Coupled high-resolution marine and terrestrial records of carbon and hydrologic cycles variations during the Paleocene–Eocene Thermal Maximum (PETM)

Abstract

The Paleocene–Eocene Thermal Maximum is characterized by a massive perturbation of the global carbon cycle reflected in a large, negative carbon isotope excursion associated with rapid global warming and changes in the hydrologic system. The magnitude of the carbon isotope excursion from terrestrial carbonates and organic carbon is generally larger relative to marine carbonates. However, high-resolution marine and terrestrial isotopic records from the same locality for direct comparison are limited. Here we present coupled carbon isotope records from terrestrial biomarkers (δ 13C n-alkane ), marine bulk carbonates (δ 13C carbonate), and bulk organic carbon (δ 13C organic) from the continuous sedimentary record of the Forada section in northern Italy in order to evaluate the magnitude and phase relationships between terrestrial and marine environments. Consistent with previous reports, we find that the carbon isotope excursion established from δ 13C n-alkane values is more negative than those established from δ 13C carbonate and δ 13C organic values. In contrast to the majority of PETM records, all Forada δ 13C records show a sharp 13C-enrichment immediately following the onset of the carbon isotope excursion. Further, the terrestrial δ 13C n-alkane record lags δ 13C carbonate/δ 13C organic trends by ~ 4–5 kyr—offsets that reflect the long residence time of soil organic carbon. Hydrogen isotope records from higher-plant leaf waxes (δD n-alkane ) and sea-surface temperatures (TEX 86) were established to assess hydrologic and ocean temperature trends. We find δD n-alkane values trend more positive, associated with higher temperatures prior to the onset of the carbon isotope excursion, and conclude that regional changes in the hydrologic cycle likely occurred before the onset of the carbon isotope anomaly.