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1.
Environ Monit Assess ; 184(1): 549-59, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21866434

RESUMO

It has become apparent that the threat of an organic pollutant in soil is directly related to its bioavailable fraction and that the use of total contaminant concentrations as a measure of potential contaminant exposure to plants or soil organisms is inappropriate. In light of this, non-exhaustive extraction techniques are being investigated to assess their appropriateness in determining bioavailability. To find a suitable and rapid extraction method to predict phenanthrene bioavailability, multiple extraction techniques (i.e., mild hydroxypropyl-ß-cyclodextrin (HPCD) and organic solvents extraction) were investigated in soil spiked to a range of phenanthrene levels (i.e., 1.12, 8.52, 73, 136, and 335 µg g( - 1) dry soil). The bioaccumulation of phenanthrene in earthworm (Eisenia fetida) was used as the reference system for bioavailability. Correlation results for phenanthrene suggested that mild HPCD extraction was a better method to predict bioavailability of phenanthrene in soil compared with organic solvents extraction. Aged (i.e., 150 days) and fresh (i.e., 0 day) soil samples were used to evaluate the extraction efficiency and the effect of soil contact time on the availability of phenanthrene. The percentage of phenanthrene accumulated by earthworms and percent recoveries by mild extractants changed significantly with aging time. Thus, aging significantly reduced the earthworm uptake and chemical extractability of phenanthrene. In general, among organic extractants, methanol showed recoveries comparable to those of mild HPCD for both aged and unaged soil matrices. Hence, this extractant can be suitable after HPCD to evaluate risk of contaminated soils.


Assuntos
Fracionamento Químico/métodos , Fenantrenos/farmacocinética , Poluentes do Solo/farmacocinética , Solo/química , 2-Hidroxipropil-beta-Ciclodextrina , Animais , Disponibilidade Biológica , Monitoramento Ambiental/métodos , Oligoquetos , Fenantrenos/química , Plantas , Poluentes do Solo/química , Fatores de Tempo , beta-Ciclodextrinas/química
2.
Arch Environ Contam Toxicol ; 60(1): 107-15, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-20437042

RESUMO

Bioavailability of organic pollutants in soil is currently a much-debated issue in risk assessment of contaminated sites. Ecorisk of an organic pollutant in soil is strongly influenced by the properties of the soil and its contamination history. To evaluate the effect of aging on the availability of pyrene, earthworm (Eisenia fetida) accumulation and chemical extraction by exhaustive and nonexhaustive techniques in soil spiked with a range of pyrene levels (1.07, 9.72, 88.4, 152, and 429 µg g⁻¹ dry soil) were measured in this study using both unaged (i.e., 0 days) and aged (i.e., 69, 150, and 222 days) soil samples. The results showed that the amount of pyrene accumulated by earthworms did not change greatly with aging time under different high-dose contamination levels, but changed significantly at lower concentrations. Moreover, aging (after 222 days) significantly decreased biological and chemical availability of pyrene. Furthermore, the relationship between earthworm bioaccumulation, hydroxypropyl-ß-cyclodextrin (HPCD), and organic solvent extraction was investigated in order to find a suitable and rapid method to predict pyrene bioavailability. Results showed that, at different levels of pyrene, the mean values of earthworm uptake and HPCD extractability were 10-40% and 10-65%, respectively. Correlation (r² = 0.985) and extraction results for pyrene suggested that mild HPCD extraction was a better method to predict bioavailability of pyrene in soil compared with organic solvent extraction.


Assuntos
Monitoramento Ambiental/métodos , Oligoquetos/metabolismo , Pirenos/análise , Poluentes do Solo/análise , beta-Ciclodextrinas/análise , 2-Hidroxipropil-beta-Ciclodextrina , Animais , Biodegradação Ambiental , Pirenos/metabolismo , Solo/análise , Poluentes do Solo/metabolismo , Solventes/análise , Solventes/metabolismo , beta-Ciclodextrinas/metabolismo
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