Hemispheric-wide climate response to regional COVID-19-related aerosol emission reductions: the prominent role of atmospheric circulation adjustments

The national and global restrictions in response to the COVID-19 pandemic led to a sudden, albeit temporary, emission reduction of many greenhouse gases (GHGs) and anthropogenic aerosols, whose near-term climate impact were previously found to be negligible when focusing on global- and/or annual-mean scales. Our study aims to investigate the monthly scale coupled climate-and-circulation response to regional, COVID-19-related aerosol emission reductions, using the output from 10 Earth system models participating in the Covid model intercomparison project (CovidMIP). We focus on January–February and March–May 2020, which represent the seasons of largest emission changes in sulfate (SO2) and black carbon (BC). During January–February (JF), a marked decrease in aerosol emissions over eastern China, the main emission region, resulted in a lower aerosol burden, leading to an increase in surface downwelling radiation and ensuing surface warming. Regional sea-level pressure and circulation adjustments drive a precipitation increase over the Maritime Continent, embedded in a negative Pacific Decadal Oscillation (PDO)- and/or El Niño–Southern Oscillation (ENSO)-like response over the Pacific, in turn associated with a northwestward displacement and zonal shrinking of the Indo-Pacific Walker cell. Remote climate anomalies across the Northern Hemisphere, including a weakening of the Siberian High and Aleutian Low, as well as anomalous temperature patterns in the northern mid-latitudes, arise primarily as a result of stationary Rossby wave trains generated over East Asia. The anomalous climate pattern and driving dynamical mechanism reverse polarity between JF and MAM (March–May) 2020, which is shown to be consistent with an underlying shift of the dominant region of SO2 emission reduction from eastern China in JF to India in MAM. Our findings highlight the prominent role of large-scale dynamical adjustments in generating a hemispheric-wide aerosol climate imprint even on short timescales, which are largely consistent with longer-term (decadal) trends. Furthermore, our analysis shows the sensitivity of the climate response to the geographical location of the aerosol emission region, even after relatively small, but abrupt, emission changes. Scientific advances in understanding the climate impact of regional aerosol perturbations, especially the rapidly evolving emissions over China and India, are critically needed to reduce current uncertainties in near-future climate projections and to develop scientifically informed hazard mitigation and adaptation policies.</p

Melting of Major Glaciers in Himalayas: Role of Desert Dust and Anthropogenic Aerosols

The Himalayan and Tibet Glaciers, that are among the largest bodies of ice and fresh water resource outside of the polar ice caps, face a significant threat of accelerated meltdown in coming decades due to climate variability and change. The rate of retreat of these glaciers and changes in their terminus (frontal dynamics) is highly variable across the Himalayan range. These large freshwater sources are critical to human activities for food production, human consumption and a whole host of other applications, especially over the Indo-Gangetic (IG) plains. They are also situated in a geo-politically sensitive area surrounded by China, India, Pakistan, Nepal and Bhutan where more than a billion people depend on them. The major rivers of the Asian continent such as the Ganga (also known as Ganges), Brahmaputra, Indus, Yamuna, Sutluj etc., originate and pass through these regions and they have greater importance due to their multi-use downstream: hydro power, agriculture, aquaculture, flood control, and as a freshwater resource. Recent studies over the Himalayan Glaciers using ground-based and space-based observations, and computer models indicate a long-term trend of climate variability and change that may accelerate melting of the Himalayan Glaciers.https://digitalcommons.chapman.edu/sees_books/1001/thumbnail.jp

Aerosol meteorology of Maritime Continent for the 2012 7SEAS southwest monsoon intensive study - Part 2: Philippine receptor observations of fine-scale aerosol behavior

