Organic Compounds, Radiocarbon, Trace Elements and Atmospheric Transport Illuminating Sources of Elemental Carbon in a 300‐Year Svalbard Ice Core

Author:

Ruppel M. M.12ORCID,Khedr M.34ORCID,Liu X.34ORCID,Beaudon E.5ORCID,Szidat S.67ORCID,Tunved P.8,Ström J.8,Koponen H.9,Sippula O.910,Isaksson E.11,Gallet J.‐C.11ORCID,Hermanson M.12ORCID,Manninen S.2,Schnelle‐Kreis J.4ORCID

Affiliation:

1. Atmospheric Composition Unit Finnish Meteorological Institute Helsinki Finland

2. Faculty of Biological and Environmental Sciences Ecosystems and Environment Research Programme University of Helsinki Helsinki Finland

3. Joint Mass Spectrometry Center University of Rostock Rostock Germany

4. Joint Mass Spectrometry Center Cooperation Group Comprehensive Molecular Analytics Helmholtz Zentrum München German Research Center for Environmental Health Neuherberg Germany

5. Byrd Polar and Climate Research Center The Ohio State University Columbus OH USA

6. Department of Chemistry Biochemistry and Pharmaceutical Sciences University of Bern Bern Switzerland

7. Oeschger Centre for Climate Change Research University of Bern Bern Switzerland

8. Department of Environmental Science Stockholm University Stockholm Sweden

9. Department of Environmental and Biological Sciences University of Eastern Finland Kuopio Finland

10. Department of Chemistry University of Eastern Finland Joensuu Finland

11. Norwegian Polar Institute Tromsø Norway

12. Hermanson & Associates (LLC) Haarlem The Netherlands

Abstract

AbstractBlack carbon (BC) particles produced by incomplete combustion of biomass and fossil fuels warm the atmosphere and decrease the reflectivity of snow and ice, hastening their melt. Although the significance of BC in Arctic climate change is widely acknowledged, observations on its deposition and sources are few. We present BC source types in a 300‐year (1700–2005) Svalbard ice core by analysis of particle‐bound organic compounds, radiocarbon, and trace elements. According to the radiocarbon results, 58% of the deposited elemental carbon (EC, thermal‐optical proxy of BC) is of non‐fossil origin throughout the record, while the organic compounds suggest a higher percentage (68%). The contribution of fossil fuels to EC is suggested to have been elevated between 1860 and 1920, particularly based on the organics and trace element data. A second increase in fossil fuel sources seems to have occurred near the end of the record: according to radiocarbon measurements between 1960 and 1990, while the organics and trace element data suggest that the contribution of fossil fuels has increased since the 1970s to the end of the record, along with observed increasing EC deposition. Modeled atmospheric transport between 1948 and 2004 shows that increasing EC deposition observed at the glacier during that period can be associated with increased atmospheric transport from Far East Asia. Further observational BC source data are essential to help target climate change mitigation efforts. The combination of robust radiocarbon with organic compound analyses requiring low sample amounts seems a promising approach for comprehensive Arctic BC source apportionment.

Funder

Academy of Finland

Koneen Säätiö

Publisher

American Geophysical Union (AGU)

Subject

Space and Planetary Science,Earth and Planetary Sciences (miscellaneous),Atmospheric Science,Geophysics

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