Tourmaline combined with Phanerochaete chrysosporium to remediate agricultural soil contaminated with PAHs and OCPs

Journal of Hazardous Materials

Volumn 264, Issue , 2014, Pages 439-448

  Wang, Cuiping ^a   Yu, Li ^a   Zhang, Zhiyuan ^a   Wang, Baolin ^a   Sun, Hongwen ^a  

^a NANKAI UNIVERSITY   (China)

Author keywords

PAHs and OCPs; PCR DGGE bacterial diversity; Remediation; Soil enzyme activities; Soil humic acid; Tourmaline

Indexed keywords

BIOLOGICAL MATERIALS; BIOREMEDIATION; DEGRADATION; ORGANIC ACIDS; POLYCYCLIC AROMATIC HYDROCARBONS; POLYMERASE CHAIN REACTION; REMEDIATION; SILICATE MINERALS; SOILS;

BACTERIAL DIVERSITY; PAHS AND OCPS; SOIL ENZYME ACTIVITY; SOIL HUMIC ACIDS; TOURMALINE;

SOIL POLLUTION;

MINERAL; ORGANOCHLORINE PESTICIDE; POLYCYCLIC AROMATIC HYDROCARBON; TOURMALINE; UNCLASSIFIED DRUG;

AGRICULTURAL SOIL; BACTERIUM; BIODEGRADATION; BIOREMEDIATION; ENZYME ACTIVITY; FUNGUS; HUMIC ACID; PAH; SOIL POLLUTION; SOIL REMEDIATION; SPECIES DIVERSITY; TOURMALINE;

ARTICLE; CHINA; CONTROLLED STUDY; DEGRADATION; MICROBIAL COMMUNITY; NONHUMAN; PHANEROCHAETE; SOIL; SOIL POLLUTION; SOIL TREATMENT; WASTE COMPONENT REMOVAL;

CHINA; DAGU RIVER; SHANDONG; TIANJIN;

BACTERIA (MICROORGANISMS); PHANEROCHAETE CHRYSOSPORIUM;

PAHS AND OCPS; PCR-DGGE BACTERIAL DIVERSITY; REMEDIATION; SOIL ENZYME ACTIVITIES; SOIL HUMIC ACID; TOURMALINE;

BIODEGRADATION, ENVIRONMENTAL; BORON COMPOUNDS; HYDROCARBONS, CHLORINATED; MINERALS; PHANEROCHAETE; POLYCYCLIC HYDROCARBONS, AROMATIC; SILICATES; SOIL MICROBIOLOGY; SOIL POLLUTANTS;

EID: 84890028472     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2013.10.073     Document Type: Article

References (32)

