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Microbial mechanisms mediate divergent ecosystem responses to nitrogen and phosphorus enrichment

  • Zehao Lv
  • , Gangsheng Wang
  • , Daifeng Xiang
  • , Xiankai Lu
  • , Mingkai Jiang
  • , Donghai Wu
  • , Qinggong Mao
  • , Shuhao Zhou
  • , Shanshan Qi
  • , Zirui Mu
  • , Yilei Zhong
  • , Mianhai Zheng
  • , Jiangming Mo
  • Wuhan University
  • CAS - South China Institute of Botany
  • Zhejiang University

Research output: Contribution to journalArticlepeer-review

Abstract

Anthropogenic nitrogen (N) and phosphorus (P) deposition are intensifying nutrient imbalances in ecosystems. However, the microbial mechanisms governing ecosystem responses to chronic N–P enrichment remain poorly resolved and are inadequately represented in ecosystem models. Here, we integrated multi-source and multi-scale observations, from functional genes and enzymes to ecosystem fluxes, into a newly developed microbial-enzyme-mediated Carbon–Nitrogen–Phosphorus model (MEND-CNP). This model-microbiome fusion enables multi-year continuous simulations of nutrient enrichment in a subtropical forest, offering mechanistic insights beyond the reach of experiments alone. Our results refined and extended the Nitrogen Saturation Hypotheses (NSH) by resolving microbial pathways previously unaccounted for in model frameworks. Specifically, after N saturation, N addition enhanced denitrification, suppressed biological N fixation, and reduced soil C:N ratios. We further demonstrated that excess N-induced acidification constrained nitrifying microorganisms and their associated enzymes, thereby mechanistically explaining the observed declines in nitrification in subtropical forests, in contrast to NSH paradigms derived from temperate ecosystems. We also identified process-level controls of increased N2O emissions, including accelerated NO3 to N2O conversion and suppressed N2O to N2 reduction. Furthermore, P addition stimulated microbial biomass and elevated microbial N demand, reversing N cycling trajectories induced by N enrichment. This divergent effect was further influenced by N availability, revealing a spectrum of single- and multi-element limitations. By embedding gene-informed microbial physiology into a process-based CNP framework, our study established a mechanistic bridge between microbiome dynamics and ecosystem-scale nutrient cycling, advancing predictive understanding of biogeochemical feedbacks under accelerating global change.

Original languageEnglish
Article number110245
Number of pages14
JournalSoil Biology and Biochemistry
Volume221
DOIs
Publication statusPublished - Oct 2026
Externally publishedYes

Keywords

  • Carbon–nitrogen–phosphorus cycle
  • Model-microbiome fusion
  • Nitrogen saturation hypotheses
  • Nutrient addition
  • Phosphorus limitation

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