Aquacrop: Calculation Procedures
Aquacrop: Calculation Procedures
Calculation procedures
AquaCrop
Version 7.1
Reference manual
August 2023
Chapter 3
Calculation procedures
AquaCrop
Version 7.1
Reference manual
August 2023
By Dirk RAES, Pasquale STEDUTO, Theodore C. HSIAO, and Elias FERERES with the
contribution of the AquaCrop Network
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Chapter 1. AquaCrop – FAO crop-water productivity model to
simulate yield response to water
Chapter 2. Users guide
3.12 Partition of biomass into yield part (yield formation) .............................. 133
3.12.1 Reference Harvest Index (HIo) ............................................................................................ 134
3.12.2 Building up of Harvest Index .............................................................................................. 134
▪ Building up of Harvest Index for leafy vegetable crops..................................................... 134
▪ Building up of Harvest Index for root/tuber crops ............................................................ 135
▪ Building up of Harvest Index for fruit/grain producing crops ........................................... 136
3.12.3 Adjustment of HIo for inadequate photosynthesis............................................................. 137
3.12.4 Adjustment of HIo for water stress before the start of yield formation............................ 138
3.12.5 Adjustment of HIo for failure of pollination (only for fruit/grain producing crops) ........... 141
▪ Flowering ........................................................................................................................... 141
▪ Failure of pollination ......................................................................................................... 141
3.12.6 Adjustment of HIo for water stress during yield formation................................................ 145
▪ Upward adjustment of HIo................................................................................................. 145
▪ Downward adjustment of HIo ............................................................................................ 147
▪ Combined effect on HIo ..................................................................................................... 148
3.12.7 Total effect of water and temperature stress on the Harvest Index ................................. 149
3.12.8 Crop dry yield (YW) in weed infested fields........................................................................ 151
3.12.9 Dry and Fresh yield ........................................................................................................ 151
3.16 Simulation of the combined effect of soil fertility and soil salinity stress
................................................................................................................................ 162
References ............................................................................................................. 163
Annexes
I. Crop parameters
II. Indicative values for lengths of crop development stages
III. Indicative values for soil salinity tolerance for some agriculture crops
IV. ETo Calculation procedures
AquaCrop is a general model, in that it is meant for a wide range of herbaceous crops,
including forage, vegetable, grain, fruit, oil, and root and tuber crops.
Examples of crop development and production for specific climate and growing conditions
estimated by AquaCrop are given in a lot of papers published in peer reviewed journals. A
digital library of references to all AquaCrop publications can be found on:
[Link]
A set of training videos are posted in an ‘AquaCrop training’ channel of YouTube. The list
of videos is provided in Chapter 5 of the AquaCrop Reference Manuel. For the playlist go
the AquaCrop website of FAO: [Link]
atmosphere
air
rainfall
ETo temperature
CO2
(b)
GDD
CC CCpot
CCact
(a) 1
1
time
evapo- irrigation
rainfall
Zr
transpiration
surface
runoff 2 Trans-
piration
soil field capacity (f)
w ater WP*
balance (c)
wilting point
(d) 3 Biomass
capillary deep
rise percolation
(g)
HI
(e)
groundw ater table 4 Yield
Figure 1. – Calculation scheme of AquaCrop with indication of the 4 steps, and the
processes (dotted arrows) affected by water stress (a to e) and temperature stress (f
to g). CC is the green canopy cover; Zr the rooting depth; ETo the reference
evapotranspiration; WP* the normalized biomass water productivity; HI the harvest index;
and GDD the growing degree day.
Water stress: (a) slows canopy expansion, (b) accelerates canopy senescence, (c) decreases root
deepening but only if severe, (d) reduces stomatal opening and transpiration, and (e) affects harvest
index. Cold temperature stress (f) reduces crop transpiration. Hot or cold temperature stress (g)
inhibits pollination and reduces HI. AquaCrop considers also the effect of weed infestation,
soil fertility and soil salinity stress on canopy development, crop transpiration and biomass
production.
0.0
field capacity
Dr
(mm)
(mm)
TAW
permanent Wr
wilting point
0.0
capillary (DP)
rise deep
(CR) percolation
Water is added to the soil reservoir by rainfall and irrigation. When the rainfall intensity is
too high, part of the precipitation might be lost by surface runoff and only a fraction will
infiltrate. The infiltrated water cannot always be retained in the root zone. When the root
zone is too wet, part of the soil water percolates out of the root zone and is lost as deep
percolation. Water can also be transported upward to the root zone by capillary rise from
a shallow groundwater table. Processes such as soil evaporation and crop transpiration
remove water from the reservoir.
Fig. 3.1b – Soil water profile (θ-z) and the top soil and root zone depicted as a
reservoir with indication of the stored water (W) and depletion (D)
The stored soil water in the root zone expressed as a depth is given by:
Vol% gravel
Wr = 1000 Zr 1 − (Eq. 3.1a)
100
where Wr soil water content of the root zone expressed as a depth [mm];
average volumetric water content in the fine soil fraction of the
root zone [m3(water)/m3(fine soil)];
Zr effective rooting depth [m];
Vol%gravel volume percentage of the gravel fraction in the root zone.
where WZtop soil water content of the top soil expressed as a depth [mm];
θtop average volumetric water content in the fine soil fraction of the top
soil [m3(water)/m3(fine soil)];
Ztop thickness of the top soil [m];
Vol%gravel volume percentage of the gravel fraction in the top soil.
0.0
field capacity
TAW
W FC
TAW
depletion (mm)
D : soil water
permanent
wilting point
W PW P
0.0
Figure 3.1c – The soil water content in the considered soil volume at Field Capacity
(WFC) and at Permanent Wilting Point (WPWP), and the Total Available soil Water
(TAW)
no stress 1.0
co
n ve
x
stress coefficient
0.8
0.6
Ks
0.4 lin
ea
r
log
0.2
ist
i c
Figure 3.2a – The stress coefficient (Ks) for various degrees of stress and
for different shapes of the Ks curve
The relative stress level (Srel) and the shape of the Ks curve determines the magnitude of
the effect of the stress on the process between the thresholds. Srel is 0.0 at the upper
threshold and 1.0 at the lower threshold (Fig. 3.2a). The shape can be linear, convex, or
logistic.
▪ Linear shape
If a linear shape is considered, the effect of stress on the process is directly proportional
to the relative stress:
where Srel (≤ 1) is the relative stress level and fshape is the shape factor. The shape factor is
positive (fshape > 0) for convex curves.
▪ Logistic shape
For the logistic shape, Ks for various Srel is given by:
Sn S x
Ks = (Eq. 3.2c)
S n + (S x − S n ) exp−r (1− Srel )
where Sn and Sx are the relative stress levels at the lower and upper threshold respectively,
and r the rate factor. Given that Ks is 0.5 midway the lower and upper threshold, the rate
factor can be obtained by solving Eq. 3.2c for Ks = 0.5 and Srel = 0.5. Since Srel is zero at
the lower threshold, a small value for Sn has to be considered. After solving Eq. 3.2c, Ks
has to be corrected for the considered small value.
Figure 3.2b – The water stress coefficient (Ks) for various degrees of root zone
depletion (Dr)
Since the stress response curves are defined for an evaporating power of the atmosphere
(ETo) of 5 mm/day, the upper and lower thresholds for water stress (p) needs to be adjusted
for ETo:
0 padj = p given + f adj (0.04 (5 − ET0 ) ) (log10 (10 − 9 p given )) 1 (Eq. 3.2d)
where fadj (default value = 1) is a program parameter which can be varied to increase (> 1)
or decrease (< 1) the adjustment. The log term in the equation makes the adjustment greater
when the soil is wet then when it is dry, based on the likely restriction of transpiration (and
hence less impact of evaporative demand) when the soil is dry.
Table 3.2a – Considered soil water stress coefficients and their effect on crop growth
Soil water stress Direct effect Target
coefficient model
parameter
Ksaer Reduces crop transpiration Trx
Soil water stress coefficient
for water logging (aeration
stress)
Ksexp,w Reduces canopy expansion and (depending CGC and
Soil water stress coefficient on timing and strength of the stress) might HI
for canopy expansion have a positive effect on the Harvest Index
Kspol,w Affects pollination and (depending on HIo
Soil water stress coefficient duration and strength of the stress) might
for pollination have a negative effect on the Harvest Index
Kssen Reduces green canopy cover CC
Soil water stress coefficient
for canopy senescence
Kssto Reduces crop transpiration and the root zone Trx, dZ and
Soil water stress coefficient expansion, and (depending on timing and HI
for stomatal closure strength of the stress) might have a negative
effect on the Harvest Index
Figure 3.2c – Comparison between the root zone depletion (Dr) and the depletion in
the top soil (DZtop) to determine which part of the soil profile is the wettest and
controls the water stress
The thickness of the top soil (Ztop), is a program parameter, which can be altered by the
user.
Table 3.2b – Considered air temperature stress coefficients and their effect on crop
growth
Air temperature stress Direct effect Target
coefficient model
parameter
KsTr Reduces crop transpiration KcTr,x
Cold stress coefficient for
crop transpiration
Kspol,c Affects pollination and (depending on HIo
Cold stress coefficient for duration and strength of the stress) might
pollination have a negative effect on the Harvest Index
Kspol,h Affects pollination and (depending on HIo
Heat stress coefficient for duration and strength of the stress) might
pollination have a negative effect on the Harvest Index
Stress indicators for air temperature stress are growing degrees (KsTr), minimum air
temperature (Kspol,c) or maximum air temperature (Kspol,h). If it is a cold stress, the process
is completely halted (Ks = 0) at and below the lower threshold, and not affected (Ks = 1)
at and above the upper threshold (Fig. 3.2d). For heat stress it is the other way round: below
the lower threshold of the maximum air temperature Ks is 1, and above the upper threshold
Ks becomes zero. For air temperatures stresses a logistic shape of the Ks curve is
considered.
no stress 1.00
air temperature stress coefficient
0.80
0.60
Ks
0.40
0.20
Figure 3.2d – The cold stress coefficient (Ks) for various air temperatures
Table 3.2c – Considered soil fertility stress coefficients and their effect on crop growth
Soil fertility stress coefficient Direct effect Target
model
parameter
KsCCx Reduces canopy cover CCx
Stress coefficient for maximum
Canopy Cover
Ksexp,f Reduces canopy expansion CGC
Stress coefficient for canopy
expansion
KsWP Reduces biomass production WP*
Stress coefficient for Biomass
Water Productivity
no stress 1.0
soil fertilty stress coefficient
0.8
0.6
Ks
0.4
0.2
Figure 3.2e – The soil fertility stress coefficient (Ks) for various levels of stress, with
indication of the calibration point (square) determining the shape of the Ks curve
The simulation of the effect of soil fertility stress is described in section 3.14 (‘Simulation
of the effect of soil fertility stress’) of this chapter.
Table 3.2d – Soil salinity stress coefficient and its effect on crop production
Soil salinity stress Direct effect Target
coefficient model
parameter
Kssalt Reduces biomass production CC and
Soil salinity stress coefficient KcTr
The average electrical conductivity of saturation soil-paste extract (ECe) from the root zone
is the indicator for soil salinity stress. At the lower threshold of soil salinity (ECen) the
stress starts to affect biomass production and Kssalt becomes smaller than 1. At and above
the upper threshold for soil salinity (ECex) the stress becomes so severe that biomass
production ceases and Kssalt is zero (Fig. 3.2f). The shape of the Ks curve is linear. Values
for ECen and ECex for many agriculture crops are given by Ayers and Westcot (1985) in
the Irrigation and Drainage Paper Nr. 29 (see Annex III).
0.6 60 %
Brel
lin
ea
0.4
r
40 %
0.2 20 %
Figure 3.2f – Soil salinity stress (Kssalt ) and relative biomass production for various
electrical conductivity of the soil-paste extract
To simulate the effect of soil salinity on biomass production (B), AquaCrop considers a set
of stress coefficients which (i) affect canopy development (similar as the effect of soil
fertility stress) and (ii) induces stomatal closure. The stress coefficients considered by
Table 3.2e – Considered soil salinity stress coefficients and their effect on crop growth
Soil salinity stress coefficient Direct effect Target
model
parameter
KsCCx Reduces canopy cover CCx
Stress coefficient for maximum
Canopy Cover
Ksexp,f Reduces canopy expansion CGC
Stress coefficient for canopy
expansion
Kssto,salt Reduces crop transpiration Kssto
Soil salinity stress coefficient
for stomatal closure
The simulation of the effect of soil salinity stress is described in section 3.15 (‘Simulation
of the effect of soil salinity stress’) of this chapter.
The simulation of the effect of soil fertility and soil salinity stress is described in section
3.16 (‘Simulation of the effect of soil fertility and soil salinity stress’) of this chapter.
Growing degree days (GDD) are calculated by subtracting the base temperature (Tbase)
from the average air temperature, Tavg (Fig. 3.3):
The base temperature (Tbase) is the temperature below which crop development does not
progress. In AquaCrop an upper threshold temperature (Tupper) is considered as well. The
upper temperature threshold specifies the temperature above which crop development no
longer increases with an increase in air temperature.
McMaster and Wilhelm (1997) present two methods for calculating Tavg in Eq. 3.3a. The
authors report that Method 1 predominates among researchers and practitioners involved
with small grain cereals such as wheat and barley. Method 2 is the most commonly used in
calculating GDD for corn, but it is used for other crops as well. In AquaCrop a 3rd method
is added.
3.3.1 Method 1
The average air temperature (Tavg) is given by:
Tavg =
(Tx + Tn ) (Eq. 3.3b)
2
3.3.2 Method 2
In this method the comparison to Tbase and Tupper occurs before the calculation of the
average temperature. Tn and Tx are adjusted if they drop below Tbase or exceed Tupper before
Tavg is calculated. The average temperature is given by:
Tavg =
(T x
*
+ Tn* ) (Eq. 3.3c)
2
where Tx* and Tn* are the adjusted maximum and/or minimum air temperatures. The
following rules apply:
- Tx* is the maximum air temperature (Tx* = Tx)
If Tx is greater than Tupper, then Tx* = Tupper,
If Tx is smaller than Tbase, then Tx* = Tbase
- Tn* is the minimum air temperature (Tn* = Tn)
If Tn is greater than Tupper, then Tn* = Tupper,
If Tn is smaller than Tbase, then Tn* = Tbase
3.3.3 Method 3
As in method 2, the comparison to Tbase and Tupper occurs before the calculation of the
average temperature. However the check is only on the maximum air temperature. The
average temperature is given by:
Tavg =
(T
x
*
+ Tn ) (Eq. 3.3d)
2
where Tx* is the adjusted maximum air temperature and Tn the minimum air temperature.
The following rules apply:
- Tx* is the maximum air temperature (Tx* = Tx)
If Tx is greater than Tupper, then Tx* = Tupper,
If Tx is smaller than Tbase, then Tx* = Tbase
- Tn is not adjusted. However if Tn exceeds Tupper, Tn will be set equal to Tupper.
Once Tavg is calculated, it is checked if the average air temperature is above the base
temperature. If Tavg is less than Tbase, then Tavg is taken as Tbase (resulting in 0 °C day on
that day).
