Beruflich Dokumente
Kultur Dokumente
D g1 r
c
=r
a
(6)
where D is the slope of the saturation vapor pressure curve
(kPa/8C), r the air density (kg/m
3
), C
p
the specic heat of dry air
at constant pressure (J/(kg K)), Dthe water vapor decit (kPa), r
a
the aerodynamic resistance (s/m) and r
c
is the surface canopy
resistance (s/m).
The surface canopy resistance r
c
, which depends on
climate factors and available soil water, can be expressed as
follows (Jarvis, 1976):
r
c
r
STmin
LAI
e
i
F
i
X
i
(7)
where r
STmin
is the minimal stomatal resistance of individual
leaves under optimal conditions (taken as 146 s/m). LAI
e
is the
effective LAI and equals to actual LAI for LAI 2, LAI/2 for
LAI ! 4, and 2 for intermediate values of LAI. X
i
is a specic
environmental variable, and F
i
(X
i
) is the stress function of X
i
,
with 0 F
i
(X
i
) 1. Ignoring the concentration of CO
2
, the
remaining environmental stress functions are as follows (Jar-
vis, 1976):
F
1
S
S
1100
_ _
1100 a
1
S a
1
_ _
(8)
F
2
T
T T
L
T
H
T
THa2=a2TL
a
2
T
L
T
H
a
2
THa2=a2TL
(9)
F
3
D e
a
3
D
(10)
F
4
u
1 u !u
F
u u
W
u
F
u
W
u
F
<u <u
W
0 u u
W
_
_
(11)
where S is the incoming photosynthetically active radiation
ux (W/m
2
), T the air temperature (K), u
F
is the soil water
content at eld capacity (cm
3
/cm
3
), u
W
the soil moisture con-
tent at wilting point (cm
3
/cm
3
), and u is the actual soil moist-
ure content in the root-zone (cm
3
/cm
3
). T
H
and T
L
are the
upper and lower temperature limits outside of which tran-
spiration is assumed to cease (8C) and are set at values of
40 and 0 8C (Harris et al., 2004). The a
1
, a
2
and a
3
, derived by
multi-variate optimization, are 57.67, 25.78 and 9.65, respec-
tively.
The aerodynamic resistance r
a
can be expressed as (Perrier,
1975a,b)
r
a
lnz d=h
c
d lnz d=z
0
k
2
u
(12)
where k is Karman constant (0.40), z the reference height (m),
h
c
is mean crop height (m), d the zero plane displacement (m),
u the wind speed at the reference height (m/s), and z
0
is the
roughness length of the crop relative to momentum transfer
(m).
Roughness length (z
0
) and zero plane displacement (d) are
dened as functions of crop height and leaf area index (LAI)
(Brenner and Incoll, 1997), given by
d 1:1h
c
ln1 X
0:25
(13)
z
0
z
0
0
0:3h
c
X
0:5
0 <X<0:2
0:3h
c
1 d=h
c
0:2 <X<1:5
_
(14)
where X = c
d
LAI, c
d
is the mean drag coefcient (taken as
0.07) (Brenner and Incoll, 1997), and z
0
0
is the roughness
length of bare soil surface (0.01 m) (Van Bavel and Hillel,
1976).
2.4.2. ShuttleworthWallace model
The ShuttleworthWallace (SW) model assumes that there is
blending of heat uxes from the leaves and the soil in the
mean canopy airow at the height of the effective canopy
source (Shuttleworth and Wallace, 1985). The SW model is
expressed as follows:
lET lE lT C
s
sw
PM
s
sw
C
p
sw
PM
p
sw
(15)
PM
s
sw
DA
sw
rC
P
D Dr
s
a
A
sw
A
s
sw
=r
a
a
r
s
a
D g1 r
s
s
=r
a
a
r
s
a
(16)
PM
p
sw
DA
sw
rC
P
D Dr
p
a
A
s
sw
=r
a
a
r
p
a
D g1 r
p
s
=r
a
a
r
p
a
(17)
C
s
sw
1
1 R
s
sw
R
a
sw
=R
p
sw
R
s
sw
R
a
sw
(18)
Fig. 1 Spatial variation of soil water content at 0100 cm
soil profile after irrigation (28 May 2006).
