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Enhanced kinetics of solid-phase microextraction and biodegradation of polycyclic aromatic hydrocarbons in the presence of dissolved organic matter.

Authors :
Haftka JJ
Parsons JR
Govers HA
Ortega-Calvo JJ
Source :
Environmental toxicology and chemistry [Environ Toxicol Chem] 2008 Jul; Vol. 27 (7), pp. 1526-32.
Publication Year :
2008

Abstract

The uptake kinetics of fluorene, phenanthrene, fluoranthene, pyrene, and benzo[e]pyrene by solid-phase microextraction fibers was studied in the presence of dissolved organic matter (DOM) obtained from sediment pore water and resulted in increased fiber absorption and desorption rate coefficients. Compared to the control without DOM, these rate coefficients were increased at a DOM concentration of 36.62 mg/L by a factor of 1.27 to 2.21 and 1.31 to 2.10 for fluorene and benzo[e]pyrene, respectively. The calculated values for the fiber absorption and desorption rate coefficients show that diffusion through an unstirred boundary layer (UBL) surrounding the fiber probably forms the rate-limiting step of the process. The mineralization of aqueous-phase phenanthrene and pyrene by a representative polycyclic aromatic hydrocarbon (PAH)-degrading bacterium (Mycobacterium gilvum VM552) also was found to be enhanced by DOM. The initial degradation rates of phenanthrene (9.03 (microg/L) and pyrene (1.96 microg/L) were significantly higher compared to the control values and were enhanced by a factor of 1.32 and 1.26 at a DOM concentration of 43.14 and 42.15 mg/L, respectively. We suggest that such an enhancement results from the combination of faster uptake kinetics of the water-dissolved compounds in the UBL surrounding microbial cells and direct access of the bacteria to DOM-associated PAHs. These enhanced kinetic effects of DOM may have strong implications in sediment processes like desorption, nonequilibrium exposure, and biodegradation.

Details

Language :
English
ISSN :
0730-7268
Volume :
27
Issue :
7
Database :
MEDLINE
Journal :
Environmental toxicology and chemistry
Publication Type :
Academic Journal
Accession number :
18260699
Full Text :
https://doi.org/10.1897/07-544