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Titel Bioavailability and Sources of Lead in the Terrestrial Environment of Egypt
VerfasserIn Ezzat Marzouk, Waleed Shetaya, Mohamed Elkassas, Elham Mohamed, Elizabeth Bailey, Scott Young
Konferenz EGU General Assembly 2016
Medientyp Artikel
Sprache en
Digitales Dokument PDF
Erschienen In: GRA - Volume 18 (2016)
Datensatznummer 250122626
Publikation (Nr.) Volltext-Dokument vorhandenEGU/EGU2016-1711.pdf
 
Zusammenfassung
Lead (Pb) is considered a major contemporary eco-toxicological threat with smelting operations and fossil fuel combustion regarded as the major sources in the environment. The majority of studies characterising Pb in soil have sought to determine: (i) its source, from 206,207,208Pb isotope ratios, (ii) its distribution among operationally defined soil fractions and (iii) its lability as defined by chemical extraction or isotopic exchangeability. The objectives of the current work were: (i) to source-apportion the soil Pb burden in Egypt between petrol, geological and other origins over a wide range of soil characteristics and diverse locations; (ii) to quantify the isotopically exchangeable fraction of Pb (PbE) as a measure of Pb reactivity; and (iii) to develop multivariate relationships to predict soil Pb lability. Combined determinations of SEP fractionation, isotopic lability and natural isotopic abundances were used as a means of characterizing Pb in ∼ 150 Egyptian soils (selected to cover a wide range of soil properties, locations and Pb exposure). Results showed a wide range of % PbEvalues (∼ 5 – 40 % of the total soil Pb concentration, Pbtotal). However, PbE showed no consistent correspondence to any single fraction of the SEP. Non-labile Pb (Pbtotal – PbE) showed reasonable agreement with the SEP ‘residual’ fraction in relatively uncontaminated soils from both inland and shoreline soils. However, in other soils, notably those from contaminated peri-urban and urban locations, the non-residual fractions (bound to oxides and humus) included non-labile forms of Pb. Up to 90% of the observed variability in the %PbE in soils from the inland and shoreline areas (uncontaminated) could be explained by soil factors, including variation in soil pH, soil organic matter content, total Pb and P concentrations. However, in the case of the contaminated peri-urban and urban soils the figure was only 33% implying a significant contaminant ‘source’ effect on Pb lability. Isotopic ratios (206Pb/207Pb and 208Pb/207Pb) fell on a mixing line between end-members attributed to petrol and regional geogenic Pb sources and clearly showed a distinction between Pb from geogenic and anthropogenic sources (mainly petrol-derived Pb). In contaminated locations, there was clear evidence that petrol-derived Pb, in average, remained considerably more labile than Pb from the soil parent material. However, in all samples, both petrol-derived and geogenic Pb contributed to the labile fraction depending on soil conditions.