a g r i c ul t ur a l a nd f or e s t me t e o r o l og y 1 4 8 ( 2 0 0 8 ) 1 6 2 9 1 6 4 0 1632
C
p
sw
1
1 R
p
sw
R
a
sw
=R
s
sw
R
p
sw
R
a
sw
(19)
R
s
sw
D gr
s
a
gr
s
s
(20)
R
p
sw
D gr
p
a
gr
p
s
(21)
R
a
sw
D gr
a
a
(22)
where lE is the latent heat ux of evaporation from the soil
surface (W/m
2
), lT the latent heat of transpiration from
canopy (W/m
2
), r
p
s
the canopy resistance (s/m), r
p
a
the aero-
dynamic resistance of the canopy to in-canopy ow (s/m), r
s
s
the soil surface resistance (s/m), r
a
a
and r
s
a
the aerodynamic
resistances from the reference height to in-canopy heat
exchange plane height and from there to the soil surface (s/
m), respectively, A
sw
andA
s
sw
are the total available energy and
the available energy to the soil (W/m
2
), respectively, which are
dened as follows:
A
sw
R
n
G (23)
A
s
sw
R
s
nsw
G (24)
where R
s
nsw
is net radiation uxes into the soil surface
(W/m
2
).
The radiation reaching the soil surface can be calculated
using Beers law as follows:
R
s
nsw
R
n
expCLAI (25)
where C is the extinction coefcient of light attenuation, 0.68
for fully grown plant (Sene, 1994). And the extinction coef-
cient is 0 for bare soil and 0.24 for the experimental vineyard
by the linear interpolation when the vegetative cover of vine-
yard is 0.35.
2.4.2.1. Canopy resistance. The canopy resistance r
p
s
is related
to environmental variables (Jarvis, 1976):
r
p
s
r
STmin
LAI
e
i
F
i
X
i
(26)
where the parameters are computed in Eqs. (8)(11).
2.4.2.2. Aerodynamic resistances. The aerodynamic resis-
tances r
a
a
and r
s
a
are calculated from the vertical wind prole
at the eld and the eddy diffusion coefcient. Above the
canopy height, the eddy diffusion coefcient (K) is given by
K ku
z d (27)
where u
*
is the friction velocity (m/s).
Beneath the canopy height, the exponential decrease of the
eddy diffusion coefcient (K) through the canopy is given as
follows:
K K
h
exp n 1
z
n
_ _ _ _
(28)
where K
h
is the eddy diffusion coefcient at the top of canopy
(m
2
/s), and n is the extinction coefcient of the eddy diffusion.
Brutsaert (1982) indicated that n = 2.5 when h
c
< 1 m; n = 4.25
whenh
c
> 10 m. Inour study, n = 2.6 by the linear interpolation
when h
c
is 1.5 m. K
h
is determined as follows:
K
h
ku
h
c
d (29)
The aerodynamic resistances r
a
a
and r
s
a
are obtained by
integrating the eddy diffusion coefcients from the soil
surface to the level of the preferred sink of momentum in
the canopy, and from there to the reference height (Shuttle-
worth and Gurney, 1990), as follows:
r
a
a
1
Ku
ln
z d
h
c
d
_ _
h
c
nK
h
exp n 1
z
0
d
h
c
_ _ _ _
1
_ _
(30)
r
s
a
h
c
expn
nK
h
exp
nz
0
0
h
c
_ _
exp n
z
0
d
h
c
_ _ _ _ _ _
(31)
The bulk boundary layer resistance of canopy is calculated
as (Shuttleworth and Wallace, 1985)
r
p
a
r
b
2LAI
(32)
where r
b
is the meanboundary layer resistance (s/m), takenfor
50 s/m (Brisson et al., 1998).
2.4.2.3. Soil surface resistance. The soil surface resistance (r
s
s
)
is the resistance to water vapor movement fromthe interior to
the surface of the soil, and is assumed to depend strongly on
the water content of an upper soil surface layer (u
s
). The soil
surface resistance was calculated as (Anadranistakis et al.,
2000)
r
s
s
r
s
s min
f u
s
(33)
where r
s
s min
is the minimum soil surface resistance, which
corresponds to soil moisture at eld capacity and its value is
assumed equal to 100 s/m (Camillo and Gurney, 1986; Thomp-
son et al., 1981), u
s
is the water content of an upper soil surface
layer (cm
3
/cm
3
).
