
Internal Water Facilitates Thermal Resetting of Clumped Isotopes in Biogenic Aragonite
Author(s) -
Nooitgedacht C. W.,
van der Lubbe H. J. L.,
Ziegler M.,
Staudigel P. T.
Publication year - 2021
Publication title -
geochemistry, geophysics, geosystems
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.928
H-Index - 136
ISSN - 1525-2027
DOI - 10.1029/2021gc009730
Subject(s) - aragonite , calcite , carbonate , isotopes of oxygen , geology , diagenesis , mineralogy , calcium carbonate , speleothem , carbonate compensation depth , stable isotope ratio , carbonate minerals , environmental chemistry , geochemistry , chemistry , ecology , cave , physics , organic chemistry , quantum mechanics , biology
Biogenic and inorganic calcium carbonates contain considerable amounts of internal water, both as free and organically associated water. The oxygen isotopic compositions (δ 18 O) of internal water and hosting carbonate are analyzed for various carbonates before and after heating at 175°C for 90 minutes. During heating, the δ 18 O values of internal water significantly increased in biogenic aragonites and speleothem calcite, whereas the δ 18 O carbonate values were lowered. Correspondingly, an aragonitic bivalve’s clumped‐isotope distribution (Δ 47 ) changed during heating, increasing reconstructed paleotemperatures. In contrast, an inorganic aragonite crystal, containing a comparable amount of internal water, showed no oxygen isotope exchange, and its Δ 47 values remained unaltered during heating, implying that there is a link between internal oxygen isotope exchange and Δ 47 resetting. This alteration process occurred without any detectable transformation from aragonite to calcite. Our results therefore reveal a mechanism that facilitates oxygen isotope exchange between biogenic aragonite and its internal water, while simultaneously resetting the Δ 47 values, without affecting mineralogy. Future studies may therefore apply coupled water‐carbonate analyses to scrutinize these kinds of diagenetic alteration processes. It appears that in biogenic aragonites, more carbonate is available for exchange reactions with the internal water reservoir than in inorganic aragonites, a feature that can be attributed to the distribution of organic‐associated water and/or high surface area fluid inclusions. This water‐aragonite exchange occurs at lower temperatures than those required for solid‐state bond reordering at the same timescale, and thus likely has occurred earlier during the burial of biogenic aragonites.