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Aerosol size distribution and radiative forcing response to anthropogenically driven historical changes in biogenic secondary organic aerosol formation

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Figure 1. Absolute change inthe years 1000 and 2000 in mg m (a) isoprene, (c) monoterpene, and (e) sesquiterpene emissions between the years 1000–1010 and 1980–1990in mg m−2 day−1 from the MEGAN terpenoid reconstruction, and absolute change in (b) isoprene
Table 1. Summary of the GEOS-Chem-TOMAS simulations performed in this study. Biogenic emissions for year 1000 and 2000 usingMEGAN are decadal-averaged emissions for 1000–1010 and 1980–1990, respectively, whereas LPJ-GUESS biogenic emissions are annual-aver
Figure 2. Mean millennial fixed-yield biogenic SOA formation from (a) MEGAN emissions and (b) LPJ-GUESS emissions between theperiods 1000–2000 in mg m−2 day−1
Table 2. Summary of global, annual mean percent changes in N3, N10, N40, and N80 (number of particles with diameter greater than3, 10, 40, and 80 nm, respectively) when changing BVOC emissions from year 1000 to year 2000 using the MEGAN and LPJ-GUESSrecons
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