Abstract
Ocean acidification damages calcareous organisms, such as calcifying algae, foraminifera, corals, and shells. In this study, we made a device equipped with a Clark-type oxygen electrode and a pH-stat to examine how the most abundant calcifying phytoplankton, the coccolithophorid Emiliania huxleyi, responded to acidification and alkalization of the seawater medium. When E. huxleyi was incubated at pH 8.2, close to oceanic pH, the medium was alkalized during photosynthesis, and the alkalization rate [determined as μmol HCl added (mg Chl)−1 h−1] was identical to the activity of photosynthesis [determined as μmol O2 evolved (mg Chl)−1 h−1]. When pH was maintained at 7.2 by the pH-stat, alkalization activity was stimulated and exceeded photosynthetic activity, resulting in an increase in the ratio of alkalization to photosynthesis (Alk/PS). On the other hand, no alkalization and photosynthesis were observed at pH 9.2. In contrast, acidification of seawater was observed in the dark because of the release of respiratory CO2 from cells at pH 8.2–9.2, but not at pH 7.2. When orthophosphate was rapidly depleted within a day in the batch culture, intracellular calcification gradually increased, and both photosynthesis and alkalization decreased gradually. During the period the Alk/PS ratio also decreased gradually. These results indicate that E. huxleyi possesses an ability to compensate for the acidification of seawater when photosynthesis is more actively driven than respiration. These results suggest that the E. huxleyi cells may not be severely damaged by oceanic acidification during photosynthesis because of their homeostatic function to avoid negative effects on cellular activity. Finally, we concluded that E. huxleyi cells possess a buffering ability to reduce acidification effects when photosynthesis is actively driven.
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