CCo CCx
green canopy cover (CC)
CGC CDC
CCo, CGC and CCx determine the time required to reach maximum canopy cover. If CCo
and CGC are large, the maximum canopy (CCx) is reached quickly. If crop development
starts with a small CCo, the period to reach maximum canopy cover will be longer. The
1.0
CC = CC x
green canopy cover (CC)
0.8
0.6 Eq. 2
CC = 0.5 CC x
0.4
0.2 Eq. 1
CC = CC o
0.0
sowing time (day)
mid
initial crop development season
stage stage
CC = 0.10 CC = 0.98 CC x
time required to reach full canopy
CC = CC o et CGC (Eq.3.4a)
CC = CCx − 0.25
(CCx )2 e −t CGC (Eq. 3.4b)
CCo
▪ Delayed germination
When the soil water content in the top soil is below the threshold at the moment of the user
specified or generated sowing date, germination is not simulated. The germination is
delayed, as long as the soil water content in the top soil remains below the threshold. During
the period of delayed germination, the time advances and the number of delayed days is
tracked.
When, as a result of rain and/or irrigation, the soil water content raises above the threshold,
the crop will germinate and AquaCrop (Fig. 3.4b/2):
(i) shifts the start of the growing cycle with the number of delayed days, but also
adjusts the length of the growing cycle to the thermal regime of the shifted growing
cycle. If due to the delayed germination, part of the crop development ends up in a
warmer/cooler period than before, the growing cycle becomes shorter/longer than
previously determined, and
(ii) extends the simulation period so that its end coincides with the adjusted date of
maturity.
CC
3.33 CDC
t
CC = CC x 1 − 0.05 e x + 2.29 − 1
(Eq. 3.4c)
The Canopy Decline Coefficient (CDC) is a measure for the speed of decline of the green
canopy once it is triggered. A large CDC results in a steep decline of the canopy, while the
canopy senescence will be more gradually by selecting a smaller CDC (Fig. 3.4c).
The constants in the numerator and denominator of the exponent in Eq. 3.4c, makes the
simulation of duration of senescence less divergent for different CCx (Fig. 3.4d).
0.0
0.4 50
75
0.10
0.150
0.200
0.2
0
0.0
0 10 20 30 40 50 60
time (days)
Figure 3.4c – Decline of green canopy cover during senescence for various canopy
decline coefficients (CDC) as described by Eq. 3.4c. All lines have initial green
canopy cover at 0.9 and starting time at 0
100.0
50.0
CC at time of senescence (CCx)
25.0
10.0
log scale
5.0
1.0
0.1
0 20 40 60 80 100
relative time (%)
Figure 3.4d – Relative time for the canopy to reach zero%, for various CCx at the
start of senescence (for CDC = 0.004 per GDD)
Procedures have been worked out to guarantee that the length of the season in any year
remain between the (fixed or generated) start and end dates of the season. It consisted in
stretching the length of the mid-season in a non-planting/sowing year, so that the time to
reach senescence and crop maturity remains identical for a ‘1st’ and a ‘not 1st season’ (Fig.
The time ‘t0’ in Figure 3.4d/2, is the time at which the crop germinates (in case of sowing)
or recovers (in case of transplanting) in the 1st season (planting/sowing year). For a ‘not 1st
season’, t0 is still required to simulate the canopy development at the 1st day of regrowth
CC = CC o et CGC (Eq.3.4a)
CC = CCx − 0.25
(CCx )2 e −t CGC (Eq. 3.4b)
CCo
CCini is the canopy cover at the start of regrowth, and given by the plant density (at
planting/sowing year) and the size of the individual plant (cm²) when regrowth starts
(ccini). In the case of regrowth, ccini cc0.
Figure 3.4d/3 – The correction factor fCCx (Eq. 3.4c/3) adjusting the maximum
canopy cover (line 1) and the correction factor fCCo (Eq. 3.4c/4) adjusting the
minimum canopy cover (line 2) for the successive years with ny = 7 years and kn =
0.1. The arched area gives the range for kn (from 0.05 at the top to 0.80 at the
bottom of the area).
The canopy development over the successive years (with nx = 7 years and kn = 0.1) as
simulated by AquaCrop is plotted in Figure 3.4d/4. To maintain high yielding stands, re-
establishment of the stand might be required after 6 to 7 years.
10
15
The natural self-thinning results in a gradual decrease of the maximum canopy cover (CCx)
that can be reached without water stress over the years. Since initially the self-thinning is
compensated by an increase in the number of shoots per plant, the decrease of CCx does
not decrease from the first year, but becomes only visible in later years when the plant
population becomes smaller (Fig. 3.4d/3). The correction factor to adjust CCx for year i is
given by:
(n − 1)
f CCx ,i = 0.9 + 0.1 1 − k n i
( )n y − 1
(Eq. 3.4c/3)
where ni is the year number (from 1 to ny), and ny the number of years at which CCx declines
to 90% of its initial value of the 1st year. Since the decline of the initial canopy cover (CCo)
is directly proportional to the natural self-thinning, its correction factor decreases linear in
time (Fig. 3.4d/3) and is given by:
n −1
fCCo ,i = 1 − i (Eq. 3.4c/4)
no − 1
where ni is the year number (from 1 to ny) and no the year where CCx and CCo both becomes
zero:
( )
no = 1 + n y − 1 10 kn (Eq. 3.4c/5)
▪ Multiple harvests
For crops that are cut several times per season, AquaCrop simulates regrowth after each
cut (Fig. 3.4d/5)
The canopy cover after cutting (CCini), and the generation or timing of the harvest events
are specified in the field management file. By considering the CCini from the input in the
field management file, the development of the canopy cover is simulated after each cut
(Equation 1 and 2). Soil water, soil fertility, soil salinity stress may slow down the canopy
development (see 3.5 “Green canopy cover for stress conditions”).
▪ Transfer of assimilates
Perennial herbaceous forage crops transfer a considerable fraction of the assimilates to their
below-ground parts after mid-season (Fig. 3.4d/6). At the start of the next season, a fraction
of the stored assimilates are remobilized by transferring them from the below-ground parts
to the above-ground parts of the crop (see Section 3.11.4 “Transfer of assimilates for
perennial herbaceous forage crops”).
Figure 3.4d/6 – Mobilization and storage stage during which assimilates are
transferred between the above and below ground parts of the crop
▪ Annual crops
In the presence of unlimited soil fertility, the total canopy cover of crop and weeds (CCTOT)
can be larger than the crop canopy cover in weed free conditions (CCWF) especially when
weeds not only suppress the crop but also expand in the free space between the individual
plants (Fig. 3.4e).
Figure 3.4e – Total canopy cover of crop and weeds (CCTOT), crop canopy cover
under weed-free conditions (CCWF – reference) and crop canopy cover in a weed
infested field (CCW), with indication of the adjustment factor for canopy expansion
(fweed) and the relative cover of the weeds (RC).
CCTOT is simulated by multiplying the initial (CCoWF) and maximum crop canopy cover
(CCxWF) for weed-free conditions, with an adjustment factor fweed:
CCo TOT = f weed CCoWF (Eq. 3.4d)
CCx TOT = f weed CCxWF (Eq. 3.4e)
where CCoTOT and CCxTOT are respectively the total initial and total maximum canopy
cover of crop and weeds. The adjustment factor for canopy cover in a weed infested field
(fweed) is given by:
1 e f shape RC − 1 1
f weed = 1 − 1 − f
e shape − 1 (Eq. 3.4f)
CCxWF CCxWF
where CCxWF (fraction) is the maximum crop canopy cover under weed-free conditions,
RC the relative cover of weeds (fraction) and fshape a shape factor (Fig. 3.4f) expressing the
expansion of the canopy cover due to weed infestation. Given that CCTOT cannot exceed 1,
the maximum value of fweed is (1/CCxWF).
1
10
=-
Maximum total canopy cover
e
ap
fsh
0.95
(crop and weeds)
)
ult
fshape = + 100
fa
(de
0.9 0 .01
=-
pe
f sha
0.85
10
+
=
e
ap
f sh
0.8
0 0.2 0.4 0.6 0.8 1
relative w eed cover (RC)
Figure 3.4f – Maximum total canopy cover of weeds and crop at mid-season
(CCx,TOT) for different relative weed covers (RC) and different shape factors (fshape)
for a field that in weed-free conditions would have a CCx of 0.8.
To assure that the length of the crop cycle is not affected, the Canopy Decline Coefficient
(CDC) needs to be adjusted as well:
CDCTOT = CDCWF
(CCxTOT + 2.29) (Eq. 3.4h)
(CCxWF + 2.29)
where CDCWF is the canopy decline coefficient under weed-free conditions.
The crop canopy development in the weed-infested field (CCW) can be derived at any time
from CCTOT (Fig. 3.4e) by considering the relative cover of weeds (RC):
CCW = CCTOT (1 − RC ) (Eq. 3.4i)
Figure 3.4f/2 – Total canopy cover of crop and weeds (CCTOT) of a perennial
herbaceous forage crop in year 7, where the open spots (as a result of natural self-
thinning) are taken over by weeds by (A) 0 % and (B) 100 %. In both cases the crop
canopy cover under weed-free conditions (CCWF – bold line for reference at year 7)
and crop canopy cover in a weed infested field (CCW) are identical.
The period of potential vegetative growth depends on how determinant is the crop’s growth
habit. For determinant crops, once peak flowering is passed and fruits or grain begin to fill,
CC has reached its maximum regardless of whether the CC at that time has or has not been
reduced by stress. For indeterminant crops the canopy development stage is stretched till
canopy senescence (Fig. 3.5b).
▪ Protection at germination:
When the crop germinates, the expansion rate of the canopy cover (CC) of the seedling is
not limited by water stress. Thanks to nutrients available in the seed, it is assumed that the
expansion of the canopy cover is its maximum rate (given by the Canopy Growth
Coefficient, CGC). Any reduction of leaf expansion due to water stress, are disregarded till
CC is 25% above the initial canopy cover (i.e. CC > 1.25 CCo).
▪ After germination:
Once CC is above 1.25 of CCo, the protection of the germinating seedling is switched off,
and the leaf growth by area expansion and therefore canopy development is sensitive to
water stress. To simulate the reduction in leaf growth as a result of water stress, the crop
growth coefficient (CGC) is adjusted for the stress effect by multiplying it with the water
stress coefficient for leaf expansion growth (Ksexp,w):
CGC adj = Ks exp,w CGC (Eq. 3.5a)
When the depletion (D) reaches its lower limit, leaf expansion is completely halted:
Dexp, lower = pexp, lower TAW (Eq.3.5c)
depletion (mm)
threshold
D : soil water
TAW
permanent
wilting point
0.0
conside re d soil v olume
(top soil or root zone)
Figure 3.5c – The upper and lower threshold for soil water depletion in the
considered soil volume affecting leaf growth by area expansion
Between the upper and lower thresholds the shape of the Ks curve determines the
magnitude of the stress (Fig. 3.5d). In AquaCrop the shape of the Ks curve can be selected
as linear or concave (see 3.2 Stresses).
no stress 1.0
0.8
water stress coefficient
Ksexp,w
0.6
0.4
0.2
D
full stress 0.0
pexp,upper pexp,lower perm anent
field capacity TAW w ilting point
Figure 3.5d – Water stress coefficient for leaf expansion growth (Ksexp,w)
for various degrees of depletion (D) in the considered soil volume
▪ Protection at germination:
Any inducing of early senescence due to water stress, are disregarded when the crop
germinates. The protection is effective till CC is 25% above the initial canopy cover (i.e.
CC > 1.25 CCo).
▪ After germination:
Once CC is above 1.25 of CCo, the protection of the germinating seedling is switched off.
Under severe water stress conditions, canopy senescence will be triggered. Early canopy
senescence will occur as soon as depletion (D) in the considered soil volume exceeds the
upper threshold:
Dsen , upper = psen TAW (Eq.3.5d)
Once the depletion in the considered soil volume reaches the lower limit (which is
permanent wilting point):
Dsen , lower = TAW (Eq. 3.5e)
the canopy decline is at full speed. The upper and lower threshold for the soil water
depletion are plotted in Figure 3.5e. Between the upper and lower threshold the rate of
canopy decline (CDC), which simulates the early canopy senescence, is adjusted to the
degree of water stress.
The canopy decline will be very small when water stress is limited, but increases with
larger water stresses. This is simulated by adjusting the canopy decline coefficient with the
water stress coefficient for senescence (Kssen). To guarantee a fast enough decline at strong
depletion, the 8th power of Kssen is considered:
(
CDCadj = 1− Ks sen
8
)
CDC (Eq. 3.5f)
TAW
TAW
depletion (mm)
D : soil water
permanent
wilting point
0.0
considered soil volume
(top soil or root zone)
Figure 3.5e – The upper and lower threshold for soil water depletion in the
considered soil volume affecting early canopy senescence
no stress 1.0
0.8
water stress coefficient
0.6
Kssen
0.4
0.2
D
full stress 0.0
psen psen,lower
field capacity TAW permanent w ilting point
Figure 3.5f – Water stress coefficient for early canopy senescence (Kssen)
for various degrees of depletion (D) in the considered soil volume
A small amount of rain or a slight expansion of the root zone in a wet subsoil, might reduce
the root zone depletion above Drsen,upper and de-activate as such the canopy senescence. To
avoid such an overreaction of the program, psen is reduced with a few percentages (β) once
early canopy senescence is triggered:
psen , adj = psen 1 − (Eq. 3.5g)
100
β is a program parameter, and its value can vary between 0 % (no adjustment) to 25 %.
During the dormant period CC gradually decreases from CCdormant (fixed at 0.05 m²/m²) to
CCo (Eq. 3.5g/2). If CCo is greater than 5 % soil cover, CC remains at CCo during the
whole of the dormant period:
1−∑ 𝐸𝑇𝑜𝑖
𝐶𝐶𝑖 = 𝐶𝐶𝑜 + (𝐿 ) (𝐶𝐶𝑑𝑜𝑟𝑚𝑎𝑛𝑡 − 𝐶𝐶𝑜) (Eq. 3.5g/2)
𝑑𝑜𝑟𝑚𝑎𝑛𝑡
where CCi the green canopy cover at day i during the dormant period (m²/m²)
CCo canopy cover at 90% emergence or after transplanting (m²/m²)
EToi sum of daily ETo during the dormant period at day i (mm)
Ldormant length of the dormant period expressed as a sum of daily ETo (mm)
If at the end of the dormant period, the crop wasn’t able to recover, CC drops to zero and
the crop is considered as permanently wilted (Fig. 3.5f/2).
Once regrowth is activated, the ageing of the canopy (inducing a progressive though small
reduction in crop transpiration and photosynthetic capacity) is reset to zero.
Although the plant will survive upon rewatering during the dormant period, regrowth can
only occur during the period of potential vegetative growth (see 3.5.1 ‘Period of potential
growth’). For determinant crops, once peak flowering is passed and fruits or grains begin
to fill, CC can no longer increase. For indeterminant crops the canopy development stage
is stretched till canopy senescence.
Limited soil fertility or soil salinity stress decreases the growing capacity of the crop (CGC)
as well as the maximum canopy cover (CCx) that can be reached at mid-season. The
adjustments of CGC and CCx for soil fertility/salinity stress are given by:
CGC adj = Ks exp, f CGC (Eq. 3.5h)
where CGC and CCx are the canopy growth coefficient (fraction or percentage per day)
and the maximum canopy cover (fraction or percentage) in the absence of soil fertility or
soil salinity stress, and Ksexp,f and KsCCx the stress coefficients.
For non-limiting soil fertility (i.e. soil fertility stress is zero) and in the absence of soil
salinity stress the stress coefficients are 1. When the soil fertility/salinity stress is complete,
crop growth is no longer possible and the Ks coefficients reach their theoretical minimum
of zero. Between the upper and lower limits the Ks coefficients vary between 1 and 0 (Fig.
