Visible near infrared reflectance spectroscopy prediction of soil heavy metal concentrations in paper mill biosolid- and liming by-product-amended agricultural soils

Citation

St. Luce, M., Ziadi, N., Gagnon, B., Karam, A. (2017). Visible near infrared reflectance spectroscopy prediction of soil heavy metal concentrations in paper mill biosolid- and liming by-product-amended agricultural soils. Geoderma, [online] 288 23-36. http://dx.doi.org/10.1016/j.geoderma.2016.10.037

Plain language summary

Conventional laboratory methods used for determining soil heavy metal concentrations in agricultural soils are time-consuming, expensive and involve hazardous chemicals. Here, the potential of visible near infrared reflectance spectroscopy (VNIRS) to rapidly and simultaneously predict total, Mehlich-3 (M3), DTPA, and water-soluble soil heavy metal concentrations was evaluated. Soil samples were collected from a loam soil (n = 64) and a loamy sand (n = 32) after repeated annual applications (3–9 years) of paper mill biosolids (PB) and liming by-products. Models were developed using 75% of the total sample set and also for each soil, with the remainder used for validating the models. Predictions for the total set were excellent for total zinc and cadmium, Mehlich-3 copper and cadmium, M3-Cu and -Cd, and DTPA-cadmium, good for total copper, nickel and molybdenum, Mehlich-3 nickel, DTPA-copper and -nickel, and water-soluble copper and nickel, but poor for Mehlich-3 zinc, DTPA-zinc, and water-soluble zinc, cadmium and molybdenum. Except for one case, site-specific models were either more accurate or provided similar results with the model of the total set in predicting site-specific concentrations. One of the most interesting findings from this study was that the strong relationship between soil organic matter and cadmium was the major predictive mechanism for cadmium in this dataset, while the prediction of other soil heavy metals was due to the combined influence of soil organic matter and iron oxides. Overall, this study showed that VNIRS has the potential to predict total, Mehlich-3, DTPA and to a lesser extent water-soluble soil heavy metals, especially when developed using site-specific samples.

Abstract

Continuous assessment of soil heavy metal concentrations in agricultural soils is critical for ensuring ecosystem health and minimizing potential adverse effects. However, conventional laboratory determinations are time-consuming, expensive and involve hazardous chemicals. We evaluated the potential of visible near infrared reflectance spectroscopy (VNIRS) to rapidly and simultaneously predict total, Mehlich-3 (M3), DTPA, and water-soluble (H2O) soil heavy metal concentrations. Soil samples were collected from a loam soil (n = 64) and a loamy sand (n = 32) after repeated annual applications (3–9 years) of paper mill biosolids (PB) and liming by-products. Models were developed using modified partial least squares regression on 75% of the total sample set and also for each soil, after removal of the spectral outliers (n = 3), with the remainder used for validation. The coefficient of determination in validation (R2V) and the ratio of performance to deviation (RPD) were used to assess model accuracy. Predictions for the total set were excellent for total Zn and Cd, M3-Cu and -Cd, and DTPA-Cd (R2V > 0.90, RPD > 3.0), good for total Cu, Ni and Mo, M3-Ni, DTPA-Cu and -Ni, and H2O-Cu and -Ni (R2V = 0.70 to 0.90, RPD = 1.70 to 3.0), but poor for M3-Zn, DTPA-Zn, and H2O-Zn, -Cd and -Mo (R2V < 0.70, RPD < 1.70). Except for one case, site-specific models were either more accurate or provided similar results with the model of the total set in predicting site-specific concentrations. The relationship with soil organic matter (SOM) was the major predictive mechanism for Cd in our dataset, while the prediction of other soil heavy metals was due to the combined influence of SOM and Fe oxides. We conclude that VNIRS has the potential to predict total, M3, DTPA and to a lesser extent water-soluble soil heavy metals, especially when developed using site-specific samples.