http://www.nature.com/nature/journal/v507/n7492/full/nature13030.html


Sulphide oxidation and carbonate dissolution as a source of CO2 over geological 
timescales


Mark A. Torres, A. Joshua West & Gaojun Li

Nature 507, 346–349 (20 March 2014) doi:10.1038/nature13030


The observed stability of Earth’s climate over millions of years is thought to 
depend on the rate of carbon dioxide (CO2) release from the solid Earth being 
balanced by the rate of CO2 consumption by silicate weathering1. During the 
Cenozoic era, spanning approximately the past 66 million years, the concurrent 
increases in the marine isotopic ratios of strontium, osmium and lithium2, 3, 4 
suggest that extensive uplift of mountain ranges may have stimulated CO2 
consumption by silicate weathering5, but reconstructions of sea-floor 
spreading6 do not indicate a corresponding increase in CO2 inputs from volcanic 
degassing. The resulting imbalance would have depleted the atmosphere of all 
CO2 within a few million years7. As a result, reconciling Cenozoic isotopic 
records with the need for mass balance in the long-term carbon cycle has been a 
major and unresolved challenge in geochemistry and Earth history. Here we show 
that enhanced sulphide oxidation
 coupled to carbonate dissolution can provide a transient source of CO2 to 
Earth’s atmosphere that is relevant over geological timescales. Like drawdown 
by means of silicate weathering, this source is probably enhanced by tectonic 
uplift, and so may have contributed to the relative stability of the partial 
pressure of atmospheric CO2 during the Cenozoic. A variety of other 
hypotheses8, 9, 10 have been put forward to explain the ‘Cenozoic 
isotope-weathering paradox’, and the evolution of the carbon cycle probably 
depended on multiple processes. However, an important role for sulphide 
oxidation coupled to carbonate dissolution is consistent with records of 
radiogenic isotopes2, 3, atmospheric CO2 partial pressure11, 12 and the 
evolution of the Cenozoic sulphur cycle, and could be accounted for by 
geologically reasonable changes in the global dioxygen cycle, suggesting that 
this CO2 source should be considered a potentially important but as yet
 generally unrecognized component of the long-term carbon cycle.

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