Evaluation of Photosynthetic Behaviors by Simultaneous Measurements of Leaf Reflectance and Chlorophyll Fluorescence Analyses

Summary

We describe a new technical approach to study photosynthetic responses in higher plants involving simultaneous measurements of chlorophyll a fluorescence and leaf reflectance using a PAM and a spectral radiometer for the detection of signals from the same leaf area in Arabidopsis.

Abstract

Chlorophyll a fluorescence analysis is widely used to measure photosynthetic behaviors in intact plants, and has resulted in the development of many parameters that efficiently measure photosynthesis. Leaf reflectance analysis provides several vegetation indices in ecology and agriculture, including the photochemical reflectance index (PRI), which can be used as an indicator of thermal energy dissipation during photosynthesis because it correlates with non-photochemical quenching (NPQ). However, since NPQ is a composite parameter, its validation is required to understand the nature of the PRI parameter. To obtain physiological evidence for evaluation of the PRI parameter, we simultaneously measured chlorophyll fluorescence and leaf reflectance in xanthophyll cycle defective mutant (npq1) and wild-type Arabidopsis plants. Additionally, the qZ parameter, which likely reflects the xanthophyll cycle, was extracted from the results of chlorophyll fluorescence analysis by monitoring relaxation kinetics of NPQ after switching the light off. These simultaneous measurements were carried out using a pulse-amplitude modulation (PAM) chlorophyll fluorometer and a spectral radiometer. The fiber probes from both instruments were positioned close to each other to detect signals from the same leaf position. An external light source was used to activate photosynthesis, and the measuring lights and saturated light were provided from the PAM instrument. This experimental system enabled us to monitor light-dependent PRI in the intact plant and revealed that light-dependent changes in PRI differ significantly between the wild type and npq1 mutant. Furthermore, PRI was strongly correlated with qZ, meaning that qZ reflects the xanthophyll cycle. Together, these measurements demonstrated that simultaneous measurement of leaf reflectance and chlorophyll fluorescence is a valid approach for parameter evaluation.

Introduction

Leaf reflectance is used to remotely sense vegetation indices that reflect photosynthesis or traits in plants^1,2. The normalized difference vegetation index (NDVI), which is based on infrared reflection signals, is one of the most widely known vegetation indices for the detection of chlorophyll-related properties, and it is used in the ecology and agricultural sciences as an indicator of environmental responses in trees or crops³. In field studies, although many parameters (e.g., chlorophyll index (CI), water index (WI), etc.) have been developed and used, few detailed verifications of what these parameters directly (or indirectly) detect have been performed using mutants.

Pulse-amplitude modulation (PAM) analysis of chlorophyll fluorescence is an effective method to measure photosynthetic reactions and processes involved in photosystem II (PSII)⁴. Chlorophyll fluorescence can be detected with a camera and used for screening photosynthesis mutants⁵. However, camera detection of chlorophyll fluorescence requires complex protocols such as dark treatment or light saturation pulses, which are difficult to implement in field studies.

Leaf absorbed solar light energy is mainly consumed by photosynthetic reactions. By contrast, the absorption of excess light energy can generate reactive oxygen species, which causes damage to photosynthetic molecules. The excess light energy must be dissipated as heat through non-photochemical quenching (NPQ) mechanisms⁶. The photochemical reflectance index (PRI), which reflects light-dependent changes in leaf reflectance parameters, is derived from narrow-band reflectance at 531 and 570 nm (reference wavelength)^7,8. It is reported to correlate with NPQ in chlorophyll fluorescence analysis⁹. However, since NPQ is a composite parameter that includes the xanthophyll cycle, state tradition, and photoinhibition, detailed validation is required to understand what the PRI parameter measures. We have focused on the xanthophyll cycle, a thermal dissipation system involving the de-epoxidation of xanthophyll pigments (violaxanthin to antheraxanthin and zeaxanthin) and a main component of NPQ because correlations between PRI and conversion of these pigments has been reported in previous studies⁸.

Many photosynthesis-related mutants have been isolated and identified in Arabidopsis. The npq1 mutant does not accumulate zeaxanthin because it carries a mutation in violaxanthin de-epoxidase (VDE), which catalyzes the conversion of violaxanthin to zeaxanthin¹⁰. To establish whether PRI only detects changes in xanthophyll pigments, we simultaneously measured PRI and chlorophyll fluorescence in the same leaf area in npq1 and the wild-type and then dissected NPQ at varying time scales of dark relaxation to extract the xanthophyll-related component¹¹. These simultaneous measurements provide a valuable technique for the assignment of vegetation indices. Furthermore, since PRI correlates with gross primary productivity (GPP), the ability to assign PRI precisely to one component has important applications in ecology¹².

Protocol

1. Cultivation of Arabidopsis plants

1. Soak Arabidopsis thaliana seeds in sterilized deionized water in a microtube, and incubate for 2 days at 4 °C in the dark.
2. Place approximately four of the imbibed, cold-treated seeds onto the soil surface using a micropipette. Incubate the planted pots in a growth chamber with a 16 h light (120 μmol photons m^–2 s^–1) and 8 h dark period at 22 °C and 20 °C, respectively.
3. Grow one plant per pot by thinning other seedlings after germination. Prepare at least five pots. Incubate the plants in the growth chamber for an additional 4 weeks. Three plants are used for the experiments.
4. Use the youngest, fully-opened mature leaf for photosynthesis measurements.

