2012). Based on the comparison of the life-cycle stages, Rokitta and co-workers concluded that the OA sensitivity in diploid cells originates from calcification, differences in Ci acquisition or both. A number of studies have shown that E. huxleyi has moderately high Ci affinities and uses HCO3 − as the primary Ci source (e.g., Herfort et al. 2002; Rokitta and Rost 2012; Rost et al. 2006b; Stojkovic et al. 2013), irrespective of the degree of calcification selleckchem (Trimborn et al. 2007; Rokitta and Rost 2012). These characteristics would suggest E. huxleyi to be

rather insensitive toward OA and the associated rise in CO2 concentration, contrary to most results obtained for the diplont. As discussed below, this apparent discrepancy could originate from differences

in conditions applied during short-term physiological measurements and those conditions cells experience in the long-term acclimation. Modes of Ci acquisition Our results demonstrate that the Ci source of both life-cycle stages of E. huxleyi is significantly influenced by the pH of the assay medium and the resulting carbonate chemistry (Fig. 2). With increasing pH in assay buffers, cells 17DMAG molecular weight progressively changed from predominant CO2 usage at lower pH values (≤ 8.1) to significant HCO3 − contribution at higher pH (≥ 8.3). Surprisingly, this change occurred irrespectively of the pCO2 conditions in the acclimation. To our knowledge, such a strong short-term pH-dependence in Ci acquisition has not been previously reported, which is most likely due to the fact that assays are C188-9 Uroporphyrinogen III synthase typically performed under standardized pH values.

Measuring physiological responses under one reference condition have the advantage that consequences of different acclimations can readily be compared in terms of altered capacities of certain processes, e.g., enzyme activities or transport rates. However, determination of the Ci source at one standard pH appears to impose a methodological bias, and our results, therefore, bear direct relevance to the interpretation of previous laboratory observations. In view of the short-term pH effect on Ci acquisition, the contribution of HCO3 − as a photosynthetic Ci source in E. huxleyi may have possibly been overestimated in previous studies. This overestimation is likely to be the most significant in those studies when 14C disequilibrium assays were conducted at pH 8.5 (e.g., Rokitta and Rost 2012; Rost et al. 2007). By looking at the Ci source determined at an assay pH mimicking the acclimation condition, we can now re-evaluate and in fact explain the responses of E. huxleyi toward elevated pCO2. When assessing \(f_\textCO_ 2 \) using assay buffers of pH 7.9 and 8.1 (equivalent to the acclimation pH of high and low pCO2 treatments), we observed predominant CO2 uptake under both conditions (Fig. 2).