Measurements of free amino acids (FAAs) in the marine environment to elucidate their transfer from the ocean into the atmosphere, to marine aerosol particles and to clouds, were performed at the MarParCloud (marine biological production, organic aerosol particles and marine clouds: a process chain) campaign at the Cabo Verde islands in autumn 2017. According to physical and chemical specifications such as the behavior of air masses, particulate MSA concentrations and MSA/sulfate ratios, as well as particulate mass concentrations of dust tracers, aerosol particles predominantly of marine origin with low to medium dust influences were observed. FAAs were investigated in different compartments: they were examined in two types of seawater underlying water (ULW) and in the sea surface microlayer (SML), as well as in ambient marine size-segregated aerosol particle samples at two heights (ground height based at the Cape Verde Atmospheric Observatory, CVAO, and at 744 m height on Mt. Verde) and in cloud water using concerted measurements. The âFAA concentration in the SML varied between 0.13 and 3.64 Âµmol L.sup.-1, whereas it was between 0.01 and 1.10 Âµmol L.sup.-1 in the ULW; also, a strong enrichment of âFAA (EF.sub.SML : 1.1-298.4, average of 57.2) was found in the SML. In the submicron (0.05-1.2 Âµm) aerosol particles at the CVAO, the composition of FAAs was more complex, and higher atmospheric concentrations of âFAA (up to 6.3 ng m.sup.-3) compared to the supermicron (1.2-10 Âµm) aerosol particles (maximum of 0.5 ng m.sup.-3) were observed. The total âFAA concentration (PM.sub.10) was between 1.8 and 6.8 ng m.sup.-3 and tended to increase during the campaign. Averaged âFAA concentrations in the aerosol particles on Mt. Verde were lower (submicron: 1.5 ng m.sup.-3 ; supermicron: 1.2 ng m.sup.-3) compared to the CVAO. A similar contribution percentage of âFAA to dissolved organic carbon (DOC) in the seawater (up to 7.6 %) and to water-soluble organic carbon (WSOC) in the submicron aerosol particles (up to 5.3 %) indicated a related transfer process of FAAs and DOC in the marine environment. Considering solely ocean-atmosphere transfer and neglecting atmospheric processing, high FAA enrichment factors were found in both aerosol particles in the submicron range (EF.sub.aer(âFAA) : 2x10.sup.3 -6x10.sup.3) and medium enrichment factors in the supermicron range (EF.sub.aer(âFAA) : 1x10.sup.1 -3x10.sup.1). In addition, indications for a biogenic FAA formation were observed. Furthermore, one striking finding was the high and varying FAA cloud water concentration (11.2-489.9 ng m.sup.-3 ), as well as enrichments (EF.sub.CW : 4x10.sup.3 and 1x10.sup.4 compared to the SML and ULW, respectively), which were reported here for the first time. The abundance of inorganic marine tracers (sodium, methanesulfonic acid) in cloud water suggests an influence of oceanic sources on marine clouds. Finally, the varying composition of the FAAs in the different matrices shows that their abundance and ocean-atmosphere transfer are influenced by additional biotic and abiotic formation and degradation processes. Simple physicochemical parameters (e.g., surface activity) are not sufficient to describe the concentration and enrichments of the FAAs in the marine environment. For a precise representation in organic matter (OM) transfer models, further studies are needed to unravel their drivers and understand their composition.