2018
DOI: 10.1016/j.aquatox.2018.02.018
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Evaluation of biomarkers in Mytilus galloprovincialis as an integrated measure of biofilm-membrane bioreactor (BF-MBR) system efficiency in mitigating the impact of oily wastewater discharge to marine environment: a microcosm approach

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Cited by 11 publications
(7 citation statements)
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“…The two affected clam populations were characterized by the presence of haemocyte infiltration and epithelial cell degradation during winter and autumn. This phenomenon has been well described as one of the responses to diverse environmental stressors (Pirrone et al 2018). It has previously been established that haemocyte infiltration is the cause of the inflammatory process due to a rapid release of pro-inflam-matory and vasoactive mediators (Bouallegui et al 2018).…”
Section: Discussionmentioning
confidence: 98%
“…The two affected clam populations were characterized by the presence of haemocyte infiltration and epithelial cell degradation during winter and autumn. This phenomenon has been well described as one of the responses to diverse environmental stressors (Pirrone et al 2018). It has previously been established that haemocyte infiltration is the cause of the inflammatory process due to a rapid release of pro-inflam-matory and vasoactive mediators (Bouallegui et al 2018).…”
Section: Discussionmentioning
confidence: 98%
“…to naphthenic acids. Microcosms are ideal for use in situations where environmental control and experimental repeatability are required while maintaining specific environmental conditions ( Pirrone et al, 2018 ). Moreover, the use of microcosms is well established for toxicity testing, owing primarily to the increased transferability of results between field and laboratory environments as microcosms can closely mimic those of target ecosystems ( Alexander et al, 2014 ).…”
Section: Methodsmentioning
confidence: 99%
“…For microscopy, about 800 μL of rehydrated FWM, containing 10,000 cells, were placed in a 24-well plate and grown for 24, 48, 72 or 96 h, and then processed as reported in Pirrone [ 19 ]. Briefly, samples were fixed in Karnovsky solution (2% glutaraldehyde, 4% formaldehyde in 0.1 M sodium cacodylate buffer, pH 7.4) for 24 h at 4 °C and then preserved in 0.1 M sodium cacodylate buffer at 4 °C.…”
Section: Methodsmentioning
confidence: 99%
“…For microscopy, about 800 μL of rehydrated FWM, containing 10,000 cells, were placed in a 24well plate and grown for 24, 48, 72 or 96 h, and then processed as reported in Pirrone [19]. Briefly,…”
Section: Optical and Electron Microscopymentioning
confidence: 99%
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