3.5g).
no stress 1.0
0.8
stress coefficient
0.6
Ks
0.4
0.2
Figure 3.5g – Soil fertility stress coefficient for various soil fertility/salinity stresses
(full line) with indication of the Ks and soil fertility/salinity stress used for
calibration (square)
The shape of the Ks curves can be convex, linear or concave and may differ between the 2
Ks curves. The shape of each of the curves is determined at calibration by specifying a
value between 1 and 0 for Ksexp,f and KsCCx for the particular soil fertility and soil salinity
stress at which the crop response is calibrated (see Chapter 2, ‘Calibration for soil fertility’
and ‘Calibration for soil salinity stress’).
In the late season (between the start of canopy senescence and maturity), the declines
continue and is given by Eq. 3.5j. However, since during this period also the natural
senescence kicks in, the green canopy decline is also described by Eq. 3.4c (see 3.4.5
‘Green canopy cover decline’). The CC considered in the simulation during the late season
is the smallest given by one of the two equations.
Figure 3.5h – Canopy cover in the absence (light area) and in the presence (dark
area) of soil fertility/salinity stress
The calibration for the average daily decline of the canopy cover (fCDecline) follows the same
approach as for Ksexp,f and KsCCx. In the absence of soil fertility or soil salinity stress the
decline is zero (see Chapter 2, ‘Calibration for soil fertility stress’ and ‘Calibration for soil
salinity stress’). When the stress is complete (100%), a maximum decline of 1 % per day
is assumed. Between the upper and lower limits fCDecline varies between 0 and 1 % per day.
The values for KsCCx, Ksexp,f and fCDecline are determined by the most important stress (soil
fertility or soil salinity stress) at that moment (see section 3.16 ‘Simulation of the combined
effect of soil fertility and soil salinity stress’).
In the absence of soil fertility stress and soil salinity stress, the described adjustment of the
canopy growth coefficient (section 3.5.2) and early canopy senescence (section 3.5.3)
under water stress conditions remain valid for weed infested fields. It is however required
to replace CCo, CCx and CDC by their corresponding values in weed infested fields
CCoTOT, CCxTOT and CDCTOT.
In case of limited soil fertility or soil salinity stress, CCTOT is entirely determined by the
available soil nutrients or the presence of salts in the absence of water stress (Fig. 3.5i). As
such the expansion of CC by fweed for unlimited soil fertility and the absence of salinity
stress cannot be considered. Given that weeds and crop are assumed to be equally sensitive
to water, temperature, salinity and fertility stress, CCTOT will be the same as the (limited)
crop canopy cover under weed-free conditions (CCWF). The adjustments of CCWF to soil
fertility and soil salinity stress are described in section 3.5.5. In case soil fertility or salinity
stress limits canopy development, CCo, CCx and CDC should not be replaced by their
corresponding values in weed infested fields (since fweed is 1).
The crop canopy development in the weed-infested field (CCW) can be derived at any time
from CCTOT (Fig. 3.5i) by considering the relative cover of weeds (RC):
𝐶𝐶𝑊 = 𝐶𝐶𝑇𝑂𝑇 (1 − 𝑅𝐶) (Eq. 3.5k)
Since root growth is more resistant to water stress than leaf growth, root development is
not affected when canopy expansion starts to be reduced.
Root development is affected:
- if the soil water stress in the root zone starts to affect crop transpiration;
- if the soil water content below the expanding root zone is too dry;
- in soil horizons with low permeability restricting root growth.
t0
t −
Z = Z o + (Z x − Z o ) n
2
(Eq. 3.6a)
t
tx − 0
2
The development of the effective root zone starts when Z exceeds the minimum effective
rooting depth (Zn) and advances till the maximum effective rooting depth (Zx) is reached
(Fig. 3.6a). At any time the effective rooting depth Z is given by
Zn Z Z x (Eq. 3.6b)
The shape factor n, which is crop specific, determines the decreasing speed of the root zone
expansion in time. For values larger than 1, the expansion of the root zone is more
important just after planting than later in the season. The larger the value of n, the stronger
the discrepancy between the expansion rates at the beginning and end of the period for root
zone expansion. The expansion of the effective root zone is constant (linear) when n is 1.
The starting depth of the root zone expansion curve Zo is a program parameter and
expressed as a fraction of Zn. The average expansion rate of the effective root zone can
never exceed a maximum value (fixed at 5 cm/day).
to/2 Zx
average
expansion rate
to
tx
The reduction in the expansion of effective rooting depth is determined by the magnitude
of the Kssto and a (negative) shape factor, fshape. The shape factor, fshape, is a program
parameter which can be adjusted by the user. The effect of water stress on the reduction of
the root zone expansion is:
- strong for fshape = 0, and given by the linear relationship:
dZ adj= Ks sto dZ (Eq. 3.6c)
not affected
dZadj = dZ
root zone expansion
8
=-
-4
e)
)=
ap
-1
pe
f(sh
=
e)
ha
ap
f(s
h 0
f(s e)
=
h ap
f(s
completely
halted
dZadj = 0 0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1
Figure 3.6b – The effect of water stress on the reduction of root zone expansion for
various shape factors (fshape) and water stress in the root zone (Kssto)
The root deepening rate is described by Eq.3.6a as long as the expanding front is in non-
restrictive horizons. In a restrictive soil horizon, the expansion is slowed down (line 2b, in
Fig. 3.6c) or inhibited (line 2a, in Fig 3.6c) depending on its penetrability:
penetrabilityhorion
dZ adj = dZ (Eq. 3.6e)
100
where dZadj and dZ are the expanding rates in respectively restrictive and non-restrictive
soil horizons, and penetrabilityhorizon the penetrability (expressed as a percentage) of the
horizon.
Below the restrictive soil layer, the root zone expansion is normal again, and no longer
restricted. However, due to the delay in expanding, the effective rooting depth can no
longer reach its maximum value.
sowin g e m e rge n ce
tran splan tin g
time
Zo
Zn
rooting depth
to/2 Zx
2a
to re strictive soil laye r 2b
1
tx
Figure 3.6c – Development of the effective rooting depth (1) in the absence and (2) in
the presence of a restrictive soil layer (2a) which inhibits the expansion of the root
zone (penetrability = 0 %); and (2b) which slows down the expansion of the root
zone (0% < penetrability < 100%)
Figure 3.6d – Root zone expansion (Zrexp) at the expansion front (bold line) and
water stress coefficient for stomata closure, Kssto (dotted line) for various soil water
depletions.
If the soil water depletion at the expansion front exceeds pZr,exp TAW, the root zone
deepening is slowed down. The expansion rate (Zrexp) is plotted in Fig. 3.6d as a percentage
of dZ (the non-restrictive expanding rate).
In AquaCrop the time increment is fixed at one day and the depth increment (z) is by
default 0.1 m. The soil profile is such divided into soil compartments (12 by default) with
thickness z (Fig 3.7b). The hydraulic characteristics of each compartment are that of the
soil horizon to which it belongs. If a crop is selected with a deep effective root zone,
AquaCrop will adjust the size of the compartments (z) to cover the entire root zone. For
deep root zones, z is not constant but increases exponentially with depth, so that
infiltration, soil evaporation and crop transpiration from the top soil horizon can be
described with sufficient detail. Program settings allow the user to adjust the number and
size of the soil compartments.
horizon 1 3
4
5
6
7
Soil 8
horizon 2 9
10
11
12
Since the magnitude of the changes in soil water content, simulated in each of the
subroutines, depends on the actual soil water content, the sequence of the calculations
might theoretically have an influence on the final simulation result. The effect however
will be small since the time step is restricted to one day. Further on, major changes in soil
water content of the soil profile as a result of infiltration, internal redistribution of soil
water and drainage, will only occur in a wet soil profile. But since in a wet soil the
evaporation and transpiration are at their maximum rate, evapotranspiration is at that
moment only dictated by the atmospheric water demand and crop development and hence
independent of the soil water content in the soil profile. On the other hand, when the soil
profile is dry, the simulated evaporation and transpiration rate depends strongly on the soil
water content but at that moment soil water flow in the soil profile does not take place.
runoff
Runoff subroutine
i,j
= i,j-1
+ i,t
+ i,t
+ i,t
+ i,t
+ i,t
Deep Capillary
percolation rise
Figure 3.7c – Calculation scheme of the soil water balance in AquaCrop
▪ Drainage function
To simulate the redistribution of water into a soil layer, the drainage out of a soil profile,
and the infiltration of rainfall and/or irrigation, AquaCrop makes use of a drainage function
(Raes, 1982; Raes et al., 1988; Raes et al., 2006):
i ei − FC − 1
= ( SAT − FC ) sat − FC (Eq. 3.7a)
t e −1
Where i/t decrease in soil water content at depth i, during time step t
[[Link]-1];
drainage characteristic [-];
i actual soil water content at depth i [m3.m-3];
SAT soil water content at saturation [m3.m-3];
FC soil water content at field capacity [m3.m-3];
t time step [day].
0.4
soil water content
1.0
field capacity
0 1 2 3 4 5 6 7 8 9 10
time (day)
The drainage function describes the amount of water lost by free drainage over time
between saturation and field capacity (Fig. 3.7d). The function is assumed to be
exponential. When field capacity is reached further drainage of the soil is disregarded. The
drainage function mimics quite realistically the infiltration and internal drainage as
observed in the field (Raes, 1982; Feyen, 1987; Hess, 1999; Wiyo, 1999; Barrios Gonzales,
1999, Raes et al., 2006).
DP = 1000 z t (Eq. 3.7c)
t
where the soil water content of the draining soil profile [m3.m-3];
Δθ/Δt drainage ability given by Eq. 3.6a [[Link]-1];
z the thickness of the draining soil profile [m];
t the time step (1 day).
Given the soil water content of compartment 1, the decrease in soil water content during
time step t is given by Eq. 3.7a. The amount of water D1 (mm) that percolates out of the
top compartment at the end of a time step is given by:
1
D1 = 1000 z1 t (Eq. 3.7d)
t
Subsequently the soil water content of the top compartment is updated. The same
calculations are repeated for the successive compartments. It is thereby assumed that the
cumulative drainage amount Di = D1 + D2 + … will pass through any compartment as
long as its drainage ability is greater than or equal to the drainage ability of the upperlying
compartment. By comparing drainage abilities and not soil water contents, the calculation
procedure is independent of the soil layer to which succeeding compartments may belong.
5 D/Z5
6 D/Z6
7
soil depth
9
deep percolation (DP)
Figure 3.7e – Schematic presentation of a draining soil profile (left) with indication
of the soil water content before (full line) and at the end (dotted line) of the process
of internal redistribution of the water, and the calculated cumulative drainage
(right)
In each compartment, the cumulative drainage amount Di that passes through should be
smaller than or equal to the maximum infiltration rate of the soil layer to which the soil
compartment belongs. If not so, part of the Di will be stored in that compartment, or if
required in the compartments above, until the remaining part of Di equals the infiltration
rate of the soil layer.
RO =
P − I a 2 (Eq. 3.7e)
P + S − Ia
100
S = 254 − 1 (Eq. 3.7f)
CN
The initial abstraction (Ia) in Eq. 3.7e is fixed at 0.05 S. Recent research (Hawkins et al.,
2002) found that this may be a more appropriate value for Ia than the previous assumed
value of 0.20S in previous AquaCrop versions.
The runoff process is described by Eq. 3.7e. Rain that falls on unsaturated soil infiltrates,
increasing the soil water content until the topsoil becomes saturated (P = 0.05S), after
which additional rainfall becomes surface runoff. A soil with a high Curve Number (CN)
will have a small potential storage (S) and may loose a large amount of rainfall as runoff.
The default Curve Numbers in AquaCrop are the average values for the four distinguished
hydrologic soil groups for the ‘small grain’ hydrologic soil-cover complex with good
hydrologic conditions as provided by USDA in the National Engineering Handbook
(USDA, 2004). The same criteria used by USDA for the assignment of hydrologic soil
groups (based on Ksat) are used in AquaCrop for the classification of the soils in the
hydrologic soil groups (Table 3.7a).
Table 3.7a – Hydrologic soil groups, the corresponding range for the saturated
hydraulic conductivity (Ksat) of the top horizon, and default CN values (assuming
an initial abstraction of 5 % of S) for antecedent moisture class II (AMCII).
Hydrologic soil Saturated hydraulic conductivity (Ksat) CN default value
group mm/day for AMC II
A > 864 46
B 864 – 347 61
C 346 – 36 72
D ≤ 35 77
The user can specify a CN value different from the default, but should thereby not consider
the effect of land use and cover, since these effects are considered when specifying the
In AquaCrop the specified CN value as soil profile characteristic is the value that belongs
to the antecedent moisture class AMC II (CNAMC II). This value is considered when the soil
water content in the top soil is half way between Field Capacity and Permanent Wilting
Point. At run time, the specified Curve Number (CNAMC II) is adjusted for the simulated
wetness of the top soil layer. To adjust CN to the antecedent moisture class, relationships
derived from CN values for various AMC presented by Smedema and Rycroft (1983) are
used. The relationships used in AquaCrop to derive CNAMC I and CNAMC II from CNAMC II
are:
The storage capacity of a soil is indeed somewhat larger (smaller CN value) if it is dry than
when it is wet. By linear interpolation between the corresponding CN values at various
antecedent moisture classes, CN is adjusted to the wetness of the topsoil.
The calculation of the relative wetness of the topsoil extends to a depth of 0.3 meter. In the
calculation, the soil water content at the soil surface has a larger weight than the soil water
content at 0.3 meter (Fig. 3.7f):
exp f d / dx − 1
wrel = 1 − (Eq. 3.7i)
exp f − 1
Program settings allow the user to switch off the adjustment of CN for soil wetness and to
adjust the default thickness of 0.3 m. Current thinking (Hawkins (personal communication)
2002) is that the AMC-I and AMC-III CN’s are ‘error-bands’ to describe departure of
surface runoff from all kind of sources, including soil moisture. There seems to be no much
literature references to show real consistent impacts of prior soil water content on surface
runoff on the scale proposed by USDA.
soil depth
For simplicity, irrigation is assumed to be fully controlled; hence the runoff subroutine (for
rainfall) is bypassed for irrigation water infiltration and tailwater is assumed to be zero. If
surface runoff from the field is important when irrigating, the above assumption requires
that irrigation be specified as a net application amount.
The maximum amount that can infiltrate the soil, either as rainfall or irrigation, is limited
by saturated hydraulic conductivity of the topsoil layer. Excess water, is considered as lost
by surface runoff.
Since field management and crop type might affect surface runoff, the user can adjust CNsoil
when specifying the effect of field surface practices affecting surface runoff. The specified
CNsoil, can be adjusted by considering the crop type (if different from ‘small grain’),
treatment and hydrologic conditions. Further-on specific field practices such as tied ridges
and soil bunds might prevent soil surface runoff. In that case the runoff subroutine is
bypassed. When the field is surrounded by soil bunds, water that cannot infiltrate as a result
of excessive rainfall or irrigation will be stored between the bunds. The storage capacity is
however limited by the height of the bunds. Water that overtops the bunds is assumed to
be lost by surface runoff.
The calculation procedure is not completely independent of the thickness of the soil
compartments. However, the simulation mimics quite realistic the infiltration process, by
taking into account the initial wetness of the soil profile, the amount of water that infiltrates
during the time step, the infiltration rate and drainage characteristics of the various soil
layers of the soil profile.
The relationship between capillary rise and the depth of the groundwater table is given by
the exponential equation:
ln( z ) − b
CR = exp (Eq. 3.7j)
a
where CR is the expected capillary rise ([Link]-1), z the depth (m) of the water table below
the soil surface and a and b parameters specific for the soil type and its hydraulic
characteristics. Since the magnitude of capillary rise is strongly affected by the shape of
the water retention curve and the K-h relationship, the a and b parameters of the equation
varies with the textural class (Fig. 3.7g).
