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JPR Advance Access originally published online on December 18, 2008
Journal of Plankton Research 2009 31(3):325-336; doi:10.1093/plankt/fbn117
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© The Author 2008. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org

Employing Chlorella protothecoides for metal bioavailability studies under acidic conditions

Zhi Ling Zeng1,2,*, Neal W. Menzies1,2 and Graham Kerven1

1 School of Land, Crop and Food Sciences, The University of Queensland, St Lucia, QLD 4072, Australia 2 Centre for Mined Land Rehabilitation, The University of Queenland, St Lucia, QLD 4072, Australia

* CORRESPONDING AUTHOR: z.zeng{at}uq.edu.au

Received on April 18, 2008; accepted on November 14, 2008


   Abstract

We report the challenges and resolutions facing the use of Chlorella protothecoides for metal bioavailability and toxicity research under acidic conditions. In our study, we found that a simplified growth medium recommended for metal bioavailability research did not support the optimum growth of C. protothecoides at pH 5.5, possibly due to nutrient deficiencies, rendering it unsuitable for bioavailability studies under acidic conditions. On the other hand, a modified Woods Hole MBL growth medium supplying all macro and micro nutrients, with chelators Tris and EDTA removed, and (NH4)2Fe(SO4)2 supplemented as the source of iron, produced excellent growth of the algae under identical conditions. This medium is therefore recommended as the alternative growth medium. While a pH increase of up to 2 units a day was observed in unbuffered media during algal growth, incorporation of CO2 into the aeration stream at a fixed partial pressure stabilized the medium pH. By initiating the metal (e.g. Cu) treatment at a culture optical density (750 nm) of ~0.04, where the algal population was just entering the rapid growth phase, the Chlorella assay was completed within 48 h. This minimized metal speciation changes and nutrient limitation that may occur over longer test durations. As demonstrated with the case of Cu, a cell density of ~7.5 x 105 cells mL–1 at the time of metal addition, caused only 5% initial loss of solution Cu, addressing the concern that such an initial cell density might deplete the metal from solution as a result of metal binding to algal cells. Overall, this study provides a valid means of employing Chlorella for metal bioavailability and toxicity research under acidic conditions, which ensures that algal growth is not impeded by nutrient deficiency, experimental duration is short, and more importantly, solution pH and metal speciation do not change significantly over the experimental period.


Corresponding editor: William Li


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