Impact of Ocean Acidification on the geochemistry of the coralline algae Lithothamnion glaciale

Federica Ragazzola1, Laura C Foster2, Christopher J Jones3, Thomas B Scott3, Jan Fietzke4, Matt R Kilburn5 and Daniela N Schmidt6, (1)University of Porstmouth, Institute of Marine Sciences, School of Biological Sciences, Portsmouth, United Kingdom, (2)Marine Conservation Society, ross on wye, United Kingdom, (3)University of Bristol, Interface Analysis Centre, Bristol, United Kingdom, (4)GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany, (5)University of Western Australia, Centre for Microscopy, Characterisation and Analysis & ARC Centre of Excellence for Core to Crust Fluid Systems, Crawley, WA, Australia, (6)University of Bristol, Bristol, United Kingdom
Abstract:
Coralline algae are not only the most common but also the most wide-spread framework builders north and south of the low latitude coral belt. Their ability to withstand physical stresses in high energy environments relies on their skeleton which is composed of high Mg-calcite. High Mg-calcite is the most soluble form of calcium carbonate and therefore potentially vulnerable to the change in carbonate chemistry resulting from the absorption of anthropogenic CO2 by the ocean. The cold water coralline alga Lithothamnion glaciale was cultured for 3 months under control conditions and high CO2 concentrations (589 µatm). The experimental condition were set at 7±0.5°C with 20 µmol photons m-2sec-1 in 12 h light/ dark cycle. Electron microprobe and NanoSIMS analysis showed high Mg calcite bands around the algae cells in the control material. In contrast, under elevated CO2 the banding is lost and overall Mg concentrations are lower. The loss of the Mg bands can be interpreted as loss of biological control on the biomineralization process. This reduction in Mg in the carbonate undermines the accuracy of the Mg/Ca ratio as proxy for past temperatures in time intervals with significantly different carbonate chemistry.