| 1. |
- Bardakov, Roman, 1992-, et al.
(författare)
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The Role of Convective Up- and Downdrafts in the Transport of Trace Gases in the Amazon
- 2022
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Ingår i: Journal of Geophysical Research - Atmospheres. - : American Geophysical Union (AGU). - 2169-897X .- 2169-8996. ; 127:18
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Tidskriftsartikel (refereegranskat)abstract
- Deep convective clouds can redistribute gaseous species and particulate matter among different layers of the troposphere with important implications for atmospheric chemistry and climate. The large number of atmospheric trace gases of different volatility makes it challenging to predict their partitioning between hydrometeors and gas phase inside highly dynamic deep convective clouds. In this study, we use an ensemble of 51,200 trajectories simulated with a cloud-resolving model to characterize up- and downdrafts within Amazonian deep convective clouds. We also estimate the transport of a set of hypothetical non-reactive gases of different volatility, within the up- and downdrafts. We find that convective air parcels originating from the boundary layer (i.e., originating at 0.5 km altitude), can transport up to 25% of an intermediate volatility gas species (e.g., methyl hydrogen peroxide) and up to 60% of high volatility gas species (e.g., n-butane) to the cloud outflow above 10 km through the mean convective updraft. At the same time, the same type of gases can be transported to the boundary layer from the middle troposphere (i.e., originating at 5 km) within the mean convective downdraft with an efficiency close to 100%. Low volatility gases (e.g., nitric acid) are not efficiently transported, neither by the updrafts nor downdrafts, if the gas is assumed to be fully retained in a droplet upon freezing. The derived properties of the mean up- and downdraft can be used in future studies for investigating convective transport of a larger set of reactive trace gases.
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| 2. |
- Bardakov, Roman, 1992-
(författare)
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Transport and chemical processing of trace gases in deep convective clouds
- 2021
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Deep convective clouds can efficiently transport trace gases from the planetary boundary layer to the upper troposphere. Once there, some gases will contribute to new particle formation and growth, eventually producing aerosols that are large enough to influence cloud properties, the radiative budget of the Earth, and climate. The magnitude and exact pathways of the convective transport of many organic and inorganic compounds are, however, still unclear. This dissertation presents a framework to study vertical transport of gas mixtures by deep convective clouds. The method consists of a chemical box model that is driven by cloud air parcel trajectory data generated by large-eddy simulation. This combination allows us to examine detailed gas-cloud interactions as well as complex systems of gas-phase chemical reactions. A large ensemble of simulated cloud trajectories was used to identify and characterize convective up- and downdrafts in the Amazon region. The analysis showed that air parcels starting close to the surface (at 0.5 km) experienced a substantially larger probability of reaching the upper troposphere (above 10 km) than parcels starting at the top of the boundary layer. Furthermore, the framework was used to estimate the vertical transport of isoprene, isoprene oxidation products, ammonia, and several non-reactive trace gases. We found that a typical Amazonian deep convective cloud can transport around 30% of the boundary layer isoprene to the cloud outflow if the efficiency of the gas uptake on ice is high and there is no lightning within the cloud. If the efficiency of gas uptake on ice is low and lightning within the cloud is extensive, all isoprene will be oxidized. Several low-volatility isoprene oxidation products will then have relatively high concentrations in the outflow, which potentially could lead to new particle formation and growth. Another result was that up to 10% of the boundary layer ammonia can reach the cloud outflow, where it in some environments can nucleate synergistically with nitric and sulfuric acid. A key uncertainty in our estimates is the efficiency of gas uptake by ice particles.
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| 3. |
- Wang, Mingyi, et al.
(författare)
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Synergistic HNO3–H2SO4–NH3 upper tropospheric particle formation
- 2022
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Ingår i: Nature. - : Springer Science and Business Media LLC. - 0028-0836 .- 1476-4687. ; 605:7910, s. 483-489
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Tidskriftsartikel (refereegranskat)abstract
- New particle formation in the upper free troposphere is a major global source of cloud condensation nuclei (CCN). However, the precursor vapours that drive the process are not well understood. With experiments performed under upper tropospheric conditions in the CERN CLOUD chamber, we show that nitric acid, sulfuric acid and ammonia form particles synergistically, at rates that are orders of magnitude faster than those from any two of the three components. The importance of this mechanism depends on the availability of ammonia, which was previously thought to be efficiently scavenged by cloud droplets during convection. However, surprisingly high concentrations of ammonia and ammonium nitrate have recently been observed in the upper troposphere over the Asian monsoon region. Once particles have formed, co-condensation of ammonia and abundant nitric acid alone is sufficient to drive rapid growth to CCN sizes with only trace sulfate. Moreover, our measurements show that these CCN are also highly efficient ice nucleating particles—comparable to desert dust. Our model simulations confirm that ammonia is efficiently convected aloft during the Asian monsoon, driving rapid, multi-acid HNO3–H2SO4–NH3 nucleation in the upper troposphere and producing ice nucleating particles that spread across the mid-latitude Northern Hemisphere.
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