Possible glendonite mineral pseudomorphs in the aftermath of the end-Permian extinction

Abstract Glendonites (from the precursor of ikaite, CaCO3.6H2O) preferentially precipitate within sediments in cold waters (− 2 to 7°C) via either organotrophic or methanogenic sulphate reduction. Here, we report the first occurrence of possible glendonites associated with the end Permian mass extin...

Full description

Saved in:
Bibliographic Details
Main Authors: Musaab Al-Sarmi, Rachel Wood
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-025-85443-y
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1841544697678397440
author Musaab Al-Sarmi
Rachel Wood
author_facet Musaab Al-Sarmi
Rachel Wood
author_sort Musaab Al-Sarmi
collection DOAJ
description Abstract Glendonites (from the precursor of ikaite, CaCO3.6H2O) preferentially precipitate within sediments in cold waters (− 2 to 7°C) via either organotrophic or methanogenic sulphate reduction. Here, we report the first occurrence of possible glendonites associated with the end Permian mass extinction in the earliest Triassic (ca. 252 Million years ago, Ma) subtropical marine carbonates on the Arabian Plateau, Oman. The authigenic carbonate crystals are small (< 2 mm) and precipitated either on bedding planes or reworked within micro cross-laminations, erosional scours, or lags at the base of calcisiltite turbidites, supporting a syn-depositional origin. The observed shape and macrostructure bear resemblance to that of glendonites. SEM and cathodoluminescent imaging reveals unzoned internal structures with three mineral phases: irregular, pseudo-hexagonal and spherical low-Mg calcite crystals (Type 1), low-Mg calcite cement (Type 2), and a later void-filling silica cement (Type 3). The pseudomorphs show δ13C values from − 0.14‰ to − 0.85‰ (mean − 0.43‰; n = 5) that are more positive than the associated micritic matrix, where values range from − 0.92‰ to − 2.39‰ (mean − 1.64‰; n = 7), indicating that oceanic dissolved inorganic carbon (DIC) was the primary carbon source rather than either methane or organic matter. These δ13C values significantly differ from typical δ13C signatures of authentic glendonites, except for Ordovician examples. If these are glendonites, we infer that they could have precipitated due to the unusually elevated alkalinity and pH (> 9) oceanic conditions present in the aftermath of the end-Permian extinction associated with highly disrupted carbon cycle dynamics, possibly accompanied with the upwelling of cold, anoxic oceanic water.
format Article
id doaj-art-c80d51be74ae454bb4a2e8ee2a1a8819
institution Kabale University
issn 2045-2322
language English
publishDate 2025-01-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj-art-c80d51be74ae454bb4a2e8ee2a1a88192025-01-12T12:20:52ZengNature PortfolioScientific Reports2045-23222025-01-0115111010.1038/s41598-025-85443-yPossible glendonite mineral pseudomorphs in the aftermath of the end-Permian extinctionMusaab Al-Sarmi0Rachel Wood1Grant Institute, School of Geosciences, University of EdinburghGrant Institute, School of Geosciences, University of EdinburghAbstract Glendonites (from the precursor of ikaite, CaCO3.6H2O) preferentially precipitate within sediments in cold waters (− 2 to 7°C) via either organotrophic or methanogenic sulphate reduction. Here, we report the first occurrence of possible glendonites associated with the end Permian mass extinction in the earliest Triassic (ca. 252 Million years ago, Ma) subtropical marine carbonates on the Arabian Plateau, Oman. The authigenic carbonate crystals are small (< 2 mm) and precipitated either on bedding planes or reworked within micro cross-laminations, erosional scours, or lags at the base of calcisiltite turbidites, supporting a syn-depositional origin. The observed shape and macrostructure bear resemblance to that of glendonites. SEM and cathodoluminescent imaging reveals unzoned internal structures with three mineral phases: irregular, pseudo-hexagonal and spherical low-Mg calcite crystals (Type 1), low-Mg calcite cement (Type 2), and a later void-filling silica cement (Type 3). The pseudomorphs show δ13C values from − 0.14‰ to − 0.85‰ (mean − 0.43‰; n = 5) that are more positive than the associated micritic matrix, where values range from − 0.92‰ to − 2.39‰ (mean − 1.64‰; n = 7), indicating that oceanic dissolved inorganic carbon (DIC) was the primary carbon source rather than either methane or organic matter. These δ13C values significantly differ from typical δ13C signatures of authentic glendonites, except for Ordovician examples. If these are glendonites, we infer that they could have precipitated due to the unusually elevated alkalinity and pH (> 9) oceanic conditions present in the aftermath of the end-Permian extinction associated with highly disrupted carbon cycle dynamics, possibly accompanied with the upwelling of cold, anoxic oceanic water.https://doi.org/10.1038/s41598-025-85443-y
spellingShingle Musaab Al-Sarmi
Rachel Wood
Possible glendonite mineral pseudomorphs in the aftermath of the end-Permian extinction
Scientific Reports
title Possible glendonite mineral pseudomorphs in the aftermath of the end-Permian extinction
title_full Possible glendonite mineral pseudomorphs in the aftermath of the end-Permian extinction
title_fullStr Possible glendonite mineral pseudomorphs in the aftermath of the end-Permian extinction
title_full_unstemmed Possible glendonite mineral pseudomorphs in the aftermath of the end-Permian extinction
title_short Possible glendonite mineral pseudomorphs in the aftermath of the end-Permian extinction
title_sort possible glendonite mineral pseudomorphs in the aftermath of the end permian extinction
url https://doi.org/10.1038/s41598-025-85443-y
work_keys_str_mv AT musaabalsarmi possibleglendonitemineralpseudomorphsintheaftermathoftheendpermianextinction
AT rachelwood possibleglendonitemineralpseudomorphsintheaftermathoftheendpermianextinction