scholarly journals Integrating biomass, sulphate and sea-salt aerosol responses into a microphysical chemical parcel model: implications for climate studies

2007 ◽  
Vol 365 (1860) ◽  
pp. 2659-2674 ◽  
Author(s):  
S Ghosh ◽  
M.H Smith ◽  
A Rap
Keyword(s):  
Radiative Forcing ◽  
General Circulation ◽  
Aerosol Particles ◽  
Cloud Droplet ◽  
Sea Salt ◽  
Radiative Properties ◽  
Radiation Budget ◽  
Sulphate Aerosol ◽  
Salt Loading ◽  
Sea Salt Aerosol

Aerosols are known to influence significantly the radiative budget of the Earth. Although the direct effect (whereby aerosols scatter and absorb solar and thermal infrared radiation) has a large perturbing influence on the radiation budget, the indirect effect (whereby aerosols modify the microphysical and hence the radiative properties and amounts of clouds) poses a greater challenge to climate modellers. This is because aerosols undergo chemical and physical changes while in the atmosphere, notably within clouds, and are removed largely by precipitation. The way in which aerosols are processed by clouds depends on the type, abundance and the mixing state of the aerosols concerned. A parametrization with sulphate and sea-salt aerosol has been successfully integrated within the Hadley Centre general circulation model (GCM). The results of this combined parametrization indicate a significantly reduced role, compared with previous estimates, for sulphate aerosol in cloud droplet nucleation and, consequently, in indirect radiative forcing. However, in this bicomponent system, the cloud droplet number concentration, N d (a crucial parameter that is used in GCMs for radiative transfer calculations), is a smoothly varying function of the sulphate aerosol loading. Apart from sea-salt and sulphate aerosol particles, biomass aerosol particles are also present widely in the troposphere. We find that biomass smoke can significantly perturb the activation and growth of both sulphate and sea-salt particles. For a fixed salt loading, N d increases linearly with modest increases in sulphate and smoke masses, but significant nonlinearities are observed at higher non-sea-salt mass loadings. This non-intuitive N d variation poses a fresh challenge to climate modellers.

scholarly journals Climate hypersensitivity to solar forcing?

2000 ◽  
Vol 18 (5) ◽  
pp. 583-588 ◽  
Author(s):  
W. Soon ◽  
E. Posmentier ◽  
S. Baliunas
Keyword(s):  
Radiative Forcing ◽  
General Circulation ◽  
Solar Physics ◽  
Stratospheric Ozone ◽  
General Circulation Models ◽  
Static Stability ◽  
Radiative Properties ◽  
Balance Model ◽  
Solar Forcing ◽  
Solar Uv

Abstract. We compare the equilibrium climate responses of a quasi-dynamical energy balance model to radiative forcing by equivalent changes in CO2, solar total irradiance (Stot) and solar UV (SUV). The response is largest in the SUV case, in which the imposed UV radiative forcing is preferentially absorbed in the layer above 250 mb, in contrast to the weak response from global-columnar radiative loading by increases in CO2 or Stot. The hypersensitive response of the climate system to solar UV forcing is caused by strongly coupled feedback involving vertical static stability, tropical thick cirrus ice clouds and stratospheric ozone. This mechanism offers a plausible explanation of the apparent hypersensitivity of climate to solar forcing, as suggested by analyses of recent climatic records. The model hypersensitivity strongly depends on climate parameters, especially cloud radiative properties, but is effective for arguably realistic values of these parameters. The proposed solar forcing mechanism should be further confirmed using other models (e.g., general circulation models) that may better capture radiative and dynamical couplings of the troposphere and stratosphere.Key words: Meteorology and atmospheric dynamics (climatology · general or miscellaneous) · Solar physics · astrophysics · and astronomy (ultraviolet emissions)

scholarly journals The effect of physical and chemical aerosol properties on warm cloud droplet activation

2005 ◽  
Vol 5 (5) ◽  
pp. 8507-8646 ◽  
Author(s):  
G. McFiggans ◽  
P. Artaxo ◽  
U. Baltensperger ◽  
H. Coe ◽  
M. C. Facchini ◽  
...  
Keyword(s):  
Atmospheric Aerosol ◽  
Radiative Forcing ◽  
Cloud Droplet ◽  
Size Composition ◽  
Radiative Properties ◽  
Atmospheric Measurements ◽  
Derived Properties ◽  
Aerosol Effects ◽  
Physical And Chemical ◽  
Aerosol Properties