Figure 3.7g –Textural triangle with indication of the 12 different soil types and the 4
soil Classes considered for the determination of the a and b parameters of Eq. 6.1a.
I. Sandy soils (dark area), II. Loamy soils (grey area),
III. Sandy clayey soils (white area) and IV. Silty clayey soils (dark area)
Table 3.7b – Equation 3.7k and 3.7l for the 4 soil Classes with indication of the
considered range for the saturated hydraulic conductivity (Ksat) (Janssens, 2006)
Soil Class Range a b
Ksat Eq. 3.7k Eq. 3.7l
[Link]-1
I. Sandy soils 200
sand, loamy sand, to – 0.3112 – 10-5 Ksat – 1.4936 + 0.2416
sandy loam 2000 ln(Ksat)
3
4
2
1.0 1
1.5
2.0
2.5
1. Sandy soils
2. Loamy soils
3. Sandy clayey
4. Silty clayey
3.0
Figure 3.7h – Capillary rise to a bare soil surface, as obtained with Eq. 6.1a, for the
4 considered soil Classes and for various depths of a shallow groundwater table and
by assuming a typical saturated hydraulic conductivity (Ksat) of 500 mm/day for
Class I (Sandy soils), 250 mm/day for Class II (Loamy soils), 100 mm/day for Class
III (Sandy clayey soils) and 25 mm/day for Class IV (Silty clayey soils)
To generate default values for the a and b soil parameters (Eq. 3.7j), AquaCrop determines:
- in a first step the class of the soil type for each of the soil layers. The classification is
obtained by comparing the volumetric water content at saturation, field capacity and
permanent wilting point of each soil layer with the expected ranges of those soil water
contents in the 4 classes (Tab. 3.7c);
- in the next step, the a and b soil parameters for each soil layer with Eq. 3.7k and 3.7l
(Tab. 3.7b) by considering (i) the soil class and (ii) the specified saturated hydraulic
conductivity (Ksat).
Table 3.7c – Ranges considered for the soil water content at saturation, field capacity
and permanent wilting point for the 4 soil classes
Soil water content (vol %)
Soil class Saturation Field Capacity Permanent Wilting
Point
I. Sandy soils 32 – 51 9 – 28 4 – 15
II. Loamy soils 42 – 55 23 – 42 6 – 20
III. Sandy clayey 40 – 53 25 – 45 16 – 34
soils
IV. Silty clayey soils 49 – 58 40 – 58 20 - 42
In the Soil profile characteristic menu, the soil class and the default values are displayed.
If required the user can calibrate the a and b soil parameters by considering the simulated
capillary rise for various depths of the groundwater table (see Chapter 2, section 2.13 Soil
profile characteristics).
To simulate drainage and capillary rise correctly, AquaCrop needs to know this equilibrium
state (called adjusted Field Capacity). In AquaCrop a parabolic function is used to describe
the adjustment of FC in the presence of the groundwater table:
where θFC soil water content at FC in the absence of a groundwater table (m3 m-3)
ΔθFC,i increase in FC at height zi above the groundwater table (m3 m-3)
θFCadj,i adjusted FC at height zi above the groundwater table (m3 m-3)
θsat soil water content at saturation (m3 m-3)
zi height above the groundwater table (m)
x height above the groundwater table where FC is no longer adjusted
FC
ad
j
Figure 3.7i – Soil water profile in equilibrium with the groundwater table
At a height of x meter or more above the groundwater table, the adjustment of Field
Capacity is neglected. At the groundwater table, FCadj,i is equal to sat, and at a height of x
meter or more above the groundwater table (where zi ≥ x), FCadj,i is equal to FC (Fig. 3.7i).
The value for x can be derived from the soil matrix potential at Field Capacity (FC) which
varies between -10 kPa (for the more sandy soils) to -20 kPa (for the more loamy and
clayey soils) when expressed as energy per unit volume. This corresponds with a head
(energy per unit weight) of about – 1 m water (pF 2.0) up to – 2 m (pF 2.3). By considering
indicative values for the soil water content at FC of 10 vol% for the more sandy and 30 vol
− 10
2 + 0.3 FC
30 − 10
10
x= (Eq. 3.7o)
100
where FC the soil water content at FC (vol %) varying between 10 and 30 vol% (Tab.
3.7d).
Table 3.7d – The soil water content at Field Capacity (FC) and the height (x) above
which the effect of the groundwater table on FC can be neglected (Eq. 3.7o)
FC (vol%) x (meter)
FC 10 vol% 1.00
15 1.19
20 1.41
25 1.68
FC 30 vol% 2.00
▪ Calculation procedure
Concept
The calculation starts at the bottom compartment (n) of the soil profile, and moves step by
step upwards to the upper lying compartments (i+1, i, i-1, ..) till the top compartment (1)
is reached (Fig 6.4a). The calculation procedure consists of the following steps:
1. Calculation of the maximum amount of water that can be transported upward by
capillary rise to the node (center) of the compartment (CRmax,i) by considering the depth
of the groundwater table below the center of the soil compartment (zi) and the
characteristics of the soil layer (Eq. 3.7j);
2. Storage of water in that compartment till i is equal to FCadj,i or all the CRmax,i has been
stored. The amount of water stored in compartment i is:
( )
IF θi ≤ θFCadj,I THEN Wstored ,i = 1000 FCadj,i − i zi f CR ,i CRmax,i (Eq. 3.7p)
ELSE Wstored ,i = 0 (Eq. 3.7q)
where Δzi is the thickness of the compartment (m), fCR,i the capillary rise factor (Eq.
3.7u), and Wstored,i the stored amount of water (mm) in the compartment. The amount
of water still to store is obtained by subtraction the stored amount of water from CRmax,i
CR
compartment soil water content
1
i-1
CRmax i
FCadj i
i
i+1
FCa
CR
dj
ma
x
zi
groundwater table
Figure 3.7j – The maximum amount of water that can be transported upward by
capillary rise (CRmax,i) and the adjusted field capacity (FCadj,i) for the node of
compartment i, at a height of zi meter above the groundwater table
3. As long as Wremain is not zero, the calculation continues by moving to the next upper
lying compartment (i-1). The calculations restart with step 1, i.e. with the calculation
of CRmax for that compartment (CRmax,i-1). The calculation will continue with the
minimum of CRmax,i-1 and Wremain. This control takes care of (i) water already stored in
the underlying compartments and (ii) possible changes of layers in the soil profile when
moving upward (whereby the restricted capillary capacity of an underlying soil layer,
limits the upward flow to the upper lying soil layers).
The calculation stops if all the water has been stored (Wremain becomes 0) or the soil surface
is reached (i = 1). The total amount of water that has been moved upward by capillary rise
to the soil profile is given by the sum of the water stored in each of the compartments:
n
CR = Wstored ,i (Eq. 3.7s)
i =1
i − PWP
relative wetness = (Eq. 3.7t)
FCadj, i − PWP
where i is the soil water content at a height zi above the groundwater table, and PWP and
FCadj,i the soil water content at the Permanent Wilting Point and the adjusted Field Capacity
respectively.
The restrictions for upward water movement as a result of a low potential gradient is
estimated by considering a power function of the relative wetness and is expressed by a
capillary rise factor (fCR,i):
x
i − PWP
f CR , i = 1− (Eq. 3.7u)
−
FCadj , i PWP
The capillary rise factor, fCR,i, varies with the soil water content (i) and ranges between 1
and 0 (Fig. 3.7k). The capillary rise factor considers on the one hand the driving force for
upward water movement and on the other hand the hydraulic conductivity.
If the top soil is dry, the potential gradient is strong and the driving force for water
movement is strong as well (fCR = 1). The wetter the soil profile, the smaller the potential
gradient and the smaller the upward water movement (fCR < 1). If the soil water content at
a given height above the groundwater table is equal to FCadj,i, upward water movement is
fully inhibited due to the absence of any water potential gradient. The power (x) in Equation
6.4f is a program parameter and set at 16 for testing.
x= 3
x
0.8
=
30 2
x=
x =16
16
f CR
0.6
0.4
x=
5
0.2
0.0
(WP+FC)
WP FCadj
2
soil water content
Figure 3.7k – The capillary rise factor (Eq. 3.7u) for different soil water content in
the soil profile above the groundwater table and values for the power x.
The power (x) in Equation 3.7u is a program parameter which can vary between 5 and 30
(with 16 as default). With the program parameter the user can adjust the simulated capillary
rise. Increasing the required soil water content gradient (by reducing x) will limit upward
flow from the groundwater table, while reducing the required soil water content gradient
(by increasing x) will facilitate the capillary rise to the soil profile.
If the total soil profile is draining (n > FCadj,n), the calculation process does not start at all.
As long as water moves out of the bottom compartment, capillary rise to the soil profile is
inhibited. After a thorough drainage, the upward movement of water can not restart
immediately since all over the soil profile, i is equal to FCadj,i and fCR,i is zero (Eq. 3.7u).
Capillary rise is restored when sufficient water is extracted out of the soil profile by crop
transpiration and/or soil evaporation and fCR,i becomes larger than 0 (Fig. 3.7u).
If during the season the water table enters in the root zone, the roots under the groundwater
table will become inactive and might die off. If later in the season the water table drops, it
is assumed that the part of the root zone that was flooded becomes active again and that
the root zone expands till Zx is reached.
The sensitivity of the crop to water logging is specified by the soil water content
(anaerobiosis point) at which the aeration of the root zone will be deficient for the crop and
starts to affect crop transpiration (section 3.10 Crop transpiration). To simulate the
resistance of crops to short periods of waterlogging, the full effect will only be reached
after a specified number of days.
By weighing the reference evapotranspiration rates and air temperatures in the previous,
actual and next 10-day period or month, daily ETo rates, and the daily maximum and
minimum air temperatures are obtained in AquaCrop. The calculation procedure is based
on the interpolation procedure presented by Gommes (1983). The same interpolation
procedure is applied for 10-day and monthly rainfall data but since it is highly unlikely that
rainfall is homogenously distributed over all the days of the 10-day period or month, some
further processing is required to determine the amount of rainfall that is (i) lost by surface
runoff, (ii) stored in the top soil as effective rainfall, (iii) lost by deep percolation and (iv)
by soil evaporation (Fig. 3.7f).
surface
runoff
effective
rainfall
deep
percolation
The following procedures are available in AquaCrop to determine the effective rainfall
when 10-day or monthly rainfall data is given as input:
- 100 percent effective
- USDA-SCS procedure
- Expressed as a percentage of rainfall
USDA-SCS procedure
SCS scientists analysed 50 years of rainfall records at 22 locations throughout the United
Sates of America to predict effective rainfall (SCS, 1993). A daily soil water balance
incorporating crop evapotranspiration, rainfall, irrigation and the storage capacity of the
root zone was used to determine the effective rainfall (Tab. 3.6e). By considering the
monthly crop evapotranspiration (ETcm) and rainfall (Pm), the monthly effective rainfall
(Pem) is obtained by the following empirical equation (USDA, 1970):
( )
Pem = 0.70917 Pm0.82416 − 0.11556 10 0.02426 ETcm (Eq.3.7v)
where Pem, Pm and ETcm are given in inches (1 inch = 25.4 mm). In the above equation
ETcm is the sum of the soil evaporation and crop transpiration by assuming that the
processes are not affected by water stress. The difference between rainfall (Pm) and the
estimated effective rainfall (Pem) is regarded as being lost by deep percolation.
Table 3.7e – Effective rainfall (expressed as a percentage of monthly rainfall) for various
levels of crop evapotranspiration and for a root zone with a RAW of 75 mm, as determined
by the USDA-SCS procedure.
Monthly crop evapotranspiration [mm/month]
30 60 90 120 150 180 210 240
Monthly Rain Effective rainfall
[mm/month] [%]
10 58 62 66 71 75 81 86 92
20 63 68 72 77 82 88 94 100
30 63 67 72 77 82 88 94 100
40 62 66 71 76 81 86 92 99
50 61 65 70 74 79 85 91 97
60 60 64 68 73 78 83 89 95
70 59 63 67 72 77 82 88 93
80 58 62 66 71 76 81 86 92
90 57 61 65 70 74 80 85 91
100 56 60 64 69 73 78 84 90
120 55 59 63 67 72 77 82 87
140 54 58 61 66 70 75 80 85
160 53 56 60 64 69 74 79 84
180 52 55 59 63 68 72 77 82
200 51 55 58 62 67 71 76 81
The percentage will depend on the rainfall amount, the evapotranspiration rate and soil
type. Indicative values are given in Table 3.7e. The percentage can be obtained with greater
accuracy by simulating the drainage out of the root zone for those years were daily rainfall
data is available (or available in a nearby representative station). As such the characteristics
of the climate, cropping period, irrigation schedules and drainage characteristics of the soil
can be fully considered.
REW + 1
Eadj = n E
(Eq. 3.7w)
20
where REW is the readily evaporable water (mm) and n a program parameter which may
vary between 1 (strong reduction) and 10 (light reduction). Its default value is 5.
The optimal setting of the program parameter can be obtained by simulating the soil
evaporation for those years were daily rainfall data is available (or available in a nearby
representative station). As such the characteristics of the climate (rainfall distribution and
evaporating power of the atmosphere), the degree of canopy cover and the characteristics
of the soil type can be fully considered.
Since the solute transport in the macro pores bypass the soil water in the matrix, a diffusion
process has to be considered to describe the transfer of solutes from macro pores to the
micro pores in the soil matrix. The driving force for this horizontal diffusion process is the
salt concentration gradient that exists between the water solution in the macro pores and
micro pores. To avoid the building up of high salt concentrations at a particular depth, a
vertical salt diffusion is also considered. The driving force for this vertical redistribution
process is the salt concentration gradient that builds up at various soil depths in the soil
profile.
Vertical upward salt movement is the result of capillary rise from a saline groundwater
table and water movement in response to soil evaporation. The vertical upward salt
movement depends on the wetness of the top of the soil profile and the salinity and depth
of the groundwater table (see Chapter 3, section 3.7 Soil water balance). Due to soil
evaporation water will evaporate at the soil surface while the dissolved salts remain in the
top compartment.
3.8.2 Cells
To describe the movement and retention of soil water and salt in the soil profile, AquaCrop
divides the soil profile in various soil compartments (12 by default) with thickness Δz (Fig.
3.7b). To simulate the convection and diffusion of salts, a soil compartment is further
divided into a number of cells where salts can be stored (Fig. 3.8a).
diffusion
diffusion z
diffusion
field saturation
capacity
Figure 3.8a – Convection and diffusion of salts in the cells of a soil compartment
The number of cells (n), which may range from 2 to 11, depends on the soil type of the soil
horizon. Since salts are strongly attached to the clay particles a clayey horizon will contain
more cells than a sandy horizon. The inverse of the saturated hydraulic conductivity (Ksat)
is used as an index for the clay content. The number of cells is obtained by considering the
Ksat of the soil horizon to which the soil compartment belongs:
1000
2 n = ROUND1.6 + 11 (Eq. 3.8a)
Ksat
where Ksat is saturated hydraulic conductivity (mm/day) of the soil horizon. The volume
of a cell, which is a fraction of the total pore volume, is given by:
where Wcell is the volume of the cell in mm(water), θsat the soil water content at saturation
(m3/m3) of the soil horizon, n the number of cells, Δz the thickness of the soil compartment
(m), and Vol%gravel the volume percentage of the gravel in the soil horizon to which the
compartment belongs. A cell is in fact a representation of a volume of pores with a
particular mean diameter. Cells with a low number have small diameters, while cells with
a high number have large diameters (Fig. 3.8a).
