Abstract

The development of calcification by the coccolithophores had a profound impact on ocean carbon cycling, but the evolutionary steps leading to the formation of these complex biomineralized structures are not clear. Heterococcoliths consisting of intricately shaped calcite crystals are formed intracellularly by the diploid life cycle phase. Holococcoliths consisting of simple rhombic crystals can be produced by the haploid life cycle stage but are thought to be formed extracellularly, representing an independent evolutionary origin of calcification. We use advanced microscopy techniques to determine the nature of coccolith formation and complex crystal formation in coccolithophore life cycle stages. We find that holococcoliths are formed in intracellular compartments in a similar manner to heterococcoliths. However, we show that silicon is not required for holococcolith formation and that the requirement for silicon in certain coccolithophore species relates specifically to the process of crystal morphogenesis in heterococcoliths. We therefore propose an evolutionary scheme in which the lower complexity holococcoliths represent an ancestral form of calcification in coccolithophores. The subsequent recruitment of a silicon-dependent mechanism for crystal morphogenesis in the diploid life cycle stage led to the emergence of the intricately shaped heterococcoliths, enabling the formation of the elaborate coccospheres that underpin the ecological success of coccolithophores.

Highlights

  • Coccolithophores, unicellular pelagic algae belonging to the Haptophyta, are among the most important contributors to global carbon (C) and calcium (Ca) cycles

  • Important questions remain around mechanisms that shape growing calcite crystals and the evolutionary steps that resulted in the formation of these complex biominerals

  • Previous Transmission electron microscopy (TEM) studies of holococcolithogenesis in C. braarudii revealed no evidence of intracellular crystals (Manton & Leedale, 1963; Klaveness, 1973; Rowson et al, 1986)

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Summary

Introduction

Coccolithophores, unicellular pelagic algae belonging to the Haptophyta, are among the most important contributors to global carbon (C) and calcium (Ca) cycles. Coccolithophores form elaborately shaped calcite platelets called coccoliths and assemble them into a hollow coccosphere in which the cell resides. The precise function of calcification might vary between species (Monteiro et al, 2016), heterococcolith formation is a highly conserved trait, suggesting that coccoliths and coccospheres are instrumental in coccolithophore ecology (Young, 1994; Bown et al, 2004). The ability to regulate the growth of calcite crystals in this manner was a key innovation in coccolithophore biology, allowing the formation of complex heterococcolith morphologies and distinct coccosphere architecture, such as the interlocking coccosphere of placolith-bearing species and the complex coccospheres of appendage-bearing species (Dixon, 1900; Gaarder, 1967). Important questions remain around mechanisms that shape growing calcite crystals and the evolutionary steps that resulted in the formation of these complex biominerals

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