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Phytoremediation potential of Acorus calamus in soils co-contaminated with cadmium and polycyclic aromatic hydrocarbons.

ABSTRACT: Phytoremediation is a promising technology for the remediation of sites co-contaminated with inorganic (heavy metal) and organic pollutants. A greenhouse experiment was conducted to investigate the independent and interactive effects of cadmium (Cd) and polycyclic aromatic hydrocarbons (PAHs) on the growth of the wetland plant Acorus calamus and its ability to uptake, accumulate, and remove pollutants from soils. Our results showed that growth and biomass of A. calamus were significantly influenced by the interaction of Cd and PAHs after 60 days of growth. The combined treatment of low Cd and low PAHs increased plant biomass and Cd accumulation in plant tissues, thus enhancing Cd removal. Dissipation of PAHs from soils was not significantly influenced by Cd addition or by the presence of plants. Correlation analysis also indicated a positive relationship between residual concentrations of phenantherene and pyrene (PAHs), whereas enzyme activities (dehydrogenase and polyphenol oxidase) were negatively correlated with each other. Cluster analysis was used to evaluate the similarity between different treatments during phytoremediation of Cd and PAHs. Our results suggest that A. calamus might be useful for phytoremediation of co-contaminated soil.

SUBMITTER: Jeelani N

PROVIDER: S-EPMC5556126 | biostudies-other | 2017 Aug

REPOSITORIES: biostudies-other

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Project description:Bacterial strains of the genus Sphingomonas are often isolated from contaminated soils for their ability to use polycyclic aromatic hydrocarbons (PAH) as the sole source of carbon and energy. The direct detection of Sphingomonas strains in contaminated soils, either indigenous or inoculated, is, as such, of interest for bioremediation purposes. In this study, a culture-independent PCR-based detection method using specific primers targeting the Sphingomonas 16S rRNA gene combined with denaturing gradient gel electrophoresis (DGGE) was developed to assess Sphingomonas diversity in PAH-contaminated soils. PCR using the new primer pair on a set of template DNAs of different bacterial genera showed that the method was selective for bacteria belonging to the family Sphingomonadaceae.Single-band DGGE profiles were obtained for most Sphingomonas strains tested. Strains belonging to the same species had identical DGGE fingerprints, and in most cases, these fingerprints were typical for one species. Inoculated strains could be detected at a cell concentration of 10(4) CFU g of soil(-1). The analysis of Sphingomonas population structures of several PAH-contaminated soils by the new PCR-DGGE method revealed that soils containing the highest phenanthrene concentrations showed the lowest Sphingomonas diversity. Sequence analysis of cloned PCR products amplified from soil DNA revealed new 16S rRNA gene Sphingomonas sequences significantly different from sequences from known cultivated isolates (i.e., sequences from environmental clones grouped phylogenetically with other environmental clone sequences available on the web and that possibly originated from several potential new species). In conclusion, the newly designed Sphingomonas-specific PCR-DGGE detection technique successfully analyzed the Sphingomonas communities from polluted soils at the species level and revealed different Sphingomonas members not previously detected by culture-dependent detection techniques.

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Phytoremediation potential of Acorus calamus in soils co-contaminated with cadmium and polycyclic aromatic hydrocarbons.

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