Tripati, A. and Thiagarajan, N. and Eiler, J. (2008) 'Clumped isotope' thermometery in foraminifera. Geochimica et Cosmochimica Acta, 72 (12). A956. ISSN 0016-7037. doi:10.1016/j.gca.2008.05.024. https://resolver.caltech.edu/CaltechAUTHORS:20130726-090003454
Full text is not posted in this repository. Consult Related URLs below.
Use this Persistent URL to link to this item: https://resolver.caltech.edu/CaltechAUTHORS:20130726-090003454
Abstract
Accurate constraints on past ocean temperature and composition are critical for documenting climate change and resolving its causes. Most inorganic and organic geochemical paleothermometers are fundamentally underconstrained because they reflect seawater composition as well as temperature. In addition, some of the most frequently used thermometers — ^(18)O/^(16)O and Mg/Ca ratios in biogenic carbonate — deviate from inorganic calibrations and can exhibit species-specific temperature dependencies. These offsets or ‘vital effects’ are poorly understood and lend an unquantifiable source of uncertainty to reconstructions of past temperature. Here we report ‘clumped isotope’ [1] measurements of benthic and planktic foraminifera from sediment core-tops showing that the proportion of ^(13)C-^(18)O bonds in calcite and aragonite shells exhibits the same temperature dependence as inorganic calcite. The ‘clumping’ of heavy isotopes into bonds with each other is independent of the isotopic composition of the water in which the mineral precipitated, and thus avoids the ambiguity intrinsic to some other thermometers. These observations suggest the clumped isotope thermometer can yield accurate determinations of past seawater temperature, even when applied to the remains of extinct taxa. The lack of discernable ‘vital effects’ in foraminifera and other forms of biogenic calcite and aragonite [1-4] indicates that these organisms precipitate calcium carbonate in isotopic equilibrium with the dissolved inorganic carbon (DIC) pool from which they calcify. The lack of difference between calcite and aragonite may indicate that the ‘clumping’ of these heavy isotopes into bonds with each other reflects the thermodynamically-controlled exchange of stable isotopes amongst DIC species in water, rather than similar exchange equilibria within the solid precipitates [5].
Item Type: | Article | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Related URLs: |
| |||||||||
Additional Information: | © 2008 Published by Elsevier Ltd. | |||||||||
Issue or Number: | 12 | |||||||||
DOI: | 10.1016/j.gca.2008.05.024 | |||||||||
Record Number: | CaltechAUTHORS:20130726-090003454 | |||||||||
Persistent URL: | https://resolver.caltech.edu/CaltechAUTHORS:20130726-090003454 | |||||||||
Official Citation: | Goldschmidt Abstracts 2008- T, Geochimica et Cosmochimica Acta, Volume 72, Issue 12, Supplement, July 2008, Pages A924-A963, ISSN 0016-7037, http://dx.doi.org/10.1016/j.gca.2008.05.024. | |||||||||
Usage Policy: | No commercial reproduction, distribution, display or performance rights in this work are provided. | |||||||||
ID Code: | 39607 | |||||||||
Collection: | CaltechAUTHORS | |||||||||
Deposited By: | Tony Diaz | |||||||||
Deposited On: | 29 Jul 2013 21:57 | |||||||||
Last Modified: | 09 Nov 2021 23:45 |
Repository Staff Only: item control page