Microborings reveal alternating agitation, resting and sleeping stages of modern marine ooids

Author:

Mono Phyllis12ORCID,Hoffmann René2ORCID,Wisshak Max3ORCID,Lokier Stephen W.4ORCID,Pederson Chelsea L.5ORCID,Hennhoefer Dominik6ORCID,Diaz Mara R.7ORCID,Swart Peter K.7ORCID,Nehrke Gernot8ORCID,Immenhauser Adrian29ORCID

Affiliation:

1. Institute for Earth System Science and Remote Sensing University of Leipzig Talstr. 35 Leipzig 04103 Germany

2. Institute of Geology, Mineralogy, and Geophysics Ruhr‐Universität Bochum Universitätsstrasse 150 Bochum 44801 Germany

3. Marine Research Department Senckenberg am Meer Wilhelmshaven 26382 Germany

4. School of Built and Natural Environment University of Derby Kedleston Road Derby DE22 1GB UK

5. School of Ocean Science and Engineering University of Southern Mississippi, Stennis Space Center 1020 Balch Boulevard Kiln MS 39556 USA

6. Hessisches Landesmuseum Darmstadt Friedensplatz 1 Darmstadt 64283 Germany

7. Department of Marine Geosciences Rosenstiel School of Marine, Atmospheric, and Earth Science University of Miami 4600 Rickenbacker Causeway Miami Florida 33149 USA

8. Alfred‐Wegener‐Institut Helmholtz‐Zentrum für Polar‐ und Meeresforschung Bremerhaven 27570 Germany

9. Fraunhofer Research Institution for Energy Infrastructures and Geothermal Systems Am Hochschulcampus 1 Bochum 44801 Germany

Abstract

ABSTRACTOoids are abundant carbonate grains throughout much of Earth's history, but their formation is not well understood. Here, an in‐depth study of microbial bioerosion features of Holocene ooids from the Schooner Cays ooid shoals (Great Bahama Bank, Eleuthera, Bahamas) and the Shalil al Ud ooid shoals in the Arabian/Persian Gulf (Abu Dhabi, United Arab Emirates) is presented. No obvious differences were found in ooid size distribution, cortex layer thickness, the composition of nuclei or euendolithic community when comparing ooids from both locations. Microendolithic borings are present in most studied ooid surfaces, but the intensity of (micro‐)bioerosion varies significantly. Applying an epoxy vacuum cast‐embedding technique allowed the identification of ichnotaxa and their inferred producers (various genera of diatoms, cyanobacteria, coccolithophores and unspecified bacteria). Euendolithic taxa have specific low‐light tolerances and light optima. This implies that information about the relative bathymetry (seafloor versus burial within an ooid shoal) and ecology for ooid cortex formation can be obtained via the presence or absence of their respective ichnotaxa. The history of a statistically significant number of ooid cortices can be translated into dune dynamics and the temporal variations thereof by allocating the inferred index producer to a defined burial or light penetration zone. In this context, ooid formation can be divided into four stages: (i) an agitation stage in the water column, characterized by the colonization of grains by photoautotrophs; (ii) a resting stage, characterized by temporary burial of the ooid, leading to immobilization and a shift towards heterotrophs; (iii) a sleeping stage, characterized by prolonged burial and colonization by organotrophs; and (iv) a reactivation stage, characterized by a resurfacing of the ooid and a subsequent shift towards photoautotrophs. The sleeping stage is presumably a stage of ooid degradation where bioerosion, mainly by heterotrophic fungi and bacteria is particularly active.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Stratigraphy,Geology,General Medicine

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