PP51D-08
Biomineralization in foraminifera
Friday, 18 December 2015: 09:45
2012 (Moscone West)
Lennart de Nooijer1, Takashi Toyofuku2, Jelle Bijma3 and Gert-Jan Reichart1, (1)Royal Netherlands Institute for Sea Research, Den Burg, 1790, Netherlands, (2)JAMSTEC Japan Agency for Marine-Earth Science and Technology, Kanagawa, Japan, (3)Alfred-Wegener Inst, Bremenhaven, Germany
Abstract:
Foraminifera are popular tools in paleoceanography since incorporation of minor/ major elements and fractionation of stable isotopes into their carbonate shells depend on environmental conditions (e.g. temperature, salinity, pH). Their shell chemistry is markedly different from that of inorganically precipitated CaCO3, reflecting that calcification is a process under strong biological control. The cellular components responsible for calcification are only partly identified in foraminifera and include the involvement of organic templates, trans-membrane ion transporters and selective ion removal. Recent results suggest that transmembrane exchange of H+ for Ca2+ is directly responsible for calcification. The resulting high pH inside and lowered pH outside the foraminifer results in an efficient CO2 ‘trap’ after which carbon dioxide is converted to carbonate prior to calcification. Amongst others, this explains how some foraminifera are able to calcify in undersaturated seawater and may explain their moderate response to ocean acidification. Minor and trace metals incorporated into test carbonate reflect the processes involved in biomineralization and can thus be used to unravel the different factors and processes involved. Still, a more detailed understanding of the processes involved in foraminiferal calcification is needed to explain observed (inter-species) differences in partition coefficients for the incorporation of minor and trace metals and isotopic fractionation.