Seawater carbonate chemistry and biological processes during experiments with phytoplankton Emiliania huxleyi (CS369), 2009

Increasing atmospheric CO2 concentration affects calcification in most planktonic calcifiers. Both reduced or stimulated calcification under high CO2 have been reported in the widespread coccolithophore Emiliania huxleyi. This might affect the response of cells to photosynthetically active radiation (PAR; 400-700 nm) and ultraviolet radiation (UVR; 280-400 nm) by altering the thickness of the coccolith layer. Here we show that in the absence of UVR, the calcification rates in E. huxleyi decrease under lowered pH levels (pHNBS of 7.9 and 7.6; pCO2 of 81 and 178 Pa or 804 and 1759 ppmv, respectively) leading to thinned coccolith layers, whereas photosynthetic carbon fixation was slightly enhanced at pH 7.9 but remained unaffected at pH 7.6. Exposure to UVR (UV-A 19.5 W m**-2, UV-B 0.67 W m**-2) in addition to PAR (88.5 W m**-2), however, results in significant inhibition of both photosynthesis and calcification, and these rates are further inhibited with increasing acidification. The combined effects of UVR and seawater acidification resulted in the inhibition of calcification rates by 96% and 99% and that of photosynthesis by 6% and 15%, at pH 7.9 and 7.6, respectively. This differential inhibition of calcification and photosynthesis leads to significant reduction of the ratio of calcification to photosynthesis. Seawater acidification enhanced the transmission of harmful UVR by about 26% through a reduction of the coccolith layer of 31%. Our data indicate that the effect of a high-CO2 and low-pH ocean on E. huxleyi (because of reduced calcification associated with changes in the carbonate system) enhances the detrimental effects of UVR on the main pelagic calcifier.

Seawater carbonate chemistry and carbon and oxygen isotopes during experiments with planktonic foraminifera Orbulina universa and Globigerina bulloides, 1997

Stable oxygen and carbon isotope measurements on biogenic calcite and aragonite have become standard tools for reconstructing past oceanographic and climatic change. In aquatic organisms, 18O/16O ratios in the shell carbonate are a function of the ratio in the sea water and the calcification temperature (Epstein et al., 1953). In contrast, 13C/12C ratios are controlled by the ratio of dissolved inorganic carbon in sea water and physiological processes such as respiration and symbiont photosynthesis (Spero et al., 1991, doi:10.1029/91PA02022). These geochemical proxies have been used with analyses of foraminifera shells to reconstruct global ice volumes (Shackleton and Opdyke, 1973, doi:10.1016/0033-5894(73)90052-5), surface and deep ocean temperatures (Broecker, 1986, doi:10.1016/0033-5894(86)90087-6; Labeyrie et al., 1987, doi:10.1038/327477a0), ocean circulation changes (Duplessy et al., 1988, doi:10.1029/PA003i003p00343) and glacial-interglacial exchange between the terrestrial and oceanic carbon pools (Sackleton, 1977). Here, we report experimental measurements on living symbiotic and non-symbiotic plankton foraminifera (Orbulina universa and Globigerina bulloides respectively) showing that the 13C/12C and 18O/16O ratios of the calcite shells decrease with increasing seawater [CO3 2-]. Because glacial-period oceans had higher pH and [CO3 2-] than today (Sanyal et al., 1995, doi:10.1038/373234a0), these new relationships confound the standard interpretation of glacial foraminiferal stable-isotope data. In particular, the hypothesis that the glacial-interglacial shift in the 13C/12C ratio was due to a transfer of terrestrial carbon into the ocean(Shackleton ,1977) can be explained alternatively by an increase in ocean alkalinity (Lea et al., 1996). A carbonate-concentration effect could also help explain some of the extreme stable-isotope variations during the Proterozoic and Phanerozoic aeons (Kaufman et al., 1993, doi:10.1016/0012-821X(93)90254-7).