Abstract

AbstractCarbonate clumped isotope thermometry is based on the ordering of 13C and 18O in the carbonate lattice and is based on the relative abundance of 13C18O16O in CO2 produced through acid digestion of carbonate minerals. The major advantage of this technique is its non‐dependency on the δ18O value of water from which the carbonate precipitated. Ghosh et al. (2007, https://doi.org/10.1016/j.gca.2007.03.015) previously published calibration data for fish otoliths referenced to heated gases and used the Gonfiantini 17O parameter set in their data evaluation. Herein, we present a new clumped isotope (Δ47) calibration for aragonitic fish otoliths in the absolute reference frame using the International Union of Pure and Applied Chemistry 17O correction. Our revised calibration equation for otolith is: . To test the accuracy of this calibration, we apply it to otoliths of modern Lutjanus lutjanus from the Bay of Bengal. The estimated average temperature (22.3°C ± 4.2°C) for the Bay of Bengal and δ18OV‐SMOW composition of waters of −1.7‰ (±0.5) are consistent with the onsite observations. We also apply the new calibration to well‐preserved otoliths of “genus Ambassidarum” sp. and “genus Gobiidarum” sp. from lower Miocene (Burdigalian) sediments of the Quilon Formation, India to quantify coastal water conditions. Estimated average environmental water temperatures in their habitats were 12.9°C ± 1.7°C, and the average δ18OV‐SMOW of ambient waters calculated yielded a value between −3.5‰ and −2.6‰ (V‐SMOW) (mean: −2.9‰ ± 0.4) and −4.4‰, respectively. These results indicate δ18O values reflect the kinetic effects impacting the δ18O of fish otoliths independently of Δ47, although we cannot fully preclude diagenesis.

Highlights

  • Otoliths are accretionary body parts deposited within the inner ear of fishes

  • If we use the newly determined nominal ∆47 values for the ETH standards, in addition to IAEA-C1 and IAEA-C2 and the equation obtained for otoliths on the I-Carbon Dioxide Equilibrium Scale (CDES), is as follows:

  • Even if the carbonate standards anchored to the otolith data set are limited to ETH 1–4, the Δ47-T calibration equation in Intercarb-Carbon Dioxide Equilibrium Scale (I-CDES) is indistinguishable from Equation 3

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Summary

Introduction

Otoliths are accretionary body parts deposited within the inner ear of fishes They accrete new crystalline and protein material onto their exterior surface daily. Previous studies employing the δ18O composition of otoliths demonstrated that the accretionary growth layers is in equilibrium with the water in which the host fish lives (Kalish, 1991b; Patterson et al, 2013; Thorrold et al, 1997). This equilibrium relationship has been applied to track environmental temperatures and migration routes for species of modern fish, constrained by the water δ18O value (Campana & Neilson, 1985)

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