[1] The paper presents the current status of the Maritime Aerosol Network (MAN), which has been developed as a component of the Aerosol Robotic Network (AERONET). MAN deploys Microtops handheld Sun photometers and utilizes the calibration procedure and data processing (Version 2) traceable to AERONET. A web site dedicated to the MAN activity is described. A brief historical perspective is given to aerosol optical depth (AOD) measurements over the oceans. A short summary of the existing data, collected on board ships of opportunity during the NASA Sensor Intercomparison and Merger for Biological and Interdisciplinary Oceanic Studies (SIMBIOS) Project is presented. Globally averaged oceanic aerosol optical depth (derived from island-based AERONET measurements) at 500 nm is $0.11 and Angstrom parameter (computed within spectral range 440-870 nm) is calculated to be $0.6. First results from the cruises contributing to the Maritime Aerosol Network are shown. MAN ship-based aerosol optical depth compares well to simultaneous island and near-coastal AERONET site AOD.

[1] Photomineralization of terrigenous dissolved organic matter (tDOM) in the Arctic Ocean is limited by persistent sea ice cover that reduces the amount of ultraviolet (UV) radiation reaching the underlying water column. UV-dependent processes are likely to accelerate as a result of shrinking sea ice extent and decreasing ice thickness caused by climatic warming over this region. In this study, we made the first quantitative estimates of photomineralization of tDOM in a coastal Arctic ecosystem under current and future sea ice regimes. We used an optical-photochemical coupled model incorporating water column optics and experimental measurements of photoproduction of dissolved inorganic carbon (DIC), the main carbon product of DOM photochemistry. Apparent quantum yields of DIC photoproduction were determined on water samples from the Mackenzie River estuary, the Mackenzie Shelf, and Amundsen Gulf. UV irradiances just below the sea surface were estimated by combining satellite backscattered and passive microwave radiance measurements with a radiative transfer model. The mean annual DIC photoproduction between 1979 and 2003 was estimated as 66.5 ± 18.5 Gg carbon in the surface waters of the southeastern Beaufort Sea, where UV absorption is dominated by chromophoric dissolved organic matter discharged by the Mackenzie River. This value is equivalent to 10% of bacterial respiration rates, 8% of new primary production rates and 2.8 ± 0.6% of the 1.3 Tg of dissolved organic carbon (DOC) discharged annually by the Mackenzie River into the area. During periods of reduced ice cover such as 1998, the latter value could rise to 5.1% of the annual riverine DOC discharge. Under an ice-free scenario, the model predicted that 150.5 Gg of DIC would be photochemically produced, mineralizing 6.2% of the DOC input from the Mackenzie River. These results show that the predicted trend of ongoing contraction of sea ice cover will greatly accelerate the photomineralization of tDOM in Arctic surface waters.

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Abstract. The Maritime Aerosol Network (MAN) has been collecting data over the oceans since November 2006. Over 80 cruises were completed through early 2010 with deployments continuing. Measurement areas included various parts of the Atlantic Ocean, the Northern and Southern Pacific Ocean, the South Indian Ocean, the Southern Ocean, the Arctic Ocean and inland seas. MAN deploys Microtops handheld sunphotometers and utilizes a calibration procedure and data processing traceable to AERONET. Data collection included areas that previously had no aerosol optical depth (AOD) coverage at all, particularly vast areas of the Southern Ocean. The MAN data archive provides a valuable resource for aerosol studies in maritime environments. In the current paper we present results of AOD measurements over the oceans, and make a comparison with satellite AOD retrievals and model simulations.

Multi-year sets of ground-based sun-photometer measurements conducted at 12 Arctic sites and 9 Antarctic sites were examined to determine daily mean values of aerosol optical thickness () at visible and near-infrared wavelengths, from which best-fit values of Ångström"s exponent  were calculated. Analysing these data, the monthly mean values of (0.50 µm) and  and the relative frequency histograms of the daily mean values of both parameters were determined for winterspring and summer-autumn in the Arctic and for austral summer in Antarctica. The Arctic and Antarctic covariance plots of the seasonal median values of  versus (0.50 µm) showed: (i) a considerable increase in (0.50 µm) for the Arctic aerosol from summer to winter-spring, without marked changes in ; and (ii) a marked increase in (0.50 µm) passing from the Antarctic Plateau to coastal sites, whereas  decreased considerably due to the larger fraction of sea-salt aerosol. Good agreement was found when comparing ground-based sun-photometer measurements of () and  at Arctic and Antarctic coastal sites with Microtops measurements conducted during numerous AERONET/MAN cruises from 2006 to 2013 in three Arctic Ocean sectors and in coastal and offshore regions of the Southern Atlantic, Pacific, and Indian Oceans, and the Antarctic Peninsula. Lidar measurements were also examined to characterise vertical profiles of the aerosol backscattering coefficient measured throughout the year at Ny-Ålesund. Satellite-based MODIS, MISR, and AATSR retrievals of () over large parts of the oceanic polar regions during spring and summer were in close agreement with ship-borne and coastal ground-based sun-photometer measurements. An overview of the chemical composition of fine and accumulation/coarse mode particles is also presented, based on in-situ measurements at Arctic and Antarctic sites. Fourteen log-normal aerosol number size-distributions were defined to represent the average features of fine and accumulation/coarse mode particles for Arctic haze, summer background aerosol, Asian dust and boreal forest fire smoke, and for various background austral summer aerosol types at coastal 4 and high-altitude Antarctic sites. The main columnar aerosol optical characteristics were determined for all particle modes, based on in-situ measurements of the scattering and absorption coefficients. Diurnally averaged direct aerosol-induced radiative forcing and efficiency were calculated for a set of multimodal aerosol extinction models, using various Bidirectional Reflectance Distribution Function models over vegetation-covered, oceanic and snow-covered surfaces. These gave a reliable measure of the pronounced effects of aerosols on the radiation balance of the surface-atmosphere system over polar regions.