Publication | Open Access
Differential NO<sub>3</sub><sup>−</sup> dependent patterns of NO<sub>3</sub><sup>−</sup> uptake in <i>Pinus pinaster, Rhizopogon roseolus</i> and their ectomycorrhizal association
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Citations
41
References
2002
Year
• A different NO<sub>3</sub> <sup>-</sup> dependent pattern of NO<sub>3</sub> <sup>-</sup> uptake at low [NO<sub>3</sub> <sup>-</sup> ] (0-0.1 mM) is shown in Pinus pinaster and in the ectomycorrhizal fungus Rhizopogon roseolus. In ectomycorrhizal symbiosis, the fungal pattern is pre-eminent. • Net NO<sub>3</sub> <sup>-</sup> uptake rates were deduced in plant and fungus from solution depletion measurements. Net NO<sub>3</sub> <sup>-</sup> fluxes were estimated at the surface of mycorrhizal and nonmycorrhizal short roots, using NO<sub>3</sub> <sup>-</sup> selective microelectrodes. • In NO<sub>3</sub> <sup>-</sup> starved seedlings, maximum NO<sub>3</sub> <sup>-</sup> uptake rates were reached after 3 d of incubation in 0.05 mM NO<sub>3</sub> <sup>-</sup> . In R. roseolus mycelia, NO<sub>3</sub> <sup>-</sup> uptake rates did not change after withdrawing NO<sub>3</sub> <sup>-</sup> for up to 7 d, or after adding NO<sub>3</sub> <sup>-</sup> for 3 d. Net NO<sub>3</sub> <sup>-</sup> fluxes in nonmycorrhizal short roots were increased twofold by a 3-d exposure to NO<sub>3</sub> <sup>-</sup> whereas in ectomycorrhiza they were similar irrespective of the NO<sub>3</sub> <sup>-</sup> pretreatment, but always higher than the fluxes measured in nonmycorrhizal roots. • Ectomycorrhiza have a greater capacity to use NO<sub>3</sub> <sup>-</sup> than nonmycorrhizal short roots, whatever the NO<sub>3</sub> <sup>-</sup> concentration in the solution. This may give mycorrhizal plants a greater ability to use fluctuating concentrations of NO<sub>3</sub> <sup>-</sup> in the soil solution.
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