Abstract

Abstract. Over the last few decades, a suite of inorganic proxies based on foraminiferal calcite have been developed, some of which are now widely used for palaeoenvironmental reconstructions. Studies of foraminiferal shell chemistry have largely focused on cations and oxyanions, while much less is known about the incorporation of anions. The halogens fluoride and chloride are conservative in the ocean, which makes them candidates for reconstructing palaeoceanographic parameters. However, their potential as a palaeoproxy has hardly been explored, and fundamental insight into their incorporation is required. Here we used nanoscale secondary ion mass spectrometry (NanoSIMS) to investigate, for the first time, the distribution of Cl and F within shell walls of four benthic species of foraminifera. In the rotaliid species Ammonia tepida and Amphistegina lessonii, Cl and F were distributed highly heterogeneously within the shell walls, forming bands that were co-located with the bands observed in the distribution of phosphorus (significant positive correlation of both Cl and F with P; p<0.01). In the miliolid species Sorites marginalis and Archaias angulatus, the distribution of Cl and F was much more homogeneous without discernible bands. In these species, Cl and P were spatially positively correlated (p<0.01), whereas no correlation was observed between Cl and F or between F and P. Additionally, their F content was about an order of magnitude higher than in the rotaliid species. The high variance in the Cl and F content in the studied foraminifera specimens could not be attributed to environmental parameters. Based on these findings, we suggest that Cl and F are predominately associated with organic linings in the rotaliid species. We further propose that Cl may be incorporated as a solid solution of chlorapatite or may be associated with organic molecules in the calcite in the miliolid species. The high F content and the lack of a correlation between Cl and F or P in the miliolid foraminifera suggest a fundamentally different incorporation mechanism. Overall, our data clearly show that the calcification pathway employed by the studied foraminifera governs the incorporation and distribution of Cl, F, P, and other elements in their calcite shells.

Highlights

  • Foraminifera are widely used to reconstruct palaeoenvironments and climates based on relative species abundances and the chemical or isotopic composition of their shells

  • Apart from the carbon and oxygen isotopic composition, most inorganic proxies based on foraminiferal calcite involve cations or their isotopes (Boyle, 1981; Elderfield et al, 1996; Lea et al, 1999; Allen et al, 2016), which can substitute for calcium in the calcite lattice

  • We suggest that association with organic linings is the primary mode of incorporation of both elements in the foraminiferal shells in A. lessonii

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Summary

Introduction

Foraminifera are widely used to reconstruct palaeoenvironments and climates based on relative species abundances and the chemical or isotopic composition of their shells. Apart from the carbon and oxygen isotopic composition, most inorganic proxies based on foraminiferal calcite involve cations or their isotopes (Boyle, 1981; Elderfield et al, 1996; Lea et al, 1999; Allen et al, 2016), which can substitute for calcium in the calcite lattice. While seawater is enriched with the halogens chlorine and bromine with respect to the primary mantle (Kendrick, 2018), fluorine is strongly depleted in seawater, with calcium carbonates being the major sink of dissolved fluoride in the oceans (Carpenter, 1969)

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