Abstract. Multiple year-round records of bulk and size-segregated composition of aerosol were obtained at the inland site of Concordia located at Dome C in East Antarctica. In parallel, sampling of acidic gases on denuder tubes was carried out to quantify the concentrations of HCl and HNO₃ present in the gas phase. These time series are used to examine aerosol present over central Antarctica in terms of chloride depletion relative to sodium with respect to freshly emitted sea-salt aerosol as well as depletion of sulfate relative to sodium with respect to the composition of seawater. A depletion of chloride relative to sodium is observed over most of the year, reaching a maximum of ∼ 20ngm⁻³ in spring when there are still large sea-salt amounts and acidic components start to recover. The role of acidic sulfur aerosol and nitric acid in replacing chloride from sea-salt particles is here discussed. HCl is found to be around twice more abundant than the amount of chloride lost by sea-salt aerosol, suggesting that either HCl is more efficiently transported to Concordia than sea-salt aerosol or re-emission from the snow pack over the Antarctic plateau represents an additional significant HCl source. The size-segregated composition of aerosol collected in winter (from 2006 to 2011) indicates a mean sulfate to sodium ratio of sea-salt aerosol present over central Antarctica of 0.16±0.05, suggesting that, on average, the sea-ice and open-ocean emissions equally contribute to sea-salt aerosol load of the inland Antarctic atmosphere. The temporal variability of the sulfate depletion relative to sodium was examined at the light of air mass backward trajectories, showing an overall decreasing trend of the ratio (i.e., a stronger sulfate depletion relative to sodium) when air masses arriving at Dome C had traveled a longer time over sea ice than over open ocean. The findings are shown to be useful to discuss sea-salt ice records extracted at deep drilling sites located inland Antarctica.

Abstract. Triple oxygen isotopic compositions (Δ¹⁷O = δ¹⁷O−0.52 × δ¹⁸O) of atmospheric sulfate (SO₄²⁻) and nitrate (NO₃⁻) in the atmosphere reflect the relative contribution of oxidation pathways involved in their formation processes, which potentially provides information to reveal missing reactions in atmospheric chemistry models. However, there remain many theoretical assumptions for the controlling factors of Δ¹⁷O(SO₄²⁻) and Δ¹⁷O(NO₃⁻) values in those model estimations. To test one of those assumption that Δ¹⁷O values of ozone (O₃) have a flat value and do not influence the seasonality of Δ¹⁷O(SO₄²⁻) and Δ¹⁷O(NO₃⁻) values, we performed the first simultaneous measurement of Δ¹⁷O values of atmospheric sulfate, nitrate, and ozone collected at Dumont d'Urville (DDU) Station (66°40′S, 140°01′E) throughout 2011. Δ¹⁷O values of sulfate and nitrate exhibited seasonal variation characterized by minima in the austral summer and maxima in winter, within the ranges of 0.9–3.4 and 23.0–41.9‰, respectively. In contrast, Δ¹⁷O values of ozone showed no significant seasonal variation, with values of 26±1‰ throughout the year. These contrasting seasonal trends suggest that seasonality in Δ¹⁷O(SO₄²⁻) and Δ¹⁷O(NO₃⁻) values is not the result of changes in Δ¹⁷O(O₃), but of the changes in oxidation chemistry. The trends with summer minima and winter maxima for Δ¹⁷O(SO₄²⁻) and Δ¹⁷O(NO₃⁻) values are caused by sunlight-driven changes in the relative contribution of O₃ oxidation to the oxidation by HO_x, RO_x, and H₂O₂. In addition to that general trend, by comparing Δ¹⁷O(SO₄²⁻) and Δ¹⁷O(NO₃⁻) values to ozone mixing ratios, we found that Δ¹⁷O(SO₄²⁻) values observed in spring (September to November) were lower than in fall (March to May), while there was no significant spring and fall difference in Δ¹⁷O(NO₃⁻) values. The relatively lower sensitivity of Δ¹⁷O(SO₄²⁻) values to the ozone mixing ratio in spring compared to fall is possibly explained by (i) the increased contribution of SO₂ oxidations by OH and H₂O₂ caused by NO_x emission from snowpack and/or (ii) SO₂ oxidation by hypohalous acids (HOX = HOCl+HOBr) in the aqueous phase.

