Search

Measurements of lipids as representative species for different lipid classes in the marine environment have been performed to characterize their oceanic sources and their transfer from the ocean into the atmosphere to marine aerosol particles. To this end, a set of lipid classes (hydrocarbons (HC), fatty acid methyl esters (ME), free fatty acids (FFA), alcohols (ALC), 1,3-diacylglycerols (1,3 DG), 1,2-diacylglycerols (1,2 DG), monoacylglycerols (MG), wax esters (WE), triacylglycerols (TG), phospholipids (PP) including phosphatidylglycerols (PG), phosphatidylethanolamine (PE), phosphatidylcholines (PC), glycolipids (GL) including sulfoquinovosyldiacylglycerols (SQDG), monogalactosyl-diacylglycerols (MGDG), digalactosyldiacylglycerols (DGDG) and sterols (ST)) is investigated in both the dissolved and particulate fraction in seawater, differentiated between underlying water (ULW) and the sea surface microlayer (SML), and in ambient submicron aerosol particle samples (PM1) at the Cape Verde Atmospheric Observatory (CVAO) applying concerted measurements. The different lipids are found in all marine compartments but in different compositions. At this point, a certain variability is observed for the concentration of dissolved (∑DLULW: 39.8-128.5 μg L\-1, ∑DLSML: 55.7-121.5 μg L\-1) and particulate (∑PLULW: 36.4-93.5 μg L\-1, ∑PLSML: 61.0-118.1 μg L\-1) lipids in seawater of the tropical North Atlantic Ocean along the campaign. Only slight SML enrichments are observed for the lipids with an enrichment factor EFSML of 1.1-1.4 (DL) and 1.0-1.7 (PL). On PM1 aerosol particles, a total lipid concentration between 75.2-219.5 ng m\-3 (averaged: 119.9 ng m\-3) is measured with high atmospheric concentration of TG (averaged: 21.9 ng m\-3) as a potential indicator for freshly emitted sea spray. Besides phytoplankton sources, bacteria influence the lipid concentrations in seawater and on the aerosol particles, so that the phytoplankton tracer (chlorophyll-a) cannot sufficiently explain the lipid abundance. The concentration and enrichment of lipids in the SML is not related to physicochemical properties describing the surface activity. For aerosol, however, the high enrichment of lipids (as a sum) corresponds well with the consideration of their high surface activity, thus the EFaer (enrichment factor on submicron aerosol particles compared to SML) ranges between 9 × 104-7 × 105. Regarding the single lipid groups on the aerosol particles, a weak relation between EFaer and lipophilicity (expressed by the KOW value) was identified, which was absent for the SML. However, overall simple physico-chemical descriptors are not sufficient to fully explain the transfer of lipids. As our findings show that additional processes such as formation and degradation influence the ocean-atmosphere transfer of both OM in general and of lipids in particular, they have to be considered in OM transfer models. Moreover, our data suggest that the extend of enrichment of lipid classes constituents on the aerosol particles might be related to the distribution of the lipid within the bubble-air-water-interface. Lipids, which are preferably arranged within the bubble interface, namely TG and ALC, are transferred to the aerosol particles to the highest extend. Finally, the connection between ice nucleation particles (INP) in seawater, which are active already at higher temperatures (\-10 °C to \-15 °C), and the lipid classes PE and FFA suggests that lipids formed in the ocean have the potential to contribute to (biogenic) INP activity when transferred to the atmosphere. [ABSTRACT FROM AUTHOR]

Number concentrations of ice nucleating particles (NINP) in the Arctic were derived from ground-based filter samples. Examined samples had been collected in Alert (Nunavut, Northern Canadian Archipelago on Ellesmere Island), Utqiagvik, formerly known as Barrow (Alaska), Ny Ålesund (Svalbard) and at the Villum Research Station (VRS, North Greenland). For the former two stations, examined filters span a full yearly cycle. For VRS, 10 weekly samples, mostly from different month of one year, were included. Samples from Ny Ålesund were collected during the months from March until September of one year. At all four stations, highest concentrations were found in the summer months from roughly June to September. For those stations with sufficient data coverage, an annual cycle can be seen. The spectra of NINP observed at the highest temperatures, i.e., those obtained for summer month, showed the presence of INP that nucleate ice up to - 5°C. It is know from literature that ice activivity observed at such high temperatures indicates the presence of ice active material of biogenic origin. Spectra observed at the lowest temperatures, i.e., those derived for winter month, were on the lower end of respective values reported in literature. An analysis concerning the origin of INP that were ice active at high temperatures was carried out, using back-trajectories and satellite information. Both, terrestrial locations in the Arctic and the adjacent sea were found to be possible source areas for highly active INP. [ABSTRACT FROM AUTHOR]