Abstract

Abstract. Sulfuric acid (H2SO4) is commonly accepted as a key precursor for atmospheric new particle formation (NPF). However, direct measurements of [H2SO4] remain challenging, thereby preventing the determination of this important quantity, and, consequently, a complete understanding of its contribution to the NPF process. Several proxies have been developed to bridge the gaps, but their ability to predict [H2SO4] under very specific conditions, such as those encountered in volcanic plumes (including, in particular, high sulfur dioxide mixing ratios), has not been evaluated so far. In this context, the main objective of the present study was to develop new proxies for daytime [H2SO4] under volcanic plume conditions and compare their performance to that of the proxies available in the literature. Specifically, the data collected at Maïdo during the OCTAVE (Oxygenated organic Compounds in the Tropical Atmosphere: variability and atmosphere–biosphere Exchanges) 2018 campaign, in the volcanic eruption plume of the Piton de la Fournaise, were first used to derive seven proxies based on knowledge of the sulfur dioxide (SO2) mixing ratio, global radiation, condensation sink (CS) and relative humidity (RH). A specific combination of some or all of these variables was tested in each of the seven proxies. In three of them (F1–F3), all considered variables were given equal weight in the prediction of [H2SO4], whereas adjusted powers were allowed (and determined during the fitting procedure) for the different variables in the other four proxies (A1–A4). Overall, proxies A1–A4 were found to perform better than proxies F1–F3, with, in particular, improved predictive ability for [H2SO4] > 2 × 108 cm−3. The CS was observed to play an important role in regulating [H2SO4], whereas the inclusion of RH did not improve the predictions. A last expression accounting for an additional sink term related to cluster formation, S1, was also tested and showed a very good predictive ability over the whole range of measured [H2SO4]. In a second step, the newly developed proxies were further evaluated using airborne measurements performed in the passive degassing plume of Etna during the STRAP (Synergie Transdisciplinaire pour Répondre aux Aléas liés aux Panaches volcaniques) 2016 campaign. Increased correlations between observed and predicted [H2SO4] were obtained when the dependence of predicted [H2SO4] on the CS was the lowest and when the dependence on [SO2] was concurrently the highest. The best predictions were finally retrieved by the simple formulation of F2 (in which [SO2] and radiation alone were assumed to explain the variations in [H2SO4] with equal contributions), with a pre-factor adapted to the STRAP data. All in all, our results illustrate the fairly good capacity of the proxies available in the literature to describe [H2SO4] under volcanic plume conditions, but they concurrently highlight the benefit of the newly developed proxies for the prediction of the highest concentrations ([H2SO4] > 2–3 × 108 cm−3). Moreover, the contrasting behaviours of the new proxies in the two investigated datasets indicate that in volcanic plumes, like in other environments, the relevance of a proxy can be affected by changes in environmental conditions and that location-specific coefficients do logically improve the predictions.

Highlights

  • Sulfuric acid (H2SO4) is commonly accepted as a key precursor for atmospheric new particle formation (NPF) and is, considered as the main driving species of cluster formation in air quality and climate models (Semeniuk and Dastoor, 2018)

  • Only the data collected in the volcanic eruption plume of the Piton de la Fournaise were effectively used to perform the fitting procedures, and the measurements obtained in the passive degassing plume of Etna were used in a second step to further test the newly derived proxies on a different dataset

  • While the questions related to the use of a proxy at different locations and/or under different conditions have been raised in earlier studies, such questions obviously apply to the volcanic plume, where the conditions are subject to very rapid change and certainly differ depending on the type of plume

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Summary

Introduction

Sulfuric acid (H2SO4) is commonly accepted as a key precursor for atmospheric new particle formation (NPF) and is, considered as the main driving species of cluster formation in air quality and climate models (Semeniuk and Dastoor, 2018) While it may not always be determinant in the process (Kirkby et al, 2016; Rose et al, 2018), evidence for the contribution of H2SO4 to the formation and initial growth of particles has been reported from chamber experiments (Kirkby et al, 2011; Duplissy et al, 2016; Lehtipalo et al, 2018) and atmospheric measurements performed in various environments (Frege et al, 2017; Jokinen et al, 2018; Yan et al, 2018). Using indirect quantification of [H2SO4], Rose et al (2019) concurrently reported a fair agreement between measured cluster formation rates and the values derived from the recent parameterization of water–sulfuric acid binary nucleation by Määttänen et al (2018), which predicted a likely significant contribution of ion-induced nucleation in the volcanic plume for [H2SO4] below ∼ 8 × 108 cm−3

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