According to Thompson et al. (1981), f(u
s
) is approximately
expressed as follows:
f u
s
2:5
u
F
u
s
_ _
1:5 (34)
2.4.3. Clumping model
The Clumping (C) model, based on SW model, separates the
soil surface into fractional areas inside and outside the
inuence of the canopy. This model can be expressed as
follows (Brenner and Incoll, 1997):
lET lE
s
lE
bs
lT
f C
s
c
PM
s
c
C
p
c
PM
p
c
1 f C
bs
c
PM
bs
c
(35)
where lE
s
is the latent heat of evaporation fromsoil under the
plant (W/m
2
), lE
bs
the latent heat of evaporation frombare soil
(W/m
2
), f is the fractional vegetative cover and is about 0.35
over the whole growing season. The terms used in Eq. (35) are
expressed as
PM
p
c
DA
c
rC
p
D Dr
p
a
A
s
c
=r
a
a
r
p
a
D g1 r
p
s
=r
a
a
r
p
a
(36)
a g r i c ul t ur a l a nd f o r e s t me t e o r ol o gy 1 4 8 ( 2 0 0 8 ) 1 6 2 9 1 6 4 0 1633
PM
s
c
DA
c
rC
p
D Dr
s
a
A
p
c
=r
a
a
r
s
a
D g1 r
s
s
=r
a
a
r
s
a
(37)
PM
bs
c
DA
bs
c
rC
p
D=r
a
a
r
bs
a
D g1 r
bs
s
=r
a
a
r
bs
a
(38)
C
s
c
R
bs
c
R
p
c
R
s
c
R
a
c
=R
s
c
R
p
c
R
bs
c
1 f R
s
c
R
p
c
R
a
c
fR
bs
c
R
s
c
R
a
c
fR
bs
c
R
p
c
R
a
c
(39)
C
p
c
R
bs
c
R
s
c
R
p
c
R
a
c
=R
s
c
R
p
c
R
bs
c
1 f R
s
c
R
p
c
R
a
c
fR
bs
c
R
s
c
R
a
c
fR
bs
c
R
p
c
R
a
c
(40)
C
bs
c
R
s
c
R
p
c
R
bs
c
R
a
c
=R
s
c
R
p
c
R
bs
c
1 f R
s
c
R
p
c
R
a
c
fR
bs
c
R
s
c
R
a
c
fR
bs
c
R
p
c
R
a
c
(41)
R
s
c
D gr
s
a
gr
s
s
(42)
R
p
c
D gr
p
a
gr
p
s
(43)
R
bs
c
D gr
bs
a
gr
bs
s
(44)
R
a
c
D gr
a
a
(45)
where A
c
, A
p
c
, A
s
c
and A
bs
c
are energy available to evapotran-
spiration, to the plant, to soil under shrubandbare soil (W/m
2
),
respectively, r
bs
a
the eddy diffusion resistances fromin-canopy
heat exchange plane height to the soil surface (s/m), r
bs
s
the soil
surface resistance of bare soil (s/m).
2.4.3.1. Available energy. The incoming radiation (R
n
) is
divided into the radiation absorbed by the plant (R
p
n
) and the
radiation absorbed by the soil (R
s
n
). If the energy stored in the
plant is assumed to be negligible, then:
R
s
nc
R
n
e
CLAI= f
(46)
R
p
nc
R
n
R
s
nc
(47)
A
s
c
R
s
nc
G
s
(48)
A
bs
c
R
n
G
bs
(49)
A
p
c
R
p
nc
(50)
where R
p
nc
and R
s
nc
are the radiation absorbed by the plant and
the radiation absorbed by the soil (W/m
2
), respectively, G
s
and
G
bs
the ground heat ux under plant and bare soil (W/m
2
),
respectively, C is the extinctioncoefcient of light attenuation,
0.68 for fully grown plant (Sene, 1994).
