Abstract

Direct evidence of intense chemical weathering induced by volcanism is rare in sedimentary successions. Here, we undertake a multiproxy analysis (including organic carbon isotopes, mercury (Hg) concentrations and isotopes, chemical index of alteration (CIA), and clay minerals) of two well-dated Triassic–Jurassic (T–J) boundary sections representing high- and low/middle-paleolatitude sites. Both sections show increasing CIA in association with Hg peaks near the T–J boundary. We interpret these results as reflecting volcanism-induced intensification of continental chemical weathering, which is also supported by negative mass-independent fractionation (MIF) of odd Hg isotopes. The interval of enhanced chemical weathering persisted for ~2 million years, which is consistent with carbon-cycle model results of the time needed to drawdown excess atmospheric CO2 following a carbon release event. Lastly, these data also demonstrate that high-latitude continental settings are more sensitive than low/middle-latitude sites to shifts in weathering intensity during climatic warming events.

Highlights

  • Volcanic source Mixing trend Erosional HgIncreasing terrestrial sourcesPost-ME ME Pre-ME Qilixia section ME Pre-MEVolcanic Continental plants-0.1 Erosional Hg

  • The Central Atlantic Magmatic Province (CAMP) coincided with ~3–6‰ negative carbon isotope excursions (CIEs) in both carbonates and organic matter, which have been used to constrain its onset and duration[4,6,9,39,40]

  • The presence of negative CIEs in carbonate and organic carbon isotope profiles of both marine and terrestrial T–J boundary sections serves to demonstrate the global extent of the underlying carbon-cycle perturbations[4,6,7,8,9,39,40]

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Summary

Introduction

~200 kyr (Fig. 2), suggesting a protracted shift in tropicalsubtropical conditions relative to high-latitude settings. This pattern is consistent with predictions of more rapid temperature increases at high-latitude sites during the initial stages of warming (similar to the modern[61]). CO2 by silicate weathering at a million-year timescale following a major emission event such as the CAMP eruptions[11,42]. LOSCAR is suitable for investigation of the effects of carbon-cycle perturbations on atmospheric CO2 concentrations and silicate weathering rates at timescales ranging from centuries to millions of years[62,63,64,65].

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