Aerosols interact with radiation and clouds. Substantial progress made over the past 40 years in observing, understanding, and modeling these processes helped quantify the imbalance in the Earth's radiation budget caused by anthropogenic aerosols, called aerosol radiative forcing, but uncertainties remain large. This review provides a new range of aerosol radiative forcing over the industrial era based on multiple, traceable, and arguable lines of evidence, including modeling approaches, theoretical considerations, and observations. Improved understanding of aerosol absorption and the causes of trends in surface radiative fluxes constrain the forcing from aerosol-radiation interactions. A robust theoretical foundation and convincing evidence constrain the forcing caused by aerosol-driven increases in liquid cloud droplet number concentration. However, the influence of anthropogenic aerosols on cloud liquid water content and cloud fraction is less clear, and the influence on mixed-phase and ice clouds remains poorly constrained. Observed changes in surface temperature and radiative fluxes provide additional constraints. These multiple lines of evidence lead to a 68% confidence interval for the total aerosol effective radiative forcing of -1.6 to -0.6 W m −2 , or -2.0 to -0.4 W m −2 with a 90% likelihood. Those intervals are of similar width to the last Intergovernmental Panel on Climate Change assessment but shifted toward more negative values. The uncertainty will narrow in the future by continuing to critically combine multiple lines of evidence, especially those addressing industrial-era changes in aerosol sources and aerosol effects on liquid cloud amount and on ice clouds. Plain Language SummaryHuman activities emit into the atmosphere small liquid and solid particles called aerosols. Those aerosols change the energy budget of the Earth and trigger climate changes, by scattering and absorbing solar and terrestrial radiation and playing important roles in the formation of

Anthropogenic aerosol interacts strongly with incoming solar radiation, perturbing the Earth's energy budget and precipitation on both local and global scales. Understanding these changes in precipitation has proven particularly difficult for the case of absorbing aerosol, which absorbs a significant amount of incoming solar radiation and hence acts as a source of localized diabatic heating to the atmosphere. In this work, we use an ensemble of atmosphere-only climate model simulations forced by identical aerosol absorption perturbations across the globe to develop a basic physical understanding of how this localized heating impacts the atmosphere and how these changes impact on precipitation both globally and locally. In agreement with previous studies we find that aerosol absorption causes a decrease in global-mean precipitation, but we also show that even for identical aerosol optical depth perturbations, the global-mean precipitation change varies by over an order-of-magnitude depending on the location of the aerosol burden. Our experiments also demonstrate that the local precipitation response to aerosol absorption is opposite in sign between the tropics and the extratropics, as found by previous work. We then show that this contrasting response can be understood in terms of different mechanisms by which the large-scale circulation responds to heating in the extratropics and in the tropics. We provide a simple theory to explain variations in the local precipitation response to tropical aerosol absorption. Our work highlights that the spatial pattern of aerosol absorption and its interactions with circulation are a key determinant of its overall climate impact and must be taken into account when developing our understanding of aerosol-climate interactions.

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