4.6 Article

A Do-It-Yourself phenotyping system: measuring growth and morphology throughout the diel cycle in rosette shaped plants

期刊

PLANT METHODS
卷 13, 期 -, 页码 -

出版社

BIOMED CENTRAL LTD
DOI: 10.1186/s13007-017-0247-6

关键词

2D; Arabidopsis thaliana; Near-infrared LED array; Image analysis; Low cost; Rubisco

资金

  1. UK Biotechnology and Biological Sciences Research Council [BB/M006468/1, BB/N02334X/1, BB/P023487/1]
  2. University of Edinburgh (UoE) Innovation Initiative Grant Scheme
  3. EPSRC DTP Ph.D. fellowship [EP/N509644/1]
  4. BBSRC [BB/P023487/1, BB/M006468/1, BB/N02334X/1] Funding Source: UKRI
  5. EPSRC [EP/N509644/1, 1785349] Funding Source: UKRI
  6. Biotechnology and Biological Sciences Research Council [BB/P023487/1, BB/M006468/1, BB/N02334X/1] Funding Source: researchfish

向作者/读者索取更多资源

Background: Improvements 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. Results: We 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, wildtype 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. Conclusion: Our 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.

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