Radiative properties of the arctic aerosol

1982 ◽  
Vol 16 (12) ◽  
pp. 2967-2977 ◽  
Author(s):  
E.M Patterson ◽  
B.T Marshall ◽  
K.A Rahn
2021 ◽  
Author(s):  
Yvette Gramlich ◽  
Sophie Haslett ◽  
Karolina Siegel ◽  
Gabriel Freitas ◽  
Radovan Krejci ◽  
...  

<p>The number of cloud seeds, e.g. cloud condensation nuclei (CCN) and ice nucleation particles (INP), in the pristine Arctic shows a large range throughout the year, thereby influencing the radiative properties of Arctic clouds. However, little is known about the chemical properties of CCN and INP in this region. This study aims to investigate the chemical properties of aerosol particles and trace gases that are of importance for cloud formation in the Arctic environment, with focus on the organic fraction.</p><p>Over the course of one full year (fall 2019 until fall 2020), we deployed a filter-inlet for gases and aerosols coupled to a chemical ionization high-resolution time-of-flight mass spectrometer (FIGAERO-CIMS) using iodide as reagent ion at the Zeppelin Observatory in Svalbard (480 m a.s.l.), as part of the Ny-Ålesund Aerosol Cloud Experiment (NASCENT). The FIGAERO-CIMS is able to measure organic trace gases and aerosol particles semi-simultaneously. The instrument was connected to an inlet switching between a counterflow virtual impactor (CVI) inlet and a total air inlet. This setup allows to study the differences in chemical composition of organic aerosol particles and trace gases at molecular level that are involved in Arctic cloud formation compared to ambient non-activated aerosol.</p><p>We observed organic signal above background in both gas and particle phase all year round. A comparison between the gas phase mass spectra of cloud-free and cloudy conditions shows lower signal for some organics inside the cloud, indicating that some trace gases are scavenged by cloud hydrometeors whilst others are not. In this presentation we will discuss the chemical characteristics of the gases exhibiting different behavior during clear sky and cloudy conditions, and the implications for partitioning of organic compounds between the gas, aerosol particle and cloud hydrometeor (droplet/ice) phase.</p>


2017 ◽  
Author(s):  
Gwennolé Guyot ◽  
Frans Olofson ◽  
Peter Tunved ◽  
Christophe Gourbeyre ◽  
Guy Fevbre ◽  
...  

Abstract. This study will focus on cloud microphysical and optical characterization of three different types of episodes encountered during the ground based CLIMSLIP-NyA campaign performed in Ny-Alesund, Svalbard: the Mixed Phase Cloud (MPC), snow precipitation and Blowing Snow (BS) events. These in situ cloud measurements will be combined with aerosol measurements and air mass backtrajectory simulations to qualify and parameterize the arctic aerosol cloud interaction and to assess the influence of anthropogenic pollution transported into the Arctic. The results show a cloud bimodal distribution with the droplet mode at 10 µm and the crystal mode centered at 250 µm, for the MPC cases. The precipitation cases presents a crystal distribution centered around 350 µm with mostly of dendritic shape. The BS cases show a higher concentration but smaller crystals, centered between 150 and 200 µm, with mainly irregular crystals. A polluted case, where aerosol properties are influenced by anthropogenic emission from Europe and East Asia, was compared to a clean case with local aerosol sources. These anthropogenic emissions seem to cause higher Black Carbon, aerosol and droplet concentrations, a more pronounced accumulation mode, smaller droplet sizes and a higher activation fraction Fa. Moreover, the activation diameter decreases as the droplet diameter increases and Fa increases showing that smaller particles are activated and droplets grow when the aerosol number decreases. This is in agreement with the first (Twomey) and second (Albrecht) aerosol indirect effect. The quantification of the variations of droplet concentration and size leads to IE (Indirect Effect) and NE (Nucleation Efficiency) coefficients values around 0.2 and 0.43, respectively. These values are close to those found by other studies in the arctic region which confirms these parameterizations of arctic aerosol-cloud interaction in climate models.


1985 ◽  
Vol 19 (12) ◽  
pp. 2083-2097 ◽  
Author(s):  
Niels Z. Heidam
Keyword(s):  

2011 ◽  
Vol 11 (22) ◽  
pp. 11335-11350 ◽  
Author(s):  
M. Martin ◽  
R. Y.-W. Chang ◽  
B. Sierau ◽  
S. Sjogren ◽  
E. Swietlicki ◽  
...  

Abstract. We present an aerosol – cloud condensation nuclei (CCN) closure study on summer high Arctic aerosol based on measurements that were carried out in 2008 during the Arctic Summer Cloud Ocean Study (ASCOS) on board the Swedish ice breaker Oden. The data presented here were collected during a three-week time period in the pack ice (>85° N) when the icebreaker Oden was moored to an ice floe and drifted passively during the most biological active period into autumn freeze up conditions. CCN number concentrations were obtained using two CCN counters measuring at different supersaturations. The directly measured CCN number concentration was then compared with a CCN number concentration calculated using both bulk aerosol mass composition data from an aerosol mass spectrometer (AMS) and aerosol number size distributions obtained from a differential mobility particle sizer, assuming κ-Köhler theory, surface tension of water and an internally mixed aerosol. The last assumption was supported by measurements made with a hygroscopic tandem differential mobility analyzer (HTDMA) for particles >70 nm. For the two highest measured supersaturations, 0.73 and 0.41%, closure could not be achieved with the investigated settings concerning hygroscopicity and density. The calculated CCN number concentration was always higher than the measured one for those two supersaturations. This might be caused by a relative larger insoluble organic mass fraction of the smaller particles that activate at these supersaturations, which are thus less good CCN than the larger particles. On average, 36% of the mass measured with the AMS was organic mass. At 0.20, 0.15 and 0.10% supersaturation, closure could be achieved with different combinations of hygroscopic parameters and densities within the uncertainty range of the fit. The best agreement of the calculated CCN number concentration with the observed one was achieved when the organic fraction of the aerosol was treated as nearly water insoluble (κorg=0.02), leading to a mean total κ, κtot, of 0.33 ± 0.13. However, several settings led to closure and κorg=0.2 is found to be an upper limit at 0.1% supersaturation. κorg≤0.2 leads to a κtot range of 0.33 ± 013 to 0.50 ± 0.11. Thus, the organic material ranges from being sparingly soluble to effectively insoluble. These results suggest that an increase in organic mass fraction in particles of a certain size would lead to a suppression of the Arctic CCN activity.


Author(s):  
S. Generoso ◽  
F.-M. Bréon ◽  
F. Chevallier ◽  
Y. Balkanski ◽  
M. Schulz ◽  
...  

1992 ◽  
Vol 26 (9) ◽  
pp. 1747-1762 ◽  
Author(s):  
James R. Anderson ◽  
Peter R. Buseck ◽  
Daniel A. Saucy ◽  
Josef M. Pacyna

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