Source-dependent absorption Ångström exponent in the Los Angeles Basin: Multi-time resolution factor analyses of ambient PM2.5 and aerosol optical absorption
Advanced receptor models can leverage the information derived from optical and chemical variables as input by a variety of instruments at different time resolutions to extract the source specific absorption Ångström exponent (AAE) from aerosol absorption. The multilinear engine (ME-2), a Positive Matrix Factorization (PMF) solver, serves as a proficient tool for performing such analyses, thereby overcoming the constraints imposed by the assumptions in current optical source apportionment methods such as the Aethalometer approach since the use of a-priori AAE values introduces additional uncertainty into the results of optical methods. Comprehensive PM<sub>2.5</sub> chemical speciation datasets, and aerosol absorption coefficients (b<sub>abs</sub>, λ) at seven wavelengths measured by an Aethalometer (AE33), were used in multi-time source apportionment (MT-PMF). The study focused on two locations in the Los Angeles (LA) Basin: Central LA (CELA, Main St.), an urban area surrounded by major freeways, and Rubidoux (RIVR), a residential area surrounded by local roads. Factor profiles and temporal variations of their contributions were obtained. Additionally, factor displacements (DISP) and profile constraints were applied. Five-factor solutions were obtained at both sites. At CELA, the resolved factors included traffic + crustal matter (traffic+ Cr_M), secondary sulfate + nitrate (SSN), biomass burning (BB), diesel emissions (DIE) and aged sea salt (ASS). Moreover, source-dependent AAE values at CELA were obtained without a-priori assumption, with values of 1.46 for traffic+ Cr_M, 1.45 for DIE and 2.37 for BB. At RIVR, the resolved factors were traffic+ Cr_M (AAE = 1.24), particulate sulfate, particulate nitrate, BB (AAE = 3.00) and aged sea salt. PM<sub>2.5</sub> composition differed at both locations. SSN accounted for the largest fraction of the ambient PM<sub>2.5</sub> mass concentration, their sum at the CELA site averaged 40 % of the PM<sub>2.5</sub> mass while the same species represented 77 % at RIVR.
Authors
- Andrés Alástuey (ORCID: https://orcid.org/0000-0002-5453-5495)
- Marco Pandolfi (ORCID: https://orcid.org/0000-0002-7493-7213)
- Xavier Querol (ORCID: https://orcid.org/0000-0002-6549-9899)
- Marjan Savadkoohi
- Uwayemi M. Sofowote
- Philip Karl Hopke (ORCID: https://orcid.org/0000-0003-2367-9661)
Institutions
- Ministry of the Environment, Conservation and Parks (CA)
- Clarkson University (US)
- Ministry of Environment (CA)
- Institute of Environmental Assessment and Water Research (ES)
- Universitat Politècnica de Catalunya (ES)
Publication Details
- Journal
- The Science of The Total Environment
- Published
- 2024-12-20
- DOI
- https://doi.org/10.1016/j.scitotenv.2024.178095
- Citations
- 3
- Primary Topic
- Atmospheric chemistry and aerosols
- Type
- article
- Field-Weighted Citation Impact
- 1.13