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Location: The Automated controlled-environment phenotyping at the Donald Danforth Plant Science Center Bellwether Foundation Phenotyping Facility
The Scanalyzer 3D platform consists of multiple digital imaging chambers connected to the Conviron growth house by a conveyor belt system, resulting in a continuous imaging loop. Plants are imaged from the top and/or multiple sides, followed by digital construction of images for analysis.
RGB imaging allows visualization and quantification of plant color and structural morphology, such as leaf area, stem diameter and plant height.
NIR imaging enables visualization of water distribution in plants in the near infrared spectrum of 900–1700 nm.
Fluorescent imaging uses red light excitation to visualize chlorophyll fluorescence between 680 – 900 nm. The system is equipped with a dark adaptation tunnel preceding the fluorescent imaging chamber, allowing the analysis of photosystem II efficiency.
The LemnaTec software suite is used to program and control the Scanalyzer platform, analyze the digital images and mine resulting data. Data and images are saved and stored on a secure server for further review or reanalysis.
Duration: 10 days on LemnaTec platform
Experimental Design:
3 replicates of 190 BAP lines were grown in a randomized complete block design
Watering regimes = 30% FC and 100% FC
Drought conditions were imposed 10 days after planting
Plants were imaged daily for 10 days (11-20 DAP) and sampled at 20 days after planting
Experiment was repeated twice to phenotype the full BAP (Reps 1A and 1B)
Kansas State University - coming 2017
HudsonAlpha Institute for Biotechnology, Alabama - coming 2017
Genomic data includes whole-genome resequencing data from the HudsonAlpha Institute for Biotechnology, Alabama for 384 samples for accessions from the sorghum Bioenergy Association Panel (BAP) and genotyping-by-sequencing (GBS) data from Kansas State University for 768 samples from a population of sorghum recombinant inbred lines (RIL).
Experimental Design:
384 BAP samples were sequenced to an average depth of ~25x.
Shotgun sequencing (127-bp paired-end) was done using an Illumina X10 instrument at the HudsonAlpha Institute for Biotechnology.
Variant calling was done using a computational pipeline at the Danforth Center.
See the Data Products page to get access to raw and derived data products.
Experimental Design:
768 RIL samples were sequenced using a GBS approach.
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Season 1 sorghum (April - July 2016) Season 2 sorghum (August - November 2016) Durum wheat (January 2017 -
Three hundred thirty one lines were planted in Season 1.
Under scanner system
West of scanner system
The Lemnatec Scanalyzer Field Gantry System is the largest field crop analytics robot in the world. This high-throughput phenotyping field-scanning robot has a 30-ton steel gantry that autonomously moves along two 200-meter steel rails while continuously imaging the crops growing below it with a diverse array of cameras and sensors.
Twelve sensors are attached to the gantry system. Detailed information for each sensor including name, variable measured, and field of view are available here. The planned sensor missions and their objectives for 2016 are available here.
emergence vigor emergence final stand counts plant heights node and tiller counts on marked plants phenology growth stage data leaf desiccation ratings radiation interception managements Incomplete harvest yield data
One hundred and seventy-six lines were planted in Season 2.
Under scanner system - same as season 1
same as season 1
plant heights managements emergence vigor emergence final stand counts node and tiller counts on marked plants leaf length and width on marked plants, one date
Experiment
Reps
Treatments
Experimental design
BAP
3
30 lines (12 PS, 12 sweet, 6 grain)
RCB with sorghum types nested in groups
Night illumination
3
5 illumination levels x 2 PS lines (with check line separating illumination levels)
RCB
Row #
3
6 adjacent plot scenarios: 3 lines (forage, sweet, PS) x 2 sides (east or west)
RCB but not balanced with all treatments in all reps
Biomass
3
5 sampling times x 3 lines (forage, sweet, PS)
RCB with sampling time as a repeated measure
Density
3
3 densities (5, 15, 30 cm) x 3 lines (forage, sweet, PS)
RCB
RILs
3
130 RILs plus 10 repeats of a single line/rep
Incomplete Block (row-column alpha lattice design)
Uniformity
17
2 lines (forage, PS)
None - Same line planted in single range
Experiment
Reps
Treatments
Experimental design
BAP
1
30 lines (12 PS, 12 sweet, 6 grain)
None - single rep planted for observation
RILs
3
60 RILs
Incomplete Block (row-column alpha lattice design)