Paleocene-Eocene carbon isotope excursion in organic carbon and pedogenic carbonate; direct comparison in a continental stratigraphic section
Paleocene-Eocene carbon isotope excursion in organic carbon and pedogenic carbonate; direct comparison in a continental stratigraphic section
Geology (Boulder) (July 2004) 32 (7): 553-556
- Bighorn Basin
- C-13/C-12
- carbon
- Cenozoic
- chemostratigraphy
- correlation
- diagenesis
- Eocene
- fine-grained materials
- geochemistry
- greenhouse effect
- isotope ratios
- isotopes
- Leg 113
- lower Eocene
- Ocean Drilling Program
- organic carbon
- organic compounds
- Paleocene
- paleoclimatology
- Paleogene
- paleotemperature
- Park County Wyoming
- sedimentary rocks
- stable isotopes
- stratigraphic boundary
- Tertiary
- United States
- upper Paleocene
- Wyoming
- Polecat Bench
- Paleocene-Eocene boundary
The negative carbon isotope excursion at the Paleocene-Eocene boundary is a chemostratigraphic marker widely used for correlation of marine and continental stratigraphic sections. It is linked to massive dissociation of sedimentary methane hydrates and helps to explain an important greenhouse thermal event (Paleocene-Eocene thermal maximum), marine extinctions, and mammalian faunal change on three continents. We show that the carbon isotope excursion recorded in dispersed organic carbon (DOC) from fine-grained terrestrial sedimentary rocks at Polecat Bench, Wyoming, is very similar to that described in two high-resolution studies of pedogenic soil-nodule carbonate from the same section. All show a rapid onset, an approximately 40 m series of excursion values, and a slower recovery. However, the carbon isotope excursion in soil-nodule carbonate starts and ends approximately 3-5 m lower stratigraphically than that in DOC. We hypothesize that enhanced diffusion of atmospheric CO (sub 2) and subsurface diagenesis in an environment of good drainage and elevated temperature and pCO (sub 2) may explain this offset. The reliability of delta (super 13) C in DOC is attributed to mixing and averaging of isotopic signals from different organic compounds and tissues.