scholarly journals Large difference in aerosol radiative effects from BVOC-SOA treatment in three ESMs

2020 ◽  
Author(s):  
Moa K. Sporre ◽  
Sara M. Blichner ◽  
Roland Schrödner ◽  
Inger H. H. Karset ◽  
Terje K. Berntsen ◽  
...  
Keyword(s):  
Aerosol Particles ◽  
Particle Formation ◽  
Earth System ◽  
New Particle Formation ◽  
Aerosol Formation ◽  
Radiative Effects ◽  
Sensitivity Experiments ◽  
Aerosol Radiative Effects ◽  
The Impact ◽  
Aerosol Radiative

Abstract. Biogenic volatile organic compounds (BVOCs) emitted from vegetation are oxidized in the atmosphere and can form aerosol particles either by contributing to new particle formation or by condensing onto existing aerosol particles. As the understanding of the importance of BVOCs for aerosol formation has increased over the past 10 years these processes have made their way into Earth System Models (ESMs). In this study, sensitivity experiments are run with three different ESMs, (the Norwegian Earth System Model (NorESM), EC-Earth and ECHAM) to investigate how the direct and indirect aerosol radiative effects are affected by changes in the formation of secondary organic aerosol (SOA) from BVOCs. In the first two sensitivity model experiments, the yields of SOA precursors from oxidation of BVOCs are changed by ± 50 %. For the third sensitivity test, the formed oxidation products do not participate in the formation of new particles, but are only allowed to condense onto existing aerosols. In the last two sensitivity experiments, the emissions of BVOC compounds (isoprene and monoterpenes) are turned off, one at a time. The results show that the impact on the direct radiative effect (DRE) are linked to the changes in the SOA production in the models, where more SOA leads to a stronger DRE and vice versa. The magnitude by which the DRE changes (maximally 0.15 W m−2 globally averaged) in response to the SOA changes however varies between the models, with EC-Earth displaying the largest changes. The results for the cloud radiative effects (CRE) are more complicated than for the DRE. The changes in CRE differ more among the ESMs and for some sensitivity experiments they even have different signs. The most sensitive models are NorESM and EC-Earth, which has CRE changes of up to 0.82 W m−2. The varying responses in the different models are connected to where in the aerosol size distributions the changes in mass and number due to SOA formation occur, in combination with the aerosol number concentration levels in the models. We also find that interactive gas-phase chemistry as well as the new particle formation parameterization have important implications for the DRE and CRE in some of the sensitivity experiments. The results from this study indicate that BVOC-SOA treatment in ESMs can have a substantial impact on the modelled climate but that the sensitivity varies greatly between the models. Since BVOC emissions have changed historically and will continue to change in the future, the spread in model results found in this study introduces uncertainty into ESM estimates of aerosol forcing from land-use change and BVOC feedback strengths.

scholarly journals Large difference in aerosol radiative effects from BVOC-SOA treatment in three Earth system models

2020 ◽  
Vol 20 (14) ◽  
pp. 8953-8973 ◽  
Author(s):  
Moa K. Sporre ◽  
Sara M. Blichner ◽  
Roland Schrödner ◽  
Inger H. H. Karset ◽  
Terje K. Berntsen ◽  
...  
Keyword(s):  
Aerosol Particles ◽  
Particle Formation ◽  
Earth System ◽  
New Particle Formation ◽  
Radiative Effects ◽  
System Models ◽  
Sensitivity Experiments ◽  
Aerosol Radiative Effects ◽  
Earth System Models ◽  
Aerosol Radiative