2.4.3.2. Resistance for clumping model. The Clumping (C)
model, based on the SW model, newly introduces the
resistance of the bare soil surface (r
bs
s
) and the aerodynamic
resistance between the bare soil surface and the mean surface
owheight (r
bs
a
). The resistance of the bare soil surface (r
bs
s
) can
be calculated using Eqs. (33) and (34), but in which soil water
content is the water content of bare soil surface. The
aerodynamic resistance between the bare soil surface and
the mean surface ow height (r
bs
a
) can be calculated by
assuming that the bare soil surface is totally unaffected by
adjacent vegetation so that its aerodynamic resistance equals
r
b
a
, which is dened by
r
b
a
ln
z
m
=z
0
0
2
k
2
u
m
(51)
where z
m
is the mean surface ow height (m), which is
assumed 0.75h
c
(Brenner and Incoll, 1997), and u
m
is the wind
speed at z
m
(m/s).
Actual aerodynamic resistance (r
bs
a
) varies between r
b
a
and
r
s
a
. Since the form of the functional relationship of this change
is not known, r
bs
a
varied linearly between r
b
a
and r
s
a
as f varies
from 0 to 1 (Brenner and Incoll, 1997). Moreover, the
calculation of other resistance is similar to those of SW
model.
2.5. Evaluation of model performance
In this study, we decided to use four statistics following
recommendations by Legates and McCabe (1999) and they
are: the modied coefcient of efciency (E
1
), the modied
index of agreement (d
1
), mean absolute error (MAE) and the
mean (
P) between the methods. The modied coefcient (E
1
)
is dened as
E
1
1:0
N
i1
jQ
i
P
i
j
N
i1
jQ
i
Qj
(52)
where Q
i
is observed value,
Q the mean observed value, P
i
modeled value. The modied index of agreement (d
1
) is given
by
d
1
1:0
N
i1
jQ
i
P
i
j
N
i1
jQ
i
Qj jP
i
Qj
(53)
3. Results and discussion
3.1. Micro-climate parameters and reference
evapotranspiration
Mostly days of the growing season were observed with daily
values of R
s
and R
n
between 3.5029.90 MJ/(m
2
d) and 1.58
17.96 MJ/(m
2
d), and the ratio of R
n
0.410.80 (Fig. 2a).
Atmospheric conditions at the vineyard were very dry
and hot where average values of T
a
, D and u were between
6.8 and 25.1 8C, 0.14 and 2.16 kPa and 0.13 and 2.40 m/s,
respectively (Fig. 2b, c and d). The maximum ratio of R
n
was
measured in July and August, July and August were also the
months with the frequent precipitation, about 127 mm. The
maximum diurnal D and T
a
were 4.754 kPa and 36.3 8C.
Reference evapotranspiration (ET
0
), estimated by the Pen-
manMonteith equation (Allen et al., 1998), during the whole
growing season was 499 mm. Monthly reference ET
0
was
highest in June with 123 mm while reference ET
0
appeared to
be lowest in September with 59 mm (Fig. 2e).
a g r i c ul t ur a l a nd f or e s t me t e o r o l og y 1 4 8 ( 2 0 0 8 ) 1 6 2 9 1 6 4 0 1634
3.2. Comparison of evapotranspiration measured by the
Bowen ratio-energy balance and soil water balance methods
Daily average evapotranspiration (ET) calculated over 7-day
periods using the soil water balance method (ET
WB
) was
compared with the corresponding daily average ET measured
by the Bowen ratio-energy balance method (ET
BREB
) as shown
in Fig. 3. The regression equation between ET
BREB
and ET
WB
was ET
BREB
= 0.9817ET
WB
(R
2
= 0.7664). The regression was not
statistically different from line 1:1 and the root mean squared
error (RMSE) between the two methods was 0.37 mm per day,
indicating a good agreement between the estimated ET by the
two methods. During the whole growing season, the LAI was
02 m
2
/m
2
and f was about 0.35, thus the measured ET
variation by the BREB method could be used as the standard
value to judge the estimated daily ET fromthe PM, SWand C
models. However, these results did not fully mean that the
BREB method was going to work properly on a 30-min periods,
because (1) this study did not take into account the effect of
shade of rows during the course of the day (Spano et al., 2000).
So, there were potential errors in the measurement of G on 30-
minperiod. However, ondaily basis, these errors were not very
important because daily cumulative values of G always were
close to zero. (2) Overestimation could be counterbalanced by
underestimation during daytime or the nighttime. It could
have important errors in the estimation of vineyard ET on 30-
min time intervals, especially under advection conditions.
