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Is the ocean surface a source of nitrous acid (HONO) in the marine boundary layer?

Authors :
Crilley, Leigh R.
Kramer, Louisa J.
Pope, Francis D.
Reed, Chris
Lee, James D.
Carpenter, Lucy J.
Hollis, Lloyd D. J.
Ball, Stephen M.
Bloss, William J.
Source :
Atmospheric Chemistry & Physics Discussions; 7/7/2021, p1-23, 23p
Publication Year :
2021

Abstract

Nitrous acid, HONO, is a key net photolytic precursor to OH radicals in the atmospheric boundary later. As OH is the dominant atmospheric oxidant, driving the removal of many primary pollutants and the formation of secondary species, a quantitative understanding of HONO sources is important to predict atmospheric oxidising capacity. While a number of HONO formation mechanisms have been identified, recent work has ascribed significant importance to the dark, oceansurface mediated conversion of NO<subscript>2</subscript> to HONO in the coastal marine boundary layer. In order to evaluate the role of this mechanism, here we analyse measurements of HONO and related species obtained at two contrasting coastal locations - Cape Verde (Atlantic Ocean), representative of the clean remote tropical marine boundary layer, and Weybourne (United Kingdom), representative of semi-polluted Northern European coastal waters. As expected, higher average concentrations of HONO (70 ppt) were observed in marine air for the more anthropogenically influenced Weybourne location compared to Cape Verde (HONO <5 ppt). At both sites, the approximately constant HONO/NO <subscript>2</subscript> ratio at night pointed to a low importance for the dark ocean-surface mediated conversion of NO<subscript>2</subscript> into HONO, whereas the midday maximum in the HONO/NO<subscript>2</subscript> ratios indicated significant contributions from photo-enhanced HONO formation mechanisms (or other sources). We obtained an upper limit to the rate coefficient of dark ocean-surface HONO-to-NO<subscript>2</subscript> conversion of CHONO = 0.0011 ppb hr<superscript>-1</superscript> from the Cape Verde observations; this is a factor of 5 lower than the slowest rate reported previously. These results point to significant geographical variation in the predominant HONO formation mechanisms in marine environments and indicate that caution is required when extrapolating the importance of such mechanisms from individual study locations to assess regional and/or global impacts on oxidising capacity. As a significant fraction of atmospheric processing occurs in the marine boundary layer, particularly in the tropics, better constraint of the possible ocean surface source of HONO is important for a quantitative understanding of chemical processing of primary trace gases in the global atmospheric boundary layer and associated impacts upon air pollution and climate. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16807367
Database :
Complementary Index
Journal :
Atmospheric Chemistry & Physics Discussions
Publication Type :
Academic Journal
Accession number :
151308940
Full Text :
https://doi.org/10.5194/acp-2021-532