The salt concentration in a cell can never exceed a threshold value. The threshold value is
determined by the solubility of the salt (see Chapter 2: 2.13 Soil profile characteristics,
2.13.6 Program settings). If the salt concentration in a cell exceeds the threshold value,
salts will precipitate and will be temporarily removed from the soil solution. Salts return to
the solution as soon as the salt concentration in the cell drops below the threshold value.
where EC is the electrical conductivity of the soil water in the cell (dS/m), Wcell the volume
of the cell (mm), and fdiff a salt diffusion coefficient.
The salt diffusion between adjacent cells does not only depend on differences in their salt
concentration but also on the swiftness with which salts can be rearranged between them
(fdiff). Between cells having large pore diameters, salts can move quite easily since the
forces acting on them are relatively small. Equilibrium between the salt content in those
pores is reached quickly. Due to strong adsorption forces and low hydraulic conductivity’s,
salt diffusion will be rather limited in the small pores and it might take quite a while before
equilibrium is reached between the salt concentrations in those cells. This is simulated in
AquaCrop by adjusting the diffusion process with the ease salts can diffuse. The ease of
salt movement is expressed by the diffusion coefficient (fdiff). The coefficient varies
between 1 for the macro pores (no limitation on salt diffusion) and 0 for the very smallest
pores (salts can no longer diffuse between adjacent cells). Between cells representing
macro pores the diffusion is entirely in response to salt concentration gradients (fdiff = 1).
Between cells representing the smaller pores, salt diffusion is more limited (fdiff < 1).
%
d
al
40
o b
0.4 gl
0.2 %
20
0.0
1 2 3 ... macropores
field saturation
cell capacity
Figure 3.8b – The salt diffusion coefficient (fdiff) for the various cells
and for various global diffusion factors
The salt diffusion coefficient for the various cells is plotted in Figure 3.8b, for various
global salt diffusion factors. The global diffusion factor is a program parameter that
describes the global capacity for salt diffusion and can be used to calibrate the model.
Increasing or decreasing the global salt diffusion factor alters the ease for salt diffusion and
increases or decreases the speed with which equilibrium is reached between the salt
concentrations in the adjacent cells. The default setting for the salt diffusion factor is 20 %.
In Table 3.8a the calculation procedure (Eq. 3.8d) for fdiff is presented.
GDF
(global < 50 % > 50 %
diffusion
factor)
field
capacity saturation
fdiff a bx − a a b (1− x ) − a
(Eq. 3.8d1) 1− (Eq. 3.8d2)
ab−a a b−a
a=2
GDF
(Eq. 3.8d3) GDF
a
100 a = 21 − (Eq. 3.8d5)
100
b b = 1010 ( 0.5−GDF /100) (Eq. 3.8d4) b = 1010 ( GDF /100 − 0.5) (Eq. 3.8d6)
To simulate upward salt transport in response to soil evaporation, AquaCrop considers not
only the amount of water that is extracted out of the soil profile by evaporation, but also
the wetness of the upper soil layer (Fig. 3.8c). The relative soil water content of the upper
soil layer determines the fraction of the dissolved salts that moves with the evaporating
water:
SWCrel
f salt = 10 SWC rel (Eq. 3.8e)
10
− air dry
SWCrel = (Eq. 3.8f)
sat − air dry
1.0
0.8
0.6
salt
f
0.4
0.2
0.0
0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1
SWC rel
air dry saturation
Figure 3.8c – Fraction of dissolved salts (fsalt) that moves with the evaporating water
for various relative soil water contents (SWCrel) of the upper soil layer
When the upper soil layer is sufficiently wet, soil evaporation will move an important
fraction of dissolved salts with the water that is moved by the process to the evaporating
soil surface layer. When the layer dries out, the fraction of the dissolved salts that can be
transported upward diminishes since water is no longer entirely moved by soil water flow
but also by vapour diffusion. Vertical salt movement in response to soil evaporation is no
longer considered when the soil water content of the upper soil layer becomes air dry (Fig.
3.8c).
At the start of Stage II of soil evaporation, the thickness of the upper layer (Ze,top) is set at
0.15 m (see 3.9.5 Evaporation reduction coefficient). When evaporation removes water
from the upper layer Ze,top gradually expands to a maximum depth which is a program
parameter. Its default value is 0.3 m and the range is 0.15 to 0.50m.
where Saltcell is the salt content expressed in grams salts per m2 soil surface, Wcell (Eq. 3.8b)
its volume expressed in liter per m2 (1 mm = 1 l/m2), and 0.64 a global conversion factor
used in AquaCrop to convert deciSiemens per meter in gram salts per liter (1 dS/m = 0.64
g/l).
The electrical conductivity of the soil water (ECsw) and of the saturated soil paste extract
(ECe) at a particular soil depth (soil compartment) is:
n
Salt
j =1
cell , j
Salt
j =1
cell , j
where n is the number of salt cells of the soil compartment, θ the soil water content (m3/m3),
θsat the soil water content (m3/m3) at saturation, Δz (m) the thickness of the compartment,
and Vol%gravel the volume percentage of the gravel in the soil horizon to which the
compartment belongs
The effect of soil salinity on biomass production is determined by the average ECe of the
soil water in the compartments of the effective rooting depth (see 3.15 ‘Simulation of the
effect of soil salinity stress’).
The soil water content at air dry is estimated by applying the rule of thumb, stating that the
soil water content at air dry is about half of the soil water at wilting point (θair dry ≈ 0.5 θWP).
By assuming 40 mm for Ze,surf, an agreement was found between REW (Eq. 3.9b) and the
cumulative evaporation for the energy limiting stage (Stage I evaporation), i.e., the U value
of Ritchie (1972).
(
Ke = 1− CC * Ke x ) (Eq. 3.9.c)
The maximum soil evaporation coefficient Kex for a wet non shaded soil surface is a
program parameter. The default value is 1.10 (Allen et al., 1998) and can be adjusted by
the user. When the canopy cover (CC) expands in the crop development stage, the soil
evaporation coefficient Ke declines gradually (Fig. 3.9c).
In Eq. 3.9c, the fraction of the soil surface not covered by green canopy (1-CC*) is adjusted
for micro-advective effects (Fig 3.9d). The adjustment for (1-CC*) is based on the
experimental data of Adams et al. (1976) and Villalobos and Fereres (1990):
The microadvection cause E to be less than just being proportional to CC. The extra energy
is used for crop transpiration (see 3.10 Crop transpiration).
0.8 0.8
0.4 0.4
0.2 0.2
0.0 0.0
time (canopy development)
Figure 3.9c – Decline (bars) of the soil evaporation coefficient Ke with reference to
the wet non shaded soil surface (Kex) in the crop development stage when
the green canopy cover (shaded area) increases
1.0
0.8
0.6
1 - CC*
0.4
0.2
0.0
0.0 0.2 0.4 0.6 0.8 1.0
Canopy cover (CC)
Figure 3.9d – Adjusted fraction (1-CC*) of not shaded soil surface (bold line)
for various fractions of green canopy cover (CC)
Two factors are considered for the adjustment of the soil evaporation coefficient:
- fcc a coefficient expressing the sheltering effect of the dead canopy cover [0 … 1];
- CCtop the canopy cover prior to senescence. If the canopy cover has reached its
maximum size, CCtop = CCx
( )
Keadj = (1 − f cc CC top ) 1 − CC * Ke x (Eq. 3.9e)
Notwithstanding the rule of thumb (Allen et al., 1998) to reduce the amount of soil water
evaporation by about 5% for each 10 % of soil surface that is effectively covered by an
organic mulch the default value for fcc is 0.60 and not 0.50, because a standing crop gives
better shelter against the effect of dry wind than an organic mulch that covers the soil
surface. To simulate a smooth increase of evaporation in the late season stage when
senescence occurs, fcc increases gradually from 0 (at the start of the late-season stage) to
its final value when CC is half of CCtop.
1.0 1.0
0.8 0.8
CC: green canopy cover
0.6 0.6
Ke/Kex
0.4 0.4
0.2 0.2
0.0 0.0
time (canopy decline)
Figure 3.9e – Increase (bars) of the soil evaporation coefficient Ke adjusted for
withered canopy with reference to the wet non shaded soil surface (Kex) in the late
season stage when the green canopy cover (shaded area) decreases
The adjustment for soil evaporation consists in multiplying Ke by the correction factor:
Keadj = 1 − f m
Percent cov ered by mulch
( )
1 − CC Kex
*
(Eq. 3.9f)
100
The adjustment is not applied when standing water remains on the soil surface (between
soil bunds).
( )
Keadj = f w 1− CC * Ke x (Eq. 3.9g)
The fraction fw is an irrigation parameter, and can be adjusted when selecting an irrigation
method in the Irrigation Management Menu. The adjustment for partial wetting is not
applied when:
- surface is wetted by irrigation and rain on the same day;
- surface is wetted by rain; and
- irrigation and/or rain water remains on the soil surface (between the soil bunds).
1.0
0.8
0.6 fK =
1
0.4 fK
=
4
0.2 fK
=
8
0.0
1.0 0.5 0.0
relative soil water content (Wrel)
start Stage II air dry
In stead of using the square root of time (Ritchie type of model), a mechanistic approach
is used to describe the evaporation rate in the falling rate stage. With this approach not only
time but also the amount of water extracted from the top soil by transpiration, groundwater
contribution from a shallow water table and the weather conditions (Rain and ETo) are
considered for the determination of Kr.
To account for the sharp decline in hydraulic conductivity with decreasing soil water
content, an exponential equation is used to relate Kr to the relative water content of the
upper soil layer:
exp f K Wrel − 1
0 Kr = 1 (Eq. 3.9h)
exp f K − 1
At the start of Stage II, Wrel begins to decline below 1 and becomes 0 when there exist no
longer a hydraulic gradient i.e. when Ze,top is air dry (Fig. 3.9f). The decline factor fK
depends on the hydraulic properties of the soil and can be used to calibrate Kr when
measurements of soil evaporation are available. The decline of Kr with decreasing Wrel
alters by varying the value of fK (Fig. 3.9f). When fK takes a value of 4, a good fit was
obtained between the square root of time approach (Ritchie, 1972) and the soil water
content approach used by AquaCrop in the simulation of Stage II evaporation. Even after
three weeks of evaporation (21 days) the cumulative amount of water lost by soil
evaporation remained in the same range for both approaches and for most soil textural
classes.
( )
EStageII = Kr 1− CC * Ke x ETo (Eq. 3.9j)
Since Kr varies strongly with Wrel especially at the beginning of Stage II, the routine daily
time step is inadequate and had to be divided into 20 equal fractions to obtain a differential
solution for Eq. 3.9j. At the end of each small time step, the water content of the soil profile
is updated and Kr is estimated with Eq. 3.9h. Consequently the switch from stage I to II
occurring during the day, can be simulated as well.
where KcTr,x coefficient for maximum crop transpiration (well watered soil and complete
canopy, CC = 1);
CC* actual canopy cover adjusted for micro-advective effects.
1
adjusted canopy cover (CC*)
0.8
0.6
0.4
0.2
0
0 0.2 0.4 0.6 0.8 1
Canopy cover (CC)
Figure 3.10b – Canopy cover (CC*) adjusted for micro-advective effects (bold line)
for various fractions of green canopy cover (CC)
When the canopy cover is incomplete extra energy is available for crop transpiration (Tr)
and less for soil evaporation (E). The micro-advection cause Tr to be more than just being
proportional to CC and E less than being proportional to (1-CC) (see 3.9 ‘Soil
evaporation’).
where t is the time in days after tCCx (t is zero before and at tCCx), and fage is the reduction
expressed as a fraction of CCx. The fage coefficient is a crop parameter, since it will require
some adjustment for annual crops such as sugarcane.
1.2
1.0 100 %
crop transpiration coefficient
0.8
KcTr
CC
0.6
0.4
0.2 20%
0.0
0.0 time
canopy canopy
expansion decline
Figure 3.10c – Canopy development (shaded area) and crop transpiration coefficient
KcTr (line) throughout the crop cycle for KcTr,x = 1.1, CCx = 100%, and fage
0.16%/day
The exponent a is a program parameter and can be used to accentuate (a > 1) or to minimize
(a < 1) the drop in the transpiration/photosynthetic efficiency of the declining canopy. In
the program ‘a’ can vary between an upper limit of 4 (very strong effect) and a lower limit
of 0.1 (very limited effect). Its default value is 1. The senescence factor (fsen) for various
degrees of withering (CC/CCx) and various values of the exponent ‘a’ is plotted in Fig.
3.10d.
1.0
0.9
a = 0.1
0.8
0.7
0.5
0.6 a= 1
f(sen)
0.5 a=
2
0.4 a=
0.3 4
0.2 a=
0.1
0.0
0.0 0.2 0.4 0.6 0.8 1.0
CC/CCx
no green leaves fully green
remain canopy
By considering the reduction of 5 %, when the [CO2] increase from 370 to 550 ppm
(analysis of FACE data), the correction of Kc for elevated [CO2]:
[𝐶𝑂2 −369.41]
𝐾𝑐𝑇𝑟𝑥,𝑎𝑑𝑗 = 𝐾𝑐𝑇𝑟𝑥 (1 − 0.05 ) (Eq. 3.10e/2)
550−369.41
To allow light rain to reduce the soil water stress of deep rooted crops, the root zone
depletion is compared with the depletion in the top soil at each time of the simulation (Fig.
3.2c). The comparison determines which part of the soil profile is the wettest and controls
the water stress (only for Kssto).
At the lower threshold, which corresponds with permanent wilting point, the soil water
depletion (Dsto,lower) is:
Dsto ,lower = TAW (Eq.3.10h)
The depletion coefficient psto is the fraction of TAW that can be depleted from the
considered soil volume before stomata starts to close. The p factor divides the Total
Available soil Water (TAW), in two parts: water that can be extracted without stress
(RAW) and water that is more difficult to extract (Fig. 3.10f).
no stress 1.0
0.8
water stress coefficient
0.6
Kssto
0.4
0.2
D
full stress 0.0
p(sto) p(lower)
field capacity TAW permanent wilting point
Figure 3.10e – The water stress coefficient for stomatal closure (Kssto)
for various degrees of depletion (D) in he considered soil volume
W: stored soil water
0.0
(mm)
field capacity
psto TAW
TAW
RAW
TAW
depletion (mm)
D : soil water
0.0
considered soil volume
(top soil or root zone)
Figure 3.10f – The upper and lower threshold of soil water depletion affecting
stomatal closure
In a well-watered saline soil, and in the absence of any other stresses than salt stress,
AquaCrop obtains the relative biomass production from the ‘Biomass – ECe’ relationship
(Fig. 3.2f). The partial closure of the stomata is specified by calibration for a particular
ECe (Fig. 3.10g – effect 1).
When the soil is not well-watered, water depletion in the root zone results in an increase of
the salt concentration in the remaining soil water. Although root zone depletion does not
alter ECe (the indicator for soil salinity), it increases the electrical conductivity of the soil
water (ECsw). The stronger the root zone depletion, the larger ECsw, and the more difficult
it becomes for the crop to extract water from its root zone. This results in a stronger closure
of the stomata when the soil dries out. The extra effect of ECsw on stomata closure is
specified by calibration for the crop response to salinity stress (Fig. 3.10g – effect 2).