Abstract. The largest 7 Southeast Asian Studies (7SEAS) operations period within the Maritime Continent (MC) occurred in the August–September 2012 biomass burning season. Data included were observations aboard the M/Y Vasco, dispatched to the Palawan Archipelago and Sulu Sea of the Philippines for September 2012. At these locations, the Vasco observed MC smoke and pollution entering the southwest monsoon (SWM) monsoonal trough. Here we describe the research cruise findings and the finer-scale aerosol meteorology of this convectively active region. This 2012 cruise complemented a 2-week cruise in 2011 and was generally consistent with previous findings in terms of how smoke emission and transport related to monsoonal flows, tropical cyclones (TC), and the covariance between smoke transport events and the atmosphere's thermodynamic structure. Biomass burning plumes were usually mixed with significant amounts of anthropogenic pollution. Also key to aerosol behavior were squall lines and cold pools propagating across the South China Sea (SCS) and scavenging aerosol particles in their path. However, the 2012 cruise showed much higher modulation in aerosol frequency than its 2011 counterpart. Whereas in 2011 large synoptic-scale aerosol events transported high concentrations of smoke into the Philippines over days, in 2012 measured aerosol events exhibited a much shorter-term variation, sometimes only 3–12 h. Strong monsoonal flow reversals were also experienced in 2012. Nucleation events in cleaner and polluted conditions, as well as in urban plumes, were observed. Perhaps most interestingly, several cases of squall lines preceding major aerosol events were observed, as opposed to 2011 observations where these lines largely scavenged aerosol particles from the marine boundary layer. Combined, these observations indicate pockets of high and low particle counts that are not uncommon in the region. These perturbations are difficult to observe by satellite and very difficult to model. Indeed, the Navy Aerosol Analysis and Prediction System (NAAPS) simulations captured longer period aerosol events quite well but largely failed to capture the timing of high-frequency phenomena. Ultimately, the research findings of these cruises demonstrate the real world challenges of satellite-based missions, significant aerosol life cycle questions such as those the future Aerosol/Clouds/Ecosystems (ACE) will investigate, and the importance of small-scale phenomena such as sea breezes, squall lines, and nucleation events embedded within SWM patterns in dominating aerosol life cycle and potential relationships to clouds

Climatic effects of 1950–2050 changes in US anthropogenic aerosols – Part 1: Aerosol trends and radiative forcing

We use the GEOS-Chem chemical transport model combined with the GISS general circulation model to calculate the aerosol direct and indirect (warm cloud) radiative forcings from US anthropogenic sources over the 1950–2050 period, based on historical emission inventories and future projections from the IPCC A1B scenario. The aerosol simulation is evaluated with observed spatial distributions and 1980–2010 trends of aerosol concentrations and wet deposition in the contiguous US. The radiative forcing from US anthropogenic aerosols is strongly localized over the eastern US. We find that it peaked in 1970–1990, with values over the eastern US (east of 100° W) of −2.0 W m[superscript −2] for direct forcing including contributions from sulfate (−2.0 W m[superscript −2]), nitrate (−0.2 W m[superscript −2]), organic carbon (−0.2 W m[superscript −2]), and black carbon (+0.4 W m[superscript −2]). The aerosol indirect effect is of comparable magnitude to the direct forcing. We find that the forcing declined sharply from 1990 to 2010 (by 0.8 W m−2 direct and 1.0 W m[superscript −2] indirect), mainly reflecting decreases in SO[subscript 2] emissions, and project that it will continue declining post-2010 but at a much slower rate since US SO[subscript 2] emissions have already declined by almost 60 % from their peak. This suggests that much of the warming effect of reducing US anthropogenic aerosol sources may have already been realized by 2010, however some additional warming is expected through 2020. The small positive radiative forcing from US BC emissions (+0.3 W m[superscript −2] over the eastern US in 2010) suggests that an emission control strategy focused on BC would have only limited climate benefit

Impacts of anthropogenic aerosols on regional climate: extreme events, stagnation, and the United States warming hole