Some reports also showed that most of the cases in which the
BREB method fails appear in the evening, during the night and
in the early morning or under advection condition (Unland
et al., 1996; Perez et al., 1999; Rana and Katerji, 2000). The
errors on 30-min period of BREB will be discussed based on
eddy covariance and heat pulse method in our further study.
Although the BREB method may have errors in the estimation
of vineyard ET on 30-min intervals, the reliable measured ET
by BREB could be provided adopting the certain criteria for
rejecting inaccurate data (Perez et al., 1999). Therefore, the
measured ET variation by the BREB method was still used as
the standard value to judge the estimated ET from the
evapotranspiration models. Many related studies also showed
Fig. 2 Daily value of solar radiation (R
s
), net radiation (R
n
),
air temperature (T
a
), vapor pressure deficit (D), wind speed
(u) and reference evapotranspiration (ET
0
) under different
rainfall and irrigation conditions during the growing
period in 2006.
Fig. 3 Comparison of average daily evapotranspiration
(ET) estimated by the Bowen ratio-energy balance and soil
water balance methods. *, data from 10 May to 6 October
2005; *, data from 19 May to 7 October 2006. ET
BREB
,
measured evapotranspiration by the Bowen ratio-energy
balance method, ET
WB
, measured evapotranspiration by
soil water balance method.
a g r i c ul t ur a l a nd f o r e s t me t e o r ol o gy 1 4 8 ( 2 0 0 8 ) 1 6 2 9 1 6 4 0 1635
that the BREB method can be used to validate the estimated ET
by models (Alves and Pereira, 2000; Kato et al., 2004; Mo, 1998;
Mo et al., 2000; Ortega-Farias et al., 1995; Rana et al., 1997b).
3.3. Comparison of estimated evapotranspiration by three
models and measured by Bowen ratio-energy balance method
3.3.1. Comparison of diurnal estimated and measured
evapotranspiration
Comparison and correlation between estimated diurnal ET by
the PM, SW and C models over 30-min period and measured
ET by the Bowen ratio-energy balance during the growing
period in 2006 are shown in Figs. 4 and 5 and Table 1. Fig. 4
shows that diurnal pattern of the evapotranspiration esti-
mated by the three models was similar to that of the measured
ET by the BREB, but there existed differences in the
magnitudes. The estimated ET from the C model was close
to the observed ET by the BREB, but the ET fromthe PMmodel
overestimated signicantly, especially in the midday under
clear sky conditions. The slopes of regression equation during
the whole growing period between the estimated ET from the
PM model and measured ET by the BREB was 1.29, with MAE
of 56.95 W/m
2
, E
1
of 0.205 and d
1
of 0.686, indicating that the P
M model overestimated the evapotranspiration signicantly
(Table 1). Ortega-Farias et al. (2006) also indicated that the PM
model overestimated on 20-min time intervals compared to
the measured ET by the BERB. During the period between11:00
and16:00 inthe sunny days, the PMmodel estimated daytime
variation of evapotranspiration with maximal relative error of
20.5%, which was in line with our result. The possible reasons
for the evapotranspiration overestimated by PM model are
the following: (1) the dry layer formed in the soil surface under
intensive radiation and inadequate soil water content will
sharply increase the surface resistance and prevent soil water
from evaporation in the furrow-irrigated vineyard of arid
desert oasis. Although total ET slightly increases with the
intensive solar radiation and greater vapor pressure decit, it
will be lower than the evapotranspiration determined by
meteorological variables. Thus the PM model overestimates
evapotranspiration because the surface canopy resistance in
the model cannot perfectly include the integrated canopy and
soil surface resistances. (2) Because vineyard was irrigated by
furrow irrigation, the dry layer formed in the soil surface
between the ridges, thus the surface resistance in the ridge
Fig. 4 The diurnal patterns of estimated
evapotranspiration from the PM, SW and C models over
30-min period and measured evapotranspiration by the
BREB method. The set of data is the average values of three
typical sky clear days.