Abstract. The effects of atmospheric aerosol on climate forcing may be very substantial but are quantified poorly at present; in particular, the effects of aerosols on cloud radiative properties, or the "indirect effects" are credited with the greatest range of uncertainty amongst the known causes of radiative forcing. This manuscript explores the effects that the composition and properties of atmospheric aerosol can have on the activation of droplets in warm clouds, so potentially influencing the magnitude of the indirect effect. The effects of size, composition, mixing state and various derived properties are assessed and a range of these properties provided by atmospheric measurements in a variety of locations is briefly reviewed. The suitability of a range of process-level descriptions to capture these aerosol effects is investigated by assessment of their sensitivities to uncertainties in aerosol properties and by their performance in closure studies. The treatment of these effects within global models is reviewed and suggestions for future investigations are made.

scholarly journals Large methane releases lead to strong aerosol forcing and reduced cloudiness

2011 ◽  
Vol 11 (3) ◽  
pp. 9057-9081
Author(s):  
T. Kurtén ◽  
L. Zhou ◽  
R. Makkonen ◽  
J. Merikanto ◽  
P. Räisänen ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
General Circulation ◽  
Cloud Droplet ◽  
Fold Increase ◽  
General Circulation Models ◽  
Large Temperature ◽  
Atmospheric Lifetime ◽  
Temperature Changes ◽  
Aerosol Forcing ◽  
Rapid Amplification

Abstract. The release of vast quantities of methane into the atmosphere as a result of clathrate destabilization is a potential mechanism for rapid amplification of global warming. Previous studies have calculated the enhanced warming based mainly on the radiative effect of the methane itself, with smaller contributions from the associated carbon dioxide or ozone increases. Here, we study the effect of strongly elevated methane (CH4) levels on oxidant and aerosol particle concentrations using a combination of chemistry-transport and general circulation models. A 10-fold increase in methane concentrations is predicted to significantly decrease hydroxyl radical (OH) concentrations, while moderately increasing ozone (O3). These changes lead to a 70% increase in the atmospheric lifetime of methane, and an 18% decrease in global mean cloud droplet number concentrations (CDNC). The CDNC change causes a radiative forcing that is comparable in magnitude to the longwave radiative forcing ("enhanced greenhouse effect") of the added methane. Together, the indirect CH4-O3 and CH4-OH-aerosol forcings could more than double the warming effect of large methane increases. Our findings may help explain the anomalously large temperature changes associated with historic methane releases.

Coexistence of three liquid phases in atmospheric aerosol particles

2021 ◽  
Author(s):  
Fabian Mahrt ◽  
Yuanzhou Huang ◽  
Shaun Xu ◽  
Manabu Shiraiwa ◽  
Andreas Zuend ◽  
...  
Keyword(s):  
Air Quality ◽  
Kinetic Modelling ◽  
Aerosol Particles ◽  
Nile Red ◽  
Cloud Droplet ◽  
Organic Aerosol ◽  
Reaction Rates ◽  
Phase Behaviour ◽  
Radiative Properties ◽  
Liquid Phases

<p>Aerosol particles are ubiquitous in the atmosphere and play an important role for air quality and Earth’s climate. Primary organic aerosol (POA), secondary organic aerosol (SOA), and secondary inorganic aerosol (SIA) constitute a significant mass fraction of these particles. POA, SOA, and SIA can become internally mixed within the same particle though different processes such as coagulation, gas–particle partitioning. To predict the role of these internally mixed particles in climate and air quality information on their phase behaviour is needed, i.e. information on the number and type of phases present within these particles. As an example, a particle with a single homogeneous liquid phase can have different radiative properties, reaction rates, uptake kinetics, and potential to change cloud microphysical properties by activating into a cloud droplet, compared to a particle with multiple liquid or solid phases.</p><p>In the current study we used Nile red, a solvatochromic dye, and fluorescence microscopy in order to determine the phase behaviour of POA+SOA+SIA particles. Squalane was used as a proxy of POA, ammonium sulfate was used as SIA and 1 of 23 different oxidized organic molecules were used as proxies of SOA. We demonstrate that three liquid phases often coexist within individual particles. We find that the phase behaviour strongly depends on the oxygen-to-carbon ratio of the SOA proxies. Experiments with SOA generated by dark ozonolysis of α-pinene in an environmental chamber are consistent with these observations. We also used thermodynamic and kinetic modelling to investigate the atmospheric implications of our experimental results.</p>

scholarly journals DMS atmospheric concentrations and sulphate aerosol indirect radiative forcing: a sensitivity study to the DMS source representation and oxidation

