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Volume 18, issue 19
Atmos. Chem. Phys., 18, 13969-13985, 2018
https://doi.org/10.5194/acp-18-13969-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
Atmos. Chem. Phys., 18, 13969-13985, 2018
https://doi.org/10.5194/acp-18-13969-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.

Research article 02 Oct 2018

Research article | 02 Oct 2018

Daytime HONO, NO2 and aerosol distributions from MAX-DOAS observations in Melbourne

Robert G. Ryan1,2, Steve Rhodes3, Matthew Tully3, Stephen Wilson4, Nicholas Jones4, Udo Frieß5, and Robyn Schofield1,2 Robert G. Ryan et al.
  • 1School of Earth Sciences, University of Melbourne, Melbourne, Australia
  • 2ARC Centre of Excellence for Climate System Science, Sydney, Australia
  • 3Bureau of Meteorology, Melbourne, Australia
  • 4School of Chemistry, University of Wollongong, Wollongong, Australia
  • 5Institute for Environmental Physics, University of Heidelberg, Heidelberg, Germany

Abstract. Toxic nitrogen oxides produced by high temperature combustion are prevalent in urban environments, contributing to a significant health burden. Nitrogen oxides such as NO2 and HONO in pollution are important for hydroxyl radical (OH) production and overall oxidative capacity in urban environments; however, current mechanisms cannot explain high daytime levels of HONO observed in many urban and rural locations around the world. Here we present HONO, NO2 and aerosol extinction vertical distributions retrieved from multi-axis differential optical absorption spectroscopy (MAX-DOAS) measurements in suburban Melbourne, which are the first MAX-DOAS results from the Australian continent. Using the optimal estimation algorithm HEIPRO we show that vertical profiles for NO2 and HONO can be calculated with a low dependence on the retrieval forward model and a priori parameters, despite a lack of independent co-located aerosol or trace gas measurements. Between December 2016 and April 2017 average peak NO2 values of 8±2 ppb indicated moderate traffic pollution levels, and high daytime peak values of HONO were frequently detected, averaging 220±30 ppt in the middle of the day. HONO levels measured in Melbourne were typically lower than those recorded in the morning in other places around the world, indicating minimal overnight accumulation, but peaked in the middle of the day to be commensurate with midday concentrations in locations with much higher NO2 pollution. Regular midday peaks in the diurnal cycle of HONO surface concentrations have only previously been reported in rural locations. The HONO measured implies a daytime source term 1 ppb h−1 above the predicted photostationary state (PSS) concentration and represents an OH radical source up to 4 times stronger than from ozone photolysis alone in the lowest 500 m of the troposphere. The dependence of the high midday HONO levels on soil moisture, combined with the observed diurnal and vertical profiles, provides evidence for a strong photoactivated and ground-based daytime HONO source.

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Nitrous acid (HONO) plays a crucial role in the self-cleansing capacity of the atmosphere but its formation mechanisms and spatial distributions are not well understood. This paper presents spectroscopic measurements of HONO, NO2 and aerosol measurements from Melbourne, Australia. HONO levels are at a maximum in the middle of the day, which is unprecedented for an urban area, and these measurements provide evidence for the existence of a strong ground-based, daytime nitrogen oxide source.
Nitrous acid (HONO) plays a crucial role in the self-cleansing capacity of the atmosphere but...
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