scholarly journals The value of remote marine aerosol measurements for constraining radiative forcing uncertainty

2019 ◽  
Author(s):  
Leighton A. Regayre ◽  
Julia Schmale ◽  
Jill S. Johnson ◽  
Christian Tatzelt ◽  
Andrea Baccarini ◽  
...  

Abstract. Aerosol measurements over the Southern Ocean are used to constrain aerosol-cloud interaction radiative forcing uncertainty in a global climate model. Aerosol forcing uncertainty is quantified using one million climate model variants that sample the uncertainty in nearly 30 model parameters. Ship-based measurements of cloud condensation nuclei, particle number concentrations and sulfate mass concentrations from the Antarctic Circumnavigation Expedition: Study of Preindustrial-like Aerosols and Their Climate Effects (ACE-SPACE) are used to identify observationally implausible variants and thereby reduce the spread in the simulated forcing. Southern Ocean measurements strongly constrain natural aerosol emissions: default sea spray emissions in the model need to be increased by around a factor of 3 to be consistent with measurements. Aerosol forcing uncertainty is reduced by around 7 % using these measurements, which is comparable to the 8 % reduction achieved using an extensive set of over 9000 predominantly Northern Hemisphere measurements. The radiative forcing due to aerosol–cloud interactions (RFaci) is constrained to −2.61 to −1.10 W m−2 (95 % confidence) and the effective radiative forcing from aerosol-cloud interactions (ERFaci) is constrained to −2.43 to −0.54 W m−2. When Southern Ocean and Northern Hemisphere measurements are combined, the uncertainty in RFaci is reduced by 21 % and the strongest 20 % of forcing values are ruled out as implausible. In this combined constraint the observationally plausible RFaci is around 0.17 W m−2 weaker (less negative) with credible values ranging from −2.51 to −1.17 W m−2 and from −2.18 to −1.46 W m−2 when using one standard deviation to quantify the uncertainty. The Southern Ocean and Northern Hemisphere measurement datasets are complementary because they constrain different processes. These results highlight the value of remote marine aerosol measurements.

2020 ◽  
Vol 20 (16) ◽  
pp. 10063-10072 ◽  
Author(s):  
Leighton A. Regayre ◽  
Julia Schmale ◽  
Jill S. Johnson ◽  
Christian Tatzelt ◽  
Andrea Baccarini ◽  
...  

Abstract. Aerosol measurements over the Southern Ocean are used to constrain aerosol–cloud interaction radiative forcing (RFaci) uncertainty in a global climate model. Forcing uncertainty is quantified using 1 million climate model variants that sample the uncertainty in nearly 30 model parameters. Measurements of cloud condensation nuclei and other aerosol properties from an Antarctic circumnavigation expedition strongly constrain natural aerosol emissions: default sea spray emissions need to be increased by around a factor of 3 to be consistent with measurements. Forcing uncertainty is reduced by around 7 % using this set of several hundred measurements, which is comparable to the 8 % reduction achieved using a diverse and extensive set of over 9000 predominantly Northern Hemisphere measurements. When Southern Ocean and Northern Hemisphere measurements are combined, uncertainty in RFaci is reduced by 21 %, and the strongest 20 % of forcing values are ruled out as implausible. In this combined constraint, observationally plausible RFaci is around 0.17 W m−2 weaker (less negative) with 95 % credible values ranging from −2.51 to −1.17 W m−2 (standard deviation of −2.18 to −1.46 W m−2). The Southern Ocean and Northern Hemisphere measurement datasets are complementary because they constrain different processes. These results highlight the value of remote marine aerosol measurements.


2020 ◽  
Vol 117 (32) ◽  
pp. 18998-19006 ◽  
Author(s):  
Isabel L. McCoy ◽  
Daniel T. McCoy ◽  
Robert Wood ◽  
Leighton Regayre ◽  
Duncan Watson-Parris ◽  
...  

