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[Display omitted] • Carbon sequestration potential of the clay fraction. • Determination of the carbon saturation deficit of each mineral of the clay fraction. • Identification of the equation for the prediction of carbon sequestration potential. • Identification of land uses with the greatest carbon sequestration potential. The capacity of soil to sequester carbon (C) is a key process that promotes the reduction of CO 2 in the atmosphere. Soils can absorb as much as 20% of anthropogenic carbon emissions, which can contribute to mitigate climate change. This capacity relies on the organo-mineral association, which includes different minerals, Fe and Al oxides, which have a critical soil organic carbon (SOC) sorption surface. Based on an equation of the potential C saturation deficit of fine soil particles (<20 μm/silt and clay fractions) for tropical regions, this study investigated the SOC sequestration potential of the clay fraction for soils in Piracicaba region, São Paulo State, Brazil as influenced by the clay minerals. This potential was fitted to a spatial regression model for soil depths 0–20 cm and 80 to 100 cm. In the surface layer, the sequestration potential was mostly explained by the relative abundance of soil minerals (Kaolinite, Hematite, Goethite and Gibbsite) determined using vis-NIR-SWIR spectroscopy. A direct relationship was observed with Goethite and Gibbsite, indicating that low concentrations would reduce the sequestration potential. At 80 to 100 cm depth, Kaolinite and Hematite explained most variation in SOC sequestration potential. Additionally, the C associated with the mineral fraction and the C saturation potential as a function of minerals were modeled and a strong importance of hematite in the C sequestration and stabilization cycle was identified at both depths. The individual mineral contribution to SOC sequestration potential was also mapped, which identified high contributions of goethite and gibbsite for deep soil layers. The influence of land use on the carbon sequestration potential of minerals was observed, with the greatest potential being found in areas with pasture and cropping mosaics and grassland and forest mosaics, with a high presence of kaolinite and hematite. These minerals have a greater potential for carbon sequestration at greater depths and, therefore, could be critical in climate change mitigation strategies. [ABSTRACT FROM AUTHOR]

[Display omitted] • Goethite, haematite, kaolinite and gibbsite abundances releveled by Vis-NIR-SWIR data; • Novelty framework to reach a continuums bare soil reflectance image; • Major soil mineralogical components mapping for the whole Brazilian territory; • Soil mineralogy mapping for large area by spectroscopy and Digital Soil Mapping; Minerals control many soil functions and play a crucial role in addressing global existential issues. Measuring the abundance of soil minerals is a laborious, costly, and time-consuming task; however, soil spectroscopy can be a useful tool to overcome this issue. This work aimed to map the abundance of major mineralogical components of soils in Brazil from surface to 1 m deep and at a spatial resolution of 30 m. Spectral data of the Brazilian Soil Spectral Library with Vis-NIR-SWIR was used to estimate the abundance of haematite, goethite, kaolinite, and gibbsite. These minerals were spatialized using digital soil mapping techniques. We also developed a novel framework to obtain bare soil reflectance for areas without natural or anthropic soil exposure (continuous image) and used it as covariate. Soil minerals and their abundances were successfully estimated by Vis-NIR-SWIR reflectance. Haematite predictions presented the most accurate results with Random Forest models, followed by gibbsite, kaolinite, and goethite. The spatial validation with reference mineralogical data found R2 of 0.64 (haematite), 0.40 (goethite), 0.20 (kaolinite/Kt), 0.29 (gibbsite/Gbs), and 0.40 (Kt/Kt + Gbs). The resulting maps of soil minerals were in accordance with the geology, pedology, climate, and relief of Brazil and revealed the spatial distribution of mineral abundances at a finer resolution than existing geological and pedological maps, reaching a farm level detail. [ABSTRACT FROM AUTHOR]