Abstract. Biogenic volatile organic compounds (BVOCs) emitted from vegetation are oxidised in the atmosphere and can form aerosol particles either by contributing to new particle formation or by condensing onto existing aerosol particles. As the understanding of the importance of BVOCs for aerosol formation has increased over the years, these processes have made their way into Earth system models (ESMs). In this study, sensitivity experiments are run with three different ESMs (the Norwegian Earth System Model (NorESM), EC-Earth and ECHAM) to investigate how the direct and indirect aerosol radiative effects are affected by changes in the formation of secondary organic aerosol (SOA) from BVOCs. In the first two sensitivity model experiments, the yields of SOA precursors from oxidation of BVOCs are changed by ±50 %. For the third sensitivity test, the formed oxidation products do not participate in the formation of new particles but are only allowed to condense onto existing aerosols. In the last two sensitivity experiments, the emissions of BVOC compounds (isoprene and monoterpenes) are turned off, one at a time. The goal of the study is to investigate whether it is of importance to treat SOA formation processes correctly in the models rather than to evaluate the correctness of the current treatment in the models. The results show that the impact on the direct radiative effect (DRE) is linked to the changes in the SOA production in the models, where more SOA leads to a stronger DRE and vice versa. However, the magnitude by which the DRE changes (maximally 0.15 W m−2 globally averaged) in response to the SOA changes varies between the models, with EC-Earth displaying the largest changes. The results for the cloud radiative effects (CREs) are more complicated than for the DRE. The changes in CRE differ more among the ESMs, and for some sensitivity experiments they even have different signs. The most sensitive models are NorESM and EC-Earth, which have CRE changes of up to 0.82 W m−2. The varying responses in the different models are connected to where in the aerosol size distributions the changes in mass and number due to SOA formation occur, in combination with the aerosol number concentration levels in the models. We also find that interactive gas-phase chemistry as well as the new particle formation parameterisation has important implications for the DRE and CRE in some of the sensitivity experiments. The results from this study indicate that BVOC-SOA treatment in ESMs can have a substantial impact on the modelled climate but that the sensitivity varies greatly between the models. Since BVOC emissions have changed historically and will continue to change in the future, the spread in model results found in this study implies uncertainty into ESM estimates of aerosol forcing from land-use change and BVOC feedback strengths.

Studying new particle formation from chemical emissions from sea surface using  ship-borne air-sea-interaction tanks

2021 ◽  
Author(s):  
Maija Peltola ◽  
Manon Rocco ◽  
Neill Barr ◽  
Erin Dunne ◽  
James Harnwell ◽  
...  
Keyword(s):  
Marine Biology ◽  
Cloud Condensation Nuclei ◽  
Aerosol Particles ◽  
Chemical Species ◽  
Particle Formation ◽  
Biological Properties ◽  
The European Union ◽  
New Particle Formation ◽  
Aerosol Formation ◽  
Horizon 2020

<p>Even though oceans cover over 70% of the Earth’s surface, the ways in which oceans interact with climate are not fully known. Marine micro-organisms such as phytoplankton can play an important role in regulating climate by releasing different chemical species into air. In air these chemical species can react and form new aerosol particles. If grown to large enough sizes, aerosols can influence climate by acting as cloud condensation nuclei which influence the formation and properties of clouds. Even though a connection of marine biology and climate through aerosol formation was first proposed already over 30 years ago, the processes related to this connection are still uncertain.</p><p>To unravel how seawater properties affect aerosol formation and to identify which chemical species are responsible for aerosol formation, we built two Air-Sea-Interaction Tanks (ASIT) that isolate 1000 l of seawater and 1000 l of air directly above the water. The used seawater was collected from different locations during a ship campaign on board the R/V Tangaroa in the South West Pacific Ocean, close to Chatham Rise, east of New Zealand. Seawater from one location was kept in the tanks for 2-3 days and then changed. By using seawater collected from different locations, we could obtain water with different biological populations. To monitor the seawater, we took daily samples to determine its chemical and biological properties.</p><p>The air in the tanks was continuously flushed with particle filtered air. This way the air had on average 40 min to interact with the seawater surface before being sampled. Our air sampling was continuous and consisted of aerosol and air chemistry measurements. The instrumentation included measurements of aerosol number concentration from 1 to 500 nm and  chemical species ranging from ozone and sulphur dioxide to volatile organic compounds and chemical composition of molecular clusters.</p><p>Joining the seawater and atmospheric data together can give us an idea of what chemical species are emitted from the water into the atmosphere and whether these species can form new aerosol particles. Our preliminary results show a small number of particles in the freshly nucleated size range of 1-3 nm in the ASIT headspaces, indicating that new aerosol particles can form in the ASIT headspaces. In this presentation, we will also explore which chemical species could be responsible for aerosol formation and which plankton groups could be related to the emissions of these species. Combining these results with ambient data and modelling work can shed light on how important new particle formation from marine sources is for climate.</p><p>Acknowledgements: Sea2Cloud project is funded by European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (Grant agreement No. 771369).</p>

scholarly journals Aerosol radiative effects with MACv2

2019 ◽  
Author(s):  
Stefan Kinne
Keyword(s):  
Anthropogenic Sources ◽  
Transfer Model ◽  
Strong Impact ◽  
Radiative Effects ◽  
Anthropogenic Aerosols ◽  
Anthropogenic Aerosol ◽  
Aerosol Forcing ◽  
Aerosol Radiative Effects ◽  
The Impact ◽  
Aerosol Radiative

