Abstract
Late Paleocene deposition of an organic-rich sedimentary facies on the continental shelf and slope of New Zealand and eastern Australia has been linked to short-lived climatic cooling and terrestrial denudation following sea level fall. Recent studies confirm that the organic matter in this facies, termed “Waipawa organofacies”, is primarily of terrestrial origin, with a minor marine component. It is also unusually enriched in 13C. In this study we address the cause of this enrichment. For Waipawa organofacies and its bounding facies in the Taylor White section, Hawke's Bay, paired palynofacies and carbon isotope analysis of heavy liquid-separated density fractions indicate that the heaviest δ13C values are associated with degraded phytoclasts (woody plant matter) and that the 13C enrichment may be partly due to lignin degradation. Compound-specific stable carbon isotope analyses of samples from the Taylor White and mid-Waipara (Canterbury) sections display similar trends and further reveal a residual 13C enrichment of ∼ 2.5 ‰ in higher plant biomarkers (long chain n-alkanes and fatty acids) and a ∼ 2 ‰–5 ‰ change in subordinate marine biomarkers. Using the relationship between atmospheric CO2 and C3 plant tissue δ13C values, we determine that the 3 ‰ increase in terrestrial δ13C may represent a ∼ 35 % decrease in atmospheric CO2.
Refined age control for Waipawa organofacies indicates that deposition occurred between 59.2 and 58.5 Ma, which coincides with an interval of carbonate dissolution in the deep sea that is associated with a Paleocene oxygen isotope maximum (POIM, 59.7–58.1 Ma) and the onset of the Paleocene carbon isotope maximum (PCIM, 59.3–57.4 Ma). This association suggests that Waipawa deposition occurred during a time of cool climatic conditions and increased carbon burial. This relationship is further supported by published TEX86-based sea surface temperatures that indicate a pronounced regional cooling during deposition. We suggest that reduced greenhouse gas emissions from volcanism and accelerated carbon burial, due to tectonic factors, resulted in short-lived global cooling, growth of ephemeral ice sheets and a global fall in sea level. Accompanying erosion and carbonate dissolution in deep-sea sediment archives may have hidden the evidence of this “hypothermal” event until now.
Refined age control for Waipawa organofacies indicates that deposition occurred between 59.2 and 58.5 Ma, which coincides with an interval of carbonate dissolution in the deep sea that is associated with a Paleocene oxygen isotope maximum (POIM, 59.7–58.1 Ma) and the onset of the Paleocene carbon isotope maximum (PCIM, 59.3–57.4 Ma). This association suggests that Waipawa deposition occurred during a time of cool climatic conditions and increased carbon burial. This relationship is further supported by published TEX86-based sea surface temperatures that indicate a pronounced regional cooling during deposition. We suggest that reduced greenhouse gas emissions from volcanism and accelerated carbon burial, due to tectonic factors, resulted in short-lived global cooling, growth of ephemeral ice sheets and a global fall in sea level. Accompanying erosion and carbonate dissolution in deep-sea sediment archives may have hidden the evidence of this “hypothermal” event until now.
Original language | English |
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Pages (from-to) | 1295-1320 |
Number of pages | 26 |
Journal | Climate of the Past |
Volume | 18 |
Issue number | 6 |
DOIs | |
Publication status | Published - 20 Jun 2022 |
Bibliographical note
Funding Information:Financial support. Primary funding for this study came from the Ministry of Business, Innovation and Employment (MBIE), New Zealand, as part of the GNS Science-led programme “Understanding petroleum source rocks, fluids, and plumbing systems in New Zealand basins: a critical basis for future oil and gas discoveries” (Contract C05X1507). Initial work was supported by the New Zealand Marsden Fund (Contract GNS0702). Work conducted at the University of Bristol was supported by the NERC through partial funding of the National Environmental Isotope Facility (NEIF; contract no. NE/V003917/1), the European Research Council under the European Union’s Seventh Framework Programme (FP/2007-2013) and European Research Council (grant no. 340923) for funding GC-MS capabilities, the NERC (contract no. NE/V003917/1) and the University of Bristol for funding the GC-IRMS capabilities, and funding for B. David A. Naafs from a Royal Society Tata University Research Fellowship.
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