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.

[1] We carried out a detailed size-resolved chemical characterization of particle emissions from the combustion of European conifer species, savanna grass, African hardwood, and German and Indonesian peat. Combustion particles were sampled using two sets of five-stage Berner-type cascade impactors after a buffer volume and a dilution tunnel. We determined the emission factors of water-soluble organic carbon (WSOC, 46-6700 mg kg À1 , sum of five stages), water-insoluble organic carbon (WISOC, 1300-6100 mg kg À1 ), (apparent) elemental carbon (ECa, 490-1800 mg kg À1 ), inorganic ions (68-400 mg kg À1 ), n-alkanes (0.38-910 mg kg À1 ), n-alkenes (0.45-180 mg kg À1 ), polycyclic aromatic hydrocarbons (PAHs) (1.4-28 mg kg À1 ), oxy-PAHs (0.08-1.0 mg kg À1 ), lignin decomposition products (59-620 mg kg À1 ), nitrophenols (1.4-31 mg kg À1 ), resin acids (0-110 mg kg À1 ), and cellulose and hemicellulose decomposition products (540-5900 mg kg À1 ). The combustion and particle emission characteristics of both of peat were significantly different from those of the other biofuels. Peat burning yielded significantly higher emission factors of total fine particles in comparison to the other biofuels. Very high emission factors of n-alkanes and n-alkenes were observed from peat combustion, which may be connected to the concurrently observed ''missing'' CCN in peat smoke. A highlevel ofmonosaccharide anhydrides, especiallylevoglucosan, wasdetectedfromall types of biofuel combustion. The fractions of monosaccharide anhydrides in the emitted total carbon were higher in smaller particles (aerodynamic diameter, D pa < 0.42 mm).

Abstract. We investigate the CCN activity of freshly emitted biomass burning particles and their hygroscopic growth at a relative humidity (RH) of 85 %. The particles were produced in the Mainz combustion laboratory by controlled burning of various wood types. The water uptake at sub-and supersaturations is parameterized by the hygroscopicity parameter, κ (c.f. Petters and Kreidenweis, 2007). For the wood burns, κ is low, generally around 0.06. The main emphasis of this study is a comparison of κ derived from measurements at sub-and supersaturated conditions (κ G and κ CCN ), in order to see whether the water uptake at 85 % RH can predict the CCN properties of the biomass burning particles. Differences in κ G and κ CCN can arise through solution nonidealities, the presence of slightly soluble or surface active compounds, or non-spherical particle shape. We find that κ G and κ CCN agree within experimental uncertainties (of around 30 %) for particle sizes of 100 and 150 nm; only for 50 nm particles is κ CCN larger than κ G by a factor of 2. The magnitude of this difference and its dependence on particle size is consistent with the presence of surface active organic compounds. These compounds mainly facilitate the CCN activation of small particles, which form the most concentratedCorrespondence to: U. Dusek (u.dusek@uu.nl) solution droplets at the point of activation. The 50 nm particles, however, are only activated at supersaturations higher than 1 % and are therefore of minor importance as CCN in ambient clouds. By comparison with the actual chemical composition of the biomass burning particles, we estimate that the hygroscopicity of the water-soluble organic carbon (WSOC) fraction can be represented by a κ WSOC value of approximately 0.2. The effective hygroscopicity of a typical wood burning particle can therefore be represented by a linear mixture of an inorganic component with κ ∼ = 0.6, a WSOC component with κ ∼ = 0.2, and an insoluble component with κ = 0.