Journal cover Journal topic
Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
doi:10.5194/acp-2016-684
© Author(s) 2016. This work is distributed
under the Creative Commons Attribution 3.0 License.
Research article
04 Oct 2016
Review status
This discussion paper is under review for the journal Atmospheric Chemistry and Physics (ACP).
Summertime OH reactivity from a receptor coastal site in the Mediterranean basin
Nora Zannoni1, Valerie Gros1, Roland Sarda Esteve1, Cerise Kalogridis1,2, Vincent Michoud3,4,5, Sebastien Dusanter3,4,6, Stephane Sauvage3,4, Nadine Locoge3,4, Aurelie Colomb7, and Bernard Bonsang1 1SCE, Laboratorie Scientifique du Climat et de l’Environnement, CNRS-CEA-UVSQ, 91191 Gif sur Yvette, France
2Institute of Nuclear Technology and Radiation Protection, National Centre of Scientific Research "Demokritos", 15310 Ag. Paraskevi, Attiki, Greece
3Mines Douai, Département Sciences de l’Atmosphère et Génie de l’Environnement (SAGE), 59508 Douai, France
4Universite de Lille, F-59000 Lille, France
5Laboratoire Interuniversitaire des Systèmes Atmosphériques (LISA), 61 avenue du Général de Gaulle, 94010 Créteil, France
6School of Public and Environmental Affairs, Indiana University, Bloomington, IN, USA
7LAMP, Campus universitaire des Cezeaux, 4 Avenue Blaise Pascal, 63178 Aubiere, France
Abstract. Total OH reactivity, the total loss frequency of the hydroxyl radical in ambient air, provides the total loading of reactive gases in air. We measured the total OH reactivity for the first time during summertime at a coastal receptor site located in the western Mediterranean basin. Measurements were performed at a temporary field site located in the northern cape of Corsica (France), during summer 2013 for the project CARBOSOR (CARBOn within continental pollution plumes: SOurces and Reactivity) -ChArMeX (Chemistry-Aerosols Mediterranean Experiment). Here, we compare the measured total OH reactivity with the OH reactivity inferred from the measured reactive gases. The difference between these two parameters is termed missing OH reactivity, i.e., the fraction of OH reactivity not explained by the measured compounds. The total OH reactivity at the site varied between the instrumental LoD (limit of detection = 3 s−1) to a maximum of 17 ± 6 s−1 (35 % uncertainty) and was 5 ± 4 s−1 (1σ standard deviation) on average. It varied with air temperature exhibiting a diurnal profile comparable to the one of the biogenic volatile organic compounds measured at the site. We observed a fraction of missing OH reactivity during two distinct periods (on average 56 %), associated respectively to transported aged air masses and low-wind speed conditions at the site. We suggest that oxygenated molecules, mostly formed from reactions of biogenic gases precursors, were the major contributors to the missing OH reactivity.

Citation: Zannoni, N., Gros, V., Sarda Esteve, R., Kalogridis, C., Michoud, V., Dusanter, S., Sauvage, S., Locoge, N., Colomb, A., and Bonsang, B.: Summertime OH reactivity from a receptor coastal site in the Mediterranean basin, Atmos. Chem. Phys. Discuss., doi:10.5194/acp-2016-684, in review, 2016.
Nora Zannoni et al.
Nora Zannoni et al.
Nora Zannoni et al.

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Short summary
Our manuscript presents results of hydroxyl radical (OH) reactivity from a field study conducted during summer 2013 in a western Mediterranean coastal site (Corsica, France). Here, the total OH reactivity, measured directly with the comparative reactivity method, is compared with the summed OH reactivity from the reactive gases measured with a multitude of different technologies. Our results demonstrate the relatively-high observed reactivity and the large impact of biogenic compounds.
Our manuscript presents results of hydroxyl radical (OH) reactivity from a field study conducted...
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