Soil respiration is strongly related
to the soil temperature, thus the simplest model to predict soil respiration
uses soil temperature as the single variable. In this case, an exponential
or Arrhenius equation is used,
as mentioned before. Since soil moisture is anther important factor influence
soil respiration, the power of prediction is greatly enhanced by incorporating
the influence of soil moisture. Other factors, such as LAI (Norman
et al., 1992), air temperature and precipitation (Raich
and Potter, 1995), are also added as model variables in some studies.
Here we introduce two soil respiration models, one of which only considers
the effect of soil temperature and the other takes soil moisture into consideration.
Model with
the effect of only soil temperature
Frank, el al. (2002) modeled
the effect of soil temperature to predict soil respiration in northern semiarid grasslands.
Soilflux = ((A1A2A3)z)
maximumflux
where: A1=(Tmax-T)/(Tmax-Topt)
A2=(T-Tmin)/(Topt-Tmin)
A3=(Topt-Tmin)/(Tmax-Topt)
z: shape parameter(1.5 in this case)
maximumflux: maximum measured soil
respiration flux
Figure 3 shows
the fit of the model for the grassland data. The percentage of difference
between the observed and predicted soil fluxes averaged for all observations
is 1.5% for this model.
GRESP models and its variation
In 1974, Bunnell and Tait modeled
the influence of soil temperature and soil moisture on soil respiration using
a model named as GRESP.
GRESP= ![]()
where GRESP: the
respiration rate (g CO2 m-2h-1)
T: soil temperature (degrees Celsius)
M:
soil moisture (grams of water per gram of dry weight times 100 percent)
a1: the % moisture content at half
field capacity
a2: the % moisture content at half
“maximum retentive capacity”
a3:
the theoretically maximum respiration rate at 10 ºC when moisture is non-limiting
a4:
the Q10 coefficient (sensitivity to temperature)
Although GRESP has been applied successfully to tundra, boreal
forests and temperate bogs ecosystems (Heal, 1979),
it has some limitations: (i) respiration equals to zero only when temperature
is zero; (ii) the relationship between soil respiration and temperature is
expressed as simple exponential equation without upper limit; (iii) Q10
is assumed constant.
Some variations of GRESP model have been proposed by other
researchers, e.g. the BRESP model fit by Schlentner
and Van cleve (1985), the FRESP model fit by Carlyle
and Ba Than (1988). The BRESP model differs from GRESP by adding an upper
and lower limit of the response of soil respiration to temperature.
BRESP=
where BRESP: the
respiration rate (g CO2 m-2h-1)
a1,
a2: the same as GRESP model
a3: a scaling factor, no
biological meaning
a4: the Q10 related
parameter
a5: the lower limit of soil
respiration
a6=![]()
Carlyle and Ba Than modified the model by allowing Q10
dependent on substrate moisture so that it can be applied to very dry
conditions.
FRESP=
; A4=![]()
where FRESP is the
respiration rate (g CO2 m-2h-1)
a4: a parameter linking Q10 to
substrate moisture content
a5: the lower limit for the Q10
quotient
a6=![]()
![]()
Figure 4 shows
the fit of a respiration in an eighteen-year-old pinus radiata stand with three
models. For this particular data, FRESP model fit best (r2=0.85),
while the other two models give poor fit (GRESP: r2=0.09; BRESP: r2=0.15).
Schlentner and Cleve (1985) obtained an r2 value of 0.58 for both
GRESP and BRESP for mature forests, indicating the fitness of this type of
models is site-specific.
Interested in more soil
respiration models? go here.