In forest ecosystems, rhizodeposition can lead to significant differences in the availability of soil carbon (C), nitrogen (N), and phosphorus (P) between rhizosphere and bulk soils. Soil stoichiometry affects microbial and enzyme nutrient content and determines the abundance and composition of microbes and thus regulates microbial carbon use efficiency (CUE). However, how soil stoichiometry—particularly its variation between the rhizosphere and bulk soil—regulates microbial CUE by shaping microbial biomass, extracellular enzyme stoichiometry, and community composition remains insufficiently quantified. Here, through the C:N, C:P, and N:P ratios for available soil nutrients, microbial biomass, and extracellular enzyme activities—(β-1,4-glucosidase (BG), β-1,4-N-acetylglucosaminodase (NAG), leucine aminopeptidase (LAP), and acid phosphatase (ACP))—and the composition and activity of microbial communities (based on sequencing of bacterial 16S rRNA and fungal ITS genes) in the rhizosphere and bulk soils of five temperate forest ecosystems in northeastern China, we aimed to unravel their integrated effects on microbial CUE. Results indicated that soil C, N, and P and their stoichiometry, microbial community composition, and microbial CUE were significantly different between rhizosphere and bulk soils among all tree species. The disproportionate variation in soil nutrient pools between the rhizosphere and non-rhizosphere regions has led to a stoichiometric imbalance. There was higher microbial CUE in the rhizosphere soil than that in the bulk soil among all tree species. However, the effect pathways of tree species on microbial CUE in the rhizosphere and bulk soils differed. The structural equation model (SEM) further suggested that tree species affected microbial CUE through distinct pathways in different soil compartments. In the rhizosphere, the effect was directly driven by available nutrient stoichiometry. In bulk soil, it was jointly mediated by both available nutrients and microbial biomass stoichiometry. These findings demonstrate that root rhizodeposition shapes microbial carbon cycling by altering soil stoichiometric imbalances, which can strengthen the current understanding of plant–microbe–soil interactions in temperate forests.
Duan et al. (2026) studied this question.