Abstract. onthly global maps for aerosol properties of the MACv2 climatology are applied in an off-line radiative transfer model to determine aerosol radiative effects. For details beyond global averages in most cases global maps are presented to visualize regional and seasonal details. Aside from the direct radiative (aerosol presence) effect, including those for aerosol components as extracted from MACv2 aerosol optics, also the major aerosol indirect radiative effect is covered. Hereby, the impact of smaller drops in water clouds due to added anthropogenic aerosol was simulated by applying a satellite retrieval based fit from locally associations between aerosol and drop concentrations over oceans. Present-day anthropogenic aerosols of MACv2 – on a global average basis – reduce the radiative net-fluxes at the top of the atmosphere (TOA) by −1.0 W/m2 and at the surface by −2.1 W/m2. Direct cooling contributions are only about half of indirect contributions (−.35 vs −.65) at TOA, but about twice at the surface (−1.45 vs −.65), as solar absorption of the direct effect warms the atmosphere by +1.1 W/m2. Natural aerosols are on average less absorbing (for a relatively larger solar TOA cooling) and larger in size (now contributing with IR greenhouse warming). Thus, average TOA direct forcing efficiencies for total and anthropogenic aerosol happen to be similar: −11 W/m2/AOD at all-sky and −24 W/m2/AOD at clear-sky conditions. The present-day direct impact by all soot (BC) is globally averaged +0.55W/m2 and at least half of it should be attributed to anthropogenic sources. Hereby any accuracy of anthropogenic impacts, not just for soot, suffers from the limited access to a pre-industrial reference. Anthropogenic uncertainty has a particular strong impact on aerosol indirect effects, which dominate the (TOA) forcing. Accounting for uncertainties in the anthropogenic definition, present-day aerosol forcing is estimated to stay within the −0.7 to −1.6 W/m2 range, with a best estimate at −1 W/m2. Calculations with model predicted temporal changes to anthropogenic AOD indicate that qualitatively the anthropogenic aerosol forcing has not changed much over the last decades and is not likely to increase over the next decades, despite strong regional shifts. These regional shifts explain most solar insolation (brightening or dimming) trends that have been observed by ground-based radiation data.

scholarly journals Formation and characteristics of ions and charged aerosol particles in a native Australian Eucalypt forest

2008 ◽  
Vol 8 (1) ◽  
pp. 129-139 ◽  
Author(s):  
T. Suni ◽  
M. Kulmala ◽  
A. Hirsikko ◽  
T. Bergman ◽  
L. Laakso ◽  
...  
Keyword(s):  
Growth Rates ◽  
Aerosol Particles ◽  
Particle Formation ◽  
Cluster Ions ◽  
Native Forest ◽  
New Particle Formation ◽  
Aerosol Formation ◽  
Eucalypt Forest ◽  
The World ◽  
Strong Source

Abstract. Biogenic aerosol formation is likely to contribute significantly to the global aerosol load. In recent years, new-particle formation has been observed in various ecosystems around the world but hardly any measurements have taken place in the terrestrial Southern Hemisphere. Here, we report the first results of atmospheric ion and charged particle concentrations as well as of new-particle formation in a Eucalypt forest in Tumbarumba, South-East Australia, from July 2005 to October 2006. The measurements were carried out with an Air Ion Spectrometer (AIS) with a size range from 0.34 to 40 nm. The Eucalypt forest was a very strong source of new aerosol particles. Daytime aerosol formation took place on 52% of days with acceptable data, which is 2–3 times as often as in the Nordic boreal zone. Average growth rates for negative/positive 1.5–3 nm particles during these formation events were 2.89/2.68 nmh−1, respectively; for 3-7 nm particles 4.26/4.03, and for 7–20 nm particles 8.90/7.58 nmh−1, respectively. The growth rates for large ions were highest when the air was coming from the native forest which suggests that the Eucalypts were a strong source of condensable vapours. Average concentrations of cluster ions (0.34–1.8 nm) were 2400/1700 cm−3 for negative/positive ions, very high compared to most other measurements around the world. One reason behind these high concentrations could be the strong radon efflux from the soils around the Tumbarumba field site. Furthermore, comparison between night-time and daytime concentrations supported the view that cluster ions are produced close to the surface within the boundary layer also at night but that large ions are mostly produced in daytime. Finally, a previously unreported phenomenon, nocturnal aerosol formation, appeared in 32% of the analysed nights but was clustered almost entirely within six months from summer to autumn in 2006. From January to May, nocturnal formation was 2.5 times as frequent as daytime formation. Therefore, it appears that in summer and autumn, nocturnal production was the major mechanism for aerosol formation in Tumbarumba.

