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25th International Meeting on Organic Geochemistry IMOG 2011

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P-005<br />

A M<strong>on</strong>te Carlo applicati<strong>on</strong> for introducing source variability in<br />

source apporti<strong>on</strong>ment calculati<strong>on</strong>s<br />

August Anderss<strong>on</strong> 1 , Rebecca Sheesley 1,2 , Jorien V<strong>on</strong>k 1,3 , Örjan Gustafss<strong>on</strong> 1<br />

1 Stockholm University, Stockholm, Sweden, 2 Baylor University, Waco, United States of America, 3 ETH,<br />

Zurich, Switzerland (corresp<strong>on</strong>ding author:august.anderss<strong>on</strong>@itm.su.se)<br />

End-member mixing analysis (EMMA) using e.g.<br />

molecular and isotopic markers are comm<strong>on</strong>ly used to<br />

decipher the relative c<strong>on</strong>tributi<strong>on</strong>s from different<br />

sources to a mixed envir<strong>on</strong>mental sample. By setting<br />

up a set of linear equati<strong>on</strong>s with N+1 sources and N<br />

source markers, the relative source c<strong>on</strong>tributi<strong>on</strong>s may<br />

be solved analytically. A major drawback of that<br />

standard approach is that the natural variability of the<br />

source markers (the end-members) is not taken into<br />

account. Here a M<strong>on</strong>te Carlo approach for accounting<br />

of the end-member variability in source calculati<strong>on</strong>s is<br />

presented.<br />

This methodology is exemplified by two applicati<strong>on</strong>s:<br />

1. Apporti<strong>on</strong>ing relative c<strong>on</strong>tributi<strong>on</strong>s to organic<br />

carb<strong>on</strong> (OC) in Arctic Ocean surface sediments from<br />

marine, riverine and erosi<strong>on</strong> sources using 13C and<br />

14C isotope [1]. Interestingly, the erosi<strong>on</strong> comp<strong>on</strong>ent<br />

was found to be around 50%, irrespective of the<br />

distance of the sampling site to the Kolyma river<br />

mouth, Figure 1.<br />

2. Apporti<strong>on</strong>ing relative c<strong>on</strong>tributi<strong>on</strong>s to carb<strong>on</strong>aceous<br />

aerosols in southern Asia from biomass combusti<strong>on</strong>,<br />

liquid petroleum combusti<strong>on</strong> and coal combusti<strong>on</strong><br />

using various polyaromatic hydrocarb<strong>on</strong> (PAH)<br />

signals as molecular source markers [2]. This study<br />

shows that the fossil fuel c<strong>on</strong>tributi<strong>on</strong> is roughly<br />

equally split between petroleum- and coal combusti<strong>on</strong><br />

sources.<br />

Taken together, these results points to the general<br />

c<strong>on</strong>clusi<strong>on</strong> that source variability influences both the<br />

calculated relative c<strong>on</strong>tributi<strong>on</strong>s from different sources<br />

and the precisi<strong>on</strong> by which it may be calculated. This<br />

c<strong>on</strong>clusi<strong>on</strong> is reinforced by analysis of synthetic data<br />

sets, designed to span the main source c<strong>on</strong>figurati<strong>on</strong>s<br />

possible.<br />

Figure 1 Relative c<strong>on</strong>tributi<strong>on</strong>s (with error bars) of<br />

riverine, erosi<strong>on</strong> and marine c<strong>on</strong>tributi<strong>on</strong>s to OC in<br />

surface sediments al<strong>on</strong>g the Kolyma paleoriver.<br />

References<br />

[1] V<strong>on</strong>k, J. et al. (2010) Biogeosciences, 7, 3153-<br />

3166<br />

[2] Sheesley, R. et al. (<strong>2011</strong>) Atmospheric<br />

Envir<strong>on</strong>ment, Accepted for publicati<strong>on</strong>.<br />

153

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