Core Ideas
We used CT‐derived parameters to explain solute, water, and air transport at field scale.
CTmatrix was found to be the best parameter to explain solute transport.
Limiting macroporosity gave the highest correlations with water and air transport.
Combining macroporosity and CTmatrix improved the relationships of water and air flow.
The characterization of soil pore space geometry is important for explaining fluxes of air, water, and solutes through soil and understanding soil hydrogeochemical functions. X‐ray computed tomography (CT) can be applied for this characterization, and in this study CT‐derived parameters were used to explain water, air, and solute transport through soil. Forty‐five soil columns (20 by 20 cm) were collected from an agricultural field in Estrup, Denmark, and subsequently scanned using a medical CT scanner. Nonreactive tracer leaching experiments were performed in the laboratory along with measurements of air permeability (Ka) and saturated hydraulic conductivity (Ksat). The CT number of the matrix (CTmatrix), which represents the moist bulk density of the soil matrix, was obtained from the CT scans as the average CT number of the voxels in the grayscale image excluding macropores and stones. The CTmatrix showed the best relationships with the solute transport characteristics, especially the time by which 5% of the applied mass of tritium was leached, known as the 5% arrival time (t0.05). The CT‐derived macroporosity (pores >1.2 mm) was correlated with Ka and log10(Ksat). The correlation improved when the limiting macroporosity (the minimum macroporosity for every 0.6‐mm layer along the soil column) was used, suggesting that soil layers with the narrowest macropore section restricted the flow through the whole soil column. Water, air, and solute transport were related with the CT‐derived parameters by using a best subsets regression analysis. The regression coefficients improved using CTmatrix, limiting macroporosity, and genus density, while the best model for t0.05 used CTmatrix only. The scanning resolution and the time for soil structure development after mechanical activities could be factors that increased the uncertainty of the relationships. Nevertheless, the results confirmed the potential of X‐ray CT visualization techniques for estimating fluxes through soil at the field scale.
The upper horizons of old vineyard soils have substantial copper contents due to the traditional use of copper-based fungicides. Total copper levels in eight vineyard soils in the Rías Baixas area of Galicia (northwestern Spain) ranged from 60 to 560 mg kg(-1) (mean +/- SD = 206 +/- 170 mg kg(-1)). The adsorption of the fungicides metalaxyl (pK(a) = 1.41) and penconazole (pK(a) = 2.83) by these soils was determined using fungicide solutions of pH 2.5 and 5.5, and desorption of fungicide adsorbed at pH 5.5 was also determined. In all cases, Freundlich equations were fitted to the data with R (2) > 0.96. Penconazole was adsorbed and retained more strongly than metalaxyl, with K(F) values more than an order of magnitude greater. In the desorption experiments, both fungicides exhibited hysteresis. Soil copper content hardly affected the adsorption of metalaxyl, but K(F) values for adsorption of penconazole increased at a rate of about 0.1 mL(n) (microg of penconazole)(1-n) (microg of Cu)(-1), which is attributed to the formation of Cu(2+)-penconazole complexes with greater affinity for soil colloids than penconazole itself. Because the dependence of K(F) for penconazole adsorption on copper content was the same at both pH values, complex formation appears not to have been affected by the solubilization of 6-17% of soil copper at pH 2.5. A similar copper dependence, or lack of dependence, was observed when 100-1000 mg kg(-1) of copper was added as Cu(NO(3))(2).2H(2)O to the solutions from which the fungicides were adsorbed.
All rights reserved. No part of this periodical may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or any information storage and retrieval system, without permission in writing from the publisher. Permission for printing and for reprinting the material contained herein has been obtained by the publisher. Facilitated Transport of Copper with Hydroxyapatite Nanoparticles in Saturated Sand Soil Chemistry H ydroxyapatite nanoparticles [Ca(PO 4 ) 6 (OH) 2 ] have been widely used to remediate soils and wastewater contaminated by metals such as Cu, Zn, Pb, Cd, and Co (Ma et al., 1994;Smičiklas et al., 2006;Wang et al., 2009). Th e fi xation of metal ions on nHAP may take place through ion exchange, surface complexation, dissolution of nHAP to form new metal phosphates, and substitution of the Ca 2+ ions in nHAP by other metal ions during recrystallization (Ma et al., 1994;Smičiklas et al., 2006). Th e small size and high surface area of nHAP make these particles especially reactive sorbents. Little attention has been paid, however, to potential environmental risks of nHAP during soil remediation. For example, nHAP signifi cantly changes the distribution of metal contaminants, such as Cu, among the mobile and immobile phases (Wang et al., 2011a). Th e transport of many chemicals can be greatly enhanced when they are associated with mobile colloids (
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