The change in planetary albedo due to aerosol−cloud interactions during the industrial era is the leading source of uncertainty in inferring Earth’s climate sensitivity to increased greenhouse gases from the historical record. The variable that controls aerosol−cloud interactions in warm clouds is droplet number concentration. Global climate models demonstrate that the present-day hemispheric contrast in cloud droplet number concentration between the pristine Southern Hemisphere and the polluted Northern Hemisphere oceans can be used as a proxy for anthropogenically driven change in cloud droplet number concentration. Remotely sensed estimates constrain this change in droplet number concentration to be between 8 cm−3and 24 cm−3. By extension, the radiative forcing since 1850 from aerosol−cloud interactions is constrained to be −1.2 W⋅m−2to −0.6 W⋅m−2. The robustness of this constraint depends upon the assumption that pristine Southern Ocean droplet number concentration is a suitable proxy for preindustrial concentrations. Droplet number concentrations calculated from satellite data over the Southern Ocean are high in austral summer. Near Antarctica, they reach values typical of Northern Hemisphere polluted outflows. These concentrations are found to agree with several in situ datasets. In contrast, climate models show systematic underpredictions of cloud droplet number concentration across the Southern Ocean. Near Antarctica, where precipitation sinks of aerosol are small, the underestimation by climate models is particularly large. This motivates the need for detailed process studies of aerosol production and aerosol−cloud interactions in pristine environments. The hemispheric difference in satellite estimated cloud droplet number concentration implies preindustrial aerosol concentrations were higher than estimated by most models.


2021 ◽  
Author(s):  
Isabel L. McCoy ◽  
Daniel T. McCoy ◽  
Robert Wood ◽  
Christopher S. Bretherton ◽  
Leighton Regayre ◽  
...  

<div> <p>The change in planetary albedo due to aerosol-cloud interactions (aci) during the industrial era is the leading source of uncertainty in inferring Earth's climate sensitivity to increased greenhouse gases from the historical record. Examining pristine environments such as the Southern Ocean (SO) helps us to understand the pre-industrial state and constrain the change in cloud brightness over the industrial period associated with aci. This study presents two methods of utilizing observations of pristine environments to examine climate models and our understanding of the pre-industrial state.</p> </div><div> <p>First, cloud droplet number concentration (<em>N<sub>d</sub></em>) is used as an indicator of aci. Global climate models (GCMs) show that the hemispheric contrast in liquid cloud <em>N<sub>d</sub></em> between the pristine SO and the polluted Northern Hemisphere observed in the present-day can be used<strong> </strong>as a proxy for the increase in <em>N<sub>d</sub></em> from the pre-industrial. A hemispheric difference constraint developed from MODIS satellite observations indicates that pre-industrial <em>N<sub>d</sub></em> may have been higher than previously thought and provides an estimate of radiative forcing associated with aci between -1.2 and -0.6 Wm<sup>-2</sup>. Comparisons with MODIS <em>N<sub>d  </sub></em>highlight significant GCM discrepancies in pristine, biologically active regions.</p> </div><div> <p>Second, aerosol and cloud microphysical observations from a recent SO aircraft campaign are used to identify two potentially important mechanisms that are incomplete or missing in GCMs: i) production of new aerosol particles through synoptic uplift, and ii) buffering of <em>N<sub>d</sub></em> against precipitation removal by small, Aitken mode aerosols entrained from the free troposphere. The latter may significantly contribute to the high, summertime SO <em>N<sub>d</sub></em> levels which persist despite precipitation depletion associated with mid-latitude storm systems. Observational comparisons with nudged Community Atmosphere Model version 6 (CAM6) hindcasts show low-biased SO <em>N<sub>d  </sub></em>is linked to under-production of free-tropospheric Aitken aerosol which drives low-biases in cloud condensation nuclei number and likely discrepancies in composition. These results have important implications for the ability of current GCMs to capture aci in pristine environments.</p> </div>


2016 ◽  
Vol 29 (14) ◽  
pp. 5175-5188 ◽  
Author(s):  
Hai Wang ◽  
Shang-Ping Xie ◽  
Qinyu Liu

Abstract Spatial patterns of climate response to changes in anthropogenic aerosols and well-mixed greenhouse gases (GHGs) are investigated using climate model simulations for the twentieth century. The climate response shows both similarities and differences in spatial pattern between aerosol and GHG runs. Common climate response between aerosol and GHG runs tends to be symmetric about the equator. This work focuses on the distinctive patterns that are unique to the anthropogenic aerosol forcing. The tropospheric cooling induced by anthropogenic aerosols is locally enhanced in the midlatitude Northern Hemisphere with a deep vertical structure around 40°N, anchoring a westerly acceleration in thermal wind balance. The aerosol-induced negative radiative forcing in the Northern Hemisphere requires a cross-equatorial Hadley circulation to compensate interhemispheric energy imbalance in the atmosphere. Associated with a southward shift of the intertropical convergence zone, this interhemispheric asymmetric mode is unique to aerosol forcing and absent in GHG runs. Comparison of key climate response pattern indices indicates that the aerosol forcing dominates the interhemispheric asymmetric climate response in historical all-forcing simulations, as well as regional precipitation change such as the drying trend over the East Asian monsoon region. While GHG forcing dominates global mean surface temperature change, its effect is on par with and often opposes the aerosol effect on precipitation, making it difficult to detect anthropogenic change in rainfall from historical observations.


