Aragonitic scleractinian corals in the Cretaceous calcitic sea.

Changes in seawater chemistry have affected the evolution of calcifying marine organisms, including their skeletal polymorph (calcite versus aragonite), which is believed to have been strongly influenced by the Mg/Ca ratio at the time these animals first emerged. However, we show that micrabaciids, a scleractinian coral clade that first appeared in the fossil record of the Cretaceous, when the ocean Mg/Ca ratio was near the lowest in the Phanerozoic (thus a priori favoring calcitic mineralogy), formed skeletons composed exclusively of aragonite. Exceptionally preserved aragonitic coralla of Micrabacia from the Late Cretaceous Ripley Formation (southeastern USA) have skeletal microstructures identical to their modern representatives. In addition, skeletons of Micrabacia from Cretaceous chalk deposits of eastern Poland are clearly diagenetically altered in a manner consistent with originally aragonitic mineralogy. These deposits have also preserved fossils of the scleractinian Coelosmilia, the skeleton of which is interpreted as originally calcitic. These findings show that if changes in seawater Mg/Ca ratio influenced the mineralogy of scleractinian corals, the outcome was taxon specific. The aragonitic mineralogy, unique skeletal microstructures and ultrastructures, and low Mg/Ca ratios in both fossil and living micrabaciids indicate that their biomineralization process is strongly controlled and has withstood major fluctuations in seawater chemistry during the past 70 m.y.

The modern analogue of a Cretaceous coral with a calcitic skeleton

Anders Meibom, Jaroslaw Hubert Stolarski

It was argued that, in contrast to all known modern scleractinian corals that form aragonite skeletons, the original mineralogy of the Cretaceous "Coelosmilia" (ca. 70-65 Ma) was calcite during a period when the Mg2+/Ca2+ ratio of the seawater was presumably the lowest in Phanerozoic (Science 2007 318: 92-94). This is consistent with the idea that scleractinians extend only partial control over their skeletal mineralogy, because calcite is the preferred calcium carbonate polymorph (over aragonite) during abiotic CaCO3 precipitation in low Mg2+/Ca2+ seawater conditions. However, subsequently it was found that a number of different Cretaceous corals formed purely aragonite coralla in the same low Mg2+/Ca2+ conditions, suggesting instead that biological control over the skeletal mineralogy differs between taxonomically different corals (Geology 2017 45:319-322) and posing the question why was "Coelosmilia’s" skeletal mineralogy affected by the seawater chemistry changes and not that of the other corals. An unusual feature of "Coelosmilia" is the infilling of a significant portion of the calice with dense, banded skeletal deposits. They are crystallographically continuous with earlier formed layers of septa, wall and axial structures, but show distinct biogeochemical signatures. To date, no modern analogs of such corals were known, and it was tempting to argue that this skeletal infilling represents secondary, purely abiotic deposits (similar to marine cements, which would be calcitic in Cretaceous seas). Here we document a living scleractinian coral that exhibits a structural organization identical to Cretaceous "Coelosmilia", including dense calicular infilling that is a species-specific feature. Surprisingly, the inner parts of these skeletal elements are composed of fibrous calcite, whereas the rest of the skeleton is aragonitic. We suggest that this modern coral is phylogenetically related to "Coelosmilia" and capable of formation of strictly biologically controlled skeletal mineralogy, which can include both aragonitic and calcitic structures. This original bipartite skeletal organization may explain several diagenetic phenomena that we observe in "Coelosmilia", and is highly relevant for the proper geochemical sampling of corals with such skeletal organization.

2019

Morphology, microstructure, crystallography, and chemistry of distinct CaCO3 deposits formed by early recruits of the scleractinian coral Pocillopora damicornis

Duncan Alexander, Melany Melissa Gilis, Anders Meibom, Jaroslaw Hubert Stolarski

Scleractinian corals begin their biomineralization process shortly after larval settlement with the formation of calcium carbonate (CaCO3) structures at the interface between the larval tissues and the substrate. The newly settled larvae exert variable degrees of control over this skeleton formation, providing an opportunity to study a range of biocarbonate structures, some of which are transient and not observed in adult coral skeletons. Here we present a morphological, structural, crystallographic, and chemical comparison between two types of aragonite deposits observed during the skeletal development of 2-days old recruits of Pocillopora damicornis: (1) Primary septum and (2) Abundant, dumbbell-like structures, quasi-randomly distributed between initial deposits of the basal plate and not present in adult coralsAt the mesoscale level, initial septa structures are formed by superimposed fan-shaped fasciculi consisting of bundles of fibers, as also observed in adult corals. This organization is not observed in the dumbbell-like structures. However, at the ultrastructural level there is great similarity between septa and dumbbell components. Both are composed of

Wiley-Blackwell2015

A modern scleractinian coral with a two-component calcite–aragonite skeleton

Anders Meibom, Jaroslaw Hubert Stolarski

One of the most conserved traits in the evolution of biomineralizing organisms is the taxon-specific selection of skeletal minerals. All modern scleractinian corals are thought to produce skeletons exclusively of the calcium-carbonate polymorph aragonite. Despite strong fluctuations in ocean chemistry (notably the Mg/Ca ratio), this feature is believed to be conserved throughout the coral fossil record, spanning more than 240 million years. Only one example, the Cretaceous scleractinian coral Coelosmilia (ca. 70 to 65 Ma), is thought to have produced a calcitic skeleton. Here, we report that the modern asymbiotic scleractinian coral Paraconotrochus antarcticus living in the Southern Ocean forms a two-component carbonate skeleton, with an inner structure made of high-Mg calcite and an outer structure composed of aragonite. P. antarcticus and Cretaceous Coelosmilia skeletons share a unique microstructure indicating a close phylogenetic relationship, consistent with the early divergence of P. antarcticus within the Vacatina (i.e., Robusta) clade, estimated to have occurred in the Mesozoic (ca. 116 Mya). Scleractinian corals thus join the group of marine organisms capable of forming bimineralic structures, which requires a highly controlled biomineralization mechanism; this capability dates back at least 100 My. Due to its relatively prolonged isolation, the Southern Ocean stands out as a repository for extant marine organisms with ancient traits.

2020

The modern analogue of a Cretaceous coral with a calcitic skeleton

Anders Meibom, Jaroslaw Hubert Stolarski

2019