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With permafrost thaw, significant amounts of organic carbon (OC) previously stored in frozen deposits are unlocked and become potentially available for microbial mineralization. This is particularly the case in ice-rich regions such as the Yedoma domain. Excess ground ice degradation exposes deep sediments and their OC stocks, but also mineral elements, to biogeochemical processes. Interactions of mineral elements and OC play a crucial role for OC stabilization and the fate of OC upon thaw, and thus regulate carbon dioxide and methane emissions. In addition, some mineral elements are limiting nutrients for plant growth or microbial metabolic activity. A large ongoing effort is to quantify OC stocks and their lability in permafrost regions, but the influence of mineral elements on the fate of OC or on biogeochemical nutrient cycles has received less attention and there is an overall lack of mineral element content analyses for permafrost sediments. Here, we combine portable X-ray fluorescence (pXRF) with a bootstrapping technique to provide i) the first large-scale Yedoma domain Mineral Concentrations Assessment (YMCA) dataset, and ii) estimates of mineral element stocks in never thawed (since deposition) ice-rich Yedoma permafrost and previously thawed and partly refrozen Alas deposits. The pXRF method for mineral element quantification is non-destructive and offers a complement to the classical dissolution and measurement by optical emission spectrometry (ICP-OES) in solution. Using this method, mineral element concentrations (Si, Al, Fe, Ca, K, Ti, Mn, Zn, Sr and Zr) were assessed on 1,292 sediment samples from the Yedoma domain with lower analytical effort and lower costs relative to the ICP-OES method. The pXRF measured concentrations were calibrated using alkaline fusion and ICP-OES measurements on a subset of 144 samples (R2 from 0.725 to 0.996). The results highlight that i) the mineral element stock in sediments of the Yedoma domain (1,387,000 km2) is higher for Si, followed by Al, Fe, K, Ca, Ti, Mn, Zr, Sr, and Zn, and that ii) the stock in Al and Fe (598 ± 213 and 288 ± 104 Gt) is in the same order of magnitude as the OC stock (327–466 Gt).

Arctic warming and permafrost degradation are modifying northern ecosystems through changes in microtopography, soil water dynamics, nutrient availability, and vegetation succession. Upon permafrost degradation, the release of deep stores of nutrients, such as nitrogen and phosphorus, from newly thawed permafrost stimulates Arctic vegetation production. More specifically, wetter lowlands show an increase in sedges (as part of graminoids), whereas drier uplands favor shrub expansion. These shifts in the composition of vegetation may influence local mineral element cycling through litter production. In this study, we evaluate the influence of permafrost degradation on mineral element foliar stocks and potential annual fluxes upon litterfall. We measured the foliar elemental composition (Al, Ca, Fe, K, Mn, P, S, Si, and Zn) of ∼ 500 samples of typical tundra plant species from two contrasting Alaskan tundra sites, i.e., an experimental sedge-dominated site (Carbon in Permafrost Experimental Heating Research, CiPEHR) and natural shrub-dominated site (Gradient). The foliar concentration of these mineral elements was species specific, with sedge leaves having relatively high Si concentration and shrub leaves having relatively high Ca and Mn concentrations. Therefore, changes in the species biomass composition of the Arctic tundra in response to permafrost thaw are expected to be the main factors that dictate changes in elemental composition of foliar stocks and maximum potential foliar fluxes upon litterfall. We observed an increase in the mineral element foliar stocks and potential annual litterfall fluxes, with Si increasing with sedge expansion in wetter sites (CiPEHR), and Ca and Mn increasing with shrub expansion in drier sites (Gradient). Consequently, we expect that sedge and shrub expansion upon permafrost thaw will lead to changes in litter elemental composition and therefore affect nutrient cycling across the sub-Arctic tundra with potential implications for further vegetation succession.

With permafrost thaw, significant amounts of organic carbon (OC) previously stored in frozen deposits are unlocked and become potentially available for microbial mineralization. This is particularly the case in ice-rich regions such as the Yedoma domain. Excess ground ice degradation exposes deep sediments and their OC stocks, but also mineral elements, to biogeochemical processes. Interactions of mineral elements and OC play a crucial role for OC stabilization and the fate of OC upon thaw, and thus regulate carbon dioxide and methane emissions. In addition, some mineral elements are limiting nutrients for plant growth or microbial metabolic activity. A large ongoing effort is to quantify OC stocks and their lability in permafrost regions, but the influence of mineral elements on the fate of OC or on biogeochemical nutrient cycles has received less attention. The reason is that there is a gap of knowledge on the mineral element content in permafrost regions. Here, we use a portable X-ray fluorescence device (pXRF) to provide (i) the first large-scale Yedoma domain Mineral Concentrations Assessment (YMCA) dataset (https://doi.pangaea.de/10.1594/PANGAEA.922724; Monhonval et al., in review), and (ii) estimates of mineral element stocks in never thawed (since deposition) ice-rich Yedoma permafrost and previously thawed and partly refrozen Alas deposits. The pXRF method for mineral element quantification is non-destructive and offers a complement to the classical dissolution and measurement by optical emission spectrometry (ICP-OES) in solution. This allowed a mineral element concentration (Si, Al, Fe, Ca, K, Ti, Mn, Zn, Sr and Zr) assessment on 1292 sediment samples from the Yedoma domain with lower analytical effort and affordable costs relative to the classical ICP-OES method. pXRF measured concentrations were calibrated using standard alkaline fusion and ICP-OES measurements on a subset of 144 samples (R2 from 0.725 to 0.996). The results highlight that (i) the most abundant mineral element in the Yedoma domain is Si (2739 ± 986 Gt) followed by Al, Fe, K, Ca, Ti, Mn, Zr, Sr, and Zn, and that (ii) Al and Fe (598 ± 213 and 288 ± 104 Gt) are present in the same order of magnitude than OC (327–466 Gt).