Cold oceans enhance terrestrial new-particle formation in near-coastal forests

The world's forests produce atmospheric aerosol by emitting volatile organic compounds (VOC) which, after being oxidized in the atmosphere, readily condense on the omnipresent nanometer-sized nuclei and grow them to climatically relevant sizes. The cooling effect of aerosols is the greatest unc...

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Main Authors: M. Kulmala, S. Sevanto, P. Briggs, E. van Gorsel, H. Cleugh, T. Kurtén, J. Bäck, H. Hakola, J. Lauros, L. Sogacheva, T. Suni
Format: Article
Language:English
Published: Copernicus Publications 2009-11-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/9/8639/2009/acp-9-8639-2009.pdf
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spelling doaj-7679cb4fd5bd4978b36426514d8e3dd12020-11-24T20:44:51ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242009-11-0192286398650Cold oceans enhance terrestrial new-particle formation in near-coastal forestsM. KulmalaS. SevantoP. BriggsE. van GorselH. CleughT. KurténJ. BäckH. HakolaJ. LaurosL. SogachevaT. SuniThe world's forests produce atmospheric aerosol by emitting volatile organic compounds (VOC) which, after being oxidized in the atmosphere, readily condense on the omnipresent nanometer-sized nuclei and grow them to climatically relevant sizes. The cooling effect of aerosols is the greatest uncertainty in current climate models and estimates of radiative forcing. Therefore, identifying the environmental factors influencing the biogenic formation of aerosols is crucial. In this paper, we connected biogenic aerosol formation events observed in a Eucalypt forest in South-East Australia during July 2005–December 2006 to air mass history using 96-h back trajectories. Formation of new particles was most frequent in the dry westerly and south-westerly air masses. According to NDVI (Normalized Difference Vegetation Index) measurements, photosynthesis was not significantly higher in this direction compared to the north-east direction. It is unlikely, therefore, that differences in photosynthesis-derived organic precursor emissions would have been significant enough to lead to the clear difference in NPF frequency between these two directions. Instead, the high evaporation rates above the Pacific Ocean resulted in humid winds from the north-east that effectively suppressed new-particle formation in the forest hundreds of kilometers inland. No other factor varied as significantly in tune with new-particle formation as humidity and we concluded that, in addition to local meteorological factors in the forest, the magnitude of evaporation from oceans hundreds of kilometers upwind can effectively suppress or enhance new-particle formation. Our findings indicate that, unlike warm waters, the cold polar oceans provide excellent clean and dry background air that enhances aerosol formation above near-coastal forests in Fennoscandia and South-East Australia. http://www.atmos-chem-phys.net/9/8639/2009/acp-9-8639-2009.pdf
collection DOAJ
language English
format Article
sources DOAJ
author M. Kulmala
S. Sevanto
P. Briggs
E. van Gorsel
H. Cleugh
T. Kurtén
J. Bäck
H. Hakola
J. Lauros
L. Sogacheva
T. Suni
spellingShingle M. Kulmala
S. Sevanto
P. Briggs
E. van Gorsel
H. Cleugh
T. Kurtén
J. Bäck
H. Hakola
J. Lauros
L. Sogacheva
T. Suni
Cold oceans enhance terrestrial new-particle formation in near-coastal forests
Atmospheric Chemistry and Physics
author_facet M. Kulmala
S. Sevanto
P. Briggs
E. van Gorsel
H. Cleugh
T. Kurtén
J. Bäck
H. Hakola
J. Lauros
L. Sogacheva
T. Suni
author_sort M. Kulmala
title Cold oceans enhance terrestrial new-particle formation in near-coastal forests
title_short Cold oceans enhance terrestrial new-particle formation in near-coastal forests
title_full Cold oceans enhance terrestrial new-particle formation in near-coastal forests
title_fullStr Cold oceans enhance terrestrial new-particle formation in near-coastal forests
title_full_unstemmed Cold oceans enhance terrestrial new-particle formation in near-coastal forests
title_sort cold oceans enhance terrestrial new-particle formation in near-coastal forests
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2009-11-01
description The world's forests produce atmospheric aerosol by emitting volatile organic compounds (VOC) which, after being oxidized in the atmosphere, readily condense on the omnipresent nanometer-sized nuclei and grow them to climatically relevant sizes. The cooling effect of aerosols is the greatest uncertainty in current climate models and estimates of radiative forcing. Therefore, identifying the environmental factors influencing the biogenic formation of aerosols is crucial. In this paper, we connected biogenic aerosol formation events observed in a Eucalypt forest in South-East Australia during July 2005–December 2006 to air mass history using 96-h back trajectories. Formation of new particles was most frequent in the dry westerly and south-westerly air masses. According to NDVI (Normalized Difference Vegetation Index) measurements, photosynthesis was not significantly higher in this direction compared to the north-east direction. It is unlikely, therefore, that differences in photosynthesis-derived organic precursor emissions would have been significant enough to lead to the clear difference in NPF frequency between these two directions. Instead, the high evaporation rates above the Pacific Ocean resulted in humid winds from the north-east that effectively suppressed new-particle formation in the forest hundreds of kilometers inland. No other factor varied as significantly in tune with new-particle formation as humidity and we concluded that, in addition to local meteorological factors in the forest, the magnitude of evaporation from oceans hundreds of kilometers upwind can effectively suppress or enhance new-particle formation. Our findings indicate that, unlike warm waters, the cold polar oceans provide excellent clean and dry background air that enhances aerosol formation above near-coastal forests in Fennoscandia and South-East Australia.
url http://www.atmos-chem-phys.net/9/8639/2009/acp-9-8639-2009.pdf
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