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Published online 17 July 2007
Published in J Environ Qual 36:1266-1272 (2007)
DOI: 10.2134/jeq2006.0370
© 2007 American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
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Passive Flux Meter Measurement of Water and Nutrient Flux in Saturated Porous Media: Bench-Scale Laboratory Tests

Jaehyun Choa, Michael D. Annablea,*, James W. Jawitzb and Kirk Hatfieldc

a Dep. of Environmental Engineering Sciences, Univ. of Florida, Gainesville, FL 32611
b Soil and Water Science Dep., Univ. of Florida, Gainesville, FL 32611
c Dep. of Civil and Coastal Engineering, Univ. of Florida, Gainesville, FL 32611


Figure 1
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Fig. 1. Schematic diagram for bench-scale flow chamber (plan view) to evaluate performance of the passive nutrient flux meter (PNFM) (shown vertically in center) including tracer elution and PO43– accumulation in the PNFM (horizontal section shown). Note that tracers are represented as straight-chain molecules with varying lengths; PO43 is represented with spheres.

 

Figure 2
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Fig. 2. Adsorption isotherm of PO43– on Lewatit S 6328A resin with a Freundlich model fit.

 

Figure 3
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Fig. 3. (A) Resident alcohol tracer elution curves along with cumulative water pore volume and (B) an example plot for retardation factor determination using four piece-wise linear segments from the nonlinear 1-hexanol elution curve. 2,4-dimethyl-3-pentanol (2,4-DMP); 2-ethyl-1-hexanol (2E1H).

 

Figure 4
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Fig. 4. Log-log relationship between retardation factor (Rd) and aqueous solubility for resident alcohol tracers. 2,4-dimethyl-3-pentanol (2,4-DMP).

 

Figure 5
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Fig. 5. Comparison between Darcy flux, q, estimated from the passive nutrient flux meter (PNFM) using the 1-hexanol and 2,4-dimethyl-3-pentanol (2,4-DMP) tracers and the actual applied values.

 

Figure 6
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Fig. 6. Comparison between passive nutrient flux meter (PNFM)-estimated and applied PO43– fluxes. Mean estimated values are shown with standard deviation (n = 4).

 





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