1. Zhang A., Fang L., Wang J., Liu W., Yuan H., Jantunen L., Li Y. Residues of currently and never used organochlorine pesticides in agricultural soils from Zhejiang Province. Chin. J. Agric. Food Chem. 2012, 60:2982-2988.
2. D'Annibale A., Ricci M., Leonardi V., Quarantino D., Mincione E., Petruccioli M. Degradation of aromatic hydrocarbons by white-rot fungi in a historically contaminated soil. Biotechnol. Bioeng. 2005, 90:723-731.
3. Prasad P.S.R. Study of structural disorder in natural tourmalines by infrared spectroscopy. Gondwana Res. 2005, 8:265-270.
4. Wang C., Liu J., Zhang Z., Wang B., Sun H. Adsorption of Cd(II), Ni(II), and Zn(II) by tourmaline at acidic conditions: Kinetics, thermodynamics, and mechanisms. Ind. Eng. Chem. Res. 2012, 51:4397-4406.
5. Xia M., Hu C., Zhang M. Effects of tourmaline addition on the dehydrogenase activity of Rhodopseudomonas palustris. Process. Biochem. 2006, 41:221-225.
6. Ni H., Li L., Li H. Tourmaline ceramic balls stimulate growth and metabolism of three fermentation microorganisms. World J. Microb. Biot. 2008, 24:725-731.
7. Iwabuchi T., Harayama S. Biochemical and molecular characterization of 1-hydroxy-2-naphthoate dioxygenase from Nocardioides sp KP7. J. Biol. Chem. 1998, 273:8332-8336.
8. Yang Y., Hunter W., Tao S., Gan J. Microbial availability of different forms of phenanthrene in soils. Environ. Sci. Technol. 2009, 43:1852-1857.
9. Yang Y., Zhang N., Xue M., Lu S., Tao S. Effects of soil organic matter on the development of the microbial polycyclic aromatic hydrocarbons (PAHs) degradation potentials. Environ. Pollut. 2011, 159:591-595.
10. Nam K., Chung N., Alexander M. Relationship between organic matter content of soil and the sequestration of phenanthrene. Environ. Sci. Technol. 1998, 32:3785-3788.
11. Liu G., Jiang N., Zhang L., Liu Z. Soil Physical and Chemical Analysis and Description of Soil Profiles 1996, Standards Press of China, Beijing, In Chinese.
12. Zhou K.L. The Science of Soil Enzymes 1987, The Science Press, Beijing, In Chinese.
13. LaParaa T.M., Nakatsu C.H., Pantea L.M., Alleman J.E. Stability of the bacterial communities supported by a seven-stage biological process treating pharmaceutical wastewater as revealed by PCR-DGGE. Water Res. 2002, 36:638-646.
14. Garbeva P., Van Veen J., Van Elsas J. Predominant Bacillus spp. in agricultural soil under different management regimes detected via PCR-DGGE. Microbiol. Ecol. 2003, 45:302-316.
15. Tao X., Lu G., Dang Z., Yang C., Yi X. A phenanthrene-degrading strain Sphingomonas sp. GY2B isolated from contaminated soils. Process Biochem. 2007, 42(42):401-408.
16. Wrenn B.A., Venosa A.D. Selective enumeration of aromatic and aliphatic hydrocarbon degrading bacteria by a most-probable-number procedure. Can. J. of microbial. 1996, 42:252-258.
17. ISO 4831 Microbiology-General Guidance for the Enumeration of Coliforms-Most Probable Number Technique 1991, International Organization for Standardization, Geneva.
18. Kohl S.D., Rice J.A. The binding of contaminants to humin: a mass balance. Chemosphere 1998, 36:251-261.
19. Kelsey J.W., Slizovskiy I.B., Peters R.D., Melnick A.M. Sterilization affects soil organic matter chemistry and bioaccumulation of spiked p,p'-DDE and anthracene by earthworms. Environ. Pollut. 2010, 158:2251-2257.
20. Ma L., hu S., Wang X., Cheng H., Liu X., Xu X. Polycyclic aromatic hydrocarbons in the surface soils from outskirts of Beijing, China. Chemosphere 2005, 58:1355-1363.
21. Long E.R., Macdonald D.D., Smith S.L., Calder F.D. Incidence of adverse biological effects with in ranges of chemical concentrations in marine and estuary sediments. J. Environ. Manage. 1995, 19:81-97.
22. Muhayimana A.S., Qi S., Wang Y., Kong X., Owago O., Zhang J. Distribution and sources of organochlorine pesticides (OCPs) in Karst Cave, Guilin, China. Acad. Arena 2009, 1:47-56.
23. Yang R., Jiang G., Zhou Q., Yuan C., Shi J. Occurrence and distribution of organochlorine pesticides in sediments collected from East China Sea. Environ. Int. 2005, 31:799-804.
24. Nhan D.D., Carvalho F.P., Am N.M., Tuan N., Yen N., Villeneuve J. Chlorinated pesticides and PCBs in sediments and molluscs from fresh water canals in the Hanoi region. Environ. Pollut. 2001, 112:311-320.
25. Zheng Z., Obbard J.P. Oxidation of polycyclic aromatic hydrocarbons (PAH) by the white rot fungus, Phanerochaete chrysosporium. Enzyme Microb. Technol. 2002, 31:3-9.
26. Hassett J.E., Zak D.R. Aspen harvest intensity decreased microbial biomass and extracellular enzyme activity, and soil nitrogen cycling. Soil Sci. Soc. Am. J. 2005, 69:227-235.
27. Tan X., Chang S., Kabzems R. Soil compaction and forest floor removal reduced microbial biomass and enzyme activities in a boreal aspen forest soil. Biol. Fertil. Soils 2008, 44:471-479.
28. Muyzer G., de Waal E.C., Uitterlinden A.G. Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction genes coding for 16S rRNA. Appl. Environ. Microbiol. 1983, 59:695-700.
29. Heuer H., Krsek M., Baker P., Smalla K.W., Elizabeth M.H. Analysis of actinomycete communities by specific amplification of genes encoding 16S rRNA and gel-electrophoretic separation in denaturing gradients. Appl. Environ. Microbiol. 1997, 63:3233-3241.
30. Zhang S., Li A., Cui D., Yang J., Ma F. Performance of enhanced biological SBR process for aniline treatment by mycelial pellet as biomass carrier. Bioresour. Technol. 2011, 102:4360-4365.
31. Mishra B., Srivastava L.L. Degradation of humic acid of a forest soil by some fungal isolates. Plant Soil 1986, 6:413-416.
32. Wang C., Sun H., Li J., Li Y., Zhang Q. Enzyme activities during degradation of polycyclic aromatic hydrocarbons by white rot fungus Phanerochaete chrysosporium in soil. Chemosphere 2009, 77:733-738.