Difference between revisions of "Constituents:Simple Constituents"

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(11.3.1 Overland Flow Plane)
(11.3.1 Overland Flow Plane)
 
(10 intermediate revisions by the same user not shown)
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For the overland flow plane kinetic rates and other inputs are specified in the '''MAPPING_TABLE_FILE'''.  For each contaminant a single value of rainfall concentration (mg L<sup>-1</sup>) is specified.  All other input values are distributed both by constituent and location on the overland flow plane with the index map and mapping table values.  The following table inputs are required.
 
For the overland flow plane kinetic rates and other inputs are specified in the '''MAPPING_TABLE_FILE'''.  For each contaminant a single value of rainfall concentration (mg L<sup>-1</sup>) is specified.  All other input values are distributed both by constituent and location on the overland flow plane with the index map and mapping table values.  The following table inputs are required.
  
#Dispersion coefficient  (m<sup>2</sup> s<sup>-1</sup>)
+
#Dispersion coefficient on the overland (m<sup>2</sup> s<sup>-1</sup>)
#Decay coefficient K (d<sup>-1</sup>)
+
#Decay coefficient in the soils and the overland K (d<sup>-1</sup>)
 
#Uptake coefficient K<sub>u</sub> (m d<sup>-1</sup>)
 
#Uptake coefficient K<sub>u</sub> (m d<sup>-1</sup>)
 
#Initial loading (Kg) or (mg Kg<sup>-1</sup>)
 
#Initial loading (Kg) or (mg Kg<sup>-1</sup>)
 
#Groundwater concentration (g m<sup>-3</sup>)
 
#Groundwater concentration (g m<sup>-3</sup>)
 
#Initial concentration (g m<sup>-3</sup>)
 
#Initial concentration (g m<sup>-3</sup>)
#Soil water distribution coefficients K<sub>d</sub> (L Kg<sup>-1</sup>)
+
#Soil water distribution coefficients in the soil K<sub>d</sub> (L Kg<sup>-1</sup>)
 
#Solubility C<sub>max</sub> (g m<sup>-3</sup>)
 
#Solubility C<sub>max</sub> (g m<sup>-3</sup>)
  
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Where:  C<sub>ponded</sub> is the concentration in the water ponded on the soil surface, C<sub>soil</sub> is the concentration in the soil pore water.  The value 86400.0 changes the reaction rate from per day to per second.  As can be seen in the equation, the direction of the flux is dependent on the relationship between the concentration of the surface water to the soil pore water volume.   
 
Where:  C<sub>ponded</sub> is the concentration in the water ponded on the soil surface, C<sub>soil</sub> is the concentration in the soil pore water.  The value 86400.0 changes the reaction rate from per day to per second.  As can be seen in the equation, the direction of the flux is dependent on the relationship between the concentration of the surface water to the soil pore water volume.   
  
For contaminants dissolved in the soil column, the uptake coefficient can be estimated from Thibodeaux, Environmental Chemodynamics 2nd Ed., Wiley, New York, 1996, pp. 276-277 using the relation:
+
While the uptake coefficient is generally considered a calibration coefficient, for contaminants in the soil column the uptake coefficient can be estimated from Thibodeaux, Environmental Chemodynamics 2nd Ed., Wiley, New York, 1996, pp. 276-277 using the relation:
 
::
 
::
 
::K<sub>u</sub> = D n<sup>4/3</sup>/(0.5 d<sub>ml</sub>)
 
::K<sub>u</sub> = D n<sup>4/3</sup>/(0.5 d<sub>ml</sub>)
 
::
 
::
where D is the diffusion coefficient of the chemical in water (m<sup>2</sup>s<sup>-d</sup>), n is the porosity, d<sub>ml</sub> is the mixing layer depth (m).
+
where D is the diffusion coefficient of the chemical in water (m<sup>2</sup> s<sup>-d</sup>), n is the porosity, d<sub>ml</sub> is the mixing layer depth (m).
  
Thibodeaux list a diffusion coefficient for nitrates of 0.000164 m<sup>2</sup>s<sup>-d</sup>.  For a typical soil with porosity of 0.4 and a mixing layer depth of 0.1 m, the uptake coefficient is 0.00048 m d<sup>-1</sup>.  Lerman, Geophysical Processes, Wiley, New York, 1979, pp. 73-121, lists diffusion coefficients for common ions.
+
Thibodeaux list a diffusion coefficient for nitrates of 0.000164 m<sup>2</sup> d<sup>-1</sup>.  For a typical soil with porosity of 0.4 and a mixing layer depth of 0.1 m, the uptake coefficient for nitrate would be 0.001 m d<sup>-1</sup>.  Lerman, Geophysical Processes, Wiley, New York, 1979, pp. 73-121, lists diffusion coefficients for common ions.  It should be noted that effective values for of uptake coefficients for nitrate used in previous modeling efforts, for example Pradhan et al. (2014), have been much lower, on the order of 10<sup>-5</sup> m d<sup>-1<sup>.
 +
 
 +
Pradhan, N. R., C. W. Downer, and B. E. Johnson, 2014.  A Physics Based Hydrologic Modeling Approach to Simulate Non-point Source Pollution for the Purposes of Calculating TMDLs and Designing Abatement Measures, Chapter 9 in Practical Aspects of Computational Chemistry-III, DOI 10.1007/978-1-4899-7445-7_1, J. Leszczynski and M. K. Shukla, eds. Springer Science+Business Media, New York.
  
