Wildfires can influence the earth’s radiative forcing through the emission of biomass-burning aerosols. To better constrain the impacts of wildfires on climate and understand their evolution under future climate scenarios, reconstructing their chemical nature, assessing their past variability, and evaluating their influence on the atmospheric composition are essential. Ice cores are unique to perform such reconstructions representing archives not only of past biomass-burning events but also of concurrent climate and environmental changes. Here, we present a novel methodology for the quantification of five biomass-burning proxies (syringic acid, vanillic acid, vanillin, syringaldehyde, and p-hydroxybenzoic acid) and one biogenic emission proxy (pinic acid) using solid phase extraction (SPE) and ultrahigh-performance liquid chromatography coupled with high-resolution mass spectrometry. This method was also optimized for untargeted screening analysis to gain a broader knowledge about the chemical composition of organic aerosols in ice and snow samples. The method provides low detection limits (0.003–0.012 ng g–1), high recoveries (74 ± 10%), and excellent reproducibility, allowing the quantification of the six proxies and the identification of 313 different molecules, mainly constituted by carbon, hydrogen, and oxygen. The effectiveness of two different sample storage strategies, i.e., re-freezing of previously molten ice samples and freezing of previously loaded SPE cartridges, was also assessed, showing that the latter approach provides more reproducible results.

<p>Ice cores are unique natural archives that provide important information about the past evolution of the Earth’s atmosphere. Whereas the inorganic atmospheric aerosol fraction is well characterized, the organic composition is less understood. The organic aerosol burden is consistently underestimated in the current state-of-the-art models, thus highlighting major gaps in our understanding of the pathways by which organic aerosols accumulate and evolve in the atmosphere. So far, organic aerosols in ice cores have been primarily reported as either bulk (e.g., water insoluble or dissolved organic carbon) or specific parameters (e.g., biomass burning tracers).<br />To provide a more comprehensive characterization of the organic fraction, we applied a non-target screening approach optimised for determining oxidation products of volatile organic compounds to a firn core collected on the Corbassière glacier (Grand Combin, Swiss Alps), in 2020, covering the period 2008-2020. In comparison with a firn core drilled two years earlier (2018), we observe a drastic disturbance of seasonal trends for certain species, such as major ions at depths corresponding to the annual layers from 2008 to 2016, induced by meltwater percolation.</p> <p>As organic tracers are present in low concentrations in the firn core, we performed solid phase extraction. The organic tracers were analysed with high-resolution mass spectrometry based on Orbitrap technology coupled with liquid chromatography. This technique makes it possible to study a wide range of individual compounds at low concentration and to identify them with MS/MS fragmentation. We can attribute molecular formulas to detected compounds by comparing the MS/MS spectra with spectral libraries (e.g., mzCloud) or reference standards. With this approach we will present a unique record of molecular composition of organic aerosol in the Corbassière firn core.<br />Furthermore, this firn core presents a unique opportunity to examine the effect of melting on the organic tracers. We found that specific burning tracers (e.g., vanillic acid, vanillin and syringaldehyde) are less affected than other biomass tracers (e.g., pinic acid) by meltwater percolation. In general, we observe a decrease in concentration of the organic tracers in the same firn core section where we also observe a decrease in major ion concentrations.</p>