Recovery of microbial diversity and activity during bioremediation following chemical oxidation of diesel contaminated soils

被引:43
作者
Sutton, Nora B. [1 ]
Langenhoff, Alette A. M. [2 ]
Lasso, Daniel Hidalgo [1 ]
van der Zaan, Bas [2 ]
van Gaans, Pauline [2 ]
Maphosa, Farai [3 ]
Smidt, Hauke [3 ]
Grotenhuis, Tim [1 ]
Rijnaarts, Huub H. M. [1 ]
机构
[1] Wageningen Univ, Dept Environm Technol, NL-6700 EV Wageningen, Netherlands
[2] Deltares, Subsurface & Groundwater Syst, NL-3508 AL Utrecht, Netherlands
[3] Wageningen Univ, Microbiol Lab, NL-6703 HB Wageningen, Netherlands
关键词
Chemical oxidation; Bioremediation; Bioavailability; Diesel contamination; DGGE; qPCR; POLYCYCLIC AROMATIC-HYDROCARBONS; GEL-ELECTROPHORESIS ANALYSIS; IN-SITU OZONATION; REAL-TIME PCR; CRUDE-OIL; BIOLOGICAL REMEDIATION; COMMUNITY COMPOSITION; BIODEGRADATION; DEGRADATION; IMPACT;
D O I
10.1007/s00253-013-5256-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To improve the coupling of in situ chemical oxidation and in situ bioremediation, a systematic analysis was performed of the effect of chemical oxidation with Fenton's reagent, modified Fenton's reagent, permanganate, or persulfate, on microbial diversity and activity during 8 weeks of incubation in two diesel-contaminated soils (peat and fill). Chemical oxidant and soil type affected the microbial community diversity and biodegradation activity; however, this was only observed following treatment with Fenton's reagent and modified Fenton's reagent, and in the biotic control without oxidation. Differences in the highest overall removal efficiencies of 69 % for peat (biotic control) and 59 % for fill (Fenton's reagent) were partially explained by changes in contaminant soil properties upon oxidation. Molecular analysis of 16S rRNA and alkane monooxygenase (alkB) gene abundances indicated that oxidation with Fenton's reagent and modified Fenton's reagent negatively affected microbial abundance. However, regeneration occurred, and final relative alkB abundances were 1-2 orders of magnitude higher in chemically treated microcosms than in the biotic control. 16S rRNA gene fragment fingerprinting with DGGE and prominent band sequencing illuminated microbial community composition and diversity differences between treatments and identified a variety of phylotypes within Alpha-, Beta-, and Gammaproteobacteria. Understanding microbial community dynamics during coupled chemical oxidation and bioremediation is integral to improved biphasic field application.
引用
收藏
页码:2751 / 2764
页数:14
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