Polar ice cores are an invaluable archive of past climate, thanks to recording a unique variety of proxies such as greenhouse gas concentrations and aerosol-related atmospheric impurity records over time-scales from decades up to hundreds of millennia (e.g., Fischer et al., 2021). The investigation of the deepest and highly thinned ice core layers remains a fundamental frontier in ice core research, being the key to unlock the oldest parts of the ice core record. As a new 1.5 million year-old ice record may soon be recovered from Antarctica (Brook et al., 2006;Fischer et al., 2013), it is also an increasingly pressing challenge. Given that each meter of such an "Oldest" ice core section expected around 2,500 m depth at Little Dome C may comprise more than 10,000 years (Lilien Abstract Understanding post-depositional processes altering the layer sequence in ice cores is especially needed to avoid misinterpretation of the oldest and most highly thinned layers. The record of soluble and insoluble impurities represents an important part of the paleoclimate proxies in ice cores but is known to be affected through interaction with the ice matrix, diffusion, and chemical reactions. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) has been recognized for its micron-scale resolution and micro-destructiveness in ice core impurity analysis. Employing LA-ICP-MS for 2D chemical imaging has already revealed a close relationship between the ice grain boundary network and impurity signals with a significant soluble component, such as Na and Mg. Here we show the latest improvements in chemical imaging with LA-ICP-MS, by increasing the spatial resolution to 20 μm and extending the simultaneous analysis to also mostly insoluble impurities, such as Al and Fe. All analytes reveal signals of dispersed spots in a sample of an East Greenland ice core. Based on their average size around 50-60 times larger than an average particle and their heterogeneous elemental ratios these spots are interpreted as particle clusters. To distinguish their origin, a simple colocalization classification reveals elemental ratios consistent with marine and mineral dust aerosol. Based on already existing data from cryo-Raman spectroscopy, we discuss potential ways to integrate the two methods in a future comparison. Such a combined approach may help constraining post-depositional changes to the dust-related insoluble impurity components, such as cluster formation and chemical reactions at grain boundaries.Plain Language Summary Aerosols of marine and terrestrial origin delivered to the polar ice sheets are archived in the ice and can be studied via the analysis of ice cores. The chemical composition and size of mineral dust can deliver important information about past climatic changes and atmospheric transport. However, it has already been shown that this insoluble material is not always passively archived in the ice but can undergo changes in its chemical composition and size, for example, by forming particle aggregates. To investigat...