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      Biogenic, anthropogenic and sea salt sulfate size-segregated aerosols in the Arctic summer

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          Abstract

          Size-segregated aerosol sulfate concentrations were measured on board the Canadian Coast Guard Ship (CCGS) <i>Amundsen</i> in the Arctic during July 2014. The objective of this study was to utilize the isotopic composition of sulfate to address the contribution of anthropogenic and biogenic sources of aerosols to the growth of the different aerosol size fractions in the Arctic atmosphere. Non-sea-salt sulfate is divided into biogenic and anthropogenic sulfate using stable isotope apportionment techniques. A considerable amount of the average sulfate concentration in the fine aerosols with a diameter &lt;  0.49 µm was from biogenic sources (&gt;  63 %), which is higher than in previous Arctic studies measuring above the ocean during fall (&lt;  15 %) (Rempillo et al., 2011) and total aerosol sulfate at higher latitudes at Alert in summer (&gt;  30 %) (Norman et al., 1999). The anthropogenic sulfate concentration was less than that of biogenic sulfate, with potential sources being long-range transport and, more locally, the <i>Amundsen</i>'s emissions. Despite attempts to minimize the influence of ship stack emissions, evidence from larger-sized particles demonstrates a contribution from local pollution.<br><br> A comparison of <i>δ</i><sup>34</sup>S values for SO<sub>2</sub> and fine aerosols was used to show that gas-to-particle conversion likely occurred during most sampling periods. <i>δ</i><sup>34</sup>S values for SO<sub>2</sub> and fine aerosols were similar, suggesting the same source for SO<sub>2</sub> and aerosol sulfate, except for two samples with a relatively high anthropogenic fraction in particles &lt;  0.49 µm in diameter (15–17 and 17–19 July). The high biogenic fraction of sulfate fine aerosol and similar isotope ratio values of these particles and SO<sub>2</sub> emphasize the role of marine organisms (e.g., phytoplankton, algae, bacteria) in the formation of fine particles above the Arctic Ocean during the productive summer months.

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          Author and article information

          Journal
          Atmospheric Chemistry and Physics
          Atmos. Chem. Phys.
          Copernicus GmbH
          1680-7324
          2016
          April 2016
          : 16
          : 8
          : 5191-5202
          Article
          10.5194/acp-16-5191-2016
          © 2016
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