Abstract. A database of 15,617 point measurements of dimethylsulfide (DMS) in surface waters along with lesser amounts of data for aqueous and particulate dirhethylsulfoniopropionate concentration, chlorophyll concentration, sea surface salinity and temperature, and wind speed has been assembled. The database was processed to create a series of climatological annual and monthly 1øxl ø latitude-longitude squares of data. The results were compared to published fields of geophysical and biological parameters. No significant correlation was found between DMS and these parameters, and no simple algorithm could be found to create monthly fields of sea surface DMS concentration based on these parameters. Instead, an annual map of sea surface DMS was produced using an algorithm similar to that employed by Conkright et al. [1994]. In this approach, a first-guess field of DMS sea surface concentration measurements is created and then a correction to this field is generated based on actual measurements. Monthly sea surface grids of DMS were obtained using a similar scheme, but the sparsity of DMS measurements made the method difficult to implement. A scheme was used which projected actual data into months of the year where no data were otherwise present.

Abstract. Absorption photometers for real time application have been available since the 1980s, but the use of filterbased instruments to derive information on aerosol properties (absorption coefficient and black carbon, BC) is still a matter of debate. Several workshops have been conducted to investigate the performance of individual instruments over the intervening years. Two workshops with large sets of aerosol absorption photometers were conducted in 2005 and 2007. The data from these instruments were corrected using existing methods before further analysis. The intercomparison shows a large variation between the responses to absorbing aerosol particles for different types of instruments. The unit to unit variability between instruments can be up to 30% for Particle Soot Absorption Photometers (PSAPs) and Aethalometers. Multi Angle Absorption Photometers (MAAPs) showed a variability of less than 5%. Reasons for the high variability were identified to be variations in sample flow and spot size. It was observed that different flow rates influence system performance with respect to response to absorption and instrumental noise. Measurements with non absorbing particles showed that the current corrections of a cross sensitivity to particle scattering are not sufficient. Remaining cross sensitivities were found to be a function of the total particle load on the filter. The large variation between the response to absorbing aerosol particles for different types of instruments indicates that current correction functions for absorption photometers are not adequate.

[1] Fifteen years of ''equivalent'' black carbon (EBC) measurements (derived from aethalometer measurements of light absorption) made at Alert in Nunavut, Canada, and Point Barrow in Alaska, United States, were compared for the long-term trends and seasonal cycle. Over the 15-year period from 1989 to 2003, the results revealed a downward trend in EBC concentrations by as much as 54% at Alert and 27% at Barrow for the all-year data, by 49% at Alert and 33% at Barrow for the winter data, and by 53% at Alert for the summer. It was difficult to quantify if there was a decline during the summer for Barrow since there was no clear trend. The difference in trends might be related to changes in circulation in the Arctic, variable source contribution, and/or scavenging of particles. The results revealed that EBC concentrations were 40% higher during the positive phase of the North Atlantic Oscillation than during the negative phase. The source contributions at the two sites were determined by using trajectory analysis techniques, which revealed that Alert came under the influence of Siberia/Europe transport while Barrow showed influence from Siberian and Pacific/Asian transport.

[1] Arctic regional climate is influenced by the radiative impact of aerosol black carbon (BC) both in the atmosphere and deposited on the snow and ice covered surfaces. The NIES (National Institute for Environmental Studies) global atmospheric transport model was used, with BC emissions from mid-latitude fossil fuel and biomass burning source regions, to simulate BC concentrations with 16 year period. The model-simulated BC agreed well with the BC observations, including the trends and seasonality, at three Arctic sites: Alert (Nunavut, Canada), Barrow (Alaska, USA), and Zepplin, Ny-Ålesund (Svalbard, Norway). The equivalent black carbon (EBC, absorption inferred BC) observations at the three Arctic locations showed an overall decline of 40% from 1990 to 2009; with most change occurring during early 1990s. Model simulations confirmed declining influence on near surface BC contribution by 70% , and atmospheric BC burden by one half from the Former Soviet Union (FSU) BC source region over 16 years. In contrast, the BC contribution from the East Asia (EA) region has little influence at the surface but atmospheric Arctic BC burden increased by 3 folds. Modelled dry deposition is dominant in the Arctic during wintertime, while wet deposition prevails at all latitudes during summer. Sensitivity analyses on the dry and wet deposition schemes indicate that parameterizations need to be refined to improve on the model performance. There are limitations in the model due to simplified parameterizations and remaining model uncertainties, which requires further exploration of source region contributions, especially from growing EA source region to Arctic BC levels in the future is warranted.

[1] During the winter and spring the North American Arctic is impacted by anthropogenic black carbon (BC) in ''Arctic Haze'' pollution from sources mainly located in Europe and Russia. This black carbon, while suspended in the atmosphere and in surface snow, has a significant effect on radiative forcing of the Arctic atmosphere. Routine ground-level observations of aerosol black carbon by optical absorption have been made at a Canadian Arctic location, Alert (82.5°N, 62.5°W), Nunavut since 1989. A 3-year intensive study was conducted to compare BC obtained by the thermal analysis and optical absorption methods, so that the seasonal variations in the ''operational'' absorption cross sections of the aerosol could be determined. A time series analysis indicated that black carbon concentrations undergo a strong seasonal variation superimposed upon a long-term trend. The latter shows a decrease of about 55% in BC concentrations between 1989 and 2002 at Alert. Factors responsible for these trends such as changes in emissions and atmospheric transport support the hypothesis that BC emissions from the former USSR are mostly responsible for the observed decreasing trend. Transport from other sectors such as North America and Europe are not as prevalent at Alert.