1.0
1
0.8
2
0.6
sto
Ks
0.4
0.2
0.0 2
FC PWP
s oil w ate r conte nt
Fig. 3.10g – The soil water coefficient for stomatal closure (Kssto) without (gray line)
and with (several alternative black lines) the effect of soil salinity stress. The decline
of Kssto (effect 1) is linked with ECe, the shift of the upper and lower threshold
(effect 2) is the effect of ECsw. The effect of ECsw on stomata closure (presented by
the alternative black lines) is specified by calibration
The effect of soil salinity stress on stomatal closure is simulated by multiplying the soil
water stress coefficient for stomatal closure (Kssto) with the soil salinity stress coefficient
for stomatal closure (Kssto,salt):
Ks sto ,adj = Ks sto ,salt Ks sto (Eq. 3.10i)
soil saturation
deficient
anaerobiosis point
soil aeration
field capacity
Figure 3.10h – The upper and lower threshold for the soil water content in the root
zone resulting in deficient aeration conditions
The effect of water logging on crop transpiration is simulated by means of a water stress
coefficient for water logging (Ksaer):
Tr = Ks aer KsTr KcTr ETo (Eq. 3.10j)
Ksaer varies linearly between the anaerobiosis point where Ksaer is 1 and soil saturation
where Ksaer is zero (Fig. 3.10i).
no stress 1.0
0.8
anaerobiosis point
RAW
water stress coefficient
0.6
Ksaer
0.4
0.2
Figure 3.10i – The water stress coefficient for water logging (Ksaer)
for various levels of soil water content (θ)
0.80
0.60
KsTr
0.40
0.20
Figure 3.10j – The air temperature stress coefficient for reduction of crop
transpiration (KsTr) for various levels of growing degrees
If the growing degrees generated in a day drops below an upper threshold (GDupper) the
crop transpiration is limited by air temperature and Ksb is smaller than 1 (Fig. 3.10j). In
AquaCrop it is assumed that transpiration is completely halted when it becomes too cold
to generate any growing degrees (KsTr = 0 for 0 °C day). Between the lower (0°C day) and
upper limit (GDupper) the variation of the adjustment factor is described by a logistic
function. The upper threshold (GDupper) is a crop parameter, and its value can be adjusted
between 0.1 and 20 °C day.
Crop transpiration in a weed infested field (TrW) is proportional to CCW (Eq. 3.5k). In the
calculation of TrW, the adjustment for micro-adjustments is based on the total canopy cover
CCTOT:
(
TrW = Ks Ks Tr CCW + CC TOT
*
)
− CC TOT Kc Tr , x ETo (Eq. 3.10l)
where Ks is the water stress coefficient, KsTr the cold stress coefficient, CCw the crop
canopy cover, CCTOT the total (crop and weeds) canopy cover, CC*TOT the total canopy
cover adjusted for micro-advective effects, KcTR,x the maximum crop transpiration
coefficient, and ETo is the evapotranspiration rate from a grass reference surface.
where Ks soil volume is the average soil water stress in the considered soil volume induced
by a shortage or an excess of water and/or aeration stress. A linear relationship between
the water stress coefficient ( Ks soil volume ) and the soil water content in the considered
soil volume is assumed.
2. Determination of the amount of water that can be extracted out of the root zone at
various depths, by considering the maximum root extraction rate and the water stress
coefficient at the various depths (soil compartments):
S i = Ks i S x , i (Eq. 3.10n)
The root extraction rate or sink term, S, (Feddes et al., 1978; Hoogland et al., 1981,
Belmans et al., 1983) expresses the amount of water that can be extracted by the roots
at a specific depth per unit of bulk volume of soil, per unit of time ([Link]-1).
Depending on the type of water stress, Ksi is either Kssto or Ksaer in Eq. 3.10n. To
determine the value of Ksi for the given θi, the assigned shape of the Ks curve (linear
or convex) is considered.
3. By integrating Eq. 3.10n over the different compartments of the root zone, the exact
amount of water that can be extracted by transpiration is obtained:
where dzi is the thickness of the soil compartment (m). The integration starts at the top
of the soil profile and is stopped when the sum is equal to the transpiration demand
given by Eq. 3.10m or the bottom of the root zone is reached.
When the maximum root extraction rate over the entire root zone (Σ 1000Sxdz) is too
small (as a result of a limited root volume), the amount of water that can be extracted
▪ Maximum root extraction rate (Sx) and the total extraction rate (Σ 1000Sxdz)
In the model the maximum root extraction rate at the top of the soil profile (Sx,top) might
be different from the maximum extraction rate at the bottom of the root zone (Sx,bottom). The
assigned Sx values at different soil depths are proportional to the specified water extraction
pattern (Fig. 3.10k). Apart from the root distribution, Sx is also determined by the total root
volume. The total root volume determines the total amount of water that can be extracted
out of the root zone, i.e. the total extraction rate (Σ 1000Sxdz).
The total extraction rate and the root distribution in the root zone are crop parameters which
can be adjusted. The default values (which are assigned when the crop is created) are:
- for root distribution: 40, 30, 20, 10% (where the values refer to the upper, second, third
and bottom quarter of the root zone as in Fig. 3.10j), and
- for total extraction rate Σ 1000Sxdz: A default 3 mm/day for each 0.10 m of rooting
depth is considered. By making Σ Sxdz very small, extremely low root volume resulting
in severely water stress even in a well-watered soil for normal climatic conditions can
be simulated.
Sx(bottom 1/ 4 ) +
2
3
(Sx(top 1/ 4) − Sx(bottom 1/ 4) )
P2 = 100 (Eq.3.10s)
4 Sx
Sx(bottom 1 / 4) +
1
3
(Sx(top 1 / 4) − Sx(bottom 1 / 4) )
P3 = 100 (Eq. 3.10t)
4 Sx
Sx(bottom 1 / 4)
P4 = 100 (Eq.3.10u)
4 Sx
SxTop and SxBottom are used throughout the simulation, to calculate at each time step,
the maximum root extraction (Sxi) at various depths Zi in the expanding root zone (i.e. the
Sxi for the different soil compartments:
Zrt − Z i
Sxi = SxBottom + SxTop − SxBottom (Eq. 3.10v)
Zrt
As such the specified water extraction pattern P1, P2, P3 and P4 in respectively the upper,
second, third and bottom quarter of the root zone remains valid at any time, as the root zone
expands during simulation.
Figure 3.10n – Root distribution or maximum root extraction (grey area) at various
moments (t1, t2 and t3) during the growing cycle
Figure 3.10p – Root distribution (water extraction pattern) at time t in a soil profile
(1) without, and (2) with restrictive soil layers (too dry and/or the presence of
physical or chemical restrictive soil layers).
To guarantee an identical total root density (total maximum root extraction) when a
restrictive soil layer limits the root zone expansion, SxBottom is adjusted, with the
correction factor, Scor:
Zx SxTop + SxBottom
2 t ,un lim
− SxTop
=
Zxt 2
S cor (Eq. 3.10w)
SxBottom
where Zxt is the limited rooting depth at time t, and Zxt,unlim the rooting depth which could
have been reached at that moment, if root deepening was unlimited.
The adjusted SxBottom is given by:
Tr
SxBottomadjust = S cor SxBottom 0.060 m 3 .m −3 .day −1 (Eq. 3.10x)
Tr
x
Eq. 3.10v, which specifies the maximum root extraction (Sxi) at various depths Zi in the
root zone, becomes :
Zr − Z i
Sxi = (Scor ) SxBottom + SxTop − (Scor ) SxBottom t 0.060 m 3 .m −3 .day −1
Zrt
(Eq. 3.10y)
where Zrt is the rooting depth at time t.
The restriction of 0.060 m3/[Link] in Eq. 3.10x and 3.10y, refers to the limitations of the
maximum root extraction.
Tr
m = WP* (Eq. 3.11a)
ETo
Tr
B = WP* (Eq. 3.11b)
ETo
Since AquaCrop does not simulate biomass partitioning among various organs, variations
in partitioning along the season are simulated by increasing or reducing WP*. The
calculation scheme for the above-ground biomass is presented in Fig. 3.11a/2, with
indication of the crop parameters which can be used to calibrate the transfer of assimilates:
- Lstorage: the duration of the storage period;
- S: the maximum fraction of produced assimilates that are stored in the below-ground
parts during the storage stage;
- M: the fraction of stored assimilates of the previous season, that are remobilized at the
start of the season.
Some leguminous crops may have WP* values below 15 g/m² due to their biological
nitrogen fixation process.
²
m
g/
g/
5
0
:3
:3
P*
P*
W
W
²
/m
0g
s
2
op
*:
Dry above-ground biomass WP
cr
C4
²
/m
15g
P*:
ps W
cro
C 3
Sum (Tr/ET0)
Figure 3.11b – The relationship between the dry above-ground biomass and the
total amount of water transpired for C3 and C4 crops after normalization for CO2
and climate (ETo)
*
WPadj
= 1 + f type ( f CO 2 − 1) WP * (Eq. 3.11c)
The coefficient between square brackets, considers the difference between the reference
value and the atmospheric composition for that year (fCO2) and the crop type (ftype).
In Figure 3.11c/1, the adjustment of WP* for various atmospheric CO2 concentrations (Eq.
3.11c) is plotted for various crop types (ftype). In Table 3.11c/1 the adjustment of WP* for
various atmospheric CO2 concentrations (Eq. 3.11c) for C3 crops (ftype = 1) and for two
different approaches of the correction coefficient for CO2 (fCO2) are listed.
1.5
1 + ftype (fCO2 - 1)
1.4
. 00
e) = 1
f(typ
1.3 op
cr
C3
1.2 f(type) = 0.50
f(type) = 0.25
1.1 C4 crop
f(type) = 0.00
1.0
0.9
0.8
320 340 360 380 400 420 440 460 480 500 520 540 560
CO2 in ppm
Figure 3.11c/1 – Correction for WP* as given by Eq. 3.11c (with the default fsink of
0.5 for fCO2) considering various atmospheric CO2 concentration and various
coefficients for crop type: ftype = 1.00 (WP* ≤ 20 g/m2); 0.50 (WP* = 30 g/m2); 0.25
(WP* = 35 g/m2); and 0.00 (WP* ≥ 40 g/m2).
0 f type =
(40 − WP *) 1
(40 − 20)
(Eq. 3.11d)
The Eq. 3.11d considers the distinction between C4 crops with a typical WP* of 30 up to
35 g/m2 and C3 crops with a typical WP* of 15 up to 20 g/m2 (Fig. 3.11b)
f CO 2 =
(C a, i / Ca , o )
1 + (Ca , i − Ca , o ) (1 − w)bSted + w ( f sin k bSted + (1 − f sin k )bFACE )
(Eq. 3.11e/1)
To consider the discrepancy between the observed (FACE experiments) and theoretical
adjustment (Steduto et al., 2007) of WP*, two coefficients (bSted and bFACE) are considered.
The weighing factor (w) makes that in Eq. 3.11e/1 bFACE gradually replaces bSted starting
from the reference atmospheric CO2 concentration (Ca,o = 369.41 ppm) and becomes fully
applicable for Ca,i equal to 550 ppm:
(550 − Ca ,i )
0 w = 1 − 1
(550 − Co,i )
(Eq. 3.11f)
For Ca,i smaller than or equal to Ca,o, the weighing factor is zero (w = 0), while for Ca,i =
550 ppm, w becomes 1. The threshold of 550 ppm is selected as the representing value for
the elevated [CO2] maintained in the FACE experiments.
The crop sink strength coefficient in Eq. 3.11e/1 considers that the theoretical adjustment
(with bSted) might not be entirely valid when (i) soil fertility is not properly adjusted to the
higher productivity under elevated CO2 concentration, and/or (ii) the sink capacity of the
current crop variety is unable to take care of the elevated CO2 concentration.
Table 3.11c/2 – Range of indicative values for fsink for 10 crops available in the
database of AquaCrop (Vanuytrecht et al., 2011)
Crop Class and indicative value range for fsink
Cereals
- Maize Low (0.0 – 0.2)
- Rice Low (0.0 – 0.2)
- Wheat Low (0.0 – 0.2)
- Sunflower Low (0.0 – 0.2)
Legumes
- Soybean Moderate low (0.2 – 0.4)
Indeterminate crops
- Tomato Moderate low (0.2 – 0.4)
- Quinoa Moderate low (0.2 – 0.4)
Woody species
- Cotton Moderate high (0.4 – 0.6)
Root and tuber crops
- Potato High (0.4 – 0.6)
- Sugar beet High (0.4 – 0.6)
The crop sink strength coefficient (fsink) can be altered according to the sink strength of the
crop considered, which is determined by crop characteristics and field management. The
value can be as high as one (the theoretical approach) or as low as zero (based on an
The values of fsink reported in Table 3.11c/2 should be considered as a good starting value
but not as definitive. If projections of future agricultural productivity are to be made in
areas where nutrient deficiency is excepted fsink should be reduced. If projections are to be
made for species with improved cultivars with a higher responsiveness to [CO2] are likely
to be bred (e.g. high value crops like vegetables) the values for fsink can be higher than the
indicative value in Table 3.11c/2.
Figure 3.11c/2 – Gross leaf photosynthesis (left ordinate) for various ambient CO2
concentrations for C3 and C4 crops (after Yin and Struik, 2009), and the derived
corresponding adjusted correction coefficient for CO2 (fCO2,adj) at the right ordinate.
The decreasing trend in crop response to elevated CO2 is well documented in literature (e.g.
Akita and Moss, 1973; Chapin et al., 2011; Kirschbaum, 2011; Kromdijk and Long, 2016;
Yin and Struik, 2009). However, the exact crop response differs between publications and
The adjustment for the correction coefficient for CO2 is based on values for the gross leaf
photosynthesis (Fig. 3.11c/2) given by Yin and Struik (2009). For the C3 crop, the leaf
photosynthesis is:
- 22.7 μmol/m2.s at 369.41 ppm (point A), which is the reference CO2 concentration at
the year 2000. There is no need to correct WP* (Tab. 3.11c/1) and the corresponding
correction coefficient for CO2 (fCO2,adj) is consequently 1 (right ordinate Fig. 3.11c/2);
- 27.5 μmol/m2.s at 550 ppm (point B0), which is the CO2 concentration maintained in
most FACE experiments. Since the leaf photosynthesis is 21 % larger than at the
reference point, fCO2,adj should also be 1.21 at this Ca,i. The resulting fCO2,adj of 1.21
corresponds well with the observed value of 1.23 derived by Vanuytrecht et al. (2011)
from the FACE experiments (Eq. 3.11e/1 with fsink = 0; Tab. 3.11c/1);
- 35.9 μmol/m2.s (point C) at 2,000 ppm, which is 58 % larger than the leaf
photosynthesis at the reference point. Hence at point C the fCO2,adj should be 1.58 (right
ordinate Fig. 3.11c/2).
In Fig. 3.11c/2, the curve AB0C (given by Yin and Struik, 2009) can also be used to specify
the adjustment of WP* for CO2 (fCO2,adj) for the approach based on FACE experiments
(when fsink = 0) for high CO2 concentrations. The corresponding value fCO2,adj is given at
the right ordinate.
For the theoretical adjustment (Eq. 3.11e/1 with fsink = 1), Eq. 3.11e/1 yields a fCO2 of 1.453
at 550 ppm (Tab. 3.11c/1). This corresponds with point B1 in Fig. 3.11c/2. Hence the curve
AB1C specifies fCO2,adj for the theoretical adjustment (when fsink = 1) for high CO2
concentrations.
