Abstract. A total of 252 emission plumes of ships operating in the
Mediterranean Sea and around the Arabian Peninsula were investigated using a
comprehensive dataset of gas- and submicron-particle-phase properties
measured during the 2-month shipborne AQABA (Air Quality and Climate Change in the Arabian Basin) field campaign in summer
2017. The post-measurement identification of the corresponding ship
emission events in the measured data included the determination of the plume
sources (up to 38 km away) as well as the plume ages (up to 115 min) and
was based on commercially available historical records of the Automatic
Identification System. The dispersion lifetime of chemically inert CO2
in the ship emission plumes was determined as 70±15 min, resulting
in levels indistinguishable from the marine background after 260±60 min. Emission factors (EFs) as quantities that are independent of plume
dilution were calculated and used for the investigation of influences on
ship emission plumes caused by ship characteristics and the combustion
process as well as by atmospheric processes during the early stage of
exhaust release and during plume ageing. Combustion efficiency and therefore
emission factors of black carbon and NOx were identified to depend
mostly on the vessel speed and gross tonnage. Moreover, larger ships,
associated with higher engine power, were found to use fuel with higher
sulfur content and have higher gas-phase SO2, particulate sulfate,
particulate organics, and particulate matter EFs. Despite the independence of
EFs of dilution, a significant influence of the ambient wind speed on the
particle number and mass EFs was observed that can be traced back to
enhanced particle coagulation in the case of slower dilution and suppressed
vapour condensation on particles in the case of faster dilution of the emission
plume. Atmospheric reactions and processes in ship emission plumes were
investigated that include NOx and O3 chemistry, gas-to-particle
conversion of NOx and SO2, and the neutralisation of acids in the
particle phase through the uptake of ambient gas-phase ammonia, the latter
two of which cause the inorganic particulate content to increase and the
organic fraction to decrease with increasing plume age. The results allow for us to
describe the influences on (or processes in) ship emission plumes
quantitatively by parameterisations, which could be used for further
refinement of atmospheric models, and to identify which of these processes
are the most important ones.