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Using an aerosol–climate coupled model, this paper has investigated the changes in distributions of anthropogenic and natural particles due to 4 × CO2-induced global warming, under the low emission scenario of Representative Concentration Pathway 4.5 (RCP4.5). Special attention is paid to the seasonal variations of aerosol size modes. With rising CO2 levels, surface warming, and changes in atmospheric circulations and hydrologic cycles are found during both summer (JJA) and winter (DJF). For anthropogenic particles, changes in fine anthropogenic particulate matter (PM2.5, particles with diameters smaller than 2.5 μm) decrease over high-latitude regions and increase over the tropics in both DJF and JJA. Global mean column concentrations of PM2.5 decrease by approximately 0.19 mg m−2, and concentrations of coarse anthropogenic particles (CPM, particles with diameters larger than 2.5 μm) increase by 0.005 mg m−2 in JJA. Changes in anthropogenic particles in DJF are similar to those in JJA, but the magnitudes of maximum regional changes are much smaller than those in JJA. The coarse anthropogenic particles (CPM, particles with diameters larger than 2.5 μm) increase over northern Africa and the Arabian Peninsula during JJA, whereas changes in anthropogenic CPM during DJF are minimal. During both JJA and DJF, changes in anthropogenic CPM are about two orders of magnitude smaller than those of anthropogenic PM2.5. Enhanced wet deposition by large-scale precipitation under rising CO2-induced surface warming is the critical factor affecting changes in anthropogenic particles. For natural particles, the distribution of change in the natural PM2.5 burden is similar to that of natural CPM, but much larger than natural CPM during each season. Both natural PM2.5 and CPM burdens increase over northern Africa and the Arabian Peninsula during JJA, but decrease over most of the continental regions during DJF. Changes in surface wind speed, divergence/convergence of surface wind, and precipitation are primary reasons for the variation of natural particles. [ABSTRACT FROM AUTHOR]

A key goal of the Paris Agreement (PA) is to reach net-zero greenhouse gas (GHG) emissions by 2050 globally, which requires mitigation efforts from all countries. Africa's rapidly growing population and gross domestic product (GDP) make this continent important for GHG emission trends. In this paper, we study the emissions of carbon dioxide (CO 2), methane (CH 4) and nitrous oxide (N 2 O) in Africa over 3 decades (1990–2018). We compare bottom-up (BU) approaches, including United Nations Convention Framework on Climate Change (UNFCCC) national inventories, FAO, PRIMAP-hist, process-based ecosystem models for CO 2 fluxes in the land use, land use change and forestry (LULUCF) sector and global atmospheric inversions. For inversions, we applied different methods to separate anthropogenic CH 4 emissions. The BU inventories show that, over the decade 2010–2018, fewer than 10 countries represented more than 75 % of African fossil CO 2 emissions. With a mean of 1373 Mt CO 2 yr -1 , total African fossil CO 2 emissions over 2010–2018 represent only 4 % of global fossil emissions. However, these emissions grew by +34% from 1990–1999 to 2000–2009 and by +31% from 2000–2009 to 2010–2018, which represents more than a doubling in 30 years. This growth rate is more than 2 times faster than the global growth rate of fossil CO 2 emissions. The anthropogenic emissions of CH 4 grew by 5 % from 1990–1999 to 2000–2009 and by 14.8 % from 2000–2009 to 2010–2018. The N 2 O emissions grew by 19.5 % from 1990–1999 to 2000–2009 and by 20.8 % from 2000–2009 to 2010–2018. When using the mean of the estimates from UNFCCC reports (including the land use sector) with corrections from outliers, Africa was a mean source of greenhouse gases of 262221863239 Mt CO 2 eq. yr -1 from all BU estimates (the subscript and superscript indicate min–max range uncertainties) and of +263717615873 Mt CO 2 eq. yr -1 from top-down (TD) methods during their overlap period from 2001 to 2017. Although the mean values are consistent, the range of TD estimates is larger than the one of the BU estimates, indicating that sparse atmospheric observations and transport model errors do not allow us to use inversions to reduce the uncertainty in BU estimates. The main source of uncertainty comes from CO 2 fluxes in the LULUCF sector, for which the spread across inversions is larger than 50 %, especially in central Africa. Moreover, estimates from national UNFCCC communications differ widely depending on whether the large sinks in a few countries are corrected to more plausible values using more recent national sources following the methodology of Grassi et al. (2022). The medians of CH 4 emissions from inversions based on satellite retrievals and surface station networks are consistent with each other within 2 % at the continental scale. The inversion ensemble also provides consistent estimates of anthropogenic CH 4 emissions with BU inventories such as PRIMAP-hist. For N 2 O, inversions systematically show higher emissions than inventories, on average about 4.5 times more than PRIMAP-hist, either because natural N 2 O sources cannot be separated accurately from anthropogenic ones in inversions or because BU estimates ignore indirect emissions and underestimate emission factors. Future improvements can be expected thanks to a denser network of monitoring atmospheric concentrations. This study helps to introduce methods to enhance the scope of use of various published datasets and allows us to compute budgets thanks to recombinations of those data products. Our results allow us to understand uncertainty and trends in emissions and removals in a region of the world where few observations exist and where most inventories are based on default IPCC guideline values. The results can therefore serve as a support tool for the Global Stocktake (GST) of the Paris Agreement. The referenced datasets related to the figures are available at 10.5281/zenodo.7347077 (Mostefaoui et al., 2022). [ABSTRACT FROM AUTHOR]