ALBERT

Description: Increasing atmospheric CO2 concentrations are potentially affecting marine ecosystems twofold, by warming and acidification. The rising amount of CO2 taken up by the ocean lowers the saturation state of calcium carbonate, complicating the formation of this key biomineral used by many marine organisms to build hard parts like skeletons or shells. Reliable time-series data of seawater pH are needed to evaluate the ongoing change and compare long-term trends and natural variability. For the high-latitude ocean, the region facing the strongest CO2 uptake, such time-series data are so far entirely lacking. Our study provides, to our knowledge, the first reconstruction of seasonal cycle and long-term trend in pH for a high-latitude ocean obtained from 2D images of stable boron isotopes from a coralline alga.

Description: Corals exert a strong biological control over their calcification processes, but there is a lack of knowledge on their capability of long-term acclimatization to ocean acidification (OA). We used a dual geochemical proxy approach to estimate the calcifying fluid pH (pHcf) and carbonate chemistry of a Mediterranean coral (Balanophyllia europaea) naturally growing along a pH gradient (range: pHTS 8.07–7.74). The pHcf derived from skeletal boron isotopic composition (δ11B) was 0.3–0.6 units above seawater values and homogeneous along the gradient (mean +/- SEM: Site 1 = 8.39 +/- 0.03, Site 2 = 8.34 +/- 0.03, Site 3 = 8.34 +/- 0.02). Also carbonate ion concentration derived from B/Ca was homogeneous [mean +/- SEM (μmol /kg): Site 1 = 579 +/- 34, Site 2 = 541 +/- 27, Site 3 = 568 +/- 30] regardless of seawater pH. Furthermore, gross calcification rate (GCR, mass of CaCO3 deposited on the skeletal unit area per unit of time), estimated by a “bio-inorganic model” (IpHRAC), was homogeneous with decreasing pH. The homogeneous GCR, internal pH and carbonate chemistry confirm that the features of the “building blocks” – the fundamental structural components – produced by the biomineralization process were substantially unaffected by increased acidification. Furthermore, the pH up-regulation observed in this study could potentially explain the previous hypothesis that less “building blocks” are produced with increasing acidification ultimately leading to increased skeletal porosity and to reduced net calcification rate computed by including the total volume of the pore space. In fact, assuming that the available energy at the three sites is the same, this energy at the low pH sites could be partitioned among fewer calicoblastic cells that consume more energy given the larger difference between external and internal pH compared to the control, leading to the production of less building blocks (i.e., formation of pores inside the skeleton structure, determining increased porosity). However, we cannot exclude that also dissolution may play a role in increasing porosity. Thus, the ability of scleractinian corals to maintain elevated pHcf relative to ambient seawater might not always be sufficient to counteract declines in net calcification under OA scenarios.