How are mineral and organic phases regulating burning-induced soil water repellency? Unravelling the crucial dynamics occurring in the Alps even at moderate fire intensities.

Wildfires play the role of ecosystem shapers in the majority of terrestrial biomes, altering canopy and litter cover and imposing strong modifications on soils. Organic matter (OM) content and composition, mineralogy, pH, aggregate stability and water repellency (WR) are among the main edaphic properties to be affected by heat. Various studies dealt with occurrence, extent and persistence of burning-induced soil WR, but the dynamics at the basis of its formation (and loss) are still widely unclear. In addition, the vast majority of research on this topic has been carried out in the Mediterranean, even if alpine environments are far from being untouched by fires. Our aims were therefore to provide insight into the key mechanisms regulating WR thermal alterations in a relatively understudied environment. Our sampling design aimed at collecting soils representative of the Western Italian Alps. Charring was simulated in the lab, at increasing temperatures (up to 300° C), on a set of A soil horizons developed under pine and beech forest covers. Water drop penetration time (WDPT) was employed to test WR persistence. Soils were analyzed in terms of organic carbon (OC) and nitrogen contents, pH, texture and iron (Fe) oxides composition (Fe-DCB and Fe-pyrophosphate extracted). Fe-speciation and OM composition of some selected samples were further characterized using Fe K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy and Fourier transform-infra red (FT-IR) spectroscopy, respectively. WR was found to be extremely variable, event at room temperature. For samples exhibiting an increase in WR upon burning intensity, maximum repellency was observed at 200° C. OC abundance (%) and coarse texture were found to be the main drivers of hydrophobicity in soil. WR was drastically lost when samples were exposed to temperatures higher than 200°C. Above this threshold, pH systematically increased and OC (%) sharply decreased. The increasingly negative charge of mineral surfaces, mirrored by pH increase, seems to result in a significant C volatilization by OM desorption, eventually leading to a super-hydrophilic behavior in soil. Fe EXAFS allowed to evaluate different thermal-dictated pathways of Fe-speciation. The formation of more crystalline Fe-forms (e.g. hematite, meghemite) was observed above 200° C. Even though a reduction in surface area should be expected when observing an increase in crystallization degree (potentially giving rise to greater WR), OM adhesion to mineral surfaces seems to be inhibited by the change induced in their charge. A reduction in the OM-bound Fe pool (pyrophosphate extracted) above 200° C could be appreciated, supporting the interpretation of oxy-hydroxides transformations and OC (%) loss. The current investigation has been carried out to capture an in-depth picture of wildfire impacts on alpine soils, targeting factors responsible for WR enhancement and shred. Identifying the mechanisms regulating wildfire-related WR is a key issue, as the formation of hydrophobic layers in soil highly favors its erosion. Addressing such matters is crucial to tackle the issue of ecosystems recovery, considering that climate-change-related alterations in wildfires regimes are already causing the occurrence of more frequent and disruptive fires.