scholarly journals Roll vortices induce new particle formation bursts in the planetary boundary layer

2020 ◽  
Author(s):  
Janne Lampilahti ◽  
Hanna Elina Manninen ◽  
Katri Leino ◽  
Riikka Väänänen ◽  
Antti Manninen ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Planetary Boundary Layer ◽  
Particle Production ◽  
Aerosol Particles ◽  
Regional Scale ◽  
Particle Formation ◽  
Forest Site ◽  
New Particle Formation ◽  
Roll Vortices ◽  
The Impact

Abstract. Recent studies have shown the importance of new particle formation (NPF) to global cloud concensation nuclei (CCN) production, as well as to air pollution in megacities. In addition to the necessary presence of low-volatility vapors that can form the new aerosol particles, both numerical and observational studies have shown that the dynamics of the planetary boundary layer (BL) plays an important role in NPF. Evidence from field observations suggests that roll vortices might be favorable for inducing NPF in a convective BL. However, direct observations and estimates on the potential importance of this phenomenon to the production of new aerosol particles are lacking. Here we show that rolls frequently induce NPF bursts along the horizontal circulations, and that the small clusters and particles originating from these bursts grow in size similar to particles typically ascribed to regional-scale atmospheric NPF. We outline a method to identify roll-induced NPF from measurements and, based on the collected data, estimate the impact of roll vortices on the overall aerosol particle production due to NPF at a boreal forest site (83 ± 34 % and 26 ± 8 % overall enhancement in particle formation for 3-nm and 10-nm particles respectively). We conclude that the formation of roll vortices should be taken into account when estimating particle number budgets in the atmospheric BL.

scholarly journals Roll vortices induce new particle formation bursts in the planetary boundary layer

2020 ◽  
Vol 20 (20) ◽  
pp. 11841-11854
Author(s):  
Janne Lampilahti ◽  
Hanna Elina Manninen ◽  
Katri Leino ◽  
Riikka Väänänen ◽  
Antti Manninen ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Planetary Boundary Layer ◽  
Particle Production ◽  
Aerosol Particles ◽  
Regional Scale ◽  
Particle Formation ◽  
Forest Site ◽  
New Particle Formation ◽  
Roll Vortices ◽  
The Impact

Abstract. Recent studies have shown the importance of new particle formation (NPF) to global cloud condensation nuclei (CCN) production, as well as to air pollution in megacities. In addition to the necessary presence of low-volatility vapors that can form new aerosol particles, both numerical and observational studies have shown that the dynamics of the planetary boundary layer (BL) plays an important role in NPF. Evidence from field observations suggests that roll vortices might be favorable for inducing NPF in a convective BL. However, direct observations and estimates of the potential importance of this phenomenon to the production of new aerosol particles are lacking. Here we show that rolls frequently induce NPF bursts along the horizontal circulations and that the small clusters and particles originating from these localized bursts grow in size similar to particles typically ascribed to atmospheric NPF that occur almost homogeneously at a regional scale. We outline a method to identify roll-induced NPF from measurements and, based on the collected data, estimate the impact of roll vortices on the overall aerosol particle production due to NPF at a boreal forest site (83 % ± 34 % and 26 % ± 8 % overall enhancement in particle formation for 3 and 10 nm particles, respectively). We conclude that the formation of roll vortices should be taken into account when estimating particle number budgets in the atmospheric BL.

