Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10110656 | Science of The Total Environment | 2005 | 13 Pages |
Abstract
Isotope dilution methods using a stable isotope tracer (207Pb) were developed for the determination of Pb availability in contaminated soils. The methods included determination of E values (isotopically exchangeable pool), L values (plant labile pool) and isotopic exchange kinetics (IEK). Isotopically exchangeable Pb was monitored at different exchange times based on measurement of the 207Pb/208Pb ratio in soil solution following addition of the tracer. The rate of decrease in the 207Pb/208Pb ratio in solution could be described by using the same IEK equation as used previously with radioisotope tracers. The amounts of isotopically exchangeable Pb in Pb-contaminated soils estimated from long-term IEK parameters were in good agreement with directly determined E values up to 15 days. However, values of some of the fitted IEK parameters cast doubts on the validity of using the IEK approach with 207Pb, most probably as a result of irreversible fixation of some of the spike by reactive surfaces in the soils. Estimation of isotopically exchangeable Pb using short-term kinetics data was unsuccessful, substantially underestimating E values. Results for the control (uncontaminated) soil were highly variable, most probably as a result of fixation of tracer by the soil and poor analytical precision due to low solution Pb concentrations. A compartmental analysis of the variation in E values with time indicates a good potential for estimating bioavailable Pb in contaminated soils. The amounts of available Pb obtained from summation of the E1min and E1 min-24 h pools (E(available)), accounting for an average of 57.62% of total soil Pb, were significantly correlated with both the L values and with Pb extracted from soil with EDTA.
Related Topics
Life Sciences
Environmental Science
Environmental Chemistry
Authors
N. Tongtavee, J. Shiowatana, Ronald G. McLaren, Colin W. Gray,