Extreme temperatures, heat waves, heavy rainfall events, drought, and extreme air pollution events have adverse effects on human health, infrastructure, agriculture and economies. The frequency, magnitude and duration of these events are expected to change in the future in response to increasing greenhouse gases and decreasing aerosols, but future climate projections are uncertain. A significant portion of this uncertainty arises from uncertainty in the effects of aerosol forcing: to what extent were the effects from greenhouse gases masked by aerosol forcing over the historical observational period, and how much will decreases in aerosol forcing influence regional and global climate over the remainder of the 21st century? The observed frequency and intensity of extreme heat and precipitation events have increased in the U.S. over the latter half of the 20th century. Using aerosol only (AER) and greenhouse gas only (GHG) simulations from 1860 to 2005 in the GFDL CM3 chemistry-climate model, I parse apart the competing influences of aerosols and greenhouse gases on these extreme events. I find that small changes in extremes in the “all forcing” simulations reflect cancellations between the effects of increasing anthropogenic aerosols and greenhouse gases. In AER, extreme high temperatures and the number of days with temperatures above the 90th percentile decline over most of the U.S., while in GHG high temperature extremes increase over most of the U.S. The spatial response patterns in AER and GHG are significantly anti-correlated, suggesting a preferred regional mode of response that is largely independent of the type of forcing. Extreme precipitation over the eastern U.S. decreases in AER, particularly in winter, and increases over the eastern and central U.S. in GHG, particularly in spring. Over the 21st century under the RCP8.5 emissions scenario, the patterns of extreme temperature and precipitation change associated with greenhouse gas forcing dominate. The temperature response pattern in AER and GHG is characterized by strong responses over the western U.S. and weak or opposite signed responses over the southeast U.S., raising the question of whether the observed U.S. “warming hole” could have a forced component. To address this question, I systematically examine observed seasonal temperature trends over all time periods of at least 10 years during 1901-2015. In the northeast and southern U.S., significant summertime cooling occurs from the early 1950s to the mid 1970s, which I partially attribute to increasing anthropogenic aerosol emissions (median fraction of the observed temperature trends explained is 0.69 and 0.17, respectively). In winter, the northeast and southern U.S. cool significantly from the early 1950s to the early 1990s, which I attribute to long-term phase changes in the North Atlantic Oscillation and the Pacific Decadal Oscillation. Rather than being a single phenomenon stemming from a single cause, both the warming hole and its dominant drivers vary by season, region, and time period. Finally, I examine historical and projected future changes in atmospheric stagnation. Stagnation, which is characterized by weak winds and an absence of precipitation, is a meteorological contributor to heat waves, extreme pollution, and drought. Using CM3, I show that regional stagnation trends over the historical period (1860-2005) are driven by changes in anthropogenic aerosol emissions, rather than rising greenhouse gases. In the northeastern and central United States, aerosol-induced changes in surface and upper level winds produce significant decreases in the number of stagnant summer days, while decreasing precipitation in the southeast US increases the number of stagnant summer days. Outside of the U.S., significant drying over eastern China in response to rising aerosol emissions contributed to increased stagnation during 1860-2005. Additionally, this region was found to be particularly sensitive to changes in local aerosol emissions, indicating that decreasing Chinese emissions in efforts to improve air quality will also decrease stagnation. In Europe, I find a dipole response pattern during the historical period wherein stagnation decreases over southern Europe and increases over northern Europe in response to global increases in aerosol emissions. In the future, declining aerosol emissions will likely lead to a reversal of the historical stagnation trends, with increasing greenhouse gases again playing a secondary role. Aerosols have a significant effect on a number of societally important extreme events, including heat waves, intense rainfall events, drought, and stagnation. Further, uncertainty in the strength of aerosol masking of historical greenhouse gas forcing is a significant source of spread in future climate projections. Quantifying these aerosol effects is therefore critical for our ability to accurately project and prepare for future changes in extreme events

Climatic Effects of 1950-2050 Changes in US Anthropogenic Aerosols

We calculate decadal aerosol direct and indirect (warm cloud) radiative forcings from US anthropogenic sources over the 1950-2050 period. Past and future aerosol distributions are constructed using GEOS-Chem and historical emission inventories and future projections from the IPCC A1B scenario. Aerosol simulations are evaluated with observed spatial distributions and 1980-2010 trends of aerosol concentrations and wet deposition in the contiguous US. Direct and indirect radiative forcing is calculated using the GISS general circulation model and monthly mean aerosol distributions from GEOS-Chem. The radiative forcing from US anthropogenic aerosols is strongly localized over the eastern US. We find that its magnitude peaked in 1970-1990, with values over the eastern US (east of 100 deg W) of 2.0Wm(exp2 for direct forcing including contributions from sulfate (2.0Wm2), nitrate (0.2Wm(exp2), organic carbon (0.2Wm(exp2), and black carbon (+0.4Wm(exp2). The uncertainties in radiative forcing due to aerosol radiative properties are estimated to be about 50 %. The aerosol indirect effect is estimated to be of comparable magnitude to the direct forcing. We find that the magnitude of the forcing declined sharply from 1990 to 2010 (by 0.8Wm(exp2) direct and 1.0Wm(exp2 indirect), mainly reflecting decreases in SO2 emissions, and project that it will continue declining post-2010 but at a much slower rate since US SO2 emissions have already declined by almost 60% from their peak. This suggests that much of the warming effect of reducing US anthropogenic aerosol sources has already been realized. The small positive radiative forcing from US BC emissions (+0.3Wm(exp2 over the eastern US in 2010; 5% of the global forcing from anthropogenic BC emissions worldwide) suggests that a US emission control strategy focused on BC would have only limited climate benefit