2003 ◽  
Vol 3 (1) ◽  
pp. 49-65 ◽  
Author(s):  
O. Boucher ◽  
C. Moulin ◽  
S. Belviso ◽  
O. Aumont ◽  
L. Bopp ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
General Circulation ◽  
Marine Boundary Layer ◽  
Circulation Model ◽  
Sensitivity Study ◽  
Sulphate Aerosol ◽  
Sulphate Aerosols ◽  
The Impact ◽  
Atmospheric Concentrations ◽  
Indirect Radiative Forcing

Abstract. The global sulphur cycle has been simulated using a general circulation model with a focus on the source and oxidation of atmospheric dimethylsulphide (DMS). The sensitivity of atmospheric DMS to the oceanic DMS climatology, the parameterisation of the sea-air transfer and to the oxidant fields have been studied. The importance of additional oxidation pathways (by O3 in the gas- and aqueous-phases and by BrO in the gas phase) not incorporated in global models has also been evaluated. While three different climatologies of the oceanic DMS concentration produce rather similar global DMS fluxes to the atmosphere at 24-27 Tg S yr -1, there are large differences in the spatial and seasonal distribution. The relative contributions of OH and NO3 radicals to DMS oxidation depends critically on which oxidant fields are prescribed in the model. Oxidation by O3 appears to be significant at high latitudes in both hemispheres. Oxidation by BrO could be significant even for BrO concentrations at sub-pptv levels in the marine boundary layer. The impact of such refinements on the DMS chemistry onto the indirect radiative forcing by anthropogenic sulphate aerosols is also discussed.

scholarly journals Climatological and radiative properties of midlatitude cirrus clouds derived by automatic evaluation of lidar measurements

2016 ◽  
Vol 16 (12) ◽  
pp. 7605-7621 ◽  
Author(s):  
Erika Kienast-Sjögren ◽  
Christian Rolf ◽  
Patric Seifert ◽  
Ulrich K. Krieger ◽  
Bei P. Luo ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
Cirrus Clouds ◽  
Radiative Properties ◽  
Radiation Budget ◽  
Shortwave Radiation ◽  
Radiative Transfer Model ◽  
Transfer Model ◽  
Data Set ◽  
Detection Scheme ◽  
Lidar Measurements

Abstract. Cirrus, i.e., high, thin clouds that are fully glaciated, play an important role in the Earth's radiation budget as they interact with both long- and shortwave radiation and affect the water vapor budget of the upper troposphere and stratosphere. Here, we present a climatology of midlatitude cirrus clouds measured with the same type of ground-based lidar at three midlatitude research stations: at the Swiss high alpine Jungfraujoch station (3580 m a.s.l.), in Zürich (Switzerland, 510 m a.s.l.), and in Jülich (Germany, 100 m a.s.l.). The analysis is based on 13 000 h of measurements from 2010 to 2014. To automatically evaluate this extensive data set, we have developed the Fast LIdar Cirrus Algorithm (FLICA), which combines a pixel-based cloud-detection scheme with the classic lidar evaluation techniques. We find mean cirrus optical depths of 0.12 on Jungfraujoch and of 0.14 and 0.17 in Zürich and Jülich, respectively. Above Jungfraujoch, subvisible cirrus clouds (τ < 0.03) have been observed during 6 % of the observation time, whereas above Zürich and Jülich fewer clouds of that type were observed. Cirrus have been observed up to altitudes of 14.4 km a.s.l. above Jungfraujoch, whereas they have only been observed to about 1 km lower at the other stations. These features highlight the advantage of the high-altitude station Jungfraujoch, which is often in the free troposphere above the polluted boundary layer, thus enabling lidar measurements of thinner and higher clouds. In addition, the measurements suggest a change in cloud morphology at Jungfraujoch above ∼ 13 km, possibly because high particle number densities form in the observed cirrus clouds, when many ice crystals nucleate in the high supersaturations following rapid uplifts in lee waves above mountainous terrain. The retrieved optical properties are used as input for a radiative transfer model to estimate the net cloud radiative forcing, CRFNET, for the analyzed cirrus clouds. All cirrus detected here have a positive CRFNET. This confirms that these thin, high cirrus have a warming effect on the Earth's climate, whereas cooling clouds typically have cloud edges too low in altitude to satisfy the FLICA criterion of temperatures below −38 °C. We find CRFNET = 0.9 W m−2 for Jungfraujoch and 1.0 W m−2 (1.7 W m−2) for Zürich (Jülich). Further, we calculate that subvisible cirrus (τ < 0.03) contribute about 5 %, thin cirrus (0.03 < τ < 0.3) about 45 %, and opaque cirrus (0.3 < τ) about 50 % of the total cirrus radiative forcing.

