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Experimental calibration of clumped isotope reodering in dolomite

Lloyd, Max K. and Ryb, Uri and Eiler, John M. (2018) Experimental calibration of clumped isotope reodering in dolomite. Geochimica et Cosmochimica Acta, 242 . pp. 1-20. ISSN 0016-7037. http://resolver.caltech.edu/CaltechAUTHORS:20180904-102656417

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Abstract

Dolomite clumped isotope compositions are indispensable for determining the temperatures and fluid sources of dolomitizing environments, but can be misleading if they have modified since formation. Carbonate Δ_(47) values are susceptible to resetting by recrystallization during diagenesis, and, even in the absence of dissolution and reprecipitation reactions, alteration by solid-state reordering during prolonged residences at elevated temperatures. In order to understand the potential of dolomite Δ_(47) values to preserve the conditions of dolomitizationin ancient sections, the kinetic parameters of solid-state reordering in this phase must be determined. We heated mm-sized crystals of near-stoichiometric dolomite in a René-type cold seal apparatus at temperatures between 409 and 717 °C for 0.1–450 h. In order to prevent the decarbonation of dolomite to calcite, periclase, and CO_2 at these conditions, the system was pressurized with CO_2 to 0.45–0.8 kbar. Over the course of 31 temperature-time points and 128 individual Δ_(47) measurements of powdered dolomite crystals from these points, we observed the evolution of dolomite Δ_(47) values from the initial (unheated) composition of the crystals (0.452 ± 0.004‰, corresponding to a formation temperature of ∼145 °C) towards high-temperature equilibrium distributions. Complete re-equilibration occurred in the 563–717 °C experiments. As with previous heating experiments using calcite and apatite, dolomite Δ_(47) exhibited complex reordering behavior inadequately described by first-order Arrhenian-style models. Instead, we fit the data using two published models for clumped isotope reordering: the transient defect/equilibrium defect model of Henkes et al. (2014), and the exchange-diffusion model of Stolper and Eiler (2015). For both models, we found optimal reordering parameters by using global least-squares minimization algorithms and estimated uncertainties on these fits with a Monte Carlo scheme that resampled individual Δ_(47) measurements and re-fit the dataset of these new mean values. Because the exact Δ_(47)–T relationship between 250 and 800 °C is uncertain, we repeated these fitting exercises using three published high-temperature Δ_(47)–T calibrations. Regardless of calibration choice, dolomite Δ_(47) rate constants determined using both models are resolvably slower than those of calcite and apatite, and predict that high-grade dolomite crystals should preserve apparent equilibrium blocking temperatures of between ∼210 and 300 °C during cooling on geologic timescales. Best agreement between model predictions and natural dolomite marbles was found when using the exchange-diffusion model and the ab initio Δ_(63)–T calibration of Schauble et al. (2006), projected into the Δ_(47) reference frame by Bonifacie et al. (2017). Therefore, we recommend modeling dolomite Δ_(47) reordering using the exchange-diffusion model and this parameter set. In simple heating scenarios, the two models disagree. The transient defect/equilibrium defect model suggests that dolomite fabrics resist detectable reordering at ambient temperatures as high as 180 °C for tens of millions of years, while the exchange-diffusion model predicts incipient partial reordering perhaps as low as 150 °C. In either case, barring later recrystallization, dolomite Δ_(47) values should be faithful recorders of the conditions of dolomitization in sedimentary sections buried no hotter than ∼150 °C for tens of millions of years.


Item Type:Article
Related URLs:
URLURL TypeDescription
https://doi.org/10.1016/j.gca.2018.08.036DOIArticle
Additional Information:© 2018 Elsevier Ltd. Received 7 February 2018, Revised 21 August 2018, Accepted 23 August 2018, Available online 1 September 2018. We thank C. Ma and N. Kitchen for assistance with instrumentation and the acquisition of key data for this work. G. Rossman offered suggestions and invaluable assistance in acquiring the dolomite sample. We are grateful to D. Stolper and M. Bonifacie for suggestions that improved this work. This project was funded by NSF EAR Award #1322058 to J.M. Eiler.
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Funding AgencyGrant Number
NSFEAR-1322058
Record Number:CaltechAUTHORS:20180904-102656417
Persistent URL:http://resolver.caltech.edu/CaltechAUTHORS:20180904-102656417
Official Citation:Max K. Lloyd, Uri Ryb, John M. Eiler, Experimental calibration of clumped isotope reordering in dolomite, Geochimica et Cosmochimica Acta, Volume 242, 2018, Pages 1-20, ISSN 0016-7037, https://doi.org/10.1016/j.gca.2018.08.036. (http://www.sciencedirect.com/science/article/pii/S0016703718304800)
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:89355
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:04 Sep 2018 17:34
Last Modified:28 Sep 2018 22:51

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