Microbially mediated plant-soil feedbacks drive patterns of plant
growth, competitive ability, succession, and community composition.
Although rare plant species maintain unique functional traits that often
facilitate negative feedbacks, there is not a consensus on the
belowground drivers nor the effects of phylogenetic origin of previously
plant-conditioned soil on aboveground traits associated with rare
species. Using a common garden, we connect belowground fungal
colonization to aboveground traits in species varying in rarity, and
soil conditions varying in the phylogenetic relatedness of conditioning
plant species, to demonstrate the mechanistic relationship between
belowground ectomycorrhizal fungal (ECM) colonization and aboveground
total plant biomass in 14 Eucalyptus species varying in their rarity
status. Specifically, we found that while the rarest species displayed
88% less total biomass than common species, the rarest species also
maintained 62% greater ECM colonization than common counterparts.
Further, negative feedbacks resulted in reduced biomass coupled with
positive feedbacks that resulted in increased ECM colonization that
varied on the basis of phylogenetic relatedness. The rarest species
decreased by 71% - 94% in total biomass but increased by 96% - 114%
in ECM colonization in phylogenetically similar and distant soil
compared to conspecific soil conditions. The effect size of ECM
colonization directly affected the effect size of total biomass in
phylogenetically distant conditions with a significant negative
correlation (r^2 = -0.83) to show that biomass may be a function of
ECM colonization acting differently among species varying in rarity.
Consequently, rare plant species may utilize stronger associations with
belowground mycorrhizal mutualists than common plant species, to
facilitate geographic, competitive, and functional persistence, even
while maintaining lower biomass.