Divergent belowground carbon allocation patterns of winter wheat shape rhizosphere microbial communities and nitrogen cycling activities

Abstract

Plant roots add carbon (C) -rich rhizodeposits to the soil, which can alter microbial activity and nitrogen (N) cycling with implications for N availability and uptake by plants. We evaluated root architecture, rhizodeposit C, and microbial community structure and function across a breeding gradient of twelve winter wheat genotypes and examined how these rhizosphere traits were related to the availability and uptake of N from fresh cover crop residues in the soil. We traced wheat-derived C into soil and microbial pools using continuous isotopic labelling (13C–CO2) and applied 15N labelled plant residues to quantify plant and microbial uptake of residue-derived N. Wheat genotypes differed in root C allocation patterns, influencing N cycling. Thicker roots released more C into soil, which enhanced N mineralization through stimulation of the microbial biomass. Microbial biomass increased N-cycling enzyme activity and residue N-uptake by wheat. Microbial communities did not differ between wheat genotypes but were strongly related to patterns in root C allocation, and several genera showed strong relationships with root C deposition and N uptake. The microbial community associated with extractable root-derived C was structurally different from the community associated with residue N uptake, indicating that N-cycling and mineralization was not necessarily carried out by the same microbial community members as those stimulated by rhizosphere C inputs. Our results indicate that differential patterns of rhizodeposition and associated belowground C allocation strategies in winter wheat can alter microbial communities and influence cycling and plant availability of residue N. Ecologically-based nutrient management in agricultural systems should consider the role of crop root traits and associated microbiomes to optimize soil nutrient dynamics.