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Biodegradation of pyrene in sand, silt and clay fractions of sediment

Microbial degradation is the dominant pathway for natural attenuation of PAHs in environmental compartments such as sediments, which in turn depends on the bioavailability of PAHs. The bioavailability of PAHs has seldom been studied at the sediment particle size scale. We evaluated biodegradation of...

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Autores principales: Cui, Xinyi, Hunter, Wesley, Yang, Yu, Chen, Yingxu, Gan, Jay
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046355/
https://www.ncbi.nlm.nih.gov/pubmed/20714921
http://dx.doi.org/10.1007/s10532-010-9399-z
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author Cui, Xinyi
Hunter, Wesley
Yang, Yu
Chen, Yingxu
Gan, Jay
author_facet Cui, Xinyi
Hunter, Wesley
Yang, Yu
Chen, Yingxu
Gan, Jay
author_sort Cui, Xinyi
collection PubMed
description Microbial degradation is the dominant pathway for natural attenuation of PAHs in environmental compartments such as sediments, which in turn depends on the bioavailability of PAHs. The bioavailability of PAHs has seldom been studied at the sediment particle size scale. We evaluated biodegradation of pyrene by Mycobacterium vanbaalenii PYR-1 as a function of sediment particle sizes, and investigated the relationship between the rate of degradation on sand, silt and clay particles with their individual desorption kinetics measured with the Tenax extraction method. Regression analysis showed that the total organic carbon (TOC), black carbon (BC), and specific surface area (SSA) of the specific particle size fractions, instead of the particle size scale itself, were closely related (P < 0.01) with the mineralization rate. While the fraction in the rapid desorption pool (F (rapid)) ranged from 0.11 to 0.38 for the whole sediments and different size groups, the fractions mineralized after 336-h incubation (0.52 to 0.72) greatly surpassed the F (rapid) values, suggesting utilization of pyrene in the slow desorption pool (F (slow)). A biodegradation model was modified by imbedding a two-phase desorption relationship describing sequential Tenax extractions. Model analysis showed that pyrene sorbed on silt and clay aggregates was directly utilized by the degrading bacteria. The enhanced bioavailability may be attributed to the higher chemical concentration, higher TOC or larger SSA in the silt and clay fractions, which appeared to overcome the reduced bioavailability of pyrene due to sorption, making pyrene on the silt and clay particles readily available to degrading microbes. This conjecture merits further investigation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10532-010-9399-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-30463552011-04-05 Biodegradation of pyrene in sand, silt and clay fractions of sediment Cui, Xinyi Hunter, Wesley Yang, Yu Chen, Yingxu Gan, Jay Biodegradation Original Paper Microbial degradation is the dominant pathway for natural attenuation of PAHs in environmental compartments such as sediments, which in turn depends on the bioavailability of PAHs. The bioavailability of PAHs has seldom been studied at the sediment particle size scale. We evaluated biodegradation of pyrene by Mycobacterium vanbaalenii PYR-1 as a function of sediment particle sizes, and investigated the relationship between the rate of degradation on sand, silt and clay particles with their individual desorption kinetics measured with the Tenax extraction method. Regression analysis showed that the total organic carbon (TOC), black carbon (BC), and specific surface area (SSA) of the specific particle size fractions, instead of the particle size scale itself, were closely related (P < 0.01) with the mineralization rate. While the fraction in the rapid desorption pool (F (rapid)) ranged from 0.11 to 0.38 for the whole sediments and different size groups, the fractions mineralized after 336-h incubation (0.52 to 0.72) greatly surpassed the F (rapid) values, suggesting utilization of pyrene in the slow desorption pool (F (slow)). A biodegradation model was modified by imbedding a two-phase desorption relationship describing sequential Tenax extractions. Model analysis showed that pyrene sorbed on silt and clay aggregates was directly utilized by the degrading bacteria. The enhanced bioavailability may be attributed to the higher chemical concentration, higher TOC or larger SSA in the silt and clay fractions, which appeared to overcome the reduced bioavailability of pyrene due to sorption, making pyrene on the silt and clay particles readily available to degrading microbes. This conjecture merits further investigation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10532-010-9399-z) contains supplementary material, which is available to authorized users. Springer Netherlands 2010-08-18 2011 /pmc/articles/PMC3046355/ /pubmed/20714921 http://dx.doi.org/10.1007/s10532-010-9399-z Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Cui, Xinyi
Hunter, Wesley
Yang, Yu
Chen, Yingxu
Gan, Jay
Biodegradation of pyrene in sand, silt and clay fractions of sediment
title Biodegradation of pyrene in sand, silt and clay fractions of sediment
title_full Biodegradation of pyrene in sand, silt and clay fractions of sediment
title_fullStr Biodegradation of pyrene in sand, silt and clay fractions of sediment
title_full_unstemmed Biodegradation of pyrene in sand, silt and clay fractions of sediment
title_short Biodegradation of pyrene in sand, silt and clay fractions of sediment
title_sort biodegradation of pyrene in sand, silt and clay fractions of sediment
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046355/
https://www.ncbi.nlm.nih.gov/pubmed/20714921
http://dx.doi.org/10.1007/s10532-010-9399-z
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