TY - JOUR
T1 - Warming-induced increase in aerosol number concentration likely to moderate climate change
AU - Paasonen, Pauli
AU - Asmi, Ari
AU - Petaja, Tuukka
AU - Kajos, Maija K.
AU - Aijala, Mikko
AU - Junninen, Heikki
AU - Holst, Thomas
AU - Abbatt, Jonathan P. D.
AU - Arneth, Almut
AU - Birmili, Wolfram
AU - van der Gon, Hugo Denier
AU - Hamed, Amar
AU - Hoffer, Andras
AU - Laakso, Lauri
AU - Laaksonen, Ari
AU - Leaitch, W. Richard
AU - Plass-Duelmer, Christian
AU - Pryor, Sara C.
AU - Raisanen, Petri
AU - Swietlicki, Erik
AU - Wiedensohler, Alfred
AU - Worsnop, Douglas R.
AU - Kerminen, Veli-Matti
AU - Kulmala, Markku
N1 - The information about affiliations in this record was updated in December 2015.
The record was previously connected to the following departments: Nuclear Physics (Faculty of Technology) (011013007), Dept of Physical Geography and Ecosystem Science (011010000)
PY - 2013
Y1 - 2013
N2 - Atmospheric aerosol particles influence the climate system directly by scattering and absorbing solar radiation, and indirectly by acting as cloud condensation nuclei(1-4). Apart from black carbon aerosol, aerosols cause a negative radiative forcing at the top of the atmosphere and substantially mitigate the warming caused by greenhouse gases(1). In the future, tightening of controls on anthropogenic aerosol and precursor vapour emissions to achieve higher air quality may weaken this beneficial effect(5-)7. Natural aerosols, too, might affect future warming(2,3,8,9). Here we analyse long-term observations of concentrations and compositions of aerosol particles and their biogenic precursor vapours in continental mid-and high-latitude environments. We use measurements of particle number size distribution together with boundary layer heights derived from reanalysis data to show that the boundary layer burden of cloud condensation nuclei increases exponentially with temperature. Our results confirm a negative feedback mechanism between the continental biosphere, aerosols and climate: aerosol cooling effects are strengthened by rising biogenic organic vapour emissions in response to warming, which in turn enhance condensation on particles and their growth to the size of cloud condensation nuclei. This natural growth mechanism produces roughly 50% of particles at the size of cloud condensation nuclei across Europe. We conclude that biosphere-atmosphere interactions are crucial for aerosol climate effects and can significantly influence the effects of anthropogenic aerosol emission controls, both on climate and air quality.
AB - Atmospheric aerosol particles influence the climate system directly by scattering and absorbing solar radiation, and indirectly by acting as cloud condensation nuclei(1-4). Apart from black carbon aerosol, aerosols cause a negative radiative forcing at the top of the atmosphere and substantially mitigate the warming caused by greenhouse gases(1). In the future, tightening of controls on anthropogenic aerosol and precursor vapour emissions to achieve higher air quality may weaken this beneficial effect(5-)7. Natural aerosols, too, might affect future warming(2,3,8,9). Here we analyse long-term observations of concentrations and compositions of aerosol particles and their biogenic precursor vapours in continental mid-and high-latitude environments. We use measurements of particle number size distribution together with boundary layer heights derived from reanalysis data to show that the boundary layer burden of cloud condensation nuclei increases exponentially with temperature. Our results confirm a negative feedback mechanism between the continental biosphere, aerosols and climate: aerosol cooling effects are strengthened by rising biogenic organic vapour emissions in response to warming, which in turn enhance condensation on particles and their growth to the size of cloud condensation nuclei. This natural growth mechanism produces roughly 50% of particles at the size of cloud condensation nuclei across Europe. We conclude that biosphere-atmosphere interactions are crucial for aerosol climate effects and can significantly influence the effects of anthropogenic aerosol emission controls, both on climate and air quality.
U2 - 10.1038/NGEO1800
DO - 10.1038/NGEO1800
M3 - Article
SN - 1752-0908
VL - 6
SP - 438
EP - 442
JO - Nature Geoscience
JF - Nature Geoscience
IS - 6
ER -