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Li 6400xt photosynthesis measurement system

Manufactured by LI COR
Sourced in United States

The LI-6400XT is a portable photosynthesis measurement system designed to measure gas exchange and environmental parameters. It is equipped with a leaf chamber to enclose a leaf sample and various sensors to monitor environmental conditions such as temperature, humidity, and light intensity. The system is capable of measuring parameters related to photosynthesis, respiration, and transpiration.

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8 protocols using li 6400xt photosynthesis measurement system

1

Evaluating Water-Use Efficiency in Plants

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The net photosynthetic rate (μmol m–2 s–1), stomatal conductance (gs, mol m–2 s–1), and transpiration rate (E, mmol m–2 s–1) were measured at 9:00–11:00 a.m. with a portable LI-6400XT photosynthesis measurement system (LI-COR Inc., Lincoln, NE, United States). WUEi (μmol mmol–1) was calculated according to the following equation:
The chlorophyll contents were determined by using the method described by Jawale et al. (2017) (link). Plant height was determined by tapeline and the unit was cm, stem diameter was determined by using a Vernier caliper and the unit was mm, the measurement was conducted on the junction of root and stem, and leaf area was determined by using a leaf area meter (handheld laser leaf area meter, CI, 203) and the unit was cm2. The dry weights of the plants were measured at the end of the treatment. The plants were dried in an oven at 80°C. Plant dry weights of aboveground (DWa) and underground parts (DWu) were determined using an electronic analytical balance. The root/shoot ratio (R/S) was calculated as follows: R/S = DWa/DWu. The single fruit weight and fruit weight per plant were determined using an electronic analytical balance after the fruit was ripe. The economic water-use efficiency (WUEe, g L–1) and biomass water-use efficiency (WUEb, g L–1) were calculated according to the following equations:
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2

Photosynthetic parameters and chlorophyll content

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Healthy leaves of the same orientation were selected on 9 May to measure their photosynthesis parameters according to Chen et al. [39 (link)] and Zhang et al. [41 (link)]. The photosynthetic rate (Pn), transpiration rate (Tr), stomatal conductance (Gs), intercellular carbon dioxide concentration (Ci), and water use efficiency (WUE) were monitored using a portable LI-6400XT photosynthesis measurement system (LI-COR Inc., Lincoln, NE, USA) with photosynthetically active radiation of 1000 μmol m−2 s−1 at 8:00~10:00 a.m. Meanwhile, the chlorophyll a and chlorophyll b contents of P. heterophylla leaves were determined with acetone–ethanol (v/v, 2:1) extraction using a UV-5800PC spectrophotometer at 663 nm and 645 nm, respectively. The chlorophyll content in P. heterophylla leaves was the sum of the chlorophyll a and chlorophyll b contents.
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3

Photosynthesis Parameters of P. ternata

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Fifteen P. ternata plants, on the east, west, south, north, and in the middle of each plot, were randomly selected at the vigorous growth period (May 15) for investigation of their photosynthesis parameters. The chlorophyll content of the fully-expanded leaves of P. ternata was monitored by a SPAD-502Plus chlorophyll meter (Konica Minolta Inc., Osaka, Japan). Meanwhile, their Pn, Ci, Gs, and Tr contents were monitored by a portable LI-6400XT photosynthesis measurement system (LI-COR Inc., Lincoln, NE, USA), with the photosynthetically active radiation of 1000 μmol m−2 s−1 at 8:00–10:00 a.m. [27 (link),28 (link)].
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4

Physiological Traits of Kiwifruit Leaves

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The phenolics, flavonoids, soluble protein, malonaldehyde (MDA), resistance enzyme activities and photosynthetic characteristics of kiwifruit leaves were determined on 25 August 2021. Total phenolics and total flavonoids were determined using an UV-5800PC spectrophotometer at 280 nm (OD280) and 325 nm (OD325) with 20 mL 1% (v/v) HCl-methyl alcohol at 3 °C for 1 h without light extraction [32 (link)]. The soluble protein, MDA, catalase (CAT), peroxidase (POD), polyphenoloxidase (PPO) and superoxide dismutase (SOD) activities of kiwifruit leaves were determined as described by Zhang et al. [33 (link)]. The chlorophyll content of kiwifruit leaves was measured using an UV-5800PC spectrophotometer at 645 nm (OD645) and 663 nm (OD663) with an acetone–ethanol (v/v, 2:1) extraction. A portable LI-6400XT photosynthesis measurement system (LI-COR Inc., Lincoln, NE, USA) was used for monitoring the photosynthetic rate (Pn) and transpiration rate (Tr) of kiwifruit leaves at 8:00–10:00 a.m. on 25 August 2021. Water use efficiency (WUE) of kiwifruit was Pn/Tr.
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5

