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Coralline algal Mg-O bond strength as a marine pCO2 proxy
Author(s) -
Maren Pauly,
Nicholas A. Kamenos,
Penelope Donohue,
E. LeDrew
Publication year - 2015
Publication title -
geology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.609
H-Index - 215
eISSN - 1943-2682
pISSN - 0091-7613
DOI - 10.1130/g36386.1
Subject(s) - calcite , ocean acidification , coralline algae , carbonate , algae , geology , proxy (statistics) , mineralogy , oceanography , environmental chemistry , chemistry , ecology , biology , seawater , organic chemistry , machine learning , computer science , reef
Past ocean acidification recorded in the geological record facilitates the understanding of rates and influences of contemporary pCO 2 enrichment. Most pH reconstructions are made using boron, however there is some uncertainty associated with vital effects and isotopic fractionation. Here we present a new structural proxy for carbonate chemistry; Mg-O bond strength in coralline algae. Coralline algae were incubated in control (380 matm pCO 2 ), moderate (750 matm pCO 2 ), and high (1000 matm pCO 2 ) acidification conditions for 24 months. Raman spectroscopy was used to determine skeletal Mg-O bond strength. There was a positive linear relationship between pCO 2 concentration and bond strength mediated by positional disorder in the calcite lattice when accounting for seasonal temperature. The structural preservation of the carbonate chemistry system in coralline algal high-Mg calcite represents an alternative approach to reconstructing marine carbonate chemistry. Significantly, it also provides an important mechanism for reconstructing historic atmospheric CO 2 concentrations.

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