Fig. 5 Comparison of estimated evapotranspiration from
the PM, SW and C models over 30-min period and the
measured by the BREB method from 1 May to 7 October
2006. lET
PM
, lET
SW
and lET
C
represent the estimated
evapotranspiration from PM, SW and C models,
respectively. lET
BREB
represents the measured
evapotranspiration by the Bowen ratio-energy balance
method.
a g r i c ul t ur a l a nd f or e s t me t e o r o l og y 1 4 8 ( 2 0 0 8 ) 1 6 2 9 1 6 4 0 1636
was far greater than the canopy resistance, which resulted in
the partition proportion of soil surface available energy into
the latent heat ux lower than that of canopy available energy
into the latent heat ux. However, the canopy resistance
model does not sufciently reect the change of leaf and soil
water condition and energy partition, leading to lower canopy
resistance, therefore, all available energy into the canopy in P
M model will overestimate the evapotranspiration. (3) The
vegetation cover of vineyard is very low, not meeting the
assumptions of the PM model.
However, some studies indicated the PM model under-
estimated ET in the early stage of crop, but the performance of
the PMmodel was goodinthe vigorous stage (Kato et al., 2004).
Suchdifference may also result fromthe canopy resistance and
soil water status. Inthe experiment of Katoet al. (2004), a sparse
canopy with full irrigation resulted in higher soil water content
and lower soil surface resistance, generally lower than the
canopy resistance. But in our experiment, because the furrow-
irrigated vineyard of arid desert oasis reduced the area of wet
soil, soil surface resistance (about 800 s/m of dry soil) was
generally higher than the canopy resistance (about 300 s/m
during the day), which resulted in ET difference fromthe result
of Katoet al. (2004). Stannard(1993) alsoindicatedthat whenthe
surface canopy resistance was much greater than the soil
surface resistance, the PMmodel severely underestimated the
evapotranspiration. Therefore, when the PM model is applied
to some specic crops and places, the relationship between the
canopy resistance in the model and environmental variables
and the value of canopy resistance will vary (Jarvis, 1976). For
sparsely vegetated canopies, the surface canopy resistance will
also include the effect of soil evaporation (Shuttleworth and
Wallace, 1985).
Since soil surface resistance was newly introducedinthe S
W and C models, thus the two models could better reect the
actual soil evaporation. The estimates of evapotranspiration
from the SW and C models were better than that from the P
M(Figs. 4 and 5 and Table 1). The slopes of regression equation
was 1.22, with MAE of 38.69 W/m
2
, E
1
of 0.460 and d
1
of 0.751,
indicating that the estimated ET by the SW model was
slightly greater than the measured ET. The estimates of
evapotranspiration from the C model were in good agreement
with the measurements, and the slopes of regressionequation
betweenthe estimated ET fromthe C model and the measured
ETby the BREBmethodwas 0.99, withMAE of 31.78 W/m
2
, E
1
of
0.556 andd
1
of 0.779. Therefore, the estimatedETfromthe SW
and C models, especially from the C model agreed well with
the measured ET.
The estimates of evapotranspiration from the SW and C
models agreed well with the measurements mainly because
these models acknowledged the differences between soil
evaporation and plant transpiration (0.57 and 0.54 of T/ET by
SW and C models, respectively). Some studies also indicated
that in the sparsely vegetated canopies, the SW and C model
estimates evapotranspiration well (Brenner and Incoll, 1997;
Domingo et al., 1999; Farahani and Bausch, 1995; Farahani and
Ahuja, 1996; Stannard, 1993; Teh et al., 2001). However, there
still existedthe difference betweenthe estimates fromthe two
models and the BREB measurements. Such difference may
result from the effect of canopy resistance and soil surface
resistance andthe inaccurate estimates of energy components
in the vegetation and soil. The reasons for the inaccurate
estimates of energy components are that: (1) the SW and C
models do not include the difference of the reectivity and
long-wave radiation between soils and canopy. Brenner and
Incoll (1997) indicated that the maximal difference of long-
wave radiation between the canopy and bare soil was about
100 W/m
2
. (2) The canopy intercept model for solar radiationis
simpler because the diurnal variation of shallowtime and area
of vineyard soil surface is not included (Zhang et al., 2001).
Brenner and Incoll (1997) assumed that the fractional shadow
area only corresponds to the vegetative cover when the sun
was directly overhand. At other times f will be larger, thus only
f usedinthe Cmodel is too simpler to describe bare soil surface
area, which also lead to the errors in the estimates of energy
components. (3) The interaction of different energy compo-
nents will affect energy ux greatly. Ham and Heilman (1991)
indicated that about 1/3 of the sensible heat ux is used for
cotton transpiration. Heilman et al. (1994) also had similar
result for grape vine inTexas, USA. Therefore, the predictedET
for the SW and C model has some differences from the
measured value by the BREB method.
