ºìÐÓÊÓÆµ

Skip to main content

Kalila Morsink

  • BA (Columbia University, 2019)
Notice of the Final Oral Examination for the Degree of Master of Science

Topic

δ^13C of mid-Pacific carbonate sediments around the time of Ocean Anoxic Event 2

School of Earth and Ocean Sciences

Date & location

  • Wednesday, February 5, 2025
  • 9:00 A.M.
  • Virtual Defence

Examining Committee

Supervisory Committee

  • Dr. Laurence Coogan, School of Earth and Ocean Sciences, University of Victoria (Co-Supervisor)
  • Dr. Blake Dyer, School of Earth and Ocean Sciences, UVic (Co-Supervisor)
  • Dr. Anne-Sofie Ahm, School of Earth and Ocean Sciences, UVic (Member)

External Examiner

  • Dr. Jeremy Owens, Department of Earth, Ocean, and Atmospheric Science, Florida State University

Chair of Oral Examination

  • Dr. Kirstin Lane, School of Exercise Science, Physical and Health Education, UVic

Abstract

The δ13C of marine carbonates is commonly used as a proxy for the global burial fraction of carbonate vs. organic carbon. At the same time, carbonate δ13C is understood to vary locally from the global ocean average due to coeval spatial variation in seawater geochemistry, especially in shallow marine settings, and/or post-depositional alteration of sediments. In Cretaceous-age shallow marine sections, Ocean Anoxic Event 2 (OAE2) is identified by a positive δ13C excursion near the Cenomanian-Turonian boundary (∼93.9 Ma). However, there are currently no OAE2 δ13C records from the Pacific basin, which at the time was ∼65% of ocean area and included most of the world’s deep ocean. Here I present new (n = 255) and previously published (n = 13) bulk carbonate δ13C and δ18O data from 10 mid-Pacific sites, measured in sediments recovered by the Deep Sea Drilling Program, which I use to test the hypothesis that there was a global change in the δ13CDIC of seawater at the time of OAE2. I use existing biostratigraphic data to target sediments of Cenomanian and Turonian age. Between sites, I compare δ13Ccarbonate and δ18Ocarbonate values associated with the same planktonic foraminifera species. My Pacific δ13Ccarbonate values range from 0.88‰ to 4.20‰ VPDB (excluding 3 samples within a 7-cm interval with -2.7‰ to -2.5‰ VPDB). They are generally lower than shallow marine bulk carbonate δ13C values where the OAE2 positive δ13C excursion has been identified, e.g., the well-known Eastbourne, UK section where Cenomanian and Turonian δ13C values range from 2.6 to 5.4‰ VPDB. To explain δ13Ccarbonate values within the Pacific, I invoke both factors local to the sites, such as proximity to a shallow semi-restricted carbonate platform in the case of the site with the shallowest paleodepth, and changes in global ocean δ13CDIC over time. An OAE2 positive δ13Ccarbonate excursion is not observed at most Pacific sites in this thesis, which has two possible explanations. One possible explanation is that a global ocean OAE2 δ13C excursion did occur, but that some process largely prevented its deposition, preservation, or recovery in the mid-Pacific. Another possible explanation is that the OAE2 δ13C excursion occurred only in the shallow epicontinental basins and continental slope environments where it is observed (including the Atlantic, Western Tethys, Neotethys, and Western Interior Seaway of North America) because organic carbon burial within these relatively restricted water masses changed their δ13CDICs but did not affect δ13CDIC in the mid-Pacific.