Letter | Published:

Aerosols implicated as a prime driver of twentieth-century North Atlantic climate variability

Nature volume 484, pages 228232 (12 April 2012) | Download Citation


  • An Erratum to this article was published on 02 May 2012


Systematic climate shifts have been linked to multidecadal variability in observed sea surface temperatures in the North Atlantic Ocean1. These links are extensive, influencing a range of climate processes such as hurricane activity2 and African Sahel3,4,5 and Amazonian5 droughts. The variability is distinct from historical global-mean temperature changes and is commonly attributed to natural ocean oscillations6,7,8,9,10. A number of studies have provided evidence that aerosols can influence long-term changes in sea surface temperatures11,12, but climate models have so far failed to reproduce these interactions6,9 and the role of aerosols in decadal variability remains unclear. Here we use a state-of-the-art Earth system climate model to show that aerosol emissions and periods of volcanic activity explain 76 per cent of the simulated multidecadal variance in detrended 1860–2005 North Atlantic sea surface temperatures. After 1950, simulated variability is within observational estimates; our estimates for 1910–1940 capture twice the warming of previous generation models but do not explain the entire observed trend. Other processes, such as ocean circulation, may also have contributed to variability in the early twentieth century. Mechanistically, we find that inclusion of aerosol–cloud microphysical effects, which were included in few previous multimodel ensembles, dominates the magnitude (80 per cent) and the spatial pattern of the total surface aerosol forcing in the North Atlantic. Our findings suggest that anthropogenic aerosol emissions influenced a range of societally important historical climate events such as peaks in hurricane activity and Sahel drought. Decadal-scale model predictions of regional Atlantic climate will probably be improved by incorporating aerosol–cloud microphysical interactions and estimates of future concentrations of aerosols, emissions of which are directly addressable by policy actions.

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We are grateful for discussion and input from D. Smith, D. Sexton, J. Murphy, M. Palmer, C. Roberts and J. Knight during the analysis and writing of this paper. We acknowledge the modelling groups, the Program for Climate Model Diagnosis and Intercomparison and the WCRP’s Working Group on Coupled Modelling for their roles in making available the WCRP CMIP3 multimodel data set. Support of this data set is provided by the Office of Science, US Department of Energy. The authors were supported by the Joint DECC/Defra Met Office Hadley Centre Climate Programme (GA01101) and the EU FP7 THOR project.

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Author notes

    • Nick J. Dunstone
    •  & Paul R. Halloran

    These authors contributed equally to this work.


  1. Met Office Hadley Centre, FitzRoy Road, Exeter EX1 3PB, UK

    • Ben B. B. Booth
    • , Nick J. Dunstone
    • , Paul R. Halloran
    • , Timothy Andrews
    •  & Nicolas Bellouin


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B.B.B.B., N.J.D. and P.R.H. jointly led the analysis, produced figures and wrote the paper. T.A. and N.B. contributed additional experiments to diagnose different aspects of the aerosol forcing, provided technical and scientific insight and commented on the manuscript.

Competing interests

The authors declare no competing financial interests.

Corresponding author

Correspondence to Ben B. B. Booth.

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    Supplementary Information

    This file contains a Supplementary Discussion, Supplementary Figures 1-8, Supplementary Tables 1-2 and additional references.

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