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Li 6800 portable photosynthetic system

Manufactured by LI COR
Sourced in United States

The LI-6800 is a portable photosynthetic system designed for researchers to measure gas exchange and fluorescence. It provides accurate and reliable data on photosynthesis, respiration, and other physiological processes in plants.

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2 protocols using li 6800 portable photosynthetic system

1

Gas Exchange Measurement of Seedlings

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The gas exchanges were measured from 9:00 to 11:00, using an LI-6800 portable photosynthetic system (LI-COR, Lincoln, NE, USA) equipped with a CO2 control module and a red–blue LED-light source. The photosynthetic-photon-flux density of the leaf chamber was set to 700 μmol m–2 s–1. The airflow rate in the leaf chamber was set as 700 μmol s–1. The concentration of CO2 in the reference chamber was set at 400 μmol mol–1 for the measurements. The net photosynthetic rate (Pn), stomatal conductance (Gs), transpiration rate (E), intercellular CO2 concentration (Ci), and CO2 concentration in the leaf chamber (Ca) were simultaneously recorded from seven seedlings per treatment.
The leaf used to measure the gas-exchange parameters were collected, promptly immersed in N2, and stored at −80 °C. The leaves were positioned with the main veins cut out on A4 paper, and a 4 × 4 cm piece of green cardboard was added as a control. Leaf images were obtained with a digital camera (7D, Canon, Inc., Tokyo, Japan), and image software (Media Cybernetics, Silver Spring, MD, USA) was utilized to measure the leaf area.
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2

Photosynthetic Responses to Drought Acclimation

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Photosynthetic parameters were measured on the third fully expanded leaf of each plant after 15 days (S2) for control (CK), drought acclimation (DA), and non-acclimation (NA) plants. The measurements were taken at 9:00 AM and 11:00 AM using an LI-6800 portable photosynthetic system (LI-COR Inc., Lincoln, NE, USA). The light-saturation point was set to µmol (photon) m -2 s -1 to measure the net photosynthetic rate and stomatal conductance using the methods reported by Du et al. (2020a) and Li et al. (2017) . The ambient temperature of each measured millet leaf was set to 30 °C. The CO 2 concentration was 400 µmol (CO 2 ) mol -1 , the relative humidity was 60%-65%, and the airflow was 500 µmol. For tissue relative water contents (RWC), the leaves and roots of CK, DA, and NA-treated plants were sampled. Fresh weights were immediately taken, and the samples were incubated in distilled water for 4 h with vigorous shaking. The turgid weights (TW) were measured after 4 h, and the tissue samples (leaf and roots) were oven-dried at 60 °C for 48 h, after which the dry weights (DW) were recorded. Tissue RWC was estimated using the equation.
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