scholarly journals Depositional ice nucleation onto hydrated NaCl particles: a new mechanism for ice formation in the troposphere

2011 ◽  
Vol 11 (8) ◽  
pp. 23139-23167 ◽  
Author(s):  
M. E. Wise ◽  
K. J. Baustian ◽  
T. Koop ◽  
M. A. Freedman ◽  
E. J. Jensen ◽  
...  
Keyword(s):  
Marine Boundary Layer ◽  
Aerosol Particles ◽  
Ice Nucleation ◽  
Sea Salt ◽  
Ice Formation ◽  
Radiation Balance ◽  
Atmospheric Conditions ◽  
Hydrated Form ◽  
Sea Salt Aerosol ◽  
Ice Nuclei

Abstract. Sea-salt aerosol particles (SSA) are ubiquitous in the marine boundary layer and over coastal areas. Therefore SSA have ability to directly and indirectly affect the Earth's radiation balance. The influence SSA have on climate is related to their water uptake and ice nucleation characteristics. In this study, optical microscopy coupled with Raman spectroscopy was used to detect the formation of an NaCl hydrate that could form under atmospheric conditions. NaCl(s) particles deliquesced at the well established value of 75.7 ± 2.5 % RH. NaCl(aq) particles effloresced to a mixture of hydrated and non-hydrated particles at temperatures between 236 and 252 K. The aqueous particles effloresced into the non-hydrated form at temperatures warmer than 252 K. At temperatures colder than 236 K all particles effloresced into the hydrated form. The deliquescence relative humidities (DRH) of hydrated NaCl(s) particles ranged from 76.6 to 93.2 % RH. Based on the measured DRH and efflorescence relative humidities (ERH), we estimate crystalline NaCl particles could be in the hydrated form 40–80 % of the time in the troposphere. Additionally, the ice nucleating abilities of NaCl(s) and hydrated NaCl(s) were determined at temperatures ranging from 221 to 238 K. NaCl(s) particles depositionally nucleated ice at an average Sice value of 1.11 ± 0.07. Hydrated NaCl(s) particles depositionally nucleated ice at an average Sice value of 1.02 ± 0.04. When a mixture of hydrated and anhydrous NaCl(s) particles was present in the same sample, ice preferentially nucleated on the hydrated particles 100 % of the time. While both types of particles are efficient ice nuclei, hydrated NaCl(s) particles are better ice nuclei than NaCl(s) particles.

scholarly journals Modelling sea salt aerosol and its direct and indirect effects on climate

2007 ◽  
Vol 7 (5) ◽  
pp. 14939-14987 ◽  
Author(s):  
X. Ma ◽  
K. von Salzen ◽  
J. Li
Keyword(s):  
Radiative Forcing ◽  
Climate Model ◽  
Global Climate ◽  
Global Climate Model ◽  
Sea Salt ◽  
Size Distributions ◽  
Size Dependent ◽  
Sea Salt Aerosol ◽  
Direct Forcing ◽  
Log Normal

Abstract. A size-dependent sea salt aerosol parameterization was developed based on the piecewise log-normal approximation (PLA) for aerosol size distributions. Results of this parameterization from simulations with a global climate model produce good agreement with observations at the surface and for vertically-integrated volume size distributions. The global and annual mean of the sea salt burden is 10.1 mg m−2. The direct radiative forcing is calculated to be −1.52 and −0.60 W m−2 for clear sky and all sky, respectively. The first indirect radiative forcing is about twice as large as the direct forcing for all-sky (−1.34 W m−2). The results also show that the total indirect forcing of sea salt is −2.9 W m−2 if climatic feedbacks are taken into account. The sensitivity of the forcings to changes in the burdens and sizes of sea salt particles was also investigated based on additional simulations with a different sea salt source function.

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