2005
DOI: 10.1016/j.apsoil.2005.01.003
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Characterization of soil health in an Italian polluted site by using microorganisms as bioindicators

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Cited by 141 publications
(80 citation statements)
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“…Thus far, only few studies focused on the microbial processes that occur in geothermal plants in the context of microbiologically mediated operational failure (Sand 2003;Pryfogle 2005;Alawi et al 2011;Lerm et al 2011a, b). As microorganisms are directly influenced by their environment, they can be used as bioindicators (Avidano et al 2005;Steube et al 2009) while reflecting changes in reservoir and topside conditions caused by aquifer utilization. In this study, the microbial community structure in a deep saline aquifer in the NGB that is used for temporary aquifer heat storage was investigated.…”
Section: Introductionmentioning
confidence: 99%
“…Thus far, only few studies focused on the microbial processes that occur in geothermal plants in the context of microbiologically mediated operational failure (Sand 2003;Pryfogle 2005;Alawi et al 2011;Lerm et al 2011a, b). As microorganisms are directly influenced by their environment, they can be used as bioindicators (Avidano et al 2005;Steube et al 2009) while reflecting changes in reservoir and topside conditions caused by aquifer utilization. In this study, the microbial community structure in a deep saline aquifer in the NGB that is used for temporary aquifer heat storage was investigated.…”
Section: Introductionmentioning
confidence: 99%
“…Most methods described above focus on profiling soil microbial biomass and diversity (Table 1). These soil attributes are relatively easy to measure and have been widely associated with "soil health" [186,187]. For example, agricultural soils with low microbial biomass and diversity are linked to yield decline in sugarcane [188].…”
Section: Choice Of Methods and Complimentary Approachesmentioning
confidence: 99%
“…After extraction, the polymerase chain reaction (PCR) was performed for the amplification of the 16S-rDNA sequence (primer sequence are in Table 2). 1 µL (2 -5 ng) of extracted DNA was used as a template for PCR, using universal primers fD1 and rD1 to amplify the 16S-rRNA gene in almost its full length [25]. Conditions for each of the PCR reactions were kept as previously described [26].…”
Section: Identification Of Microorganismsmentioning
confidence: 99%