Abstract

Well-preserved skeletons of Paleocene and Eocene scleractinians andoctocorals (Polytremacis sp.) from Poland andUkraine were studied to reveal microborings produced in vivo by coral-associatedmicroendoliths. Microborings (mostly < 5 μm in diameter) are hardly visible, ifat all, under a petrographic microscope. Their resin casts are obtained, however,through the epoxy vacuum cast-embedding technique and observed under a scanningelectron microscope (SEM). Three-dimensional resin-filled (cast) microborings arealso clearly visible under SEM in acid-etched petrographic thin-sections.Backscattered scanning electron microscopy imaging (BSE) is useful for visualizationof the microborings during SEM study of both etched and non-etched thin-sections. Asimple but very effective method to reveal the dense network of resin casts ofmicroborings is observations of etched thin-sections under the petrographicmicroscope. Fluorescence microscopy (FL), especially with application of blue andgreen filters (Nikon’s B-1A and G-2A filter cubes), is recommended if etchingthin-sections or polished samples is not possible. However, color contrast betweenthe resin casts and the calcium carbonate of the coral skeleton was strong enoughonly in some examined thin-sections. The cathodoluminescence microscopy, the othermethod, does not require the etching of the thin-sections and is potentially usefulfor detection of microborings filled with calcite cement, although this techniquewas not applicable for the samples studied. Symbiotic coral-microendolithassociation (in broad meaning of the term symbiosis) is a common phenomenon inmodern corals, but its fossil record is very sparse. This study shows that emptymicroborings can be common in fossil corals, allowing preparation of the resincasts. Some of the tested methods permit rapid detection of resin-filledmicroborings in thin-sections even by non-specialists, and selection of samples forSEM studies. Corals from claystones and mudstones, usually less affected bydiagenesis, have higher taphonomic potential for preservation of empty microboringsthan corals from reef facies. The methods discussed here can be also applied forrapid detection of post-mortem microborings occurring in other substrates.

Highlights

  • Modern corals are commonly associated with boring microorganisms inhabiting skeletons during coral’s life (e.g., Le Campion-Alsumard et al 1995; Golubic et al 2005; Tribollet 2008)

  • The only detailed reports deal with calcite-filling microborings, that are commonly ca. 10–40 μm in diameter, large enough to be visible under a petrographic microscope (Kołodziej et al 2012, 2016)

  • Preliminary studies of corals from the Paleocene (Kołodziej and Radtke 1999; Salamon 2017) and from the Eocene revealed that the microborings in fossilized corals may be common and still empty, allowing preparation of resin casts and study under the scanning electron microscope (SEM). These results indicate that the microborings left by coral-associated microendoliths are much more common in the fossil material than previously assumed

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Summary

Introduction

Modern corals are commonly associated with boring microorganisms inhabiting skeletons during coral’s life (e.g., Le Campion-Alsumard et al 1995; Golubic et al 2005; Tribollet 2008). Preliminary studies of corals from the Paleocene (Kołodziej and Radtke 1999; Salamon 2017) and from the Eocene (this report) revealed that the microborings in fossilized corals may be common and still empty, allowing preparation of resin casts and study under the scanning electron microscope (SEM). These results indicate that the microborings left by coral-associated microendoliths are much more common in the fossil material than previously assumed. The Mandrykovka Beds are yellowish or light grey, coarse, poorly lithified, slightly clayey, detrital limestones (traditionally called calcareous detrital sands) They contain diverse microfossils and small, fragile macrofossils, among others foraminifera, corals, bryozoans, small brachiopods, worms, crustaceans, gastropods, bivalves, and fish remains.

Methods
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Microscopic methods
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Discussion and conclusions
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