2014
DOI: 10.1016/j.jhazmat.2014.05.049
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Arsenic uptake and depuration kinetics in Microcystis aeruginosa under different phosphate regimes

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Cited by 47 publications
(13 citation statements)
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“…Thirdly, the influence of dead cells of microalgae on the As metabolism cannot be overlooked because these cells may decompose or change their membrane permeability, releasing the absorbed As back to the culture media (Wang et al 2014c) and modifying intracellular As speciation (Duncan et al 2013a). Such impacts may be more significant in batch culture, in which the proportion of non-living cells keeps increasing since the nutrient supplies gradually become limited (Duncan et al 2013a).…”
Section: Concluding Remarks and Future Perspectivementioning
confidence: 99%
“…Thirdly, the influence of dead cells of microalgae on the As metabolism cannot be overlooked because these cells may decompose or change their membrane permeability, releasing the absorbed As back to the culture media (Wang et al 2014c) and modifying intracellular As speciation (Duncan et al 2013a). Such impacts may be more significant in batch culture, in which the proportion of non-living cells keeps increasing since the nutrient supplies gradually become limited (Duncan et al 2013a).…”
Section: Concluding Remarks and Future Perspectivementioning
confidence: 99%
“…A nonlinear one-compartment model considering a simultaneous As uptake and release was used to describe the measured intracellular concentration of As in algal cells for each treatment over time according to the following first-order kinetics: Herein, (μg g −1 dry weight) is the intracellular concentration of As in algal cells; (μg L −1 ) is the As concentration in medium assumed to be a constant, and t (h) is the time of As exposure; k u (L g −1 h −1 ) and k e (h −1 ) are the As uptake and release rate constants for the algae, respectively [ 5 ].…”
Section: Methods Detailsmentioning
confidence: 99%
“…To determine the As release rates from dead cells, 50 mL algal solution of each treatment were taken after 96 h incubation and rinsed with ultrapure water and the aforementioned phosphate buffer. To produce dead cells of M. aeruginosa , the samples were heated for 10 min at 50 °C using a waterbath [ 5 , 7 , 8 ]. Afterwards the treated algae were resuspended in 20 mL sterilized BG-11 media (same with their initial culture conditions) for 8 h, respectively.…”
Section: Methods Detailsmentioning
confidence: 99%
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“…A systematic examination of hydrodynamic size and sedimentation of nTiO 2 in three types of media was conducted. Additionally, arsenic, ubiquitous throughout global environments, is a noxious, nonessential metalloid that has been designated a priority pollutant [26]. Increasing concern has recently arose on how and to what extent changes in nTiO 2 cause co-occurring contaminants, such as arsenic, to react across phytoplankton-daphnia food chains [27].…”
Section: Introductionmentioning
confidence: 99%