Deep CO(2) in the end-Triassic Central Atlantic Magmatic Province

• Published in: Nature Communications
• Main Authors: Capriolo, Manfredo, Marzoli, Andrea, Aradi, László E., Callegaro, Sara, Dal Corso, Jacopo, Newton, Robert J., Mills, Benjamin J. W., Wignall, Paul B., Bartoli, Omar, Baker, Don R., Youbi, Nasrrddine, Remusat, Laurent, Spiess, Richard, Szabó, Csaba
• Format: Text
• Language: English
• Published: Nature Publishing Group UK 2020
• Subjects: Article; Ocean acidification
• Online Access: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138847/; http://www.ncbi.nlm.nih.gov/pubmed/32265448; https://doi.org/10.1038/s41467-020-15325-6

Large Igneous Province eruptions coincide with many major Phanerozoic mass extinctions, suggesting a cause-effect relationship where volcanic degassing triggers global climatic changes. In order to fully understand this relationship, it is necessary to constrain the quantity and type of degassed magmatic volatiles, and to determine the depth of their source and the timing of eruption. Here we present direct evidence of abundant CO(2) in basaltic rocks from the end-Triassic Central Atlantic Magmatic Province (CAMP), through investigation of gas exsolution bubbles preserved by melt inclusions. Our results indicate abundance of CO(2) and a mantle and/or lower-middle crustal origin for at least part of the degassed carbon. The presence of deep carbon is a key control on the emplacement mode of CAMP magmas, favouring rapid eruption pulses (a few centuries each). Our estimates suggest that the amount of CO(2) that each CAMP magmatic pulse injected into the end-Triassic atmosphere is comparable to the amount of anthropogenic emissions projected for the 21(st) century. Such large volumes of volcanic CO(2) likely contributed to end-Triassic global warming and ocean acidification.