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Salinity-dependent toxicities of zinc oxide nanoparticles to the marine diatom Thalassiosira pseudonana.
Yung, Mana M N; Wong, Stella W Y; Kwok, Kevin W H; Liu, F Z; Leung, Y H; Chan, W T; Li, X Y; Djurisic, A B; Leung, Kenneth M Y.
Affiliation
  • Yung MM; The Swire Institute of Marine Science and School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.
  • Wong SW; The Swire Institute of Marine Science and School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China.
  • Kwok KW; Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, China.
  • Liu FZ; Department of Physics, The University of Hong Kong, Pokfulam, Hong Kong, China.
  • Leung YH; Department of Physics, The University of Hong Kong, Pokfulam, Hong Kong, China.
  • Chan WT; Department of Chemistry, The University of Hong Kong, Pokfulam, Hong Kong, China.
  • Li XY; Department of Civil Engineering, The University of Hong Kong, Pokfulam, Hong Kong, China.
  • Djurisic AB; Department of Physics, The University of Hong Kong, Pokfulam, Hong Kong, China.
  • Leung KM; The Swire Institute of Marine Science and School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong, China. Electronic address: kmyleung@hku.hk.
Aquat Toxicol ; 165: 31-40, 2015 Aug.
Article in En | MEDLINE | ID: mdl-26011135
This study comprehensively investigated the influences of salinity, exposure concentration and time on the aggregate size, surface charge and dissolution of zinc oxide nanoparticles (ZnO-NPs; 20nm) in seawater, and examined the interacting effect of salinity and waterborne exposure of ZnO-NPs on the marine diatom Thalassiosira pseudonana for 96h. We found that aggregate sizes of ZnO-NPs significantly increased with increasing salinity, but generally decreased with increasing exposure concentration. Ion release decreased with increasing salinity, whereas the surface charge of the particles was not affected by salinity. The increased aggregate size and decreased ion release with increasing salinity, and consequently lower concentration of bioavailable zinc ions, resulted in decreased toxicity of ZnO-NPs at higher salinity in general in terms of growth inhibition (IC50) and chlorophyll fluorescence (EC50 - ФPo and EC50 - Ф2). However, IC50s and EC50s of ZnO-NPs were smaller than those of Zn(2+) (from ZnO-NPs ultrafiltrate and ZnCl2), indicating that dissolved Zn(2+) can only partially explain the toxicity of ZnO-NPs. SEM images showed that ZnO-NPs attached on the diatom frustule surface, suggesting that the interaction between the nanoparticles and the cell surface may acerbate the toxicity of ZnO-NPs. Our results linked the physicochemical characteristics of ZnO-NPs in seawater with their toxicities to the marine diatom and highlighted the importance of salinity as an influential environmental factor governing the aggregation, dissolution and the toxicity of ZnO-NPs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Water Pollutants, Chemical / Zinc Oxide / Diatoms / Nanoparticles / Salinity Language: En Journal: Aquat Toxicol Journal subject: BIOLOGIA / TOXICOLOGIA Year: 2015 Document type: Article Affiliation country: China Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Water Pollutants, Chemical / Zinc Oxide / Diatoms / Nanoparticles / Salinity Language: En Journal: Aquat Toxicol Journal subject: BIOLOGIA / TOXICOLOGIA Year: 2015 Document type: Article Affiliation country: China Country of publication: Netherlands