Uncertainty in the representation of biomass burning (BB) aerosol composition and optical properties in climate models contributes to a range in modeled aerosol effects on incoming solar radiation. Depending on the model, the top-of-the-atmosphere BB aerosol effect can range from cooling to warming. By relating aerosol absorption relative to extinction and carbonaceous aerosol composition from 12 observational datasets to nine state-of-the-art Earth system models/chemical transport models, we identify varying degrees of overestimation in BB aerosol absorptivity by these models. Modifications to BB aerosol refractive index, size, and mixing state improve the Community Atmosphere Model version 5 (CAM5) agreement with observations, leading to a global change in BB direct radiative effect of −0.07 W m−2, and regional changes of −2 W m−2 (Africa) and −0.5 W m−2 (South America/Temperate). Our findings suggest that current modeled BB contributes less to warming than previously thought, largely due to treatments of aerosol mixing state.

Abstract. A recent development in the representation of aerosols in climate models is the realization that some components of organic aerosol (OA), emitted from biomass and biofuel burning, can have a significant contribution to shortwave radiation absorption in the atmosphere. The absorbing fraction of OA is referred to as brown carbon (BrC). This study introduces one of the first implementations of BrC into the Community Atmosphere Model version 5 (CAM5), using a parameterization for BrC absorptivity described in Saleh et al. (2014). Nine-year experiments are run (2003–2011) with prescribed emissions and sea surface temperatures to analyze the effect of BrC in the atmosphere. Model validation is conducted via model comparison to single-scatter albedo and aerosol optical depth from the Aerosol Robotic Network (AERONET). This comparison reveals a model underestimation of single scattering albedo (SSA) in biomass burning regions for both default and BrC model runs, while a comparison between AERONET and the model absorption Ångström exponent shows a marked improvement with BrC implementation. Global annual average radiative effects are calculated due to aerosol–radiation interaction (REari; 0.13±0.01 W m−2) and aerosol–cloud interaction (REaci; 0.01±0.04 W m−2). REari is similar to other studies' estimations of BrC direct radiative effect, while REaci indicates a global reduction in low clouds due to the BrC semi-direct effect. The mechanisms for these physical changes are investigated and found to correspond with changes in global circulation patterns. Comparisons of BrC implementation approaches find that this implementation predicts a lower BrC REari in the Arctic regions than previous studies with CAM5. Implementation of BrC bleaching effect shows a significant reduction in REari (0.06±0.008 W m−2). Also, variations in OA density can lead to differences in REari and REaci, indicating the importance of specifying this property when estimating the BrC radiative effects and when comparing similar studies.

Marine stratocumulus clouds cover nearly one-quarter of the ocean surface and thus play an extremely important role in determining the global radiative balance. The semipermanent marine stratocumulus deck over the southeastern Atlantic Ocean is of particular interest, because of its interactions with seasonal biomass burning aerosols that are emitted in southern Africa. Understanding the impacts of biomass burning aerosols on stratocumulus clouds and the implications for regional and global radiative balance is still very limited. Previous studies have focused on assessing the magnitude of the warming caused by solar scattering and absorption by biomass burning aerosols over stratocumulus (the direct radiative effect) or cloud adjustments to the direct radiative effect (the semidirect effect). Here, using a nested modeling approach in conjunction with observations from multiple satellites, we demonstrate that cloud condensation nuclei activated from biomass burning aerosols entrained into the stratocumulus (the microphysical effect) can play a dominant role in determining the total radiative forcing at the top of the atmosphere, compared with their direct and semidirect radiative effects. Biomass burning aerosols over the region and period with heavy loadings can cause a substantial cooling (daily mean -8.05 W m), primarily as a result of clouds brightening by reducing the cloud droplet size (the Twomey effect) and secondarily through modulating the diurnal cycle of cloud liquid water path and coverage (the cloud lifetime effect). Our results highlight the importance of realistically representing the interactions of stratocumulus with biomass burning aerosols in global climate models in this region.

Abstract. Aerosols from open-land fires could significantly perturb the global radiation balance and induce climate change. In this study, Community Atmosphere Model version 5 (CAM5) with prescribed daily fire aerosol emissions is used to investigate the spatial and seasonal characteristics of radiative effects (REs, relative to the case of no fires) of open-fire aerosols including black carbon (BC) and particulate organic matter (POM) from 2003 to 2011. The global annual mean RE from aerosol–radiation interactions (REari) of all fire aerosols is 0.16 ± 0.01 W m−2 (1σ uncertainty), mainly due to the absorption of fire BC (0.25 ± 0.01 W m−2), while fire POM induces a small effect (−0.05 and 0.04 ± 0.01 W m−2 based on two different methods). Strong positive REari is found in the Arctic and in the oceanic regions west of southern Africa and South America as a result of amplified absorption of fire BC above low-level clouds, in general agreement with satellite observations. The global annual mean RE due to aerosol–cloud interactions (REaci) of all fire aerosols is −0.70 ± 0.05 W m−2, resulting mainly from the fire POM effect (−0.59 ± 0.03 W m−2). REari (0.43 ± 0.03 W m−2) and REaci (−1.38 ± 0.23 W m−2) in the Arctic are stronger than in the tropics (0.17 ± 0.02 and −0.82 ± 0.09 W m−2 for REari and REaci), although the fire aerosol burden is higher in the tropics. The large cloud liquid water path over land areas and low solar zenith angle of the Arctic favor the strong fire aerosol REaci (up to −15 W m−2) during the Arctic summer. Significant surface cooling, precipitation reduction and increasing amounts of low-level cloud are also found in the Arctic summer as a result of the fire aerosol REaci based on the atmosphere-only simulations. The global annual mean RE due to surface-albedo changes (REsac) over land areas (0.03 ± 0.10 W m−2) is small and statistically insignificant and is mainly due to the fire BC-in-snow effect (0.02 W m−2) with the maximum albedo effect occurring in spring (0.12 W m−2) when snow starts to melt.