Among the PM, SWandCmodels, the estimated ETby the
C model coincided closely with the BREB measurements,
which could be suitable for estimating the vineyard ET in the
region. Furthermore, the model can separate the evaporation
from soil and the transpiration from plants, thus the models
could be used to study the water use of grapevines.
3.3.2. Comparison of diurnal estimated and measured
evapotranspiration after a rainfall
The effect of rainfall on diurnal evapotranspiration was
simulated by the three models (Fig. 6). Fig. 6 shows that the
SW and C models tended to follow the general trend of
measured ET whereas the PM model underestimated the
midday ET. Because the only computational mechanisms the
PM model used to increase ET after a rainfall were a slightly
increased value of net radiation and a decreased value of
canopy resistance due to a decreased value of D. However, the
Table 1 Correlation between the estimated evapotranspiration of vineyard by three models over 30-min period and the
measured evapotranspiration by Bowen ratio-energy balance during the growing period in 2006
Model Regressive equation E
1
d
1
MAE
Q
P
PM lET
PM
= 1.29lET
BREB
0.205 0.686 56.95 61.69 100.88
SW lET
SW
= 1.22lET
BREB
0.460 0.751 38.69 61.69 90.38
C lET
C
= 0.99lET
BREB
0.556 0.779 31.78 61.69 73.65
lET
PM
, lET
SW
and lET
C
are the respective estimated evapotranspiration of vineyard from PM, SW and C models, lET
BREB
is the measured
evapotranspiration by the Bowen ratio-energy balance. E
1
is the modied coefcient of efciency; d
1
is the modied index of agreement; MAE is
the mean absolute error,
Q is the mean of lET measured by the BREB, and P is the mean of lET estimated from three models.
a g r i c ul t ur a l a nd f o r e s t me t e o r ol o gy 1 4 8 ( 2 0 0 8 ) 1 6 2 9 1 6 4 0 1637
decreased value of D also decreased the aerodynamic term,
which tended to decrease ET (Stannard, 1993). The SW and C
models explicitly accounted for bare soil evaporation after a
rainfall, thus the performances of the SW and C models were
better.
3.3.3. Comparison of diurnal estimated and measured
evapotranspiration after a frost
The diurnal patterns of estimated ET fromthe PM, SWand C
models and measuredETby the BREBmethod, after a frost, are
shown in Fig. 7. It can be seen that although the C model
generally performed well, its performance after a frost varied.
The C model (including the PM and SW models) severely
overestimated the measure value of evapotranspiration.
Because after a frost, plants might suffer chill injury,
characterized by destruction of the plants membrane and
cell framework, which inhibited or destroyed enzyme activa-
tion (Li et al., 2003), the actual value of stomata resistance was
virtually signicantly increased and the transpiration
decreased. However, the model value of stomata resistance
did not fully reect the change of grapevine stomata
resistance, which will underestimate stomata resistance
and overestimate ET value of grapevine in our study.
4. Conclusions
Insummary, the following conclusions canbe drawnfromthis
study:
(1) The Bowen ratio-energy balance method could provide
accurate estimates of vineyard ET from the arid desert
region when the Bowen ratio instrument was appropri-
ately installed on the corresponding equilibrium layer to
the evapotranspiration surface to avoid the possible heat
circulation between the studied area and adjacent dry
environment area.
(2) Generally, the diurnal variation of the estimated ET by the
PM, SW and C models was similar to those measured by
the BREB method. The estimated ET from the SW and C
models, especially from the C model agreed well with the
measured ET by the BREB, but the PM model signicantly
overestimated the ET. After a rainfall, the soil was wet, the
performances of the SW and C models were also good.
Therefore, among the three models, the C model was the
optimal model in simulating the vineyard ET in the arid
region of northwest China.
(3) Although the C model performed well after a rainfall, it
signicantly overestimated the ET after a frost because the
canopy resistance did not fully reect the dramatic
decrease of grapevine transpiration.
Acknowledgements
We are grateful for the grant support from nancial support
from the Chinese National Natural Science Fund (50679081,
50528909), the National High-Tech 863 Project of China
(2006AA100203) and PCSIRT (IRT0657).
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