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Root anatomy governs bi-directional resource transfer in mycorrhizal symbiosis

Jingjing Cao, Junjian Wang, Qingpei Yang, B. C. Guo, Tino Colombi, Oscar J. Valverde‐Barrantes, Junxiang Ding, Yue Zhang, Huifang Wu, Zhipei Feng, Xitian Yang, Deliang Kong

2025Nature Communications9 citationsDOIOpen Access PDF

Abstract

Plants form mycorrhizal symbioses to enhance nutrient acquisition, yet the biophysical principles governing carbon and nutrient exchange remain unclear. Here, we develop a theory of bi-directional carbon-nutrient transfer that integrates root anatomy, energetic costs, and mycorrhizal positioning. We show that nutrient uptake per unit carbon or energy investment declines with increasing root diameter due to higher carbon demands across thicker cortical tissues. Mycorrhizal fungi mitigate this constraint by enabling more carbon-efficient nutrient uptake, particularly when arbuscules are positioned in inner cortical layers. This spatial optimization minimizes the carbon cost of transporting nutrients to the stele. Our framework reconciles anatomical variation, symbiotic structure, and functional efficiency across root types and mycorrhizal strategies and offers a new lens for understanding the coevolution between roots and mycorrhizal fungi.

Topics & Concepts

SymbiosisNutrientMycorrhizal fungiBiologyCarbon fibersCoevolutionMutualism (biology)Root (linguistics)GreenhouseBotanyResource (disambiguation)EcologyNutrient cycleEnergy transferAgronomyMycorrhizaEnvironmental scienceRoot hairCarbon cycleRoot systemConstraint (computer-aided design)Mycorrhizal Fungi and Plant InteractionsLegume Nitrogen Fixing SymbiosisPlant nutrient uptake and metabolism
Root anatomy governs bi-directional resource transfer in mycorrhizal symbiosis | Litcius