Background and aims <p>In multi-symbiotic plant communities, interactions between below- and aboveground plant symbionts modify nutrient acquisition for host and co-occurring plants, yet the relative importance of distinct pathways remains poorly resolved.&#xa0;We aimed to determine how common mycorrhizal networks (CMNs) modulate the interactive effects of foliar endophytes and arbuscular mycorrhizal fungi (AMF) on nitrogen (N) dynamics and plant interactions in a multi-symbiotic grass-legume system.</p> Methods <p>We conducted a factorial greenhouse experiment using three-compartment microcosms. Central compartment contained <i>Trifolium repens</i>. One outer compartment held non-endophytic grass <i>Bromus catharticus</i>, and <i>Lolium multiflorum</i> (with high/low <i>Epichloë occultans</i> status) on the other. Forty-micrometre mesh allowed CMN connections while preventing root contact. We evaluated how endophyte status and CMN connection in <i>L. multiflorum</i> modified fixed-N transfer and soil N uptake within neighbouring plants using <sup>15</sup>N natural abundance.</p> Results <p>Fixed-N transfer to grasses depended on the interaction between endophyte status of <i>L. multiflorum</i> and its CMN connection. The endophyte enhanced N transfer to its host but restricted transfer to the neighbour. <i>B. catharticus</i> received fixed-N transfer only when its low-endophyte neighbour was disconnected from the CMNs. Low-endophyte <i>L. multiflorum</i> depended more on the CMNs for soil-N uptake. Growth resembled these dynamics: CMN connection enhanced biomass in both grasses under low-endophyte status, whereas high-endophyte status favoured <i>L. multiflorum</i> biomass over that of <i>B. catharticus.</i></p> Conclusions <p>Foliar endophytes and CMNs interactively shape N dynamics and competitive balance among co-occurring grasses. Endophytes regulate N partitioning, shifting plant interactions from facilitation to competition, particularly when plants remain connected through the CMN.</p>

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Foliar fungal endophytes and common mycorrhizal networks shape nitrogen dynamics in multi-symbiotic grass–legume systems

  • Mercedes Lanati,
  • Marina Omacini,
  • Agustín A. Grimoldi,
  • Pablo A. García-Parisi

摘要

Background and aims

In multi-symbiotic plant communities, interactions between below- and aboveground plant symbionts modify nutrient acquisition for host and co-occurring plants, yet the relative importance of distinct pathways remains poorly resolved. We aimed to determine how common mycorrhizal networks (CMNs) modulate the interactive effects of foliar endophytes and arbuscular mycorrhizal fungi (AMF) on nitrogen (N) dynamics and plant interactions in a multi-symbiotic grass-legume system.

Methods

We conducted a factorial greenhouse experiment using three-compartment microcosms. Central compartment contained Trifolium repens. One outer compartment held non-endophytic grass Bromus catharticus, and Lolium multiflorum (with high/low Epichloë occultans status) on the other. Forty-micrometre mesh allowed CMN connections while preventing root contact. We evaluated how endophyte status and CMN connection in L. multiflorum modified fixed-N transfer and soil N uptake within neighbouring plants using 15N natural abundance.

Results

Fixed-N transfer to grasses depended on the interaction between endophyte status of L. multiflorum and its CMN connection. The endophyte enhanced N transfer to its host but restricted transfer to the neighbour. B. catharticus received fixed-N transfer only when its low-endophyte neighbour was disconnected from the CMNs. Low-endophyte L. multiflorum depended more on the CMNs for soil-N uptake. Growth resembled these dynamics: CMN connection enhanced biomass in both grasses under low-endophyte status, whereas high-endophyte status favoured L. multiflorum biomass over that of B. catharticus.

Conclusions

Foliar endophytes and CMNs interactively shape N dynamics and competitive balance among co-occurring grasses. Endophytes regulate N partitioning, shifting plant interactions from facilitation to competition, particularly when plants remain connected through the CMN.