 
3) Contaminants dissolved in surface water decay at the rate:
 
3) Contaminants dissolved in surface water decay at the rate:
Line 52: Line 54:
 
==11.3.2 Channels==
 
==11.3.2 Channels==
  
For channels, the only reaction is decay, calculated as above.  The decay coefficient can be set as a uniform value for every stream node by specifying the value (d<sup>-1</sup>) with the '''CHAN_DECAY''' card.  In addition to setting the rate, the dispersion coefficient (m<sup>2</sup>s<sup>-1</sup>) can be defined with the '''CHAN_DISP_COEF''' card.  Inital values (g m<sup>-3</sup>) can be specified with the '''INIT_CHAN_CONC''' card.  The default value for each of these is zero.
+
For channels, the only reaction is decay, calculated as above.  The decay coefficient can be set as a uniform value for every stream node by specifying the value (d<sup>-1</sup>) with the '''CHAN_DECAY''' card.  In addition to setting the rate, the dispersion coefficient (m<sup>2</sup>s<sup>-1</sup>) can be defined with the '''CHAN_DISP_COEF''' card.  Inital values (g m<sup>-3</sup>) can be specified with the '''INIT_CHAN_CONC''' card.  The default value for each of these is zero.  The partition coefficient is the same as for the overland.
  
 
==11.3.3 Soil Column==
 
==11.3.3 Soil Column==
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where: M is the total mass in the layer (g) and V is the volume of the pore water in the soil layer (m<sup>3</sup>).
 
where: M is the total mass in the layer (g) and V is the volume of the pore water in the soil layer (m<sup>3</sup>).
  
The same reaction rates specified in the '''MAPPING_TABLE_FILE''' are used for both the soils and the overland flow.
+
The same reaction rates specified in the '''MAPPING_TABLE_FILE''' are used for both the soils and the overland flow
 +
 
 +
During simulations uptake, decay, and movement between layers will change the concentration in the surface soil layer, which can be specified as the '''MIXING_LAYER_DEPTH''', or if using '''INF_REDIST''' is the top layer depth, either '''TOP_LAYER_DEPTH''' or '''SOIL_MOIST_DEPTH''' depending on whether one or two soil infiltration layers are specified, or if using '''INF_LAYERED_SOIL''' the '''MIXING_LAYER_DEPTH''' or the top infiltration layer in the soil profile.  In any case the concentration of materials in the surface soil layer can be held static by using the '''SOIL_STATIC_CONC''' card in the project file.  This might be desirable when either the concentration in the soil is expected to held constant by addition of more constituent, such as N and P addition due to fertilizer.  Furthermore, fluxes between soil layers can be halted by using the '''SOIL_NOFLUX''' card.  This might be desirable to include if the material in the top layer is being flushed out at an excessive rate and reducing the surface soil layer concentration too rapidly.  This option may also be desirable to use if exfiltration is occurring and an excessive amount of constituent is being added to the overland flow plane.  
 
<noinclude>
 
<noinclude>
 
{{Nav|Nav11}}
 
{{Nav|Nav11}}
 
</noinclude>
 
</noinclude>

Latest revision as of 21:41, 9 January 2017

11.3 Simple Constituents

As described in Section 11.1, reactive contaminants may be treated as simple constituents. That is, all reactions are simple first order reactions with user specified kinetic rates (K). There is no limit on the number of simple constituents that can be simulated at one time.

11.3.1 Overland Flow Plane

For the overland flow plane kinetic rates and other inputs are specified in the MAPPING_TABLE_FILE. For each contaminant a single value of rainfall concentration (mg L-1) is specified. All other input values are distributed both by constituent and location on the overland flow plane with the index map and mapping table values. The following table inputs are required.

  1. Dispersion coefficient on the overland (m2 s-1)
  2. Decay coefficient in the soils and the overland K (d-1)
  3. Uptake coefficient Ku (m d-1)
  4. Initial loading (Kg) or (mg Kg-1)
  5. Groundwater concentration (g m-3)
  6. Initial concentration (g m-3)
  7. Soil water distribution coefficients in the soil Kd (L Kg-1)
  8. Solubility Cmax (g m-3)

See Section 13 for details on the MAPPING_TABLE inputs.