scholarly journals Ion-induced sulfuric acid–ammonia nucleation drives particle formation in coastal Antarctica

2018 ◽  
Vol 4 (11) ◽  
pp. eaat9744 ◽  
Author(s):  
T. Jokinen ◽  
M. Sipilä ◽  
J. Kontkanen ◽  
V. Vakkari ◽  
P. Tisler ◽  
...  
Keyword(s):  
Sulfuric Acid ◽  
Cloud Condensation Nuclei ◽  
Aerosol Particles ◽  
Particle Growth ◽  
Field Studies ◽  
Particle Formation ◽  
New Particle Formation ◽  
Aerosol Formation ◽  
Radiative Balance ◽  
Secondary Aerosol

Formation of new aerosol particles from trace gases is a major source of cloud condensation nuclei (CCN) in the global atmosphere, with potentially large effects on cloud optical properties and Earth’s radiative balance. Controlled laboratory experiments have resolved, in detail, the different nucleation pathways likely responsible for atmospheric new particle formation, yet very little is known from field studies about the molecular steps and compounds involved in different regions of the atmosphere. The scarcity of primary particle sources makes secondary aerosol formation particularly important in the Antarctic atmosphere. Here, we report on the observation of ion-induced nucleation of sulfuric acid and ammonia—a process experimentally investigated by the CERN CLOUD experiment—as a major source of secondary aerosol particles over coastal Antarctica. We further show that measured high sulfuric acid concentrations, exceeding 107 molecules cm−3, are sufficient to explain the observed new particle growth rates. Our findings show that ion-induced nucleation is the dominant particle formation mechanism, implying that galactic cosmic radiation plays a key role in new particle formation in the pristine Antarctic atmosphere.

Aerosol Radiative Effects Over India from Direct Radiation Measurements and Model Estimates

2021 ◽  
Author(s):  
Tamanna Subba ◽  
Mukunda M. Gogoi ◽  
K. Krishna Moorthy ◽  
Pradip K. Bhuyan ◽  
Binita Pathak ◽  
...  
Keyword(s):  
Radiative Effects ◽  
Direct Radiation ◽  
Aerosol Radiative Effects ◽  
Radiation Measurements ◽  
Aerosol Radiative

scholarly journals Hygroscopic properties of ultrafine aerosol particles in the boreal forest: diurnal variation, solubility and the influence of sulfuric acid

2007 ◽  
Vol 7 (1) ◽  
pp. 211-222 ◽  
Author(s):  
M. Ehn ◽  
T. Petäjä ◽  
H. Aufmhoff ◽  
P. Aalto ◽  
K. Hämeri ◽  
...  
Keyword(s):  
Sulfuric Acid ◽  
Boreal Forest ◽  
Diurnal Variation ◽  
Gas Phase ◽  
Aerosol Particles ◽  
Particle Formation ◽  
Time Of Day ◽  
New Particle Formation ◽  
Hygroscopic Growth ◽  
Hygroscopic Properties

Abstract. The hygroscopic growth of aerosol particles present in a boreal forest was measured at a relative humidity of 88%. Simultaneously the gas phase concentration of sulfuric acid, a very hygroscopic compound, was monitored. The focus was mainly on days with new particle formation by nucleation. The measured hygroscopic growth factors (GF) correlated positively with the gaseous phase sulfuric acid concentrations. The smaller the particles, the stronger the correlation, with r=0.20 for 50 nm and r=0.50 for 10 nm particles. The increase in GF due to condensing sulfuric acid is expected to be larger for particles with initially smaller masses. During new particle formation, the changes in solubility of the new particles were calculated during their growth to Aitken mode sizes. As the modal diameter increased, the solubility of the particles decreased. This indicated that the initial particle growth was due to more hygroscopic compounds, whereas the later growth during the evening and night was mainly caused by less hygroscopic or even hydrophobic compounds. For all the measured sizes, a diurnal variation in GF was observed both during days with and without particle formation. The GF was lowest at around midnight, with a mean value of 1.12–1.24 depending on particle size and if new particle formation occurred during the day, and increased to 1.25–1.34 around noon. This can be tentatively explained by day- and nighttime gas-phase chemistry; different vapors will be present depending on the time of day, and through condensation these compounds will alter the hygroscopic properties of the particles in different ways.

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