Nitrification & Ammonia Volatilization

Nitrification is the two-step bacterial oxidation of NH4+NH_4^+ to NO3NO_3^-.

Ammonia volatilization is the gaseous loss of NH3NH_3 that occurs when ammonium, NH4+NH_4^+, is surface applied to a calcareous soil or when urea, (NH2)2CO2NH_2)_2CO_2, is surface applied to any soil.

NH4+NH_4^+ surface applied to a calcareous soil:

Urea surface applied to any soil:

SWAT+ simulates nitrification and ammonia volatilization using a combination of the methods developed by Reddy et al. (1979) and Godwin et al. (1984). The total amount of nitrification and ammonia volatilization is calculated, and then partitioned between the two processes. Nitrification is a function of soil temperature and soil water content while ammonia volatilization is a function of soil temperature, depth and cation exchange capacity. Four coefficients are used in the nitrification/volatilization algorithms to account for the impact of these parameters. Nitrification/volatilization occurs only when the temperature of the soil layer exceeds 5°C.

The nitrification/volatilization temperature factor is calculated:

ηtmp,ly=0.41(Tsoil,ly5)10\eta_{tmp,ly}=0.41*\frac{(T_{soil,ly}-5)}{10} if Tsoil,ly>5T_{soil,ly}>5 3:1.3.1

where ηtmp,ly\eta_{tmp,ly} is the nitrification/volatilization temperature factor, and Tsoil,lyT_{soil,ly} is the temperature of layer lyly (°C).

The nitrification soil water factor is calculated:

ηsw,ly=SWlyWPly0.25(FClyWPly)\eta_{sw,ly}=\frac{SW_{ly}-WP_{ly}}{0.25*(FC_{ly}-WP_{ly})} if SWly<0.25FCly0.75WPlySW_{ly}<0.25*FC_{ly}-0.75*WP_{ly} 3:1.3.2

ηsw,ly=1.0\eta_{sw,ly}=1.0 if SWly0.25FCly0.75WPlySW_{ly} \ge 0.25*FC_{ly}-0.75*WP_{ly} 3:1.3.3

where ηsw,ly\eta_{sw,ly} is the nitrification soil water factor, SWlySW_{ly} is the soil water content of layer lyly on a given day (mm H2_2O), WPlyWP_{ly} is the amount of water held in the soil layer at wilting point water content (mm H2_2O), and FClyFC_{ly} is the amount of water held in the soil layer at field capacity water content (mm H2_2O).

The volatilization depth factor is calculated:

ηmidz,ly=1zmid,lyzmid,ly+exp[4.7060.0305zmid,ly]\eta_{midz,ly}=1-\frac{z_{mid,ly}}{z_{mid,ly}+exp[4.706-0.0305*z_{mid,ly}]} 3:1.3.4

where ηmidz,ly\eta_{midz,ly} is the volatilization depth factor, and zmid,lyz_{mid,ly} is the depth from the soil surface to the middle of the layer (mm).

SWAT+ does not require the user to provide information about soil cation exchange capacity. The volatilization cation exchange factor is set to a constant value:

ηcec,ly=0.15\eta_{cec,ly}=0.15 3:1.3.5

The impact of environmental factors on nitrification and ammonia volatilization in a given layer is defined by the nitrification regulator and volatilization regulator. The nitrification regulator is calculated:

ηnit,ly=ηtmp,lyηsw,ly\eta_{nit,ly}=\eta_{tmp,ly}*\eta_{sw,ly} 3:1.3.6

and the volatilization regulator is calculated:

ηvol,ly=ηtmp,lyηmidz,lyηcec,ly\eta_{vol,ly}=\eta_{tmp,ly}*\eta_{midz,ly}*\eta_{cec,ly} 3:1.3.7

where ηnit,ly\eta_{nit,ly} is the nitrification regulator, ηvol,ly\eta_{vol,ly} is the volatilization regulator, ηtmp,ly\eta_{tmp,ly} is the nitrification/volatilization temperature factor, ηsw,ly\eta_{sw,ly} is the nitrification soil water factor, and ηmidz,ly\eta_{midz,ly} is the volatilization depth factor.

The total amount of ammonium lost to nitrification and volatilization is calculated using a first-order kinetic rate equation (Reddy et al., 1979):

Nnitvol,ly=NH4ly(1expηnit,lyηvol,ly)N_{nit|vol,ly}=NH4_{ly}*(1-exp\lfloor-\eta_{nit,ly}-\eta_{vol,ly}\rfloor) 3:1.3.8

where Nnitvol,ly^{N_{nit|vol,ly}} is the amount of ammonium converted via nitrification and volatilization in layer lyly (kg N/ha), NH4lyNH4_{ly} is the amount of ammonium in layer lyly (kg N/ha), ηnit,ly\eta_{nit,ly} is the nitrification regulator, and ηvol,ly\eta_{vol,ly} is the volatilization regulator.

To partition Nnitvol,ly^{N_{nit|vol,ly}} between nitrification and volatilization, the expression by which NH4lyNH4_{ly} is multiplied in equation 3:1.3.8, is solved using each regulator individually to obtain a fraction of ammonium removed by each process:

frnit,ly=1expηnit,lyfr_{nit,ly}=1-exp\lfloor-\eta_{nit,ly}\rfloor 3:1.3.9

frvol,ly=1expηvol,lyfr_{vol,ly}=1-exp\lfloor-\eta_{vol,ly}\rfloor 3:1.3.10

where frnit,lyfr_{nit,ly} is the estimated fraction of nitrogen lost by nitrification, frvol,lyfr_{vol,ly} is the estimated fraction of nitrogen lost by volatilization, ηnit,ly\eta_{nit,ly} is the nitrification regulator, and ηvol,ly\eta_{vol,ly} is the volatilization regulator.

The amount of nitrogen removed from the ammonium pool by nitrification is then calculated:

Nnit,ly=frnit,ly(frnit,ly+frvol,ly)Nnitvol,lyN_{nit,ly}=\frac{fr_{nit,ly}}{(fr_{nit,ly}+fr_{vol,ly})}*N_{nit|vol,ly} 3:1.3.11

and the amount of nitrogen removed from the ammonium pool by volatilization is:

Nvol,ly=frvol,ly(frnit,ly+frvol,ly)Nnitvol,lyN_{vol,ly}=\frac{fr_{vol,ly}}{(fr_{nit,ly}+fr_{vol,ly})}*N_{nit|vol,ly} 3:1.3.12

where Nnit,lyN_{nit,ly} is the amount of nitrogen converted from NH4+NH_4^+ to NO3NO_3^- in layer lyly (kg N/ha), Nvol,lyN_{vol,ly} is the amount of nitrogen converted from NH4+NH_4^+ to NH3NH_3 in layer lyly (kg N/ha), frnit,lyfr_{nit,ly} is the estimated fraction of nitrogen lost by nitrification, frvol,lyfr_{vol,ly} is the estimated fraction of nitrogen lost by volatilization, and Nnitvol,ly^{N_{nit|vol,ly}} is the amount of ammonium converted via nitrification and volatilization in layer lyly (kg N/ha).

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