Abstract

BackgroundUnderstanding how elevated atmospheric CO2 (eCO2) impacts on phosphorus (P) transformation in plant rhizosphere is critical for maintaining ecological sustainability in response to climate change, especially in agricultural systems where soil P availability is low.MethodsThis study used rhizoboxes to physically separate rhizosphere regions (plant root-soil interface) into 1.5-mm segments. Wheat plants were grown in rhizoboxes under eCO2 (800 ppm) and ambient CO2 (400 ppm) in two farming soils, Chromosol and Vertosol, supplemented with phytate (organic P). Photosynthetic carbon flow in the plant-soil continuum was traced with 13CO2 labeling. Amplicon sequencing was performed on the rhizosphere-associated microbial community in the root-growth zone, and 1.5 mm and 3 mm away from the root.ResultsElevated CO2 accelerated the mineralization of phytate in the rhizosphere zones, which corresponded with increases in plant-derived 13C enrichment and the relative abundances of discreet phylogenetic clades containing Bacteroidetes and Gemmatimonadetes in the bacterial community, and Funneliformis affiliated to arbuscular mycorrhizas in the fungal community. Although the amplicon sequence variants (ASVs) associated the stimulation of phytate mineralization under eCO2 differed between the two soils, these ASVs belonged to the same phyla associated with phytase and phosphatase production. The symbiotic mycorrhizas in the rhizosphere of wheat under eCO2 benefited from increased plant C supply and increased P access from soil. Further supportive evidence was the eCO2-induced increase in the genetic pool expressing the pentose phosphate pathway, which is the central pathway for biosynthesis of RNA/DNA precursors.ConclusionsThe results suggested that an increased belowground carbon flow under eCO2 stimulated bacterial growth, changing community composition in favor of phylotypes capable of degrading aromatic P compounds. It is proposed that energy investments by bacteria into anabolic processes increase under eCO2 to level microbial P-use efficiencies and that synergies with symbiotic mycorrhizas further enhance the competition for and mineralization of organic P.33SwUUA3eFb3g78WvKtJiVVideo

Highlights

  • Phosphorus (P) is fundamentally important to soil biota as a major building block of life [1, 2]

  • The results showed that e­ CO2 shifted the bacterial community composition in the rhizosphere of wheat which was significant in the Chromosol and marginally significant in the Vertosol (Fig. 5)

  • Under e­ CO2 environments, the increased plant C efflux into the rhizosphere resulted in the stimulation of microbial activity, leading to stronger competition for P in the microbial community

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Summary

Introduction

Phosphorus (P) is fundamentally important to soil biota as a major building block of life [1, 2]. Climate change has the potential to impact organic P transformation. One of most important climate change factors, elevated atmospheric C­ O2 concentration ­(eCO2), would considerably accelerate the mineralization of soil organic P [8, 9]. The competition for P between plants and soil microbes in P-limited soils, and balancing C/P stoichiometry in microorganisms with increasing P-use efficiency for microbial population growth likely intensify the mobilization of soil organic P [10,11,12,13]. Understanding how elevated atmospheric ­CO2 ­(eCO2) impacts on phosphorus (P) transformation in plant rhizosphere is critical for maintaining ecological sustainability in response to climate change, especially in agricultural systems where soil P availability is low

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