2019 ◽  
Author(s):  
Johannes Mülmenstädt ◽  
Edward Gryspeerdt ◽  
Marc Salzmann ◽  
Po-Lun Ma ◽  
Sudhakar Dipu ◽  
...  

Abstract. Using the method of offline radiative transfer modelling within the partial radiative perturbations (PRP) approach, the effective radiative forcing (ERF) by aerosol–cloud interactions (ACI) in the ECHAM-HAMMOZ aerosol climate model is decomposed into a radiative forcing by anthropogenic cloud droplet number change and adjustments of the liquid water path and cloud fraction. The simulated radiative forcing and liquid water path adjustment are of approximately equal magnitude at −0.52 W m−2 and −0.53 W m−2, respectively, while the cloud fraction adjustment is somewhat weaker at −0.31 W m−2 (constituting 38 %, 39 %, and 23 % of the total ERFaci, respectively); geographically, all three ERF components in the simulation peak over China, the subtropical eastern ocean boundaries, the northern Atlantic and Pacific Ocean, Europe, and eastern North America (in order of prominence). Spatial correlations indicate that the temporal-mean liquid water path adjustment is proportional to the temporal-mean radiative forcing, while the relationship between cloud fraction adjustment and radiative forcing is less direct. While the estimate of warm-cloud ACI is relatively insensitive to the treatment of ice and mixed-phase cloud overlying warm cloud, there are indications that more restrictive treatments of ice in the column result in a low bias in the estimated magnitude of the liquid water path adjustment and a high bias in the estimated magnitude of the droplet number forcing. Since the present work is the first PRP decomposition of the aerosol ERF into RFaci and fast cloud adjustments, idealized experiments are conducted to provide evidence that the PRP results are accurate. The experiments show that using low-frequency (daily or monthly) time-averaged model output of the cloud property fields underestimates the ERF, but 3-hourly mean output is sufficiently frequent.


2021 ◽  
Author(s):  
Christopher Smith ◽  
Glen Harris ◽  
Matthew Palmer ◽  
Nicolas Bellouin ◽  
William Collins ◽  
...  

<p>Aerosol forcing remains the most uncertain component of the total climate forcing on the Earth system. RFMIP and AerChemMIP contained experiments that allow us to determine time-slice present day (2014 minus 1850) from 17 CMIP6 models, and transient (1850 to 2014, or 2100) aerosol forcing from 11 models. In CMIP6, aerosol present-day aerosol forcing is -1.01 (full range -1.37 to -0.63) W m<sup>-2</sup>, a range considerably narrower than comprehensive assessments of aerosol forcing from multiple lines of evidence such as AR5 (-1.9 to -0.1 W m<sup>-2</sup>) or Bellouin et al. 2020 (-2.0 to -0.35 W m<sup>-2</sup>). The transient experiments also show a diversity in time histories, with most models showing a peak negative aerosol forcing at some time between 1975 and 2010, and recent trends varying from strongly recovering to slightly strengthening aerosol forcing. Models that were run to 2100 under SSP2-4.5 all show a projected weakening aerosol forcing.</p><p>By fitting a simple relationship of how globally integrated emissions of black carbon, organic carbon and SO<sub>2</sub> relate to effective radiative forcing from aerosol-radiation interactions (ERFari) and aerosol-cloud interactions (ERFaci), an emissions to forcing relationship can be determined for these 11 RFMIP and AerChemMIP models. Using a 100,000 member Monte Carlo ensemble of historical aerosol time series, where coefficients are drawn from these model-derived distributions, and total 1850 to 2014 aerosol forcing is taken from the wider distributions of Bellouin et al. (2020), we create a best estimate historical time series for aerosol forcing (with uncertainty) that is constrained to historical warming and observed ocean heat uptake using a simple climate model. This method can also be used to predict aerosol forcing from future emissions scenarios, such as the SSPs and those derived from integrated assessment models, and provides estimates of the likely ranges for equilibrium climate sensitivity and transient climate response based on the historical aerosol forcing.</p>


Atmosphere ◽  
2021 ◽  
Vol 12 (3) ◽  
pp. 406
Author(s):  
Xiangjun Shi ◽  
Chunhan Li ◽  
Lijuan Li ◽  
Wentao Zhang ◽  
Jiaojiao Liu

