Abstract

BackgroundImprovements in high-throughput phenotyping technologies are rapidly expanding the scope and capacity of plant biology studies to measure growth traits. Nevertheless, the costs of commercial phenotyping equipment and infrastructure remain prohibitively expensive for wide-scale uptake, while academic solutions can require significant local expertise. Here we present a low-cost methodology for plant biologists to build their own phenotyping system for quantifying growth rates and phenotypic characteristics of Arabidopsis thaliana rosettes throughout the diel cycle.ResultsWe constructed an image capture system consisting of a near infra-red (NIR, 940 nm) LED panel with a mounted Raspberry Pi NoIR camera and developed a MatLab-based software module (iDIEL Plant) to characterise rosette expansion. Our software was able to accurately segment and characterise multiple rosettes within an image, regardless of plant arrangement or genotype, and batch process image sets. To further validate our system, wild-type Arabidopsis plants (Col-0) and two mutant lines with reduced Rubisco contents, pale leaves and slow growth phenotypes (1a3b and 1a2b) were grown on a single plant tray. Plants were imaged from 9 to 24 days after germination every 20 min throughout the 24 h light–dark growth cycle (i.e. the diel cycle). The resulting dataset provided a dynamic and uninterrupted characterisation of differences in rosette growth and expansion rates over time for the three lines tested.ConclusionOur methodology offers a straightforward solution for setting up automated, scalable and low-cost phenotyping facilities in a wide range of lab environments that could greatly increase the processing power and scalability of Arabidopsis soil growth experiments.

Highlights

  • Improvements in high-throughput phenotyping technologies are rapidly expanding the scope and capacity of plant biology studies to measure growth traits

  • No measurable decrease in photosynthetically active radiation (PAR) was observed when the rig was set up in the side-lit growth cabinet used for growth experiments in this study

  • When light levels were measured under the rig in a vertically lit growth chamber (Snijders Scientific model MC1000), an average decrease of 14% in PAR was observed (180–154 μmol photons ­m−2 s−1)

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Summary

Introduction

Improvements in high-throughput phenotyping technologies are rapidly expanding the scope and capacity of plant biology studies to measure growth traits. The costs of commercial phenotyping equipment and infrastructure remain prohibitively expensive for wide-scale uptake, while academic solutions can require significant local expertise. Dobrescu et al Plant Methods (2017) 13:95 high-throughput plant phenotyping tools The wider uptake of such tools has been hampered by the local expertise required for hardware and software development. The lack of accessible hardware and appropriate algorithms for trait extraction is widely considered the major bottleneck in the plant phenotyping field [5]. Several online tools are available for measuring plant traits (e.g. www.plant-image-analysis.org [6]) to supplement either commercial systems or support affordable solutions (e.g. www.phenotiki.com [5]). Many image analysis systems lack robust validation and are not well supported [6]

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