SpatialVariationsof Atmospheric Alkylated PolycyclicAromatic Hydrocarbons across the Western Pacific to the Southern Ocean:Unexpected Increasing Deposition

Spatial variations of atmospheric alkylated polycyclic aromatic hydrocarbons (Alk-PAHs) are key to understanding their long-range atmospheric transport (LRAT). However, limited Alk-PAHs data have hindered their LRAT characterizations on a global scale. In this study, 49 Alk-PAHs were measured in the atmospheric samples collected across the Western Pacific to the Southern Ocean. The summed concentration of 39 frequently detected Alk-PAHs (Σ₃₉Alk-PAHs) was 25.8 ± 25.3 ng m^–3. The concentrations of Σ₃₉Alk-PAHs significantly declined with the decrease in latitude (°N). Higher concentrations (55.8 ± 33.8 ng m^–3) were linked to continental air mass compared to oceanic/Antarctica air mass (17.0 ± 13.6 ng m^–3), highlighting continental emissions as the primary source of marine atmospheric Alk-PAHs. An unexpected increase in the G/P partitioning ratio (<i>K</i>_P) was found in samples farther away from the continent, which cannot be explained by the influence of temperature on the partitioning process. Deposition analysis suggested that gaseous concentrations and the G/P partitioning largely influenced deposition patterns. Hypothetical scenario analysis indicated that increased <i>K</i>_P under snowy conditions could enhance the total Alk-PAH deposition. These findings emphasize the need for accurate characterization of partitioning and deposition processes when studying the global fate of Alk-PAHs, particularly in remote and polar regions.