The equation for any of the curves ABC for any fsink between 0 and 1 (Fig. 3.11c/3) is given
by:
(Eq. 3.11e/2)
Figure 3.11c/3 – Correction coefficient for CO2 for various atmospheric CO2
concentrations and fsink in AquaCrop, for a C3 crop type (ftype = 1 with WP* ≤ 20
g/m2). The dotted lines are the fCO2 as given by Eq. 3.11e/1 for respectively fsink = 0,
0.5 and 1. The points A, B0, B1, and C are identical as in Figure 3.11c/2
400
ref erence (369.41 ppm)
300
200
100
0
1900 1920 1940 1960 1980 2000 2020
year
Figure 3.11c/4 – Atmospheric CO2 concentrations derived from frin and ice samples
(light bars), observed at Mauna Loa Observation (dark bars), and predicted (dotted
line) by assuming a continuous rise of 2 ppm/year, with indication of the reference
value
Figure 3.11d – Projected CO2 concentrations for 5 SSPs (solid line) and 4 RCPs
(dotted lines), available in the database of AquaCrop.
In the vegetative stage, the dry above-ground biomass is derived from the simulated
amount of water transpired by means of WP*. During yield formation, the biomass water
productivity switches gradually from WP* to WP*adj (Fig. 3.11e). For determinant crops
the transition takes place during the lag phase where the increase of the Harvest Index is
slow (see 3.12.3 Building up of Harvest Index). For indeterminant crops it is assumed that
the biomass water productivity is fully adjusted after 1/3 of the length of the yield formation
stage.
Dry above-ground biomass
transition
period
yie ld
form ation
Sum (Tr/ET0)
Figure 3.11e – The relationship between the dry above-ground biomass and the total
amount of water transpired before and during yield formation for crops rich in
lipids or proteins
KsWP is 1 for non-limiting soil fertility. The stress coefficient decreases for increasing soil
fertility stress (see 3.2. Stresses). Biomass production is no longer possible when the stress
coefficient reaches the theoretical minimum of 0.
Because the reservoir of nutrients gradually depletes when the crop develops, the effect of
soil fertility on the adjustment of WP is not linear throughout the season. As long as the
canopy is small, the daily biomass production will be rather similar to the daily production
for non-limited soil fertility, and KsWP,i at day i will be close to 1 (no fertility stress). This
is the case early in the season when sufficient nutrients are still available in the root zone.
If the crop does not experience water stress, the canopy will further develop during the
season but this will result in a progressive depletion of nutrients from the reservoir.
Consequently the daily biomass production will gradually decline when more and more
biomass is produced. This is simulated in AquaCrop by making the stress coefficient KsWP,i
a function of the relative amount of biomass produced (Brel). For every day in the season
Brel is given by the ratio between the amount of biomass produced on that day and the
maximum amount of biomass that can be obtained at the end of the season for the given
soil fertility level. The maximum amount refers to a production without any water stress
during the season.
Since Brel, after correction for temperature stress, is proportional to the relative amount of
water that has been transpired, KsWP,i for any day in the season is given by:
2
i
(Tr j / ETo j )
KsWP , i = 1 − fWP j =1 (Eq. 3.11i)
n
(Trx , j / ETo j )
j =1
where KsWP,i soil fertility stress coefficient for biomass water productivity at day
fWP maximum reduction for WP (expressed as a fraction) for the given
soil fertility level, that can be observed at the end of the season when
the crop does not experience water stress (fWP = 1 – KsWP)
∑(Trj/EToj) sum of water transpired at day i (normalized for climate)
∑(Trx,j/EToj) sum of water that will have been transpired at the end of the season
(normalized for climate) for the given soil fertility level when the
crop does not experience water stress
n number of days in the season
f WP
0.6
KsWP,i
0.4
0.2
Figure 3.11f – Soil fertility stress coefficient for various degrees of relative
transpiration (for a fWP of 0.3 or a KsWP of 0.7)
The variation of the soil fertility stress coefficient throughout the season is plotted in Fig.
3.11f. At the start of the season KsWP,i is 1 and WP* is not adjusted. As more and more
water is transpired during the season, KsWP,i will gradually decline. When the crop does
not experience any water stress throughout its cycle, the relative transpiration becomes 1
at the end of the season and KsWP,i=n = KsWP. However, if water stress hampers the canopy
development and/or result in stomatal closure, the relative transpiration will remain smaller
than 1 throughout the season, resulting in a smaller adjustment of WP (KsWP,i=n > KsWP,x).
How strongly WP*adj differs from WP*, depends on the deviation of the atmospheric CO2
concentration from its 369.47 ppm reference value, the crop type, its sink strength, the
growth stage (vegetative or yield formation), the type of products synthesized during yield
formation, the amount of biomass produced, the soil fertility and /or soil salinity stress. For
soil fertility/salinity stress, WP*adj will decline during the season as more biomass is
produced and KsWP,i gradually decreases.
Reference: Raes, D., Fereres, E., García Vila, M., Curnel, Y., Knoden, D., Kale Çelik, S.,
Ucar, Y., Türk, M., Wellens, J. 2023. Simulation of alfalfa yield with AquaCrop.
Agricultural Water Management (284), 108341.
[Link]
Perennial herbaceous forage crops transfer a considerable fraction of the assimilates to their
below-ground parts after mid-season. At the start of the next season, a fraction of the stored
assimilates are remobilized by transferring them from the below-ground to the above
ground parts of the crop (Fig. 3.11a/2). The rest is assumed to be lost during the off-season
by respiration and natural self-thinning, or remain stored in underground organs.
The transfer of assimilates is described by 3 crop parameters (Tab. 3.11n), which can be
used to calibrate the process of the transfer of the assimilates.
Table 3.11n – Crop parameters describing the transfer of assimilates (Fig. 3.11a/2)
Symbol Description Type
Lstorage Number of days at end of season during which assimilates Management
are stored in root system – only for perennial forage crops Cultivar
Calibration:
- By altering the length of the storage stage, the total amount of biomass produced in the
storage stage (∑m) can be adjusted;
- By altering the maximum percentage at the end of the storage stage, the percentage of
assimilates stored (100 ∑msto/∑m) can be adjusted;
- Only a fraction of the stored assimilates will be remobilized at the start of the next
season. This fraction (expressed as a percentage) can be used to calibrate (increase or
decrease) the remobilization of the stored assimilates at the start of the next season.
Where fi is a correction factor which is less than one during the period of assimilate storage
in below-ground organs, and greater than one during the period of remobilization of
assimilates in spring (Fig. 3.11a/2).
The net assimilate storage stage starts after mid-season when the crop transfers an
important fraction of mi to the below-ground organs. During the following spring, which
corresponds to the net remobilization stage, the stored assimilates are transferred to the
above-ground organs to contribute to enhanced growth. In the remobilization and storage
stages, fi is corrected for regrowth, since plants use the carbohydrate reserves for regrowth
both in the spring and after each cutting (Fig. 3.11n).
Since perennial herbaceous forage crops transfer a considerable fraction of the assimilates
below ground after mid-season, the daily biomass produced, mi, is reduced by a fraction
(fsto,i) that exponentially increases from 0 at the start of the net storage stage (t = 0) to a
fraction (S) of mi at the end of the season (t = 1):
(𝑒𝑥𝑝−5𝑡 −1)
𝑓𝑠𝑡𝑜,𝑖 = [ (𝑒𝑥𝑝−5−1) ] 𝑆 (Eq. 3.11r)
When the crop is harvested during the storage stage, fsto,i is temporarily reduced to consider
the assimilates required for the regrowth of the crop canopy. This is simulated by
multiplying fsto,i by an adjustment factor (ai) for regrowth (0 ≤ ai ≤ 1):
(𝐶𝐶𝑖 − 𝐶𝐶𝑐𝑢𝑡 )
𝑎𝑖 = (𝐶𝐶𝑥 − 𝐶𝐶𝑐𝑢𝑡 )
(Eq. 3.11s)
where CCcut is the canopy cover after harvest, and CCi the canopy cover at day i, which
increases during regrowth from CCcut to the maximum canopy cover, CCx. At every
harvest date, CCi = CCcut, ai is zero and storage is halted (Fig. 3.11p). When CCi reaches
CCx at the end of regrowth, ai is 1, and storage is again at maximum rate.
Figure 3.11p – Storage fraction (fsto,i) that exponentially increases during the storage
stage of assimilates (Eq. 3.11r). The adjustment factor ai for regrowth (Eq. 3.11s) is
zero on a day of harvest, and gradually increases to 1 during regrowth.
Although the percentage of assimilates transferred to the root system gradual increases
(Fig. 3.11p), the daily production of the biomass at the end of the storage stage, and as such
the stored fraction, might not be that important due to a reduction of the crop transpiration
in the late-season as a result of the natural senescence of the crop Canopy Cover at the end
of the crop cycle and/or cold stresses (Fig. 3.11q).
Figure 3.11q – Example of simulated stored assimilates in root system (Bout) during
the storage stage
where mmob,i are the assimilates remobilized from the root system on day i, expressed as a
fraction (fmob,i) of mi, and t is the relative time in the remobilization stage which gradually
decreases from 1 at the start of the season to zero at the end of the remobilization stage.
When the canopy reaches 90 percent of CCx after regrowth, remobilization is no longer
considered. This is simulated by multiplying fmob,i with an adjustment factor (ci) for
regrowth (0 ≤ ci ≤ 1):
(𝐶𝐶 − 𝐶𝐶 )
𝑐𝑖 = 0.1𝑥 𝐶𝐶 𝑖 if CCi > 0.9 CCx (Eq. 3.11w)
𝑥
At each harvest, ci is 1 and remobilization starts at its maximum rate. It stays that way until
CC has reached 90 percent of its maximum (CCx). When maximum canopy cover is
reached (CC = CCx), ci is zero and remobilization is halted until the next harvest. It is
considered that remobilization and storage do not occur at the same time.
Figure 3.11r – Mobilization fraction (fmob,i) that exponentially decreases during the
mobilization stage of assimilates (Eq. 3.11u). To stimulate growth, the adjustment
factor ci is 1 as long as CC increase. When the maximum canopy cover is reached, ci
is zero and remobilization is halted (Eq. 3.11v).
Figure 3.11s – Example of simulated mobilized assimilates from the root system
(Bin) during the mobilization stage
Since remobilization and storage cannot exist at the same time, any remaining part that still
needs to be remobilized at the start of the storage stage, is no longer considered and
assumed to be lost.
where B is the total dry above-ground biomass produced at crop maturity (Eq. 3.11b) and
HI the fraction of B that is the yield part, and Ydry is the dry yield. When water and/or
temperature stress develops during the crop cycle, the Harvest Index is adjusted to the
stresses at run time for fruit/grain producing crops and roots and tuber crops and might be
different from the reference harvest index (HIo). The adjustment can be positive or negative
and depends on the timing and the extent of the stress. The calculation scheme is presented
in Fig. 3.12a.
Figure 3.12a – Calculation scheme in AquaCrop for dry (Ydry) and fresh yield
(Yfresh)
The simulation of the building up of the Harvest Index differs along the crop types.
Distinction is made between leafy vegetable crops (Fig. 3.12b), root/tuber crops (Fig.
3.12c), and fruit/grain producing crops (Fig. 3.12d).
HIo
Harvest Index
time
germination
Figure 3.12b – Building up of Harvest Index along the growth cycle for leafy
vegetable crops
HIo
sowing time
transplanting start of tuber formation
or root enlargement
Figure 3.12c – Building up of Harvest Index for root and tuber crops
Once the increase of the Harvest Index is sufficient large to reach HIo at the end of yield
formation, the lag phase is ended and the increase of HI becomes linear (Fig. 3.12d). When
the building up of the Harvest Index is fast, the crop might have reached its reference value
(HIo) before the end of the crop cycle. Given the excess of potential fruits, the period of
building up of HI cannot be smaller in AquaCrop than the time required to have 100%
potential fruits.
70
60
HI0
50
Harvest Index (%)
40
30
20
10
0
time (days after anthesis)
lag phase linear increase of HI
During the yield formation stage, the Harvest Index for root/tuber crops and fruit/grain
producing crops, gradually increases until the Reference Harvest (HIo) is reached at about
the end of the crop growing cycle. However, when due to early canopy senescence, the
remaining green canopy cover (CC) drops below a threshold (CCmin), the Harvest Index
can no longer increase (Fig. 3.12e). In that case there is not enough green canopy left, so
that photosynthesis becomes insufficient. This results in an adjusted HI which is smaller
than HIo. The threshold green canopy cover below which the Harvest Index can no longer
increase is a program parameter.
Figure 3.12e – Harvest index development (bold line) when insufficient green canopy
cover remains during yield formation for crops with determinacy linked with
flowering
The adjustment is limited to the case of a decline of the green canopy cover due to severe
water stress, triggering an early senescence. This restriction avoids a zero HI (and no yield
formation) when CC is small (as a result of stresses) at the start of yield formation (tuber
formation or root enlargement for root/tuber crops or flowering for fruit/grain crops). The
adjustment of HI is only valid for root/tuber crops and fruit/grain producing crops, and
does not apply to leafy vegetable and forage crops.
70
60
HI ante
HI 0
50
Harvest Index (%)
40
30
20
10
0
lag phase tim e (days after anthesis)
yield formation
Figure 3.12f – Range (shaded area) in which the Harvest Index of fruit/grain
producing or root/tuber crops can increase as a result of water stress before the
start of yield formation
In AquaCrop the relative biomass is used to assess the saving in energy in the vegetative
growth stage. The relative biomass (Brel), determined at the start of flowering (tuber
formation), is the ratio between the actual biomass (B) and the potential biomass (B0):
B
Brel = (Eq. 3.12c)
B0
The actual dry above-ground biomass is the biomass derived from the cumulative amount
of water transpired at the moment of flowering. The potential value is the dry above-ground
biomass that could have been obtained in the same period in the given environment if there
was not any stress resulting in stunned growth, stomatal closure or early senescence.
HIo might be adjusted upward if Brel is smaller than 1 at the start of flowering. However, it
is the magnitude of Brel that determine the magnitude of the adjustment. A too high or a too
Range(Brel ) =
( )
ln HI ante
1 (Eq. 3.12d)
5.62
where ΔHIante allowable increase of HIo as the result of water stress before
flowering [%];
Range(Brel) range of relative biomass (Brel) in which HIo can be adjusted
[fraction].
In AquaCrop the range is linked to the allowable increase (in percentage) of HIo specified
by the user. The percentage is crop specific and gives the maximum possible increase of
HIo as a result of water stress before flowering. The higher the specified increase ΔHIante,
the larger the range for adjustment.
HIante /100
1.0
fante
0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0
lower upper
Brel limit top limit
Brel range
affecting HI 0
Figure 3.12g – Coefficient (fante) by which HIo has to be multiplied to consider the
effect of water stress before the start of yield formation, for various relative biomass
values (Brel), and a given allowable increase (ΔHIante)
Brel − Br , low
0 Ratiolow = 1 (Eq. 3.12f)
Br , top − Br , low
• For Brel between the top and the upper limit (Brel = 1):
Brel − Br , top
0 Ratioup = 1 (Eq. 3.12h)
Br , up − Br , top
The response in the Range(Brel) is assumed to be asymmetric. The top is at 1/3 of Br,up and
at 2/3 of Br,low.
▪ Flowering
In AquaCrop the pattern of flowering is assumed to be asymmetric with time (Fig. 3.12h).
The flowering distribution curve is given by:
where k is the relative time in percentage of the total flowering duration and fk is the
fraction of flowers flowering at time k.
Generally a crop will produce flowers in excess. When conditions are favorable, the crop
sets more fruits than needed for a good harvest. The excessive young fruits are aborted as
the older fruits grow. The excess (fexcess) is a crop parameter.
