TY - JOUR
T1 - Multiple oceanic sources of alkylamines in Southern Ocean atmospheres
AU - Dall'osto, Manuel
AU - Fitzsimons, Mark
AU - Brean, James
AU - Akenga, Preston
AU - Jones, A
AU - Lachlan-Cope, Tom
AU - Sotomayor, Ana
AU - Berdalet, Elisa
AU - Vaque, Dolors
AU - Harrison, Roy
AU - Mansour, Karam
AU - Rinaldi, Matteo
AU - Decesari, Stefano
AU - Beddows, David
AU - Paglione, Marco
PY - 2025/12/12
Y1 - 2025/12/12
N2 - Measurements of pre-industrial conditions are of paramount importance for understanding historical climate change. The Southern Ocean and Antarctic continent are some of the least polluted environments on planet Earth. Alkylamines can rapidly partition into aerosols, increasing their mass, as well as form new particles altogether. We demonstrate the importance of pelagic “open ocean” (OO) and sympagic “sea ice” (SI) regions in supplying distinct organic nitrogen aerosol components. In the aerosol phase, dimethylamine (DMA) and trimethylamine (TMA) are both secondary, though DMA likely originates mainly from pelagic regions, while TMA is associated mainly with sympagic regions. Parallel measurements in ice and surface waters reveal that melting sea ice contains a factor of four more TMA than coastal Antarctic Peninsula waters; and seventeen times more TMA than OO regions - suggesting additional coastal Antarctic sources. To better interpret future climate change, we recommend employing regional atmospheric chemistry models to understand these diverse aerosol sources.
AB - Measurements of pre-industrial conditions are of paramount importance for understanding historical climate change. The Southern Ocean and Antarctic continent are some of the least polluted environments on planet Earth. Alkylamines can rapidly partition into aerosols, increasing their mass, as well as form new particles altogether. We demonstrate the importance of pelagic “open ocean” (OO) and sympagic “sea ice” (SI) regions in supplying distinct organic nitrogen aerosol components. In the aerosol phase, dimethylamine (DMA) and trimethylamine (TMA) are both secondary, though DMA likely originates mainly from pelagic regions, while TMA is associated mainly with sympagic regions. Parallel measurements in ice and surface waters reveal that melting sea ice contains a factor of four more TMA than coastal Antarctic Peninsula waters; and seventeen times more TMA than OO regions - suggesting additional coastal Antarctic sources. To better interpret future climate change, we recommend employing regional atmospheric chemistry models to understand these diverse aerosol sources.
UR - https://pearl.plymouth.ac.uk/gees-research/1534/
U2 - 10.1038/s41612-025-01284-6
DO - 10.1038/s41612-025-01284-6
M3 - Article
SN - 2397-3722
VL - 9
JO - npj Climate and Atmospheric Science
JF - npj Climate and Atmospheric Science
M1 - 12
ER -