2017
DOI: 10.1016/j.nbt.2016.09.006
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Plant-assisted bioremediation of a historically PCB and heavy metal-contaminated area in Southern Italy

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Cited by 70 publications
(66 citation statements)
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“…Finally, because the same site has been used as an illegal city dump, different kinds of waste have been accumulated over time contributing to the decline in the soil quality. A preliminary characterization of the experimental site performed in 2012 showed hot spots of PCB and a diffuse HM contamination . In April 2013 about 650 poplar cuttings were planted in a site sub‐area of 785 m 2 and three data campaigns have been carried out so far: March 2013: characterization campaign ( t 0 = before poplar planting), June 2014: first monitoring campaign ( t 1 = 420 days after poplar planting), November 2015: second monitoring campaign ( t 2 = 900 days after poplar planting), …”
Section: Methodsmentioning
confidence: 99%
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“…Finally, because the same site has been used as an illegal city dump, different kinds of waste have been accumulated over time contributing to the decline in the soil quality. A preliminary characterization of the experimental site performed in 2012 showed hot spots of PCB and a diffuse HM contamination . In April 2013 about 650 poplar cuttings were planted in a site sub‐area of 785 m 2 and three data campaigns have been carried out so far: March 2013: characterization campaign ( t 0 = before poplar planting), June 2014: first monitoring campaign ( t 1 = 420 days after poplar planting), November 2015: second monitoring campaign ( t 2 = 900 days after poplar planting), …”
Section: Methodsmentioning
confidence: 99%
“…Soil sampling was performed 30 months (900 days) after poplar planting in order to analyse HMs, microbial abundance, cell viability and dehydrogenase activity (DHA) of the soil microbial community. Soil samples were collected from the HM contaminated plots (P2, P3 and P4) following the sampling procedure reported in detail in Ancona et al . Briefly, soil samples were collected: at 0 cm from the trunk, around the roots (depth: 0–30 cm) as a rhizosphere sample (R); at 0.25 m distance (depths 0–20 and 20–40 cm); and finally, at 1 m distance from the trunk (depths: 0–20 and 20–40 cm).…”
Section: Methodsmentioning
confidence: 99%
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