scholarly journals Sensitivity studies of different aerosol indirect effects in mixed-phase clouds

2009 ◽  
Vol 9 (22) ◽  
pp. 8917-8934 ◽  
Author(s):  
U. Lohmann ◽  
C. Hoose

Abstract. Aerosols affect the climate system by changing cloud characteristics. Using the global climate model ECHAM5-HAM, we investigate different aerosol effects on mixed-phase clouds: The glaciation effect, which refers to a more frequent glaciation due to anthropogenic aerosols, versus the de-activation effect, which suggests that ice nuclei become less effective because of an anthropogenic sulfate coating. The glaciation effect can partly offset the indirect aerosol effect on warm clouds and thus causes the total anthropogenic aerosol effect to be smaller. It is investigated by varying the parameterization for the Bergeron-Findeisen process and the threshold coating thickness of sulfate (SO4-crit), which is required to convert an externally mixed aerosol particle into an internally mixed particle. Differences in the net radiation at the top-of-the-atmosphere due to anthropogenic aerosols between the different sensitivity studies amount up to 0.5 W m−2. This suggests that the investigated mixed-phase processes have a major effect on the total anthropogenic aerosol effect.

2009 ◽  
Vol 9 (4) ◽  
pp. 15045-15081
Author(s):  
U. Lohmann ◽  
C. Hoose

Abstract. Aerosols affect the climate system by changing cloud characteristics. Using the global climate model ECHAM5-HAM, we investigate different aerosol effects on mixed-phase clouds: The glaciation effect, which refers to a more frequent glaciation due to anthropogenic aerosols, versus the de-activation effect, which suggests that ice nuclei become less effective because of an anthropogenic sulfate coating. The glaciation effect can partly offset the indirect aerosol effect on warm clouds and thus causes the total anthropogenic aerosol effect to be smaller. It is investigated by varying the parameterization for the Bergeron-Findeisen process and the threshold coating thickness of sulfate (SO4-crit), which is required to convert an externally mixed aerosol particle into an internally mixed particle. Differences in the net radiation at the top-of-the-atmosphere due to anthropogenic aerosols between the different sensitivity studies amount up to 0.5 W m−2. This suggests that the investigated mixed-phase processes have a major effect on the total anthropogenic aerosol effect.


2022 ◽  
pp. 1-48
Author(s):  
Yi Ming

Abstract A negative shortwave cloud feedback associated with higher extratropical liquid water content in mixed-phase clouds is a common feature of global warming simulations, and multiple mechanisms have been hypothesized. A set of process-level experiments performed with an idealized global climate model (a dynamical core with passive water and cloud tracers and full Rotstayn-Klein single-moment microphysics) show that the common picture of the liquid water path (LWP) feedback in mixed-phase clouds being controlled by the amount of ice susceptible to phase change is not robust. Dynamic condensate processes—rather than static phase partitioning—directly change with warming, with varied impacts on liquid and ice amounts. Here, three principal mechanisms are responsible for the LWP response, namely higher adiabatic cloud water content, weaker liquid-to-ice conversion through the Bergeron-Findeisen process, and faster melting of ice and snow to rain. Only melting is accompanied by a substantial loss of ice, while the adiabatic cloud water content increase gives rise to a net increase in ice water path (IWP) such that total cloud water also increases without an accompanying decrease in precipitation efficiency. Perturbed parameter experiments with a wide range of climatological LWP and IWP demonstrate a strong dependence of the LWP feedback on the climatological LWP and independence from the climatological IWP and supercooled liquid fraction. This idealized setup allows for a clean isolation of mechanisms and paints a more nuanced picture of the extratropical mixed-phase cloud water feedback than simple phase change.


2021 ◽  
Author(s):  
Ramiro Checa-Garcia ◽  
Didier Didier Hauglustaine ◽  
Yves Balkanski ◽  
Paola Formenti

<p>Glyoxal (GL) and methylglyoxal (MGL) are the smallest di-carbonyls present in the atmosphere. They hydrate easily, a process that is followed by an oligomerisation. As a consequence, it is considered that they participate actively in the formation of secondary organic aerosols (SOA) and therefore, they are being introduced in the current climate models with interactive chemistry to assess their importance on atmospheric chemistry. In our study we present the introduction of glyoxal in the INCA global model. A new closed set of gas-phase  reactions is analysed first with a box model. Then the simulated global distribution of glyoxal by the global climate model is compared with satellite observations. We show that the oxidation of volatile organic compounds and acetylene, together with the photolysis of more complex di-carbonyls allows us to reproduce well glyoxal seasonal cycle in the tropics but it requires an additional sink in several northern hemispheric regions. Additional sensitivity studies are being conducted by introducing  GL and MGL interactions with dust and SOA according to new uptake  coefficients obtained by dedicated experiments in the CESAM instrument (Chamber of Experimental Simulation of Atmospheric Multiphases). The effects of these heterogeneous chemistry processes will be quantified in the light of the new chamber measurements  and also evaluated in terms of optical properties of aged dust aerosol  and the changes in direct radiative effects  of the involved aerosol species.</p>


