Testing deep placement of an 15N tracer as a method for in situ deep root phenotyping of wheat, barley and ryegrass

Abstract Background Deep rooting is one of the most promising plant traits for improving crop yield under water-limited conditions. Most root phenotyping methods are designed for laboratory-grown plants, typically measuring very young plants not grown in soil and not allowing full development of the...

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Main Authors: Si Chen, Simon Fiil Svane, Kristian Thorup-Kristensen
Format: Article
Language:English
Published: BMC 2019-12-01
Series:Plant Methods
Subjects:
Online Access:https://doi.org/10.1186/s13007-019-0533-6
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author Si Chen
Simon Fiil Svane
Kristian Thorup-Kristensen
author_facet Si Chen
Simon Fiil Svane
Kristian Thorup-Kristensen
author_sort Si Chen
collection DOAJ
description Abstract Background Deep rooting is one of the most promising plant traits for improving crop yield under water-limited conditions. Most root phenotyping methods are designed for laboratory-grown plants, typically measuring very young plants not grown in soil and not allowing full development of the root system. Results This study introduced the 15N tracer method to detect genotypic variations of deep rooting and N uptake, and to support the minirhizotron method. The method was tested in a new semifield phenotyping facility on two genotypes of winter wheat, seven genotypes of spring barley and four genotypes of ryegrass grown along a drought stress gradient in four individual experiments. The 15N labeled fertilizer was applied at increasing soil depths from 0.4 to 1.8 m or from 0.7 to 2.8 m through a subsurface tracer supply system, and sampling of aboveground biomass was conducted to measure the 15N uptake. The results confirm that the 15N labeling system could identify the approximate extension of the root system. The results of 15N labeling as well as root measurements made by minirhizotrons showed rather high variation. However, in the spring barley experiment, we did find correlations between root observations and 15N uptake from the deepest part of the root zone. The labeled crop rows mostly had significantly higher 15N enrichment than their neighbor rows. Conclusion We concluded that the 15N tracer method is promising as a future method for deep root phenotyping because the method will be used for phenotyping for deep root function rather than deep root growth. With some modifications to the injection principle and sampling process to reduce measurement variability, we suggest that the 15N tracer method may be a useful tool for deep root phenotyping. The results demonstrated that the minirhizotrons observed roots of the tested rows rather than their neighboring rows.
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spelling doaj.art-051255cbbb864151811175173dafcf252022-12-21T22:24:00ZengBMCPlant Methods1746-48112019-12-0115111210.1186/s13007-019-0533-6Testing deep placement of an 15N tracer as a method for in situ deep root phenotyping of wheat, barley and ryegrassSi Chen0Simon Fiil Svane1Kristian Thorup-Kristensen2College of Agriculture and Biotechnology, Zhejiang UniversityDepartment of Plant and Environmental Science, University of CopenhagenDepartment of Plant and Environmental Science, University of CopenhagenAbstract Background Deep rooting is one of the most promising plant traits for improving crop yield under water-limited conditions. Most root phenotyping methods are designed for laboratory-grown plants, typically measuring very young plants not grown in soil and not allowing full development of the root system. Results This study introduced the 15N tracer method to detect genotypic variations of deep rooting and N uptake, and to support the minirhizotron method. The method was tested in a new semifield phenotyping facility on two genotypes of winter wheat, seven genotypes of spring barley and four genotypes of ryegrass grown along a drought stress gradient in four individual experiments. The 15N labeled fertilizer was applied at increasing soil depths from 0.4 to 1.8 m or from 0.7 to 2.8 m through a subsurface tracer supply system, and sampling of aboveground biomass was conducted to measure the 15N uptake. The results confirm that the 15N labeling system could identify the approximate extension of the root system. The results of 15N labeling as well as root measurements made by minirhizotrons showed rather high variation. However, in the spring barley experiment, we did find correlations between root observations and 15N uptake from the deepest part of the root zone. The labeled crop rows mostly had significantly higher 15N enrichment than their neighbor rows. Conclusion We concluded that the 15N tracer method is promising as a future method for deep root phenotyping because the method will be used for phenotyping for deep root function rather than deep root growth. With some modifications to the injection principle and sampling process to reduce measurement variability, we suggest that the 15N tracer method may be a useful tool for deep root phenotyping. The results demonstrated that the minirhizotrons observed roots of the tested rows rather than their neighboring rows.https://doi.org/10.1186/s13007-019-0533-615N tracerDeep rootingPhenotypingDrought stress gradients
spellingShingle Si Chen
Simon Fiil Svane
Kristian Thorup-Kristensen
Testing deep placement of an 15N tracer as a method for in situ deep root phenotyping of wheat, barley and ryegrass
Plant Methods
15N tracer
Deep rooting
Phenotyping
Drought stress gradients
title Testing deep placement of an 15N tracer as a method for in situ deep root phenotyping of wheat, barley and ryegrass
title_full Testing deep placement of an 15N tracer as a method for in situ deep root phenotyping of wheat, barley and ryegrass
title_fullStr Testing deep placement of an 15N tracer as a method for in situ deep root phenotyping of wheat, barley and ryegrass
title_full_unstemmed Testing deep placement of an 15N tracer as a method for in situ deep root phenotyping of wheat, barley and ryegrass
title_short Testing deep placement of an 15N tracer as a method for in situ deep root phenotyping of wheat, barley and ryegrass
title_sort testing deep placement of an 15n tracer as a method for in situ deep root phenotyping of wheat barley and ryegrass
topic 15N tracer
Deep rooting
Phenotyping
Drought stress gradients
url https://doi.org/10.1186/s13007-019-0533-6
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