To better understand the formation process of biogenic and anthropogenic secondary organic aerosols (BSOA and ASOA) in the marine atmosphere under the background of global warming, aerosol samples were collected over three summers (i.e., 2014, 2016 and 2018) from the Bering Sea (BS) to the western North Pacific (WNP). The results showed that temporally, atmospheric concentrations of isoprene-derived SOA (SOA) tracers were the lowest in 2014 regardless of the marine region, while atmospheric concentrations of monoterpenes-derived SOA (SOA) tracers in this year were the highest and the aerosols were more aged than those in the other two years. In comparison, the concentrations of β-caryophyllene-derived and toluene-derived SOA (SOA and SOA) tracers were relatively low overall. Spatially, the concentrations of SOA tracers were significantly higher over the WNP than over the BS, with SOA tracers over the BS mainly coming from marine sources, while the WNP was strongly influenced by terrestrial inputs. In particular, for land-influenced samples from the WNP, NO-channel products of SOA were more dependent on O and SO relative to HO-channel product, and the high atmospheric oxidation capacity and SO could promote the formation of later-generation SOA products. The extent of terrestrial influence was further quantified using a principal component analysis (PCA)-generalized additive model (GAM), which showed that terrestrial emissions explained more than half of the BSOA tracers' concentrations and contributed almost all of the ASOA tracer. In addition, the assessment of secondary organic carbon (SOC) highlighted the key role of anthropogenic activities in organic carbon levels in offshore areas. Our study revealed significant contributions of terrestrial natural and anthropogenic sources to different SOA over the WNP, and these relevant findings help improve knowledge about SOA in the marine atmosphere.
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http://dx.doi.org/10.1016/j.scitotenv.2022.160138 | DOI Listing |
ACS Earth Space Chem
December 2024
Université Paris-Est Créteil and Université Paris Cité, CNRS, LISA, Créteil F-94010, France.
Hydroxyacetone (HA) is an atmospheric oxidation product of isoprene and other organic precursors that can form brown carbon (BrC). Measured bulk aqueous-phase reaction rates of HA with ammonium sulfate, methylamine, and glycine suggest that these reactions cannot compete with aqueous-phase hydroxyl radical oxidation. In cloud chamber photooxidation experiments with either gaseous or particulate HA in the presence of the same N-containing species, BrC formation was minor, with similar mass absorption coefficients at 365 nm (<0.
View Article and Find Full Text PDFEnviron Sci Technol
December 2024
Institute of Low Temperature Science, Hokkaido University, Sapporo 060-0819, Japan.
Arctic haze has attracted considerable scientific interest for decades. However, limited studies have focused on the molecular composition of atmospheric particulate matter that contributes to Arctic haze. Our study collected atmospheric particles at Alert in the Canadian high Arctic from mid-February to early May 2000.
View Article and Find Full Text PDFACS Earth Space Chem
November 2024
Department of Environmental Toxicology, University of California, Davis, California 95616, United States.
Phenolic compounds, which are significant emissions from biomass burning (BB), undergo rapid photochemical reactions in both gas and aqueous phases to form secondary organic aerosol, namely, gasSOA and aqSOA, respectively. The formation of gasSOA and aqSOA involves different reaction mechanisms, leading to different product distributions. In this study, we investigate the gaseous and aqueous reactions of guaiacol-a representative BB phenol-to elucidate the compositional differences between phenolic aqSOA and gasSOA.
View Article and Find Full Text PDFSci Total Environ
December 2024
State Key Joint Laboratory of Environmental Simulation and Pollution Control, International Joint Laboratory for Regional Pollution Control, Ministry of Education (IJRC), College of Environmental Sciences and Engineering, Beijing 100871, China; Collaborative Innovation Center of Atmospheric Environment and Equipment Technology, Nanjing University of Information Science & Technology, Nanjing 210044, China. Electronic address:
Semi-volatile/intermediate-volatility organic compounds (S/IVOCs) are considered to be missing precursors of secondary organic aerosol (SOA). In this study, ambient S/IVOCs were collected in the winter of Chengdu and were analyzed by a thermal desorption-comprehensive two-dimensional gas chromatography-quadrupole mass spectrometer (TD-GC×GC-qMS). Molecular characteristics and volatility-polarity distributions of the S/IVOCs were specified.
View Article and Find Full Text PDFSci Total Environ
November 2024
Institute of Surface-Earth System Science, Tianjin University, Tianjin 300072, China. Electronic address:
Secondary organic aerosol (SOA) accounts for a large fraction of fine particulate matter (PM), but the lack of vertical observations of SOA in the urban boundary layer (UBL) limits a comprehensive understanding of its sources and formation mechanisms. In this study, PM samples were simultaneously collected at 3 m, 118 m, and 488 m on the Canton Tower in Guangzhou during winter. Typical SOA tracers, including oxidation products of isoprene (SOA), monoterpene (SOA), sesquiterpene (SOA), and toluene (ASOA), were investigated alongside meteorological parameters and gaseous/particulate pollutants.
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