foliage humdity is higher than that in the air.
In a middle range of the relative humidity of the air (
Ra=60-80%), the foliage relative humidity is greater or less than or equal to that in the air, depending upon the value of net radiation. Results obtained from heat balance analysis o
View full abstract