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Ice cores provide
valuable information on past atmospheric composition, chemistry, and
climate. Atmospheric chemistry is controlled by its "oxidation
capacity", defined by OH radical concentrations. OH concentrations
determine the lifetime of many atmospheric species, including climatically
important species such as methane. The oxygen isotopes of sulfate
and nitrate can provide the first conservative proxy for past OH
concentrations, enabling us to study the link between atmospheric
chemistry and climate.
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Photo:
ICDS 2006 |
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Our longest
record of the O-isotope composition of sulfate comes from the Vostok ice core in east Antarctica,
extending through the past 125,000 years.This figure shows the variability in the O-isotopic composition (D17O)
of sulfate, along with dDice
measurements (indicative of temperature), through the last
glacial-interglacial cycle from the Vostok (Antarctica) ice core
[Alexander et al. 2002].
Sulfate formation through oxidation of reduced sulfur species by OH is
30-50% more important during the cold glacial period, than the surrounding
interglacial periods. This change is due to changing OH
concentrations and/or cloud processing efficiency. A more
quantitative interpretation of this paleo record will be provided by a global
model of chemistry and transport. |
The
WAIS Divide project
will provide the first complete record of multiple isotope ratios of
nitrate and sulfate covering the last ~100,000 years, from the deep ice
core planned for the central ice divide of the West Antarctic Ice Sheet
(WAIS). The WAIS Divide ice core will be the highest resolution long ice
core obtained from Antarctica and we can expect important complementary
information to be available, including accurate knowledge of past
accumulation rates, temperatures, and compounds such as H2O2, CO and CH4.
These compounds play significant roles in global atmospheric chemistry and
climate. Especially great potential lies in the use of multiple isotope
signatures. The unique mass independent fractionation (MIF)
D17O signature
of ozone is observed in both nitrate and sulfate, due to the interaction
of their precursors with ozone. The development of methods to measure the
multiple-isotope composition of small samples of sulfate and nitrate makes
continuous high resolution measurements on ice cores feasible for the
first time. This project will coincide with the International Polar Year
(2007-2008), and contributes to goals of the IPY, which include the
fostering of interdisciplinary research toward enhanced understanding of
atmospheric chemistry and climate in the polar regions. |
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People: | |
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Eric Steig (lead P.I.), Becky Alexander (co-P.I.), Shelley
Kunasek, and Meredith Hastings, University of Washington
Mark H. Thiemens (co-P.I.), University of California, San Diego |
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Funding: |
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| NSF-OPP 0538049 |
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References: |
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Alexander, B., Savarino, J., Thiemens, M.H., and Delmas, R., “Climate driven changes of the oxidation pathways of atmospheric sulfur,” Geophys. Res. Lett., 29(14), 30 (2002). |
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