At invasion fronts, seedling mortality may increase if they fail to form associations with symbiotic fungi in the early developmental stages (Collier & Bidartondo, 2009). Trees that form northern treelines are obligately associated with ectomycorrhizal (EM) fungi that improve water and nutrient absorption by the host plants. EM associations may provide plants with direct access to mineralized nutrients that are released from organic matter by fungal enzyme activity (Lindahl & Tunlid, 2015;Shah et al., 2016). Such functions are particularly important in northern ecosystems, where cold temperatures reduce decomposition rates and water accessibility (Bödeker et al., 2014;Deslippe, Hartmann, Grayston, Simard, & Mohn, 2016). Thus, the availability of compatible EM fungi is crucial for successful seedling establishment and subsequent tree range expansion into novel habitats (Germino, Smith, & Resor, 2002;Nuñez et al., 2009;Policelli, Bruns, Vilgalys, & Nunez, 2019).Siberian Larix Mill. species form the longest continuous belt of Arctic treeline in Eurasia (> 5000 km) (Semerikov, Iroshnikov, & Lascoux, 2007). Given the extent of Larix distribution and the disproportionate rate of warming in the Arctic (Serreze & Barry, 2011;Overland, Walsh, & Kattsov, 2017), it is vital to clarify the migration potential of Larix trees. In primary habitats, pre-existing shrubs can provide EM fungal inocula to colonizer tree seedlings via common mycorrhizal networks (CMNs)