Belowground carbon sequestration potential of apple trees
Lead Research Organisation:
University of Reading
Department Name: Sch of Agriculture Policy and Dev
Abstract
Objectives
This project will expand our understanding of the associations between terrestrial C sequestration capacity and genotype-specific apple rootstock traits, including recalcitrance, rhizodeposition and the associated rhizosphere microbial communities. This knowledge will then enable growers to select rootstocks with greater ecosystem service capacity, in terms of their C storage abilities, which will benefit soil fertility and promote the capture of atmospheric CO2. In turn, policy makers may incorporate this information into environmental reward payment schemes.
Approaches
This project will assess a selection of widely-used apple rootstock cultivars for their C-sequestering abilities by analysing three key components:
Physical root measurements: Root recalcitrance will be assessed using biochemical methods to quantify various compounds (e.g. total C, soluble phenolics, condensed tannins, acid-insoluble fractions (lignin)). Additional measurements will be made for root thickness, decomposition rate, and root depth distribution using rhizotrons, intact cores (Dornbush, et al., 2002) and incubation of roots in microcosms.
Root exudate biochemical analysis: Rhizodeposit collection may be done either by collection of percolated (run-off) water from pot-grown rootstocks (Leisso, et al., 2017), or by dipping roots of axenically-grown rootstocks in distilled water containing silver (Ag+) as described and evaluated by Gransee & Wittenmayer (2000). Primary (sugars, organic acids) and secondary (phenolics) metabolites will be analysed by high performance liquid chromatography (HPLC) or gas chromatography-mass spectrometry (GC-MS).
Rhizosphere community analysis: Recent advances in high-throughput sequencing methods have greatly enhanced microbial community analysis. The bacterial and fungal composition of the rhizosphere community will be investigated via amplification of the universal 16S rRNA gene (bacteria) and ITS sequences (fungi). In particular, the project will focus on functional groups related to C cycling, such as methanotrophs (methane producers), methanogens (methane consumers), and AMF.
This project will expand our understanding of the associations between terrestrial C sequestration capacity and genotype-specific apple rootstock traits, including recalcitrance, rhizodeposition and the associated rhizosphere microbial communities. This knowledge will then enable growers to select rootstocks with greater ecosystem service capacity, in terms of their C storage abilities, which will benefit soil fertility and promote the capture of atmospheric CO2. In turn, policy makers may incorporate this information into environmental reward payment schemes.
Approaches
This project will assess a selection of widely-used apple rootstock cultivars for their C-sequestering abilities by analysing three key components:
Physical root measurements: Root recalcitrance will be assessed using biochemical methods to quantify various compounds (e.g. total C, soluble phenolics, condensed tannins, acid-insoluble fractions (lignin)). Additional measurements will be made for root thickness, decomposition rate, and root depth distribution using rhizotrons, intact cores (Dornbush, et al., 2002) and incubation of roots in microcosms.
Root exudate biochemical analysis: Rhizodeposit collection may be done either by collection of percolated (run-off) water from pot-grown rootstocks (Leisso, et al., 2017), or by dipping roots of axenically-grown rootstocks in distilled water containing silver (Ag+) as described and evaluated by Gransee & Wittenmayer (2000). Primary (sugars, organic acids) and secondary (phenolics) metabolites will be analysed by high performance liquid chromatography (HPLC) or gas chromatography-mass spectrometry (GC-MS).
Rhizosphere community analysis: Recent advances in high-throughput sequencing methods have greatly enhanced microbial community analysis. The bacterial and fungal composition of the rhizosphere community will be investigated via amplification of the universal 16S rRNA gene (bacteria) and ITS sequences (fungi). In particular, the project will focus on functional groups related to C cycling, such as methanotrophs (methane producers), methanogens (methane consumers), and AMF.
People |
ORCID iD |
| Flora Jane O'Brien (Primary Supervisor) | |
| Catherine Chapman (Student) |
Studentship Projects
| Project Reference | Relationship | Related To | Start | End | Student Name |
|---|---|---|---|---|---|
| BB/T508986/1 | 30/09/2019 | 29/09/2023 | |||
| 2289429 | Studentship | BB/T508986/1 | 30/09/2019 | 29/09/2023 | Catherine Chapman |