Stable isotope fractionation of strontium in coccolithophore calcite: Influence of temperature and carbonate chemistry.

Title Stable isotope fractionation of strontium in coccolithophore calcite: Influence of temperature and carbonate chemistry.
Authors M.N. Müller; A. Krabbenhöft; H. Vollstaedt; F.P. Brandini; A. Eisenhauer
Journal Geobiology
DOI 10.1111/gbi.12276
Abstract

Marine calcifying eukaryotic phytoplankton (coccolithophores) is a major contributor to the pelagic production of CaCO3 and plays an important role in the biogeochemical cycles of C, Ca and other divalent cations present in the crystal structure of calcite. The geochemical signature of coccolithophore calcite is used as palaeoproxy to reconstruct past environmental conditions and to understand the underlying physiological mechanisms (vital effects) and precipitation kinetics. Here, we present the stable Sr isotope fractionation between seawater and calcite (?88/86 Sr) of laboratory cultured coccolithophores in individual dependence of temperature and seawater carbonate chemistry. Coccolithophores were cultured within a temperature and a pCO2 range from 10 to 25°C and from 175 to 1,240 ?atm, respectively. Both environmental drivers induced a significant linear increase in coccolith stable Sr isotope fractionation. The temperature correlation at constant pCO2 for Emiliania huxleyi and Coccolithus braarudii is expressed as ?88/86 Sr = -7.611 × 10-3 T + 0.0061. The relation of ?88/86 Sr to pCO2 was tested in Emiliania huxleyi at 10 and 20°C and resulted in ?88/86 Sr = -5.394 × 10-5 pCO2 - 0.0920 and ?88/86 Sr = -5.742 × 10-5 pCO2 - 0.1351, respectively. No consistent relationship was found between coccolith ?88/86 Sr and cellular physiology impeding a direct application of fossil coccolith ?88/86 Sr as coccolithophore productivity proxy. An overall significant correlation was detected between the elemental distribution coefficient (DSr ) and ?88/86 Sr similar to inorganic calcite with a physiologically induced offset. Our observations indicate (i) that temperature and pCO2 induce specific effects on coccolith ?88/86 Sr values and (ii) that strontium elemental ratios and stable isotope fractionation are mainly controlled by precipitation kinetics when embedded into the crystal lattice and subject to vital effects during the transmembrane transport from seawater to the site of calcification. These results provide an important step to develop a coccolith ?88/86 Sr palaeoproxy complementing the existing toolbox of palaeoceanography.

Citation M.N. Müller; A. Krabbenhöft; H. Vollstaedt; F.P. Brandini; A. Eisenhauer.Stable isotope fractionation of strontium in coccolithophore calcite: Influence of temperature and carbonate chemistry.. Geobiology. 2018. doi:10.1111/gbi.12276

Related Elements

Strontium

See more Strontium products. Strontium (atomic symbol: Sr, atomic number: 38) is a Block S, Group 2, Period 5 element with an atomic weight of 87.62 . Strontium Bohr ModelThe number of electrons in each of Strontium's shells is [2, 8, 18, 8, 2] and its electron configuration is [Kr] 5s2. The strontium atom has a radius of 215 pm and a Van der Waals radius of 249 pm. Strontium was discovered by William Cruickshank in 1787 and first isolated by Humphry Davy in 1808. In its elemental form, strontium is a soft, silvery white metallic solid that quickly turns yellow when exposed to air. Elemental StrontiumCathode ray tubes in televisions are made of strontium, which are becoming increasingly displaced by other display technologies pyrotechnics and fireworks employ strontium salts to achieve a bright red color. Radioactive isotopes of strontium have been used in radioisotope thermoelectric generators (RTGs) and for certain cancer treatments. In nature, most strontium is found in celestite (as strontium sulfate) and strontianite (as strontium carbonate). Strontium was named after the Scottish town where it was discovered.

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