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Lcp narrow lamp

Manufactured by ADC BioScientific
Sourced in United Kingdom

The LCP Narrow Lamp is a laboratory equipment product manufactured by ADC BioScientific. It is a specialized light source designed for specific applications in research and analysis. The core function of the LCP Narrow Lamp is to provide a focused and controlled light output for various experimental or measurement purposes.

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5 protocols using lcp narrow lamp

1

Photosynthetic Activity Evaluation in Plants

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The photosynthetic activity of dark-acclimated plants was assessed using the LCpro-SD Gas Exchange Measurement System (ADC BioScientific Ltd., UK), based on the following parameters:–A—CO2 assimilation level (μmol m-2s-1),–E—transpiration (mmol m-2s-1),–s—stomatal conductance (mol m-2s-1),–i—intercellular CO2 concentration (vpm). Measurements were carried out in the phytotron at a constant air temperature of 298.15 K and ambient humidity of 70±5%. The measurement sequence was the same, and the drought-stressed and non-stressed plants under the same fertilizer regimes were alternately measured. For measurements in each plant, the same, youngest, fully developed leaf was selected. The gas exchange measuring settings were set up according to the methods described earlier [36 (link)]. The concentration of CO2 supplied to the measuring chamber (reference CO2) was kept at 360 vpm. The flow of air supplied to the measuring chamber (u) was maintained at 200 μmol s-1. The concentration of H2O (reference H2O) was set to ambient, i.e., the actual concentration in the environment. The intensity of the light emitted in the measuring chamber (PPFD) by the red and blue (in the proportion of 10:1) LEDs of the spectrum was set to 400 μmol m-2s-1 (LCP Narrow Lamp, ADC BioScientific Ltd., UK). Gas exchange measurements were performed in 3 biological replications.
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2

Photosynthetic and Transpiration Rates

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Photosynthesis Rate (A (μmol CO2 m-2s-1)) and the Transpiration Rate (E (mmol H2O m-2s-1)) of single leaves were measured on the same leaf as chlorophyll fluorescence, with a portable photosynthesis system (LCpro-SD, ADC Bio Scientific Ltd., UK) with a Narrow leaf chamber (area: 5.8 cm2). The CO2 concentration (Reference CO2) in the leaf chamber was kept at 360 vpm, and the leaf chamber temperature (Tch) was maintained at 26 ± 1°C. The flow rate of the air (u) was at 200 μmols-1. The Reference H2O and flow (u) stayed at the ambient level. During the measurements, PAR was 400 μmolm-2s-1 and adjusted automatically by a red-blue light-emitting diode (LED) light source (LCP Narrow Lamp, ADC Bio Scientific Ltd., UK). The setting protocols and methods of measurement were selected in accordance with the manufacturer’s instructions [15 (link), 16 (link)].
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3

Measuring Leaf Gas Exchange Parameters

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Net CO2 assimilation rate (photosynthetic rate: A) and leaf transpiration rate (E) were measured on the same fully mature leaf with a portable photosynthesis system (LCpro-SD, ADC BioScientific Ltd., Hoddesdon, UK) with a narrow leaf chamber (area: 5.8 cm2). During the period of measurements, CO2 concentration (reference CO2) in the leaf chamber was kept at 360 ppm, leaf chamber temperature was maintained at 25 ± 1 °C, the flow rate of air was kept at 200 µmol s−1 and ambient H2O concentration (Reference H2O) and PAR were adjusted automatically by a red-blue light-emitting diode (LED) light source (LCP Narrow Lamp, ADC BioScientific Ltd., UK). Water use efficiency (WUE) (4) was calculated according to the following equation: WUE=AE
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4

Leaf Photosynthesis and CO2 Exchange

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Rates of CO2 exchange in the leaf chamber to the photosynthesis rate (A) of single leaves were measured on the first young fully mature healthy leaf using a portable photosynthesis system (LCpro-SD, ADC BioScientific Ltd., Hoddesdon, UK) with a narrow leaf chamber (area: 5.8 cm2). The CO2 concentration (Reference CO2) in the leaf chamber was respectively kept at 360 vpm and the leaf chamber temperature (Tch) maintained at 26 ± 1 °C. The flow rate of air (u) was 200 µmol s−1. The H2O concentration (Reference H2O) and flow (u) were maintained at ambient values. Plant photosynthesis, for each combination of GB, was measured after 6-h dark adaptation of plants at 400 µmol m−2 s−1, adjusted automatically by a red–blue light-emitting diode (LED) light source (LCP Narrow Lamp, ADC BioScientific Ltd., Hoddesdon, UK). Settings protocols and methods of measurement were selected in accordance with the manufacturer’s instructions. The following parameters were measured: Photosynthesis rate—A (µmol m−2 s−1), transpiration rate—E (mmol m−2 s−1), sub-stomatal CO2—Ci (µmol mol−1) and stomatal conductance—Gs (mol m−2 s−1).
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5

Photosynthetic Response to Drought Stress

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The plant photosynthesis intensity values were measured twice – after drought stress imposition and after regeneration. Photosynthesis intensity was estimated on single leaves in the leaf chamber, based on CO2 exchange rate—A (mol/m2 × s), transpiration rate—E (mmol/m2 × s), sub-stomatal CO2—Ci (μmol/mol), and stomatal conductance—Gs (mol/m2 × s). The measurements were taken using a portable photosynthesis system (LCpro-SD, ADC BioScientific Ltd., Hoddesdon, United Kingdom) with a narrow leaf chamber (area: 5.8 cm2) on the first young fully developed healthy leaf. Photosynthesis measurements were carried out in triplicate (three plants) for each seed treatment at either timepoint. The CO2 concentration (reference CO2) in the leaf chamber was kept at 360 vpm, leaf chamber temperature (Tch) was set at 25°C, the flow rate of air (u) was kept at 200 μmol/s, and ambient H2O concentration (Reference H2O) was used. Photosynthetically active radiation (PAR) was kept at 400 μmol/s × m2, adjusted automatically by a red-blue light-emitting diode light source (LCP Narrow Lamp, ADC BioScientific Ltd.).
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