Multi-excitation wavelength modulated chlorophyll fluorescence meter——MULTI-COLOR-PAM
Date:2024-12-19 08:46:15

Main functions


Measurement parameters

F Oh, FM, F, FM, F V/FM, Y(II), QP, QN, NP Q, Y(no), Y(NP Q), ET R, ET R(II)λ, fear, J, τ, sigma(II)λ, PAR, PAR(II) etc.


Application areas

It is mainly used for in-depth photosynthesis mechanism research of various algae, and in-depth research on cyanobacteria, green algae, diatoms, dinoflagellates, red algae, cryptoalgae, etc. with suitable wavelengths, new measurements, and new parameters.If you choose higher plant attachments, you can also measure the leaves of higher plant.


Main technical parameters

Measured light: Provides pulse-modulated measurement light of 400, 440, 480, 540, 590 and 625 nm, 20 intensity selections, 14 frequency selections.

Actinic light: Provide continuous actinic light from 440, 480, 540, 590, 625 nm and 420-640 nm (white light), with maximum light intensity of 4000 μmol m-2yes-1;Maximum intensity of single turnover saturated flash 200 000 μmol m-2yes-1, duration 5-50 μs adjustable; multi-turnover saturated flash intensity 10 000 μmol m-2yes-1, adjustable from 1-800 ms.

Far red light: 725 nm.

Signal detection: PIN-photodiode with special phase locked amplifier (patented design), maximum time resolution of 10 μs.


Introduction to the functions of Multi-Color-PAM

The relative electron transfer rate rETR of optical system II is a very commonly used parameter.rETR = PAR × Y(II) × ETR-factor, where ETR-factor refers to the proportion of light energy absorbed by the optical system II to the total incident PAR.In most published literatures, no attempt was made to determine ETR-factor, but simply assumed that it was the same as "mode blades", that is, 50% of the PAR was distributed to the optical system II and 84% of the PAR was absorbed by photosynthetic pigments.Therefore, in existing literature, rETR is generally calculated using the formula rETR = PAR × Y(II) × 0.84 × 0.5.

Recently, the absolute electron transfer rate of optical system II can be achieved by using multi-excitation wavelength modulated chlorophyll fluorescence meter MULTI-COLOR-PAMλmeasurement.First, use MULTI-COLOR-PAM to determine the functional optical cross-sectional area of ​​optical system II at a certain wavelength Sigma(II)λ(Unit nm2) (where λ is the wavelength), then find the quantum absorption rate of optical system II PAR(II) = Sigma(II)λ× L × PAR = 0.6022 × Sigma(II)λ× PAR.where L is the Avogadro constant and the coefficient 0.6022 is to 1 μmol quanta m-2(i.e. 6.022 × 1017 quanta m-2) Convert to 0.6022 quanta nm-2, the unit of PAR(II) is quanta/(PSII × s).Next, you can calculate ETR(II)λ= PAR(II) × Y(II)/Y(II)max, where Y(II)max is the quantum yield of the optical system II after dark adaptation, that is, Fv/Fm×ETR(II)The unit is electrons/(PSII × s).

Traditional modulated chlorophyll fluorescence instruments generally can only provide one or two colors of light sources, such as halogen lamps that emit white light, blue LEDs that emit blue light, or red LEDs that emit red light, etc.The results of measuring light with different colors may vary. As shown in Figure 1A, there is a very significant difference in the rapid light curve of the green algae Chlorella Chlorella illuminated by blue light (440 nm) and red light (625 nm).The rETRmax under the irradiation is significantly smaller than that under the red light irradiation, and there is a slight downward trend in the stronger light curve rETR, which shows that the blue light is more likely to induce light suppression (Schreiber, Klughammer et al. 2011, Schreiber, Klughammer et al. 2012).From this, it can be inferred that many experimental results reported in the past literature may have misunderstandings caused by different excitation light sources used.

As mentioned above, using MULTI-COLOR-PAM, the real electron transfer rate ETR(II) can already be measuredλ.If using ETR(II)λWhat will happen if you draw a fast light curve?Figure 1B is the result obtained after converting the results of Figure 1A into absolute electron transfer rate. It can be seen that the absolute electron transfer rate is consistent whether it is irradiated with blue light or red light.This proves that the difference in the results in Figure 1A is due to the optical system II functional optical cross-sectional area of ​​algae cells at different wavelengths Sigma(II)λdifferent sizes of the , (Schreiber, Klughammer et al. 2011, Schreiber, Klughammer et al. 2012).This utilizes absolute electron transfer rate ETR(II)λThe drawn fast light curves may play an increasingly important role in future scientific research.

1.jpg2.jpg
Figure 1 Fast light curves drawn using relative electron transfer rate (A) and absolute electron transfer rate (B) respectively (cited from Schreiber et al., 2012)
The rapid light curve of Chlorella sp. was measured using MULTI-COLOR-PAM with blue light (440 nm) and red light (625 nm) as actinic light sources, respectively.
In Figure A, rETR calculation uses 0.42 as the ETR factor.
In Figure B, the functional optical cross-sectional area of ​​the optical system II obtained under the excitation of blue and red light Sigma(II)λ4.547 and 1.669 nm respectively2, calculate the absolute electron transfer rate ETR(II)440and ETR(II)625The Fv/Fm of the two groups are 0.68 and 0.66, respectively.


Purchase Guide

1. Basic hanging sample measurement

System composition: general-purpose host, standard version detection unit, optical unit of suspension, data cable, workbench, software, etc.

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Basic hanging sample measurement model



2. Basic articles on measuring leaves of higher plants

System composition: general-purpose host, standard version detection unit, special blade clip, data cable, workbench, software, etc.

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Special leaf clips for measuring leaves of higher plants



3. Other optional accessories

1. ED-101US/T: The temperature control device, installed on ED-101US/MD, is a suspension liquid temperature control; it can be connected to an external circulating water bath to control the temperature,

2. US-SQS/WB: Spherical miniature optical quantum probe, which can be inserted into the sample cup to measure PAR; controlled by the host DUAL-C.

3. PHYTO-MS: Magnetic stirrer, connected to the bottom of the optical unit ED-101US/MD to stir the suspension.

Origin: WALZ, Germany


References

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Original data source: Google Scholar

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Collection