The prescribed anthropogenic aerosol forcing recommended by Coupled Model Intercomparison Project Phase 6 (CMIP6) was implemented in an atmospheric model. With the reduced complexity of anthropogenic aerosol forcing, each component of anthropogenic aerosol effective radiative forcing (ERF) can be estimated by one or more calculation methods, especially for instantaneous radiative forcing (RF) from aerosol–radiation interactions (RFari) and aerosol–cloud interactions (RFaci). Simulation results show that the choice of calculation method might impact the magnitude and reliability of RFari. The RFaci—calculated by double radiation calls—is the definition-based Twomey effect, which previously was impossible to diagnose using the default model with physically based aerosol–cloud interactions. The RFari and RFaci determined from present-day simulations are very robust and can be used as offline simulation results. The robust RFari, RFaci, and corresponding radiative forcing efficiencies (i.e., the impact of environmental properties) are very useful for analyzing anthropogenic aerosol radiative effects. For instance, from 1975 to 2000, both RFari and RFaci showed a clear response to the spatial change of anthropogenic aerosol. The global average RF (RFari + RFaci) has enhanced (more negative) by ~6%, even with a slight decrease in the global average anthropogenic aerosol, and this can be explained by the spatial pattern of radiative forcing efficiency.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Hailing Jia ◽  
Xiaoyan Ma ◽  
Fangqun Yu ◽  
Johannes Quaas

AbstractSatellite-based estimates of radiative forcing by aerosol–cloud interactions (RFaci) are consistently smaller than those from global models, hampering accurate projections of future climate change. Here we show that the discrepancy can be substantially reduced by correcting sampling biases induced by inherent limitations of satellite measurements, which tend to artificially discard the clouds with high cloud fraction. Those missed clouds exert a stronger cooling effect, and are more sensitive to aerosol perturbations. By accounting for the sampling biases, the magnitude of RFaci (from −0.38 to −0.59 W m−2) increases by 55 % globally (133 % over land and 33 % over ocean). Notably, the RFaci further increases to −1.09 W m−2 when switching total aerosol optical depth (AOD) to fine-mode AOD that is a better proxy for CCN than AOD. In contrast to previous weak satellite-based RFaci, the improved one substantially increases (especially over land), resolving a major difference with models.


2019 ◽  
Vol 59 ◽  
pp. 11.1-11.72 ◽  
Author(s):  
Sonia M. Kreidenweis ◽  
Markus Petters ◽  
Ulrike Lohmann

Abstract This chapter reviews the history of the discovery of cloud nuclei and their impacts on cloud microphysics and the climate system. Pioneers including John Aitken, Sir John Mason, Hilding Köhler, Christian Junge, Sean Twomey, and Kenneth Whitby laid the foundations of the field. Through their contributions and those of many others, rapid progress has been made in the last 100 years in understanding the sources, evolution, and composition of the atmospheric aerosol, the interactions of particles with atmospheric water vapor, and cloud microphysical processes. Major breakthroughs in measurement capabilities and in theoretical understanding have elucidated the characteristics of cloud condensation nuclei and ice nucleating particles and the role these play in shaping cloud microphysical properties and the formation of precipitation. Despite these advances, not all their impacts on cloud formation and evolution have been resolved. The resulting radiative forcing on the climate system due to aerosol–cloud interactions remains an unacceptably large uncertainty in future climate projections. Process-level understanding of aerosol–cloud interactions remains insufficient to support technological mitigation strategies such as intentional weather modification or geoengineering to accelerating Earth-system-wide changes in temperature and weather patterns.


2021 ◽  
Author(s):  
Arshad Nair ◽  
Fangqun Yu ◽  
Pedro Campuzano Jost ◽  
Paul DeMott ◽  
Ezra Levin ◽  
...  

Abstract Cloud condensation nuclei (CCN) are mediators of aerosol–cloud interactions, which contribute to the largest uncertainty in climate change prediction. Here, we present a machine learning/artificial intelligence model that quantifies CCN from variables of aerosol composition, atmospheric trace gases, and meteorology. Comprehensive multi-campaign airborne measurements, covering varied physicochemical regimes in the troposphere, confirm the validity of and help probe the inner workings of this machine learning model: revealing for the first time that different ranges of atmospheric aerosol composition and mass correspond to distinct aerosol number size distributions. Machine learning extracts this information, important for accurate quantification of CCN, additionally from both chemistry and meteorology. This can provide a physicochemically explainable, computationally efficient, robust machine learning pathway in global climate models that only resolve aerosol composition; potentially mitigating the uncertainty of effective radiative forcing due to aerosol–cloud interactions (ERFaci) and improving confidence in assessment of anthropogenic contributions and climate change projections.


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