Three types of reactions can take place on the overland flow plane:

  1. uptake from land surface,
  2. uptake from soil,
  3. decay.

1) The uptake coefficient controls movement of contaminants into the overland flow based on the concentration deficit (solubility of the constituent and the concentration in solution). The mass flux (F) (g s-1) is computed as:

F=Ku A(Cmax -C)/86400.0

Where C is the concentration of contaminant in the ponded surface water, and A is the area of the computational grid cell (m2). The value 86400.0 converts the reaction rate into (m s-1).

2) If SOIL_CONTAM is included in the project file Ku is the transfer rate between the soil pore water and the water ponded on the land surface. In this case the mass flux (F) (g s-1) is calculated as:

F=Ku A(Cponded-Csoil)/86400.0

Where: Cponded is the concentration in the water ponded on the soil surface, Csoil is the concentration in the soil pore water. The value 86400.0 changes the reaction rate from per day to per second. As can be seen in the equation, the direction of the flux is dependent on the relationship between the concentration of the surface water to the soil pore water volume.

While the uptake coefficient is generally considered a calibration coefficient, for contaminants in the soil column the uptake coefficient can be estimated from Thibodeaux, Environmental Chemodynamics 2nd Ed., Wiley, New York, 1996, pp. 276-277 using the relation:

Ku = D n4/3/(0.5 dml)

where D is the diffusion coefficient of the chemical in water (m2 s-d), n is the porosity, dml is the mixing layer depth (m).

Thibodeaux list a diffusion coefficient for nitrates of 0.000164 m2 d-1. For a typical soil with porosity of 0.4 and a mixing layer depth of 0.1 m, the uptake coefficient for nitrate would be 0.001 m d-1. Lerman, Geophysical Processes, Wiley, New York, 1979, pp. 73-121, lists diffusion coefficients for common ions. It should be noted that effective values for of uptake coefficients for nitrate used in previous modeling efforts, for example Pradhan et al. (2014), have been much lower, on the order of 10-5 m d-1.

Pradhan, N. R., C. W. Downer, and B. E. Johnson, 2014. A Physics Based Hydrologic Modeling Approach to Simulate Non-point Source Pollution for the Purposes of Calculating TMDLs and Designing Abatement Measures, Chapter 9 in Practical Aspects of Computational Chemistry-III, DOI 10.1007/978-1-4899-7445-7_1, J. Leszczynski and M. K. Shukla, eds. Springer Science+Business Media, New York.

3) Contaminants dissolved in surface water decay at the rate:

F=KCV/86400.0

where V is the volume (m3), A times the depth.

11.3.2 Channels

For channels, the only reaction is decay, calculated as above. The decay coefficient can be set as a uniform value for every stream node by specifying the value (d-1) with the CHAN_DECAY card. In addition to setting the rate, the dispersion coefficient (m2s-1) can be defined with the CHAN_DISP_COEF card. Inital values (g m-3) can be specified with the INIT_CHAN_CONC card. The default value for each of these is zero. The partition coefficient is the same as for the overland.

11.3.3 Soil Column

When transport in the soil is specified with the SOIL_CONTAM card, exchange between the top soil layer and the surface water occurs, as well as decay in the soil pore water. The reactions are the same as described above for overland flow. The soil water distribution coefficient controls the pore water concentration. The fraction of the total that is dissolved is:

Partition.jpg

where theta is the soil moisture (fraction) and rhos is the dry soil density (Kg m-3). So that the concentration dissolved is:

Cd=fdM/V

where: M is the total mass in the layer (g) and V is the volume of the pore water in the soil layer (m3).

The same reaction rates specified in the MAPPING_TABLE_FILE are used for both the soils and the overland flow.

During simulations uptake, decay, and movement between layers will change the concentration in the surface soil layer, which can be specified as the MIXING_LAYER_DEPTH, or if using INF_REDIST is the top layer depth, either TOP_LAYER_DEPTH or SOIL_MOIST_DEPTH depending on whether one or two soil infiltration layers are specified, or if using INF_LAYERED_SOIL the MIXING_LAYER_DEPTH or the top infiltration layer in the soil profile. In any case the concentration of materials in the surface soil layer can be held static by using the SOIL_STATIC_CONC card in the project file. This might be desirable when either the concentration in the soil is expected to held constant by addition of more constituent, such as N and P addition due to fertilizer. Furthermore, fluxes between soil layers can be halted by using the SOIL_NOFLUX card. This might be desirable to include if the material in the top layer is being flushed out at an excessive rate and reducing the surface soil layer concentration too rapidly. This option may also be desirable to use if exfiltration is occurring and an excessive amount of constituent is being added to the overland flow plane.

GSSHA User's Manual

11 Constituent Transport and Fate
11.1     Simulating Reactive Constituents in GSSHA
11.2     Transport Formulations
11.3     Simple Constituents
11.4     Point and Non-point sources
11.5     Multi-phase transport