PE EIE[R-Rg RESEARCH ON - HJ Andrews Experimental Forest
PE EIE[R-Rg RESEARCH ON - HJ Andrews Experimental Forest
PE EIE[R-Rg RESEARCH ON - HJ Andrews Experimental Forest
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where T = leaf temperature, ° K<br />
S = solar radiation, gcal cm-2 min<br />
Pn = net photosynthesis rate ,<br />
mg CO 2 (g dry wt)-1 hr 1<br />
(3i = parameters to be estimate d<br />
Equation 7 was derived from equation 8 and<br />
equation 9 :<br />
P(L)=a+b 1nS (8)<br />
which had been used to fit photosynthesis dat a<br />
from several herbaceous species (Blackman an d<br />
Rutter 1946, Blackman and Wilson 1951) .<br />
Equation 8 was coupled with equation 9 suggested<br />
by data of Pisek and Winkler (1958) ,<br />
Krueger and Ferrell (1965), and others :<br />
G(T) = a + bT + cT2 (9 )<br />
Data from two species of oak were obtained<br />
from infrared gas analysis and wer e<br />
used to estimate the parameters of equation 7<br />
by stepwise multiple regression analysis . Som e<br />
of the terms of equation 7 were nonsignificant,<br />
and were thus discarded . The final<br />
model was :<br />
Pn =Qo +(3 1 T+(3 2 In S+(3 5 T In S (10 )<br />
Having estimated the parameters of equation<br />
10, the model was used to predict photo -<br />
synthesis of oak in the field . Their model gav e<br />
fair to good agreement with subsequentl y<br />
measured net photosynthesis .<br />
In terms of the criteria discussed above ,<br />
equation 10 is generally inadequate . It doe s<br />
allow for interaction between two variables but<br />
fails to take into consideration other factor s<br />
that affect photosynthetic rate (stomatal behavior,<br />
micrometeorological conditions, plan t<br />
nutrition) . The model does satisfy the requirement<br />
that the Pn model be solved as a functio n<br />
of systems variables, that is, Pn = f [S, T] .<br />
In terms of the other criteria, the model fall s<br />
short of having a great deal of theoretica l<br />
validity in that the function is one of convenience<br />
rather than having general physicalchemical<br />
meaning . It is unnecessary to discuss<br />
in detail Botkin's model with respect to the<br />
other criteria . Like most photosynthesis models,<br />
it is specified at the leaf level, where th e<br />
inputs to the leaf are measured, and the<br />
relations between the leaf subsystems are<br />
inferred .<br />
While his model has many failings, it doe s<br />
have one virtue. If one were interested in<br />
comparing Pn = f[T,L] in two species under<br />
identical conditions, this model may be adequate,<br />
given that some other factor, e .g . ,<br />
stomatal resistance, is not limiting . The fact<br />
that the parameters of the model were estimated<br />
by least-squares allows the use o f<br />
statistical tests useful in comparing such data .<br />
Energy Budget Mode l<br />
Idso and Baker (1968) based their model of<br />
photosynthesis and their earlier model (Ids o<br />
and Baker 1967) on that of Gates (1965 )<br />
which is an energy budget model where precis e<br />
measurement of incoming radiant energy is<br />
equated with outgoing energy . Thus, at equilibrium,<br />
the amount of energy leaving a leaf i s<br />
equal to that coming in . Gates ' (1965) leaf<br />
energy budget model is :<br />
where<br />
(1 +r) (S + s) (<strong>Rg</strong>' +R a)<br />
as 2 +a t 2 (11 )<br />
-e taTZ ± C±LE= 0<br />
a s = mean total absorbance of plant to<br />
sunlight and skyligh t<br />
r = reflectance of underlying ground<br />
or plane surface to sunlight and<br />
skylight, S and s<br />
at = absorbance of plant to thermal<br />
radiation, <strong>Rg</strong> and Ra<br />
e t = emissivity of plant to thermal<br />
radiatio n<br />
Tl = leaf temperature ° K<br />
C = energy gained or lost by convection<br />
cal cm-2 min- 1<br />
L = latent heat of evaporation ca l<br />
cm-2 miri- l<br />
E = transpiration rate of leaf gm cal - 2<br />
min- 1<br />
S, s, <strong>Rg</strong>, Ra = various short and lon g<br />
wave radiation inputs ca l<br />
cm-2 min 1<br />
232