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Abstract Many regions of the planet have experienced an increase in fire activity in recent decades. Although such increases are consistent with warming and drying under continued climate change, the driving mechanisms remain uncertain. Here, we investigate the effects of increasing atmospheric carbon dioxide concentrations on future fire activity using seven Earth system models. Centered on the time of carbon dioxide doubling, the multi-model mean percent change in fire carbon emissions is 66.4 ± 38.8% (versus 1850 carbon dioxide concentrations, under fixed 1850 land-use conditions). A substantial increase is associated with enhanced vegetation growth due to carbon dioxide biogeochemical impacts at 60.1 ± 46.9%. In contrast, carbon dioxide radiative impacts, including warming and drying, yield a negligible response of fire carbon emissions at 1.7 ± 9.4%. Although model representation of fire processes remains uncertain, our results show the importance of vegetation dynamics to future increases in fire activity under increasing carbon dioxide, with potentially important policy implications. 

Abstract. Recent analyses show the importance of methane shortwave absorption, which many climate models lack. In particular, Allen et al. (2023) used idealized climate model simulations to show that methane shortwave absorption mutes up to 30 % of the surface warming and 60 % of the precipitation increase associated with its longwave radiative effects. Here, we explicitly quantify the radiative and climate impacts due to shortwave absorption of the present-day methane perturbation. Our results corroborate the hypothesis that present-day methane shortwave absorption mutes the warming effects of longwave absorption. For example, the global mean cooling in response to the present-day methane shortwave absorption is -0.10±0.07 K, which offsets 28 % (7 %–55 %) of the surface warming associated with present-day methane longwave radiative effects. The precipitation increase associated with the longwave radiative effects of the present-day methane perturbation (0.012±0.006 mm d−1) is also muted by shortwave absorption but not significantly so (-0.008±0.009 mm d−1). The unique responses to methane shortwave absorption are related to its negative top-of-the-atmosphere effective radiative forcing but positive atmospheric heating and in part to methane's distinctive vertical atmospheric solar heating profile. We also find that the present-day methane shortwave radiative effects, relative to its longwave radiative effects, are about 5 times larger than those under idealized carbon dioxide perturbations. Additional analyses show consistent but non-significant differences between the longwave versus shortwave radiative effects for both methane and carbon dioxide, including a stronger (negative) climate feedback when shortwave radiative effects are included (particularly for methane). We conclude by reiterating that methane remains a potent greenhouse gas. 

Abstract. In 2020 the International Maritime Organization (IMO) implemented strict new regulations on the emissions of sulphate aerosol from the world's shipping fleet. This can be expected to lead to a reduction in aerosol-driven cooling, unmasking a portion of greenhouse gas warming. The magnitude of the effect is uncertain, however, due to the large remaining uncertainties in the climate response to aerosols. Here, we investigate this question using an 18-member ensemble of fully coupled climate simulations evenly sampling key modes of climate variability with the NCAR CESM2 model. We show that while there is a clear physical response of the climate system to the IMO regulations, including a surface temperature increase, we do not find global mean temperature influence that is significantly different from zero. The 20-year average global mean warming for 2020–2040 is +0.03 °C, with a 5–95 % confidence range of [-0.09, 0.19], reflecting the weakness of the perturbation relative to internal variability. We do, however, find a robust, non-zero regional temperature response in part of the North Atlantic. We also find that the maximum annual-mean ensemble-mean warming occurs around a decade after the perturbation in 2029, which means that the IMO regulations have likely had very limited influence on observed global warming to date. We further discuss our results in light of other, recent publications that have reached different conclusions. Overall, while the IMO regulations may contribute up to at 0.16 °C [-0.17, 0.52] to the global mean surface temperature in individual years during this decade, consistent with some early studies, such a response is unlikely to have been discernible above internal variability by the end of 2023 and is in fact consistent with zero throughout the 2020–2040 period. 

Abstract. Wildfires in the southwestern United States, particularly in northern California (nCA), have grown in size and severity in the past decade. As they have grown larger, they have been associated with large emissions of absorbing aerosols and heat into the troposphere. Utilizing satellite observations from MODIS, CERES, and AIRS as well as reanalysis from MERRA-2, the meteorology associated with fires during the wildfire season (June–October) was discerned over the nCA-NV (northern California and Nevada) region during the period 2003–2022. Wildfires in the region have a higher probability of occurring on days of positive temperature (T) anomalies and negative relative humidity (RH) anomalies, making it difficult to discern the radiative effects of aerosols that are concurrent with fires. To attempt to better isolate the effects of large fire emissions on meteorological variables, such as clouds and precipitation, variable anomalies on high fire emission days (90th percentile) were compared with low fire emission days (10th percentile) and were further stratified based on whether surface relative humidity (RHs) was anomalously high (75th percentile) or low (25th percentile) compared with typical fire season conditions. Comparing the simultaneously high fire emission and high RHs data with the simultaneously low fire emission and high RHs data, positive tropospheric T anomalies were found to be concurrent with positive AOD anomalies. Further investigation found that due to shortwave absorption, the aerosols heat the atmosphere at a rate of 0.041 ± 0.016 to 0.093 ± 0.019 K d−1, depending on whether RH conditions are anomalously positive or negative. The positive T anomalies were associated with significant negative 850–300 hPa RH anomalies during both 75th percentile RHs conditions. Furthermore, high fire emission days under high RHs conditions are associated with negative CF anomalies that are concurrent with the negative RH anomalies. This negative CF anomaly is associated with a significantly negative regional precipitation anomaly and a positive net top-of-atmosphere radiative flux anomaly (a warming effect) in certain areas. The T, RH, and CF anomalies under the simultaneously high fire emission and high RHs conditions compared with the simultaneously low fire emission and high RHs conditions have a significant spatial correlation with AOD anomalies. Additionally, the vertical profile of these variables under the same stratification is consistent with positive black carbon mass mixing ratio anomalies from MERRA-2. However, causality is difficult to discern, and further study is warranted to determine to what extent the aerosols are contributing to these anomalies. 