Global sulfur emissions in the 1990s

This paper provides global and country by country estimates of sulfur emissions for the early and mid-1990s. Raw estimates are obtained in two ways. For countries with published data we compile that data from the available sources. For the remaining countries, we use either the decomposition model estimated by Stern (1999), the first differences environmental Kuznets curve model estimated by Stern and Common (2001), or simple extrapolation depending on the availability of data on the explanatory variables. We then examine the compatibility of these estimates with the ASL estimates for 1990. Based on these and other comparisons we construct a preferred database for 1850-1999 and discuss the main movements in the 1990s. The data is available from the datasite.

Changes in the aerosol direct radiative forcing from 2001 to 2015: observational constraints and regional mechanisms

We present estimates of changes in the direct aerosol effects (DRE) and its anthropogenic component (DRF) from 2001 to 2015 using the GFDL chemistry–climate model AM3 driven by CMIP6 historical emissions. AM3 is evaluated against observed changes in the clear-sky shortwave direct aerosol effect (DREswclr) derived from the Clouds and the Earth's Radiant Energy System (CERES) over polluted regions. From 2001 to 2015, observations suggest that DREclrsw increases (i.e., less radiation is scattered to space by aerosols) over western Europe (0.7–1&thinsp;W&thinsp;m−2&thinsp;decade−1) and the eastern US (0.9–1.4&thinsp;W&thinsp;m−2&thinsp;decade−1), decreases over India (−1 to −1.6&thinsp;W&thinsp;m−2&thinsp;decade−1), and does not change significantly over eastern China. AM3 captures these observed regional changes in DREclrsw well in the US and western Europe, where they are dominated by the decline of sulfate aerosols, but not in Asia, where the model overestimates the decrease of DREclrsw. Over India, the model bias can be partly attributed to a decrease of the dust optical depth, which is not captured by our model and offsets some of the increase of anthropogenic aerosols. Over China, we find that the decline of SO2 emissions after 2007 is not represented in the CMIP6 emission inventory. Accounting for this decline, using the Modular Emission Inventory for China, and for the heterogeneous oxidation of SO2 significantly reduces the model bias. For both India and China, our simulations indicate that nitrate and black carbon contribute more to changes in DREclrsw than in the US and Europe. Indeed, our model suggests that black carbon (+0.12&thinsp;W&thinsp;m−2) dominates the relatively weak change in DRF from 2001 to 2015 (+0.03&thinsp;W&thinsp;m−2). Over this period, the changes in the forcing from nitrate and sulfate are both small and of the same magnitude (−0.03&thinsp;W&thinsp;m−2 each). This is in sharp contrast to the forcing from 1850 to 2001 in which forcings by sulfate and black carbon largely cancel each other out, with minor contributions from nitrate. The differences between these time periods can be well understood from changes in emissions alone for black carbon but not for nitrate and sulfate; this reflects non-linear changes in the photochemical production of nitrate and sulfate associated with changes in both the magnitude and spatial distribution of anthropogenic emissions.</p

Robust evidence for reversal in the aerosol effective climate forcing trend

Anthropogenic aerosols exert a cooling influence that offsets part of the greenhouse gas warming. Due to their short tropospheric lifetime of only up to several days, the aerosol forcing responds quickly to emissions. Here we present and discuss the evolution of the aerosol forcing since 2000. There are multiple lines of evidence that allow to robustly conclude that the anthropogenic aerosol effective radiative forcing – both aerosol-radiation and aerosol-cloud interactions – has become globally less negative, i.e. that the trend in aerosol effective radiative forcing changed sign from negative to positive. Bottom-up inventories show that anthropogenic primary aerosol and aerosol precursor emissions declined in most regions of the world; observations related to aerosol burden show declining trends, in particular of the fine-mode particles that make up most of the anthropogenic aerosols; satellite retrievals of cloud droplet numbers show trends consistent in sign, as do observations of top-of-atmosphere radiation. Climate model results, including a revised set that is constrained by observations of the ocean heat content evolution show a consistent sign and magnitude for a positive forcing relative to 2000 due to reduced aerosol effects. This reduction leads to an acceleration of the forcing of climate change, i.e. an increase in forcing by 0.1 to 0.3 W m-2, up to 12 % of the total climate forcing in 2019 compared to 1750 according to IPCC