2. Setting up the sample stage, photosynthetic instruments, and light source

NOTE: For this protocol, a custom-built sample stage was used for fixing leaves and detection probes (Figure 1).

1. Attach a 10 cm² steel plate with a 1 cm diameter hole onto the custom-made sample stage. The hole size in this plate can be changed to accommodate different leaf samples or plant species. The stage has a clip for fixing the detection probes and an adjuster to adjust the distance between the probes and the leaf sample.
2. Prepare thin fiber probes for measuring chlorophyll fluorescence and leaf reflectance. These thin fiber probes will be positioned closely so that they measure signals from the same leaf position.
   NOTE: A PAM chlorophyll fluorometer and a spectral radiometer were adapted for signal detection of chlorophyll a fluorescence and leaf reflectance, respectively. Both instruments use thin fiber probes with diameters of 1 mm and 2 mm, respectively.
3. Fit these two probes tightly together and wrap them with plastic tape.
4. Clip the taped probes onto the sample stage using a coaxial lens holder (see Figure 1), and position them vertical to the leaf surface.
   NOTE: The field of view of the fiber optic cable in the spectral radiometer is α = 25°. In this method, the distance between the fiber probe tips and leaf surface is shorter than 1 cm. Therefore, the measuring leaf area is almost the same as that of the fiber.
5. Attach a biforked light guide made of glass fibers to the halogen light source and irradiate the sample stage from both directions at angles of approximately 45°.
   NOTE: A halogen lamp, which is close to the wavelength distribution of natural sunlight, is used as actinic light for inducing photosynthesis. The halogen light source was adapted with a built-in cold filter, which removes long wavelengths from near infrared, to prevent increases in leaf surface temperature (λ = 400 to 800 nm).
6. Adjust the light source so that light uniformly illuminates the sample stage without casting shadows.

3. Setting up simultaneous measurements of leaf reflectance and chlorophyll fluorescence

NOTE: All steps are performed in the dark room to avoid the detection of light other than actinic light. A weak-green light (e.g., green-cellophaned light) should be turned off before the actual measurements.

1. Measuring the distance between the leaf sample and the probes on the sample stage.
   1. Place a test leaf on the leaf holder of the sample stage in the dark. Press the leaf against a steel plate on the stage (black square in Figure 1).
   2. Turn on the PAM and irradiate the leaf sample with a measuring light. The values of the chlorophyll fluorescence intensities are confirmed using PAM controlling software (see Table of Materials).
   3. Move the adjuster so that the fluorescence intensity measures approximately 100. Measure the distance between the probe and the leaf. Fix the adjuster, and record the value of the distance on the adjuster.
   4. Turn off the measuring light. Remove the test leaf.
2. Measuring the irradiance intensities of the actinic light
   NOTE: To observe light-dependent photosynthetic behaviors, actinic light of varying intensity is used to irradiate the leaf sample.
   1. Set a light quantum meter at the position where the sample leaf would be placed.
   2. Irradiate light from the halogen light source and measure the intensity.
   3. Determine which positions of the light source dial would generate intensities of 30, 60, 120, 240, and 480 μmol photons m^–2 s^–1.
      NOTE: Arabidopsis plants are grown under 120 μmol photons m^–2 s^–1; therefore, the irradiance intensities of the actinic light are selected to provide a range of small and large intensities.
   4. Mark each irradiance intensity on the dial.
3. Measure a reflection standard.
   NOTE: A reflection standard is required to calculate the leaf reflectance ratio at each irradiance intensity.
   1. Place a white plate as a reflectance standard at the position of the leaf sample.
   2. Turn on a spectral radiometer. The reflectance signal is shown by the spectral radiometer controlling software. At this time, there are no spectral data because there is no irradiating light.
   3. Turn on the halogen lamp to irradiate with 480 μmol photons m^–2 s^–1, the highest irradiance intensity in this test.
   4. Adjust the detection strength of the radiometer to avoid saturation.
   5. Record spectral reflectance between 450–850 nm at 1 nm intervals under illumination with 30, 60, 120, 240, and 480 μmol photons m^–2 s^–1.
      NOTE: A baseline electrical signal (dark current) is corrected and subtracted at every spectral measurement.

4. Simultaneous measurements of leaf reflectance and chlorophyll a fluorescence, and calculation of photosynthetic parameters

1. Set a plant at the leaf sample position.
   1. Transfer the Arabidopsis plant from the grown chamber to the controlled dark room with the same temperature and humidity as that of the growth chamber.
   2. Incubate the plant for 1 h in the dark at 22 °C to dissipate electrons from the PSII reaction center and to relax of non-photochemical quenching.
   3. Place the dark-adapted whole plant on a lab jack under the sample stage (Figure 1).
   4. Fix the sample leaf to the leaf holder so that the leaf surface is perpendicular to the detection probes.
2. Measurement of the maximum quantum yield of PSII.
   1. Turn on the PAM and start recording the curve. This value is called 0.
   2. Turn on the measuring light, and wait approximately 30 s for the curve to respond. This value is called F₀.
   3. Give a saturated pulse of 4000 μmol photons m^–2 s^–1 for 0.8 s from the PAM.
   4. Obtain the highest value of the spike in the curve with increased fluorescence intensity. This value is called F_M.
   5. Calculate the maximum quantum yield of PSII in the dark (F_V/F_M), using the following equation.
      F_V/F_M = (F_M – F₀) / F_M
3. Measurement of photosynthetic behaviors at steady state.