Coccolithophores are major contributors to global marine planktonic calcification, and in nature coccolithophores are invariably calcified through almost all of their life cycle. The response of calcification to environmental factors is essential in understanding the persistence of coccolithophores through at least 220 million years of changing global environments, and their prospects for current environmental change. So far the responses examined have been at the level of acclimation rather than adaptation in evolution. Variation in results of CO 2 manipulation experiments can be tentatively attributed to variation among genotypes rather than differences in experimental procedure. Comparisons of methods using the same genotype, and of several genotypes using a single method, suggest significant variation among genotypes. The general response is a decreased particulate inorganic carbon (PIC) to particulate organic carbon (POC) ratio in higher than present CO 2 concentrations and vice versa for lower CO 2 concentrations. Fewer studies have investigated the effect of other environmental factors. Decreased availability of phosphorus and, to a lesser extent, nitrogen, as well as decreasing photosynthetically active radiation (PAR) down to a certain low value increase PIC:POC, while variable results have been found for changes in ultraviolet radiation (UVR). Many of these results can be accommodated by considering the restriction of calcification to the G1 phase of the cell cycle and the length of this phase under different growth conditions. Fewer studies have investigated the interactions among environmental factors which change with increased CO 2 and increasing sea surface temperature; the shoaling of the thermocline will increase the mean PAR and UVR whilst decreasing nitrogen and phosphorus availability. More studies of these interactions, as well as of genetic adaptation in response to changed environmental factors, are needed.

The effect of ocean acidification conditions has been investigated in cultures of the diatom Thalassiosira pseudonana CCMP1335. Expected end-of-the-century pCO2 (aq) concentrations of 760 µatm (equivalent to pH 7.8) were compared with present-day condition (380 µatm CO2, pH 8.1). Batch culture pH changed rapidly because of CO2 (aq) assimilation and pH targets of 7.8 and 8.1 could not be sustained. Long-term (∼100 generation) pH-auxostat, continuous cultures could be maintained at target pH when cell density was kept low (<2×105 cells mL−1). After 3 months continuous culture, the C:N ratio was slightly decreased under high CO2 conditions and red fluorescence per cell was slightly increased. However, no change was detected in photosynthetic efficiency (Fv/Fm) or functional cross section of PS II (σPSII). Elevated pCO2 has been predicted to be beneficial to diatoms due to reduced cost of carbon concentration mechanisms. There was reduced transcription of one putative δ-carbonic anhydrase (CA-4) after 3 months growth at increased CO2 but 3 other δ-CAs and the small subunit of RUBISCO showed no change. There was no evidence of adaptation or clade selection of T. pseudonana after ∼100 generations at elevated CO2. On the basis of this long-term culture, pH change of this magnitude in the future ocean may have little effect on T. pseudonana in the absence of genetic adaption.

We use a meta-analysis to quantify the response of Emiliania huxleyi particulate inorganic carbon (PIC) to particulate organic carbon (POC) ratio under different laboratory conditions and changes in carbonate chemistry. There is an overarching trend of decreasing PIC : POC across all ecotypes irrespective of the strain, isolation date, isolation location, and method of acidification. The variability about this overall trend is explained by the different nutrient and light regimes used in each experiment, but there is no evidence for a strain-specific response that might be expected if strains had adapted to the average environmental conditions at the locations from which the strain was isolated; indeed, each strain shows a comparably broad physiological window. We propose that E. huxleyi PIC : POC exhibits a plastic response to carbonate conditions that can be predicted by the seawater concentrations of aqueous CO 2 , total alkalinity, and phosphate conditions. This relationship now requires field validation as well as longer-term studies of E. huxleyi response to variable environmental conditions.

Abstract. The oceans absorb about a quarter of the annually produced anthropogenic atmospheric carbon dioxide (CO2), resulting in a decrease in surface water pH, a process termed ocean acidification (OA). Surprisingly little is known about how OA affects the physiology of heterotrophic bacteria or the coupling of heterotrophic bacteria to phytoplankton when nutrients are limited. Previous experiments were, for the most part, undertaken during productive phases or following nutrient additions designed to stimulate algal blooms. Therefore, we performed an in situ large-volume mesocosm ( ∼  55 m3) experiment in the Baltic Sea by simulating different fugacities of CO2 (fCO2) extending from present to future conditions. The study was conducted in July–August after the nominal spring bloom, in order to maintain low-nutrient conditions throughout the experiment. This resulted in phytoplankton communities dominated by small-sized functional groups (picophytoplankton). There was no consistent fCO2-induced effect on bacterial protein production (BPP), cell-specific BPP (csBPP) or biovolumes (BVs) of either free-living (FL) or particle-associated (PA) heterotrophic bacteria, when considered as individual components (univariate analyses). Permutational Multivariate Analysis of Variance (PERMANOVA) revealed a significant effect of the fCO2 treatment on entire assemblages of dissolved and particulate nutrients, metabolic parameters and the bacteria–phytoplankton community. However, distance-based linear modelling only identified fCO2 as a factor explaining the variability observed amongst the microbial community composition, but not for explaining variability within the metabolic parameters. This suggests that fCO2 impacts on microbial metabolic parameters occurred indirectly through varying physicochemical parameters and microbial species composition. Cluster analyses examining the co-occurrence of different functional groups of bacteria and phytoplankton further revealed a separation of the four fCO2-treated mesocosms from both control mesocosms, indicating that complex trophic interactions might be altered in a future acidified ocean. Possible consequences for nutrient cycling and carbon export are still largely unknown, in particular in a nutrient-limited ocean.