Considerable interest exists in understanding how climate change affects wildfire activity. Here, we use the Community Earth System Model version 2 to show that future anthropogenic aerosol mitigation yields larger increases in fire activity in the Northern Hemisphere boreal forests, relative to a base simulation that lacks climate policy and has large increases in greenhouse gases. The enhanced fire response is related to a deeper layer of summertime soil drying, consistent with increased downwelling surface shortwave radiation and enhanced surface evapotranspiration. In contrast, soil column drying is muted under increasing greenhouse gases due to plant physiological responses to increased carbon dioxide and by enhanced melting of soil ice at a depth that increases soil liquid water. Although considerable uncertainty remains in the representation of fire processes in models, our results suggest that boreal forest fires may be more sensitive to future aerosol mitigation than to greenhouse gas–driven warming. 

Abstract The ocean’s major circulation system, the Atlantic Meridional Overturning Circulation (AMOC), is slowing down. Such weakening is consistent with warming associated with increasing greenhouse gases, as well as with recent decreases in industrial aerosol pollution. The impact of biomass burning aerosols on the AMOC, however, remains unexplored. Here, we use the Community Earth System Model version 1 Large Ensemble to quantify the impact of both aerosol types on the AMOC. Despite relatively small changes in North Atlantic biomass burning aerosols, significant AMOC evolution occurs, including weakening from 1920 to ~1970 followed by AMOC strengthening. These changes are largely out of phase relative to the corresponding AMOC evolution under industrial aerosols. AMOC responses are initiated by thermal changes in sea surface density flux due to altered shortwave radiation. An additional dynamical mechanism involving the North Atlantic sea-level pressure gradient is important under biomass-burning aerosols. AMOC-induced ocean salinity flux convergence acts as a positive feedback. Our results show that biomass-burning aerosols reinforce early 20th-century AMOC weakening associated with greenhouse gases and also partially mute industrial aerosol impacts on the AMOC. Recent increases in wildfires suggest biomass-burning aerosols may be an important driver of future AMOC variability. 

Abstract In the era of escalating climate change, understanding human impacts on marine heatwaves (MHWs) becomes essential. This study harnesses climate model historical and single forcing simulations to delve into the individual roles of anthropogenic greenhouse gases (GHGs) and aerosols in shaping the characteristics of global MHWs over the past several decades. The results suggest that GHG variations lead to longer-lasting, more frequent, and intense MHWs. In contrast, anthropogenic aerosols markedly curb the intensity and growth of MHWs. Further analysis of the sea surface temperature (SST) probability distribution reveals that anthropogenic GHGs and aerosols have opposing effects on the tails of the SST probability distribution, causing the tails to expand and contract, respectively. Climate extremes such as MHWs are accordingly promoted and reduced. Our study underscores the significant impacts of anthropogenic GHGs and aerosols on MHWs, which go far beyond the customary concept that these anthropogenic forcings modulate climate extremes by shifting global SST probabilities via modifying the mean-state SST. 

Abstract Although greenhouse gases absorb primarily long-wave radiation, they also absorb short-wave radiation. Recent studies have highlighted the importance of methane short-wave absorption, which enhances its stratospherically adjusted radiative forcing by up to ~ 15%. The corresponding climate impacts, however, have been only indirectly evaluated and thus remain largely unquantified. Here we present a systematic, unambiguous analysis using one model and separate simulations with and without methane short-wave absorption. We find that methane short-wave absorption counteracts ~30% of the surface warming associated with its long-wave radiative effects. An even larger impact occurs for precipitation as methane short-wave absorption offsets ~60% of the precipitation increase relative to its long-wave radiative effects. The methane short-wave-induced cooling is due largely to cloud rapid adjustments, including increased low-level clouds, which enhance the reflection of incoming short-wave radiation, and decreased high-level clouds, which enhance outgoing long-wave radiation. The cloud responses, in turn, are related to the profile of atmospheric solar heating and corresponding changes in temperature and relative humidity. Despite our findings, methane remains a potent contributor to global warming, and efforts to reduce methane emissions are vital for keeping global warming well below 2 °C above preindustrial values. 

Abstract Previous studies suggest that greenhouse gas-induced warming can lead to increased fine particulate matter concentrations and degraded air quality. However, significant uncertainties remain regarding the sign and magnitude of the response to warming and the underlying mechanisms. Here, we show that thirteen models from the Coupled Model Intercomparison Project Phase 6 all project an increase in global average concentrations of fine particulate matter in response to rising carbon dioxide concentrations, but the range of increase across models is wide. The two main contributors to this increase are increased abundance of dust and secondary organic aerosols via intensified West African monsoon and enhanced emissions of biogenic volatile organic compounds, respectively. Much of the inter-model spread is related to different treatment of biogenic volatile organic compounds. Our results highlight the importance of natural aerosols in degrading air quality under current warming, while also emphasizing that improved understanding of biogenic volatile organic compounds emissions due to climate change is essential for numerically assessing future air quality.