Characterizing R. roxburghii Leaf Resistance

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R. roxburghii leaves from the middle, east, west, south and north orientations of each tree tested were randomly collected on April 24 in 2021. A mixture of collected leaves in each plot were used for determining the disease resistance parameters of R. roxburghii leaves, including total phenolics, total flavonoids, soluble protein, soluble sugar, proline (Pro), malonaldehyde (MDA), SOD activity and polyphenoloxidase (PPO) activity, as described by Wang et al. [35 (link)] and Zhang et al. [36 (link),37 (link)]. In the meantime, the photosynthesis parameters of R. roxburghii leaves including chlorophyll content, photosynthetic rate (Pn), transpiration rate (Tr) and water use efficiency (WUE) were also measured on April 24 in 2021 according to Zhang et al. [34 (link)]. Chlorophyll content was determined by an UV-5800PC spectrophotometer at 663 nm and 645 nm with acetone–ethanol (v/v, 2:1) extraction. Additionally, a portable LI-6400XT photosynthesis measurement system (LI-COR Inc., Lincoln, NE, USA) was applied for monitoring the Pn and Tr of R. roxburghii leaves at 8:00–10:00 a.m. on April 24 in 2021.
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6

Fungicide Efficacy and Physiological Responses in R. roxburghii

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The control effect of tested fungicides for powdery mildew of R. roxburghii was investigated on May 30 in 2020 according to Li et al. [7 (link)]. The incidence rate, disease index, and control effect of tested fungicides for powdery mildew of R. roxburghii were calculated according to Equations (2)–(4), respectively. The incidence degree: 0 = no incidence, 1 = 1~2 diseased lobules with thin hyphae, 2 = 3~4 diseased lobules with thick hyphae, 3 = 5~6 diseased lobules with dense hyphae, 4 = more than 7 diseased lobules with dense hyphae.



The resistance parameters of R. roxburghii leaves, such as proline (Pro), soluble sugar, malonaldehyde (MDA), flavonoid, SOD activity and PPO activity, were determined on 30 May 2020 as described by Zhang et al. [30 (link),31 (link)]. The photosynthetic rate (Pn) of leaves in R. roxburghii was monitored using a portable LI-6400XT photosynthesis measurement system (LI-COR Inc., Lincoln, NE, USA) at 8:00–10:00 a.m. on 30 May. Chlorophyll content of R. roxburghii leaves was determined by a UV-5800PC spectrophotometer at 645 nm (OD645) and 663 nm (OD663) with an acetone–ethanol (v/v, 2:1) extraction.
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7

Photosynthesis Measurements of P-Deficient Plants

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Net CO2 assimilation rate (An) were measured on the fourth youngest fully expanded leaf from the top at 9:30 a.m. to 11:00 a.m. every 10 d from the onset of P deficiency. Three plants from each treatment group were subjected to measurement using a portable LI-6400XT photosynthesis measurement system (LI-COR, Lincoln, NE, USA). The photosynthetic active radiation (PAR), temperature, and CO2 concentration during the measurements were 300 μmol m−2 s−1, 30°C, and 400 μmol mol−1, respectively.
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8

Oligochitosan and Pyraclostrobin SC Protocol

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Five percent of oligochitosan AS was provided by Kesheng Group Co. Ltd. (Yancheng, Jiangsu, China), its trade name is Xiansheng. Thirty percent pyraclostrobin SC was produced by Jinan Zhongke Green Biological Engineering Co. Ltd. (Jinan, Shandong, China), its trade name is Cuijian. The portable LI-6400XT photosynthesis measurement system was produced by LI-COR Inc., (Lincoln, NE, USA), and the UV-5800PC spectrophotometer was produced by Shanghai Yuan Analysis Instrument Co., Ltd. (Shanghai, China).
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