Here we use a filter based technique to measure atmospheric INPs on top of filters which have been collected on board of the BAe-146 FAAM aircraft in a range of contrasting environments, from the tropics to the Arctic. INP measurements are carried out in parallel with a compositional analysis using Scanning Electron Microscopy (SEM), in order to obtain the size-segregated composition of the atmospheric aerosol particles (Sanchez-Marroquin et al., 2019). This double analysis has been applied in three field campaigns in very contrasting locations: UK, Iceland and Alaska (we also compare with a published dataset in Cape Verde where we used the same technique (Price et al., 2018)).
We clearly show that the INP concentration spectra in the different environments are very different (scattering more than 12 oC at a given concentration), but that there is also a great deal of variability at single locations (Fig. 1). Aerosol samples dominated by Saharan dust with large concentrations of INPs were collected in Cape Verde (Price et al., 2018). The samples collected in the UK were very heterogeneous in composition, and the INP concentrations were not as high as in Cape Verde at lower temperatures, but at above about -15°C some of the spectra have higher concentrations. This is consistent with a local, probably biogenic INP source which has been inferred from ground based measurements (O'Sullivan et al., 2018). Icelandic samples were dominated by the presence of local re-suspended volcanic material, which we find is an effective ice-nucleator, with the potential to contribute significantly to INP population at mid- to high-latitudes (Sanchez-Marroquin et al., In prep). Both the aerosol and INP concentrations in Alaska were very low. Our results also show that most of the measured INP concentrations can be explained based on the aerosol surface area of the sample, and particularly the presence of mineral dust.
This study helps to understand the sources and distributions of INPs at different locations, showing its high spatial variability which presumably leads to variability in ice and supercooled water content in clouds around the world. This is particularly relevant since there are very few INP measurements around the globe and we are yet to quantify all INP sources.
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CAPTION: Figure 1. INP concentration measurements at different locations. Data has been compared with the range of typical INP concentrations at various locations and sessions from (Petters and Wright, 2015). (*) All the Cape Verde data was obtained by (Price et al., 2018). Circles represent data significantly above the limit of detection while crosses represent upper limits.