Analysis and Evaluation of Sulfur Dioxide and Equivalent Black Carbon at a Southern Italian WMO/GAW Station Using the Ozone to Nitrogen Oxides Ratio Methodology as Proximity Indicator

The measurement and evaluation of the atmospheric background levels of greenhouse gases (GHGs) and aerosols are useful to determine long-term tendencies and variabilities, and pinpoint peaks attributable to anthropogenic emissions and exceptional natural emissions such as volcanoes. At the Lamezia Terme (code: LMT) World Meteorological Organization–Global Atmosphere Watch (WMO/GAW) observation site located in the south Italian region of Calabria, the “Proximity” methodology based on photochemical processes, i.e., the ratio of tropospheric ozone (O3) to nitrogen oxides (NOx) has been used to discriminate the local and remote atmospheric concentrations of GHGs. Local air masses are heavily affected by anthropogenic emissions while remote air masses are more representative of atmospheric background conditions. This study applies, to eight continuous years of measurements (2016–2023), the Proximity methodology to sulfur dioxide (SO2) for the first time, and also extends it to equivalent black carbon (eBC) to assess whether the methodology can be applied to aerosols. The results indicate that SO2 follows a peculiar pattern, with LOC (local) and BKG (background) levels being generally lower than their N–SRC (near source) and R–SRC (remote source), thus corroborating previous hypotheses on SO2 variability at LMT by which the Aeolian Arc of volcanoes and maritime traffic could be responsible for these concentration levels. The anomalous behavior of SO2 was assessed using the Proximity Progression Factor (PPF) introduced in this study, which provides a value representative of changes from local to background concentrations. This finding, combined with an evaluation of known sources on a regional scale, has been used to provide an estimate on the spatial resolution of proximity categories, which is one of the known limitations of this methodology. Furthermore, the results confirm the potential of using the Proximity methodology for aerosols, as eBC shows a pattern consistent with local sources of emissions, such as wildfires and other forms of biomass burning, being responsible for the observed peaks.

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Publication Details

Journal
Environments
Published
2025-08-09
DOI
https://doi.org/10.3390/environments12080273
Primary Topic
Atmospheric chemistry and aerosols
Type
article
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article

Analysis and Evaluation of Sulfur Dioxide and Equivalent Black Carbon at a Southern Italian WMO/GAW Station Using the Ozone to Nitrogen Oxides Ratio Methodology as Proximity Indicator

Claudia Roberta Calidonna, Teresa Lo Feudo, Daniel Gullì, Ivano Ammoscato et al.
Environments
Atmospheric chemistry and aerosols
article

Analysis and Evaluation of Sulfur Dioxide and Equivalent Black Carbon at a Southern Italian WMO/GAW Station Using the Ozone to Nitrogen Oxides Ratio Methodology as Proximity Indicator

Claudia Roberta Calidonna, Teresa Lo Feudo, Daniel Gullì, Ivano Ammoscato, Luana Malacaria, Francesco D’Amico, Salvatore Sinopoli, Giorgia De Benedetto
article en

Abstract

The measurement and evaluation of the atmospheric background levels of greenhouse gases (GHGs) and aerosols are useful to determine long-term tendencies and variabilities, and pinpoint peaks attributable to anthropogenic emissions and exceptional natural emissions such as volcanoes. At the Lamezia Terme (code: LMT) World Meteorological Organization–Global Atmosphere Watch (WMO/GAW) observation site located in the south Italian region of Calabria, the “Proximity” methodology based on photochemical processes, i.e., the ratio of tropospheric ozone (O3) to nitrogen oxides (NOx) has been used to discriminate the local and remote atmospheric concentrations of GHGs. Local air masses are heavily affected by anthropogenic emissions while remote air masses are more representative of atmospheric background conditions. This study applies, to eight continuous years of measurements (2016–2023), the Proximity methodology to sulfur dioxide (SO2) for the first time, and also extends it to equivalent black carbon (eBC) to assess whether the methodology can be applied to aerosols. The results indicate that SO2 follows a peculiar pattern, with LOC (local) and BKG (background) levels being generally lower than their N–SRC (near source) and R–SRC (remote source), thus corroborating previous hypotheses on SO2 variability at LMT by which the Aeolian Arc of volcanoes and maritime traffic could be responsible for these concentration levels. The anomalous behavior of SO2 was assessed using the Proximity Progression Factor (PPF) introduced in this study, which provides a value representative of changes from local to background concentrations. This finding, combined with an evaluation of known sources on a regional scale, has been used to provide an estimate on the spatial resolution of proximity categories, which is one of the known limitations of this methodology. Furthermore, the results confirm the potential of using the Proximity methodology for aerosols, as eBC shows a pattern consistent with local sources of emissions, such as wildfires and other forms of biomass burning, being responsible for the observed peaks.

EnvironmentsVol. 12(8)
Institute of Atmospheric Sciences and Climate (IT), University of Calabria (IT)
Openalex Percentile: Top 74%
Atmospheric chemistry and aerosols
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