Skip to main content
. 2019 Feb 8;10:47. doi: 10.3389/fpls.2019.00047

FIGURE 1.

FIGURE 1

Schematic overview of cultivation protocol and automated phenotyping protocol. (A) Plants were cultivated for 20 days prior to transplantation in control conditions (FS-WI, PSI, Czechia) and were further kept in the same conditions for the next 19 days (DAT, days after transplantation). Eight types of protein hydrolysates (A–G, I) plus control treatment were applied twice to tomato plants by spraying 5 and 12 days after transplantation. Plant phenotypic measurements were performed during the experiment using PlantScreenTM Modular System installed in semi-controlled greenhouse environment conditions in PSI Research Center (PSI, Drásov, Czechia). (B) Plant handling and automated phenotyping protocol. Tomato plants were transferred to PlantScreenTM Modular System and automated phenotyping protocol was initiated. Prior to and following the protein hydrolysates application, plants were regularly screened using the calibrated top and side view RGB camera and kinetic chlorophyll fluorescence camera for photosynthetic performance quantification. Plants were regularly watered and weighed using the automated watering and weighing station.