▪ Failure of pollination
Severe water stress, cold stress, or heat stress at flowering might induce a reduction in the
reference harvest index because insufficient flowers are pollinated to reach HIo. The effect
is dynamic, affecting only the population of flowers that is due to pollinate at the time of
the stress, but not the younger flowers due to pollinate days later or the flowers already
pollinated. To estimate HIadj AquaCrop calculates for each day of the flowering period, the
HI that can be reached with the number of flowers already pollinated:
where j number of days since the start of flowering (j = 1 at the start of flowering)
fexcess excess of the sink (percentage);
Fj fractional flowering on day j (Eq. 3.12j/2: derived from Eq. 3.12i);
To be able to account for cold and heat stress at flowering, the calculation
procedure works with calendar days;
Ksj stress factor limiting pollination on day j.
100
𝐹𝑗 = 𝐿 𝑓̅𝑗 (Eq. 3.12j/2)
𝑓𝑙𝑜𝑤𝑒𝑟𝑖𝑛𝑔
stressed period
40 38.0 %
30
Development of HI
26.7 %
20
10
0
0 1 2 3 4 5 6 7 8 9 10 11 12 13 14
Time (days)
Figure 3.12i – The development of HI at flowering and the adjusted harvest indexes
(HIadj) for a non-stressed (full) and a stressed (dotted line) flowering period of 14
days. (HIo = 38%, fexcess = 50%, and stress occurs (Ks < 1) from day 2 till day 9)
The excess of the sink made that if stress reduces pollination by a minor amount, HIo might
not be affected because the excessive young fruits are given the change to grow, instead of
dropping off, if stress is ameliorated after the flowering period and canopy photosynthesis
is adequate. An import stress, during several days at flowering, might result in a HIadj that
is smaller than the specified HIo (Fig. 3.12i). The smaller the excess of flowers (fexcess) and
the more severe the stress (Ks), the stronger the reduction of the reference harvest index.
no stress 1.0
0.8
water stress coefficient
Kspol,w
0.6
0.4
0.2
D
full stress 0.0
p(pol) p(lower)
field capacity TAW permanent wilting point
Figure 3.12j – The water stress coefficient for failure of pollination (Kspol,w)
for various degrees of depletion (D) in the considered soil volume
Since pollination is inhibited only be severe stress, the fraction of TAW that can be depleted
from the considered soil volume before pollination is affected (ppol) is large. The threshold
should be set lower than the threshold for the effect for stomatal closure (psto) and
senescence (psen). Since by then stomata are largely closed and most of the transpiration is
eliminated, the stress effect on pollination needs not to be adjusted to ETo. Because the
data on pollination failure are limited and insufficient to determine the shape of the
response curve, a linear function is considered for Kspol,w.
When the minimum air temperature on a day drops below the specified threshold
temperature (Tn,cold), the cold stress coefficient Kspol,c will be smaller than 1 (Fig. 3.12k).
Kspol,c becomes zero at the lower threshold which is set at 5 degrees below Tn,cold. A logistic
function is used as the response function between the lower temperature threshold and
Tn,cold. Similarly, when the maximum air temperature rises above the specified threshold
temperature (Tx,heat), the heat stress coefficient Kspol,h will be smaller than 1. Kspol,h
becomes zero at the upper threshold which is set at 5 degrees above Tx,heat. Outside the
stressed period, the air temperature stress coefficients Kspol,c and Kspol,h are 1.
Kspol,h
0.6 0.6
0.4 0.4
0.2 0.2
Figure 3.12k – The air temperature stress coefficients for failure of pollination
due to cold (Kspol,c) and heat (Kspol,h) stress for various air temperatures
70
60
fpost HI 0
HI 0
50
Harvest Index (%)
40
30
fpost HI 0
20
10
0
lag phase tim e (days after anthesis)
yield formation
Figure 3.12l – Range (shaded area) in which the Harvest Index of fruit/grain
producing or root/tuber crops can alter as a result of water stress during yield
formation
n (exp)
1 − Ksexp,i
f post = 1 +
i =1 a (Eq. 3.12l)
n(exp)
The adjustment of HIo is plotted in Figure 3.12m for various values of ‘a’. When a is 0.5
and the average root zone depletion during the potential period of vegetative growth is
large (Dr ≥ pexp,lower TAW), fpost↑ might increase up to 3. This will result in a HIo which is
the triple of HIo.
2.0
fpost
1.8
1.6 1
a=
1.4
a=2
1.2
no adjustment
1.0
1.0 0.8 0.6 0.4 0.2 0.0
Figure 3.12m – Values for fpost↑ if water stress after flowering occurs
for various mean water stresses affecting leaf growth (Ksexp,w) and ‘a’ values
no adjustment
1.0
b = 10
fpost
0.8
b=
2
0.6
b=
1
0.4
0.2
0.0
1.0 0.8 0.6 0.4 0.2 0.0
Figure 3.12n – Values for fpost↓ if water stress after flowering occurs for various
mean water stresses affecting crop transpiration (Kssto) and ‘b’ values
n ( yield )
(1 − Kssto , i )
10 Kssto ,i 1 −
i =1 b
f post = (Eq. 3.12n)
n( yield)
The adjustment of HIo is plotted in Figure 3.12n for various values of ‘b’. The 10th root of
Kssto in Eq. 3.12n makes that the effect of stomatal closure on HIo is small when Kssto is
close to 1, i.e. crop transpiration is only slightly hampered. Severe water stress might
strongly reduce HIo especially when b is small (close to 1).
w1 f post + (w2 − w1 )
f post = f post
(Eq. 3.12o)
w2
where w1 length of the period when vegetative growth is still possible [days];
w2 length of the period of building up the harvest Index [days];
fpost coefficient by which HIo has to be multiplied to consider the combined
effect of water stress after flowering.
Figure 3.12o – Periods in which water stress might affect HI and its effect on HIo.
(1) before yield formation; (2) during flowering; and (4) during yield formation,
with indication of (3) the period of possible vegetative growth
for (a) determinant crops and (b) indeterminant crops
The total correction of HIo at the end of the yield formation is given by:
▪ If HI is larger than HIo, its value can however never exceed a maximum specified by
the user. The allowable increase (ΔHItot) which is crop specific, is specified as a
percentage of HIo:
HI tot
HI 1 + HI 0 (Eq. 3.12q)
100
▪ As a result of water stress at and after flowering, HI might be smaller than HIo. If the
water stress during yield formation is very severe and results in a crop transpiration rate
far below its potential value, HI might become very small. HI will be zero (resulting in
no yield) if the average water content in the root zone is at wilting point during yield
formation.
70
60
HI tot
HI 0
50
Harvest Index (%)
40
30
20
10
0
lag phase tim e (days after anthesis)
yield formation
Figure 3.12p – Range (shaded area) in which the Harvest Index can increase or
decrease as a result of water stress before and after the start of yield formation
In the calculation of YW a simplification is made since it is assumed that the effect of weeds
on the harvest index is negligible. Nevertheless, it is observed in the field that weed
infestation affects yield not only through a lower biomass production (BW) but also trough
a lower number of ear bearing tillers, grains per ear and 1000-kernel weight (Wilson and
Peters, 1982, Morishita and Thill, 1988). To avoid over-parametrisation this is neglected
in AquaCrop, especially since the effect of weed stress on HI might be small compared to
the effect of weed stress on biomass production (Van Gaelen, 2011). Further-on, the
adjustment of HI might be simulated indirectly in AquaCrop, since the presence of weeds
might cause extra water stress for the crop (due to larger total transpiration of crop and
weeds). As a consequence, the simulated HI might be lower than the simulated HI in weed-
free conditions.
One way to increase WPET, and as such the production of more marketable yield per unit
of water evapo-transpired in the field, consists in reducing soil evaporation (which is in the
denominator of the equation). Reducing soil evaporation, which is a non-productive
consumption of water, can be achieved by mulches or by switching from traditional
irrigation methods to drip irrigation, which only partially wets the soil surface. By running
AquaCrop with and without the interventions, the increase in WPET can be quantified.
AquaCrop can also be used to quantify the effect of other irrigation, field and crop
management strategies on WPET (more crop per drop) in water-scarce regions. Examples
of strategies that can be analysed by AquaCrop are the effect of selecting a more suitable
crop and/or cultivar for the region, altering the time for seeding/planting, adjusting the
planting density to the rainfall and soil fertility, introducing deficit irrigation, limiting
surface run-off of valuable rainwater from the field, improving weed management, etc.
Table 3.14 - Soil fertility stress coefficients and their effect on crop growth
Soil fertility stress coefficient Direct effect Target
model
parameter
KsCCx: Stress coefficient for Reduces canopy cover CCx
maximum Canopy Cover
Ksexp,f : Stress coefficient for Reduces canopy expansion CGC
canopy expansion
fCDecline : Decline coefficient of Decline of the canopy cover once the CC
canopy cover maximum canopy cover is reached
KsWP : Stress coefficient for Reduces biomass production WP*
Biomass Water Productivity
The shape of each of the 4 soil fertility stress coefficients are fixed when calibrating the
crop response to soil fertility stress (Fig. 3.14a). The calibration process is described in
Chapter 2 (see ‘Calibration for soil fertility stress’) of the Reference Manual, by
considering the effect of soil fertility stress in a stressed field. The calibration is done in
the Crop characteristics menu.
Ks exp,f curve
1.0
soil fertilty stress coefficient
0.4
0.8 fCDecline curve
0.6 1.0
0.2
soil fertilty stress coefficient
0.2
soil fertiltiy
0.8stress
% 0.4 % %
0.0
0 20
0.6 40 60 80 100
0.2 soil fertiltiy stress
0.4
% % %
0.0
0 0.2 20 40 60 80 100
soil fertiltiy stress
0.0
0 % 20 % 40 % 60 % 80 % 100 %
soil f ertiltiy stress
Since the shapes of the 4 Ks curve are not necessary identical and the effect of stress on
WP* increases when the canopy cover increases, the Biomass – soil fertility stress
relationship is not linear (Fig. 3.14b).
100
80
relative Biomass (%)
60
40
20
0
0 20 40 60 80 100
soil fertility stress (%)
Figure 3.14b – Relationship between relative Biomass and soil fertility stress
When due to soil water or soil salinity stress, the Biomass is less than what can be expected
for the given soil fertility stress, AquaCrop decreases the soil fertility stress in its next time
step(s). As such AquaCrop considers the rise in soil fertility because a water or salinity
stressed crop is limited in its uptake of nutrients. The stronger the non-fertility stress, the
more nutrients remain in the soil reservoir and the stronger the rise in soil fertility. If at a
later stage the non-fertility stress is relieved by ample rainfall or irrigation, the soil fertility
decreases since more nutrients are taken up by the crop and eventually returns to its original
state if the Biomass production is in line with the one specified in the Field management
menu. This dynamic adjustment of the soil fertility level makes that the effect of soil
fertility stress is automatically adjusted to the effect of other stresses which affect the
biomass production.
The average electrical conductivity of the saturation soil-paste extract (ECe) from the root
zone during the growing season is the indicator for soil salinity stress in a well-watered
soil. At the lower threshold of soil salinity (ECen), Ks becomes smaller than 1 and the stress
starts to affect biomass production. Ks becomes zero at the upper threshold for soil salinity
(ECex) at which the soil salinity stress becomes so severe that biomass production ceases
(Fig. 3.15a). The shape of the Ks curve is linear. Values for ECen and ECex for many
agriculture crops are given by Ayers and Westcot (1985) in the Irrigation and Drainage
Paper Nr. 29 and presented in Annex I.
0.8 80 %
Kssalt
0.6 60 %
Brel
lin
ea
0.4
r
40 %
0.2 20 %
Figure 3.15a – The soil salinity stress (Kssalt) and relative biomass production (Brel)
for various electrical conductivity of the saturated soil-paste extract
▪ Well-watered soil
To describe the effect of soil salinity stress on crop development and production, AquaCrop
makes use of 4 stress coefficients (Table 3.15b).
Table 3.15b - Soil salinity stress coefficients and their effect on crop growth
Soil salinity stress coefficient Direct effect Target
model
parameter
KsCCx: Stress coefficient for Reduces canopy cover CCx
maximum Canopy Cover
Ksexp,f : Stress coefficient for Reduces canopy expansion CGC
canopy expansion
fCDecline : Decline coefficient of Decline of the canopy cover once the CC
canopy cover maximum canopy cover is reached
Kssto,salt : Stress coefficient for Reduces crop transpiration Kssto
stomatal closure
The shape of each of the 4 soil salinity stress coefficients are fixed when calibrating the
crop response to soil salinity stress (expressed by ECe) in a well-watered soil (Fig. 3.15b).
Ks exp,f curve
1.0
fertilty stress coefficient
0.4
0.8 fCDecline curve
soilsalinity
0.6 1.0
0.2
soil
0.0 1.0
0% 20 % 40 % 60 80 100
0.6
soilsalinity stress coefficient
0.2
soil
soil fertiltiy
0.8stress
% 0.4 % %
soilsalinity
0.0
0 20 0.6 40 60 80 100
0.2 soil fertiltiy stress
soil
0.4
% % %
0.0
0 0.2 20 40 60 80 100
soil fertiltiy stress
0.0
0 % 20 % 40 % 60 % 80 % 100 %
soil salinity stress
1.0
1
0.8
2
0.6
sto
Ks
0.4
0.2
0.0 2
FC PWP
s oil w ate r conte nt
Fig. 3.15c – The soil water coefficient for stomatal closure (Kssto) without (gray line)
and with (several alternative black lines) the effect of soil salinity stress. The decline
of Kssto (effect 1) is linked with the effect of soil salinity stress in a well-watered soil
(Fig. 3.15b), the shift of the upper and lower threshold (effect 2) is the effect of
ECsw. The effect of ECsw on stomata closure (presented by the alternative black
lines) is specified by calibration
The relative biomass production is obtained by considering the calibrated effect on canopy
development and of stomatal closure on crop transpiration in a well-watered soil. The
calculation procedure is schematically depicted in Figure 3.15d and consists of the
following 4 steps:
1. the average electrical conductivity of the saturation soil-paste extract (ECe) from the
root zone determines the soil salinity stress (Kssalt), as described in Fig. 3.15a;
2. the relative biomass (Brel) that can be produced with the salinity stress (Kssalt) is
obtained by Eq. 3.15a;
3. the salinity stress (Kssalt) determines (Fig. 3.15b) the value for (i) Kssto,salt (resulting in
stomatal closure and affecting crop transpiration, Tr), (ii) Ksexp,f (slowing down canopy
development), (iii) KsCCx (reducing the maximum canopy cover) and (iv) fCDecline
(triggering canopy decline) resulting in reduced canopy cover and reduced crop
transpiration;
4. the reduced crop transpiration, results in a reduced biomass production. As a result of
the calibration the resulting Brel is identical to the expected Brel (Eq. 3.15a) in the
absence of soil water stress.
The smaller canopy cover and stomatal closure as a result of salinity stress, results in a
reduced crop transpiration which affects the soil water balance.
▪ In presence of water-stress:
Canopy development and crop transpiration might be further affected if next to soil salinity
stress, also water stress develops during the growing season (Fig. 3.15e).
Figure 3.15e – The combined effect of soil salinity and soil water stress
on canopy development, stomatal closure, crop transpiration and biomass
production
Figure 3.16 – Schematic outline of the combined effect of soil fertility and salinity
stress on the values of the various stress coefficients: Ksexp,f (stress coefficient for
canopy expansion); KsCCx (stress coefficient for maximum canopy cover); fCDecline
(decline coefficient of canopy cover); KsWP (stress coefficient for biomass water
productivity); Kssto,salt (stress coefficient for stomatal closure);
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