Measurement of loss rates of organic compounds in snow using in situ experiments and isotopically labelled compounds

• Published in: Polar Research
• Main Authors: Erika von Schneidemesser, James J. Schauer, Martin M. Shafer, Michael H. Bergin
• Format: Article in Journal/Newspaper
• Language: English
• Published: Norwegian Polar Institute 2012
• Subjects: Snow; photochemistry; air pollution; Greenland; Arctic; Environmental sciences; GE1-350; Oceanography; GC1-1581; ice core; Ice Sheet; Polar Research
• Online Access: https://doi.org/10.3402/polar.v31i0.11597; https://doaj.org/article/14569f12078a4b1b9daf135069062d4f

Organic molecular marker compounds are widely used to identify emissions from anthropogenic and biogenic air pollution sources in atmospheric samples and in deposition. Specific organic compounds have been detected in polar regions, but their fate after deposition to snow is poorly characterized. Within this context, a series of exposure experiments were carried out to observe the post-depositional processing of organic compounds under real-world conditions in snow on the surface of the Greenland Ice Sheet, at the Summit research station. Snow was prepared from water spiked with isotopically labelled organic compounds, representative of typical molecular marker compounds emitted from anthropogenic activities. Reaction rate constants and reaction order were determined based on a decrease in concentration to a stable, non-zero, threshold concentration. Fluoranthene-d10, docosane-d46, hexadecanoic acid-d31, docosanoic acid-d43 and azelaic acid-d14 were estimated to have first order loss rates within surface snow with reaction rate constants of 0.068, 0.040, 0.070, 0.067 and 0.047 h−1, respectively. No loss of heptadecane-d36 was observed. Overall, these results suggest that organic contaminants are archived in polar snow, although significant post-depositional losses of specific organic compounds occur. This has implications for the environmental fate of organic contaminants, as well as for ice-core studies that seek to use organic molecular markers to infer past atmospheric loadings, and source emissions.