A record of carbonyl sulfide from Antarctic ice over the last 1000 years
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Date
2013-01-01
Journal Title
Journal ISSN
Volume Title
Publisher
Geochemical Society
Abstract
Carbonyl sulfide (COS) is a trace gas, present in the troposphere, and also in the stratosphere, where it contributes to the stratospheric sulfate aerosol layer. It has both natural and anthropogenic sources. Natural processes include uptake by plants, while oceans, wetlands, volcanism and biomass
burning all contribute to natural COS emissions.
We have measured COS in Antarctic ice cores from Dronning Maud Land, drilled in 1998, the DE08 core drilled at Law Dome in 1987, and the DSS0506 core drilled in 2006.
Ice samples with COS gas ages between about 1050 AD and the early 20th centrury have been examined. A large volume ice crusher at the CSIRO Marine and Atmospheric Research
laboratory was used to extract air from bubbles occluded in the ice cores. These air samples were analysed for CO2, CH4,
CO and 13CO2 at CSIRO, and then for COS and several halocarbons at the University of East Anglia on a high sensitivity gas chromatograph/tri-sector mass spectrometer
system.
Initial results indicate that good sample integrity can be achieved. Measurements from the DML samples indicate low and uniform abundances across the last few hundred years,
and at concentrations significantly below those in the modernday atmosphere. Measurements in more recent ice from DE08
show the start of increasing concentrations in the early 1900s, confirming earlier evidence that the global atmospheric
abundance of COS has increased as a result of industrial activity during the 20th century.
Description
Keywords
Carbon oxysulfide, Gases, Troposphere, Stratosphere, Aerosols, Plants, Antarctica
Citation
Allin, S. J., Sturges, W. T., Laube, J., Etheridge, D., Rubino, M., Trudinger, C., Smith, A., & Mulvaney, R. (2013). A Record of carbonyl sulfide from Antarctic Ice over the Last 1000 Years. Paper presented at the Goldschmidt 2013 Conference, Florence, Italy, 25-30 August 2013. (pp.579). doi:10.1180/minmag.2013.077.5.1. 579