Abstract. Atmospheric aging promotes internal mixing of black carbon (BC), leading to an enhancement of light absorption and radiative forcing. The relationship between BC mixing state and consequent absorption enhancement was never estimated for BC found in the Arctic region. In the present work, we aim to quantify the absorption enhancement and its impact on radiative forcing as a function of microphysical properties and mixing state of BC observed in situ at the Zeppelin Arctic station (78^∘ N) in the spring of 2012 during the CLIMSLIP (Climate impacts of short-lived pollutants in the polar region) project.

Single-particle soot photometer (SP2) measurements showed a mean mass concentration of refractory black carbon (rBC) of 39 ng m⁻³, while the rBC mass size distribution was of lognormal shape, peaking at an rBC mass-equivalent diameter (D_rBC) of around 240 nm. On average, the number fraction of particles containing a BC core with D_rBC>80 nm was less than 5 % in the size range (overall optical particle diameter) from 150 to 500 nm. The BC cores were internally mixed with other particulate matter. The median coating thickness of BC cores with 220 nm < D_rBC< 260 nm was 52 nm, resulting in a core–shell diameter ratio of 1.4, assuming a coated sphere morphology. Combining the aerosol absorption coefficient observed with an Aethalometer and the rBC mass concentration from the SP2, a mass absorption cross section (MAC) of 9.8 m² g⁻¹ was inferred at a wavelength of 550 nm. Consistent with direct observation, a similar MAC value (8.4 m² g⁻¹ at 550 nm) was obtained indirectly by using Mie theory and assuming a coated-sphere morphology with the BC mixing state constrained from the SP2 measurements. According to these calculations, the lensing effect is estimated to cause a 54 % enhancement of the MAC compared to that of bare BC particles with equal BC core size distribution. Finally, the ARTDECO radiative transfer model was used to estimate the sensitivity of the radiative balance to changes in light absorption by BC as a result of a varying degree of internal mixing at constant total BC mass. The clear-sky noontime aerosol radiative forcing over a surface with an assumed wavelength-dependent albedo of 0.76–0.89 decreased, when ignoring the absorption enhancement, by −0.12 W m⁻² compared to the base case scenario, which was constrained with mean observed aerosol properties for the Zeppelin site in Arctic spring. The exact magnitude of this forcing difference scales with environmental conditions such as the aerosol optical depth, solar zenith angle and surface albedo. Nevertheless, our investigation suggests that the absorption enhancement due to internal mixing of BC, which is a systematic effect, should be considered for quantifying the aerosol radiative forcing in the Arctic region.

Abstract. Although aerosols in the Arctic have multiple and complex impacts on the regional climate, their removal due to deposition is still not well quantified. We combined meteorological, aerosol, precipitation, and snowpack observations with simulations to derive information about the deposition of sea salt components and black carbon (BC) from November 2011 to April 2012 to the Arctic snowpack at two locations close to Ny-Ålesund, Svalbard. The dominating role of sea salt and the contribution of dust for the composition of atmospheric aerosols were reflected in the seasonal composition of the snowpack. The strong alignment of the concentrations of the major sea salt components in the aerosols, the precipitation, and the snowpack is linked to the importance of wet deposition for transfer from the atmosphere to the snowpack. This agreement was less strong for monthly snow budgets and deposition, indicating important relocation of the impurities inside the snowpack after deposition. Wet deposition was less important for the transfer of nitrate, non-sea-salt sulfate, and BC to the snow during the winter period. The average BC concentration in the snowpack remains small, with a limited impact on snow albedo and melting. Nevertheless, the observations also indicate an important redistribution of BC in the snowpack, leading to layers with enhanced concentrations. The complex behavior of bromide due to modifications during sea salt aerosol formation and remobilization in the atmosphere and in the snow were not resolved because of the lack of bromide measurements in aerosols and precipitation.