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OOID SIGNED

The Ocean's Oxygen Isotopes Deciphered: Combining Observations, Experiments and Models

Total Cost €

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EC-Contrib. €

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Partnership

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Project "OOID" data sheet

The following table provides information about the project.

Coordinator
WEIZMANN INSTITUTE OF SCIENCE 

Organization address
address: HERZL STREET 234
city: REHOVOT
postcode: 7610001
website: www.weizmann.ac.il

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Israel [IL]
 Total cost 1˙490˙596 €
 EC max contribution 1˙490˙596 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2018
 Duration (year-month-day) from 2018-09-01   to  2023-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    WEIZMANN INSTITUTE OF SCIENCE IL (REHOVOT) coordinator 1˙490˙596.00

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 Project objective

The isotopic composition of O in seawater is a fundamental property of Earth's oceans, key to paleoclimate reconstructions and to our understanding of the origin of water on Earth, the water-rock reactions that govern seawater chemistry, and the conditions under which life emerged. Despite more than five decades of research, the geologic history of seawater 18O/16O remains a topic of intense debate. Without exception, well-preserved 18O/16O records from marine precipitates reflect both the minerals' formation temperature, and the isotopic composition of seawater. This duality has prevented unique interpretation of a long-term secular trend, in which 18O/16O in sedimentary rocks (e.g., carbonates, cherts) has increased by ~15 ‰ since the Archean. Here I outline an inter-disciplinary research program to address this fundamental problem, which integrates new geochemical observations, laboratory experiments, and numerical models.

We will generate geologic records of 18O/16O in two previously untapped repositories: iron oxides and iron-bearing authigenic clays. Several characteristics of both, and preliminary results, suggest that these repositories hold the potential to settle the long-standing debate about seawater 18O/16O. We will determine the temperature dependence of mineral-water O isotope fractionation in laboratory experiments and observations of natural systems. We will experimentally test the resistance of these minerals to O isotope exchange under geologically-relevant conditions, with the aim of evaluating the potential for late-stage isotopic resetting. Finally, we will develop models of the marine O isotope cycle, which account for the processes that govern seawater 18O/16O over long timescales, and which will be used to provide a quantitative understanding of the new records. With these new insights, we will explore implications for the geologic history of seawater chemistry, atmospheric composition, climate and biology.

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