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Abstract. Changes in anthropogenic aerosol emissions have strongly contributed to global and regional trends in temperature, precipitation, and other climate characteristics and have been one of the dominant drivers of decadal trends in Asian and African precipitation. These and other influences on regional climate from changes in aerosol emissions are expected to continue and potentially strengthen in the coming decades. However, a combination of large uncertainties in emission pathways, radiative forcing, and the dynamical response to forcing makes anthropogenic aerosol a key factor in the spread of near-term climate projections, particularly on regional scales, and therefore an important one to constrain. For example, in terms of future emission pathways, the uncertainty in future global aerosol and precursor gas emissions by 2050 is as large as the total increase in emissions since 1850. In terms of aerosol effective radiative forcing, which remains the largest source of uncertainty in future climate change projections, CMIP6 models span a factor of 5, from −0.3 to −1.5 W m−2. Both of these sources of uncertainty are exacerbated on regional scales. The Regional Aerosol Model Intercomparison Project (RAMIP) will deliver experiments designed to quantify the role of regional aerosol emissions changes in near-term projections. This is unlike any prior MIP, where the focus has been on changes in global emissions and/or very idealised aerosol experiments. Perturbing regional emissions makes RAMIP novel from a scientific standpoint and links the intended analyses more directly to mitigation and adaptation policy issues. From a science perspective, there is limited information on how realistic regional aerosol emissions impact local as well as remote climate conditions. Here, RAMIP will enable an evaluation of the full range of potential influences of realistic and regionally varied aerosol emission changes on near-future climate. From the policy perspective, RAMIP addresses the burning question of how local and remote decisions affecting emissions of aerosols influence climate change in any given region. Here, RAMIP will provide the information needed to make direct links between regional climate policies and regional climate change. RAMIP experiments are designed to explore sensitivities to aerosol type and location and provide improved constraints on uncertainties driven by aerosol radiative forcing and the dynamical response to aerosol changes. The core experiments will assess the effects of differences in future global and regional (Africa and the Middle East, East Asia, North America and Europe, and South Asia) aerosol emission trajectories through 2051, while optional experiments will test the nonlinear effects of varying emission locations and aerosol types along this future trajectory. All experiments are based on the shared socioeconomic pathways and are intended to be performed with 6th Climate Model Intercomparison Project (CMIP6) generation models, initialised from the CMIP6 historical experiments, to facilitate comparisons with existing projections. Requested outputs will enable the analysis of the role of aerosol in near-future changes in, for example, temperature and precipitation means and extremes, storms, and air quality.

With continued fossil‐fuel dependence, anthropogenic aerosols over South Asia are projected to increase until the mid‐21st century along with greenhouse gases (GHGs). Using the Community Earth System Model (CESM1) Large Ensemble, we quantify the influence of aerosols and GHGs on South Asian seasonal precipitation patterns over the 21st century under a very high‐emissions (RCP 8.5) trajectory. We find that increasing local aerosol concentrations could continue to suppress precipitation over South Asia in the near‐term, delaying the emergence of precipitation increases in response to GHGs by several decades in the monsoon season and a decade in the post‐monsoon season. Emergence of this wetting signal is expected in both seasons by the mid‐21st century. Our results demonstrate that the trajectory of local aerosols together with GHGs will shape near‐future precipitation patterns over South Asia. Therefore, constraining precipitation response to different trajectories of both forcers is critical for informing near‐term adaptation efforts.

The distribution of anthropogenic aerosols’ climate effects depends on the geographic distribution of the aerosols themselves. Yet many scientific and policy discussions ignore the role of emission location when evaluating aerosols’ climate impacts. Here, we present new climate model results demonstrating divergent climate responses to a fixed amount and composition of aerosol—emulating China’s present-day emissions—emitted from 8 key geopolitical regions. The aerosols’ global-mean cooling effect is fourteen times greater when emitted from the highest impact emitting region (Western Europe) than from the lowest (India). Further, radiative forcing, a widely used climate response proxy, fails as an effective predictor of global-mean cooling for national-scale aerosol emissions in our simulations; global-mean forcing-to-cooling efficacy differs fivefold depending on emitting region. This suggests that climate accounting should differentiate between aerosols emitted from different countries and that aerosol emissions’ evolving geographic distribution will impact the global-scale magnitude and spatial distribution of climate change.

Despite distinct geographic distributions of top-of-the-atmosphere radiative forcing, anthropogenic greenhouse gases and aerosols have been found to produce similar patterns of climate response in atmosphere-and-ocean coupled climate model simulations. Understanding surface energy flux changes, a crucial pathway by which atmospheric forcing is communicated to the ocean, is a vital bridge to explaining the similar full atmosphere-and-ocean responses to these disparate forcings. Here we analyze the fast, atmosphere-driven change in surface energy flux caused by present-day greenhouse gases vs aerosols to elucidate its role in shaping the subsequent slow, coupled response. We find that the surface energy flux response patterns achieve roughly two-thirds of the anti-correlation seen in the fully coupled response, driven by Rossby waves excited by symmetric changes to the land–sea contrast. Our results suggest that atmosphere and land surface processes are capable of achieving substantial within-hemisphere homogenization in the climate response to disparate forcers on fast, societally-relevant timescales.