EGU24-9842, updated on 08 Mar 2024
https://doi.org/10.5194/egusphere-egu24-9842
EGU General Assembly 2024
© Author(s) 2024. This work is distributed under
the Creative Commons Attribution 4.0 License.

Phenomenology of organic aerosols light absorption in europe based on in situ surface observations 

Jordi Rovira1, Gang Chen2, Jesús Yus-Díez3, Grisa Močnik3, and Marco Pandolfi1
Jordi Rovira et al.
  • 1Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Barcelona, 08034, Spain
  • 2MRC Centre for Environ. and Health, Environ. Research Group, Imperial College London, London, U.K
  • 3Center for Atmospheric Research, University of Nova Gorica, Ajdovščina, Slovenia

Both chamber and field experiments have shown that a fraction of organic aerosols (OA), called brown carbon (BrC), can efficiently absorb UV-VIS radiation with important effects on radiation balance. However, the optical properties of BrC, and its climate effects, remain poorly understood because a variety of chemical compositions are involved and their fractions vary with source and formation process. We present a phenomenology of OA light absorption in Europe using Aethalometer (AE) data. AE data were used to calculate the black carbon (BC) and BrC contribution to the total measured absorption in the UV-VIS spectral range (babs,BC(l), babsBrC(l)). Fig. 1 shows the BrC absorption at 370 nm and shows that the BrC absorption was on average higher in urban than in rural sites.

Figure 1. Map of BrC absorption in rural and urban sites.

At 18 out of 41 sites, simultaneous ACSM (Aerosol Chemical Speciation Monitor) data were available allowing reporting the mass absorption cross-section (MAC), the imaginary refractive index (k), the k Angström Exponent (w) of OA particles and OA sources. We compared the experimental data the with Saleh’s classification, that groups BrC in four optical classes, namely very weakly (VW-BrC), weakly (W-BrC), moderately (M-BrC) and strongly (S-BrC) absorbing BrC. Preliminary results show that both MAC and k of POA sources were higher compared to SOA sources and that BBOA (biomass burning OA) followed by CCOA (coal combustion OA) and HOA (hydrocarbon-like OA) dominated the absorption by BrC.  Data reported indicate a relationship between w and k with higher w associated to less absorbing OA particles.

With this work we provide a robust experimental framework that can be used to better constrain the climate effect of OA particles represented in climate models. In our results we found that most of the measured ambient OA particles present from W to M absorption properties. Variations in OA k and w depend on the relative contribution of POA compared to SOA as also reflected by the higher k observed in winter compared to summer. Our results also demonstrate a strong variation of OA optical properties in Europe thus further confirming the complexity of OA absorption properties.

This work was supported by the FOCI Project (G.A. 101056783) and ARRS P1-0385. Action Cost COLOSSAL. We thank the COLOSSAL Team for providing OA sources and AE33 data.

Chen et al (2022). Env. Int. 166, 107325.

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Canagaratna et al (2015). Atmos. Chem. Phys. 15, 253-272.

Saleh et al (2020). Curr. Pollution Rep. 6, 90–104.

How to cite: Rovira, J., Chen, G., Yus-Díez, J., Močnik, G., and Pandolfi, M.: Phenomenology of organic aerosols light absorption in europe based on in situ surface observations , EGU General Assembly 2024, Vienna, Austria, 14–19 Apr 2024, EGU24-9842, https://doi.org/10.5194/egusphere-egu24-9842, 2024.