2018 ◽  
Author(s):  
Ulrike Lohmann ◽  
David Neubauer

Abstract. Clouds are important in the climate system because of their large influence on the radiation budget. On the one hand, they scatter solar radiation and with that cool the climate. On the other hand, they absorb and re-emit terrestrial radiation, which causes a warming. How clouds change in a warmer climate is one of the largest uncertainties for the equilibrium climate sensitivity (ECS). While a large spread in the cloud feedback arises from low-level clouds, it was recently shown that also mixed-phase clouds are important for ECS. If mixed-phase clouds in the current climate contain too few supercooled cloud droplets, too much ice will change to liquid water in a warmer climate. As shown by Tan et al. (2016), this overestimates the negative cloud phase feedback and underestimates ECS in the CAM global climate model (GCM). Here we are using the newest version of the ECHAM6-HAM2 GCM to investigate the importance of mixed-phase clouds for ECS. Although we also considerably underestimate the fraction of supercooled liquid water globally in the reference version of ECHAM6-HAM2 GCM, we do not obtain increases in ECS in simulations with more supercooled liquid water in the present-day climate, contrary to the findings by Tan et al. (2016). We hypothesize that it is not the global supercooled liquid water fraction that matters, but only how well low- and mid-level mixed-phase clouds with cloud top temperatures in the mixed-phase temperature range between 0 and −35 ºC are simulated. These occur most frequent in mid-latitudes, in particular over the Southern Ocean where they determine the amount of absorbed shortwave radiation. In ECHAM6-HAM2 the amount of absorbed shortwave radiation over the Southern Ocean is only overestimated if all clouds below 0 ºC consist exclusively of ice and only in this simulation is ECS is significantly smaller than in all other simulations. Hence, the negative cloud phase feedback seems to be important only if the optically thin low- and mid-level mid-latitude clouds have the wrong phase (ice instead of liquid water) in the absence of overlying clouds. In all other simulations, changes in cloud feedbacks associated with cloud amount and cloud top pressure, dominate.


2011 ◽  
Vol 11 (1) ◽  
pp. 3399-3459 ◽  
Author(s):  
M. Wang ◽  
S. Ghan ◽  
M. Ovchinnikov ◽  
X. Liu ◽  
R. Easter ◽  
...  

Abstract. Much of the large uncertainty in estimates of anthropogenic aerosol effects on climate arises from the multi-scale nature of the interactions between aerosols, clouds and large-scale dynamics, which are difficult to represent in conventional global climate models (GCMs). In this study, we use a multi-scale aerosol-climate model that treats aerosols and clouds across multiple scales to study aerosol indirect effects. This multi-scale aerosol-climate model is an extension of a multi-scale modeling framework (MMF) model that embeds a cloud-resolving model (CRM) within each grid cell of a GCM. The extension allows the explicit simulation of aerosol/cloud interactions in both stratiform and convective clouds on the global scale in a computationally feasible way. Simulated model fields, including liquid water path (LWP), ice water path, cloud fraction, shortwave and longwave cloud forcing, precipitation, water vapor, and cloud droplet number concentration are in agreement with observations. The new model performs quantitatively similar to the previous version of the MMF model in terms of simulated cloud fraction and precipitation. The simulated change in shortwave cloud forcing from anthropogenic aerosols is −0.77 W m−2, which is less than half of that in the host GCM (NCAR CAM5) (−1.79 W m−2) and is also at the low end of the estimates of most other conventional global aerosol-climate models. The smaller forcing in the MMF model is attributed to its smaller increase in LWP from preindustrial conditions (PI) to present day (PD): 3.9% in the MMF, compared with 15.6% increase in LWP in large-scale clouds in CAM5. The much smaller increase in LWP in the MMF is caused by a much smaller response in LWP to a given perturbation in cloud condensation nuclei (CCN) concentrations from PI to PD in the MMF (about one-third of that in CAM5), and, to a lesser extent, by a smaller relative increase in CCN concentrations from PI to PD in the MMF (about 26% smaller than that in CAM5). The smaller relative increase in CCN concentrations in the MMF is caused in part by a smaller increase in aerosol lifetime from PI to PD in the MMF, a positive feedback in aerosol indirect effects induced by cloud lifetime effects. The smaller response in LWP to anthropogenic aerosols in the MMF model is consistent with observations and with high resolution model studies, which may indicate that aerosol indirect effects simulated in conventional global climate models are overestimated and point to the need to use global high resolution models, such as MMF models or global CRMs, to study aerosol indirect effects. The simulated total anthropogenic aerosol effect in the MMF is −1.05 W m−2, which is close to the Murphy et al. (2009) inverse estimate of −1.1 ± 0.4 W m−2 (1σ) based on the examination of the Earth's energy balance. Further improvements in the representation of ice nucleation and low clouds are needed.


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