HR: 0800h
AN: PP41B-0546 [Abstracts]
TI: Considering the effects of diagenesis on the Ca isotope geochemical proxy
AU: * Fantle, M S
EM: mfantle@geosc.psu.edu
AF: Pennsylvania State University, Geosciences Dept., 212 Deike Bldg., University Park, PA
16802, United States
AB:
The Ca isotopic composition of marine carbonates has been proposed as an indicator of past conditions at the
Earth's surface. Some have suggested that Ca isotopes are a proxy for sea surface temperature while others
have used Ca isotopes to constrain relative weathering flux through geologic time. Recent results by Fantle and
DePaolo (2007) GCA 71(10) suggest that bulk carbonates in some sedimentary columns may experience more
reaction than previously thought. In light of this, it is critical to evaluate the fidelity of the proxy by elucidating the
effect of diagenetic processes on the Ca isotopic composition of marine carbonates in various geologic settings.
The current study uses reactive transport models to constrain the effects of recrystallization during diagenesis on
the Ca isotopic composition of marine carbonates. The study considers a sedimentary column in which: (1)
advection of a seawater-like fluid dominates the pore fluid chemistry, and (2) a minor component of the bulk
sediment reacts at a rate that is different from the bulk sediment. The modeling suggests that, in the former case,
the original isotopic composition of marine carbonates can be altered by as much as 0.4‰, given the
sorts of recrystallization rates previously suggested by modeling Sr isotopes (e.g. Richter and Liang, 1993, GCA
117(3--4)). However, the sort of enhanced reaction suggested by Fantle and DePaolo (2007) increases the
diagenetic effect substantially. In the latter case, Ca isotope variability in bulk sediments may persist even at high
recrystallization rates, due to a buffering effect on pore fluid chemistry. At low rates of bulk sediment
recrystallization, significant diagenetic alteration can occur when components within the bulk sediment react at
faster rates.
The implications of the current study are noteworthy. Current calibrations of the Ca isotope-paleotemperature
proxy indicate that the relationship between fractionation and temperature of most carbonate-producing
organisms in the surface ocean is ~0.02‰/°C. Thus, isotope shifts (0.2‰) due
to fairly large temperature changes (10°C) may be erased during diagenesis, complicating the
interpretation of paleotemperature. The key to using Ca isotopes as a proxy is selecting suitable sites and
appropriate samples, while using modeling techniques to constrain interpretations.
DE: 1009 Geochemical modeling (3610, 8410)
DE: 1041 Stable isotope geochemistry (0454, 4870)
DE: 4835 Marine inorganic chemistry (1050)
DE: 4954 Sea surface temperature
SC: Paleoceanography and Paleoclimatology [PP]
MN: 2007 Fall Meeting