4.7 Article

The ikaite to calcite transformation: Implications for palaeoclimate studies

期刊

GEOCHIMICA ET COSMOCHIMICA ACTA
卷 334, 期 -, 页码 201-216

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.gca.2022.08.001

关键词

X-ray diffractometry; Glendonite; Clumped isotope thermometry; Stable isotopes; carbonate chemistry

资金

  1. European Commission (ICECAP) [101024218]
  2. Danish Council for Independent Research-Natural Sciences [DFF-7014-00142]
  3. Research Council of Norway [223272, EP/S03305X/1]
  4. Marie Curie Actions (MSCA) [101024218] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

This study investigates the transformation of ikaite to calcite and its palaeoclimatic and palaeoenvironmental significance. The results show that the transformation temperature of ikaite can be reconstructed using clumped and stable isotope thermometry, and stable isotope and element/Ca ratios can provide information about the chemical environment of ikaite growth.
Marine sedimentary ikaite is the parent mineral to glendonite, stellate pseudomorphs found throughout the geological record which are most usually composed of calcite. Ikaite is known to be metastable at earth surface temperatures and pres-sures, readily breaking down to more stable carbonate polymorphs when exposed to warm (ambient) conditions. Yet the pro-cess of transformation of ikaite to calcite is not well understood, and there is an ongoing debate as to the palaeoclimatic significance of glendonites in the geological record. This study uses a combination of techniques to examine the breakdown of ikaite to calcite, outside of the ikaite growth medium, and to assess the palaeoclimatic and palaeoenvironmental signifi-cance of stable and clumped isotope compositions of ikaite-derived calcite. Powder X-ray diffraction shows that ikaite under-goes a quasi-solid-state transformation to calcite during heating of samples in air, yet when ikaite transforms under a high temperature differential, minor dissolution-recrystallisation may also occur with the ikaite structural waters. No significant isotopic equilibration to transformation temperature is observed in the resulting calcite. Therefore, in cases of transformation of ikaite in air, clumped and stable isotope thermometry can be used to reconstruct ikaite growth temperatures. In the case of ancient glendonites, where transformation of the ikaite occurred in contact with the interstitial waters of the host sediments over unknown timescales, it is uncertain whether the reconstructed clumped isotope temperatures reflect ikaite crystallisation or its transformation temperatures. Yet clumped and stable isotope thermometry may still be used conservatively to estimate an upper limit for bottom water temperatures. Furthermore, stable isotope along with element/Ca ratios shed light on the chemical environment of ikaite growth. Our data indicate that a range of (bio)geochemical processes may act to promote ikaite formation at different marine sedimentary sites, including bacterial sulphate reduction and anaerobic oxidation of methane. The colours of the ikaites, from light brown to dark brown, indicate a high organic matter content, favouring high rates of bacterial sulphate reduction as the main driver of ikaite precipitation. Highest Mg/Ca ratios are found in the most unstable ikaites, indicating that Mg acts to destabilise ikaite structure.

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