Resource Allocation Trade‐Offs and Rewired Mycorrhizal Networks Underlie the Adaptation of <i>Paphiopedilum purpuratum</i> to Ex Situ Conservation

ABSTRACT This study reveals how the rare orchid Paphiopedilum purpuratum adapts to ex situ conservation. Although seed production was significantly increased, the plants incurred physiological costs: reduced photosynthesis and higher oxidative stress. Importantly, host physiology—particularly nitrogen metabolism—directly influenced root fungal communities. This drove two distinct adaptive strategies in the fungal community. Mycorrhizal fungi maintained stable communities by reorganizing their interaction networks into resilient multi‐cluster structures. In contrast, non‐mycorrhizal fungi exhibited high species turnover, shifting toward beneficial taxa that potentially suppress pathogens. These findings highlight that successful ex situ conservation must address both the plant physiological trade‐offs and its restructured root microbiomes. We propose that the orchid's resilience relies on a multi‐level microbial adaptation strategy, combining a reorganized yet stable mycorrhizal core with a dynamic, beneficial non‐mycorrhizal periphery. Our work offers a new framework for protecting rare orchids—one that prioritizes sustaining these complementary fungal partnerships to ensure long‐term survival.

Publication Details

Journal
Biological Diversity
Published
2026-03-24
DOI
https://doi.org/10.1002/bod2.70022
Primary Topic
Plant and animal studies
Type
article
Field-Weighted Citation Impact
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article

Resource Allocation Trade‐Offs and Rewired Mycorrhizal Networks Underlie the Adaptation of Paphiopedilum purpuratum to Ex Situ Conservation

Biological Diversity
Plant and animal studies
article

Resource Allocation Trade‐Offs and Rewired Mycorrhizal Networks Underlie the Adaptation of Paphiopedilum purpuratum to Ex Situ Conservation

article en

Abstract

ABSTRACT This study reveals how the rare orchid Paphiopedilum purpuratum adapts to ex situ conservation. Although seed production was significantly increased, the plants incurred physiological costs: reduced photosynthesis and higher oxidative stress. Importantly, host physiology—particularly nitrogen metabolism—directly influenced root fungal communities. This drove two distinct adaptive strategies in the fungal community. Mycorrhizal fungi maintained stable communities by reorganizing their interaction networks into resilient multi‐cluster structures. In contrast, non‐mycorrhizal fungi exhibited high species turnover, shifting toward beneficial taxa that potentially suppress pathogens. These findings highlight that successful ex situ conservation must address both the plant physiological trade‐offs and its restructured root microbiomes. We propose that the orchid's resilience relies on a multi‐level microbial adaptation strategy, combining a reorganized yet stable mycorrhizal core with a dynamic, beneficial non‐mycorrhizal periphery. Our work offers a new framework for protecting rare orchids—one that prioritizes sustaining these complementary fungal partnerships to ensure long‐term survival.

Biological Diversity
Partnerships for the goals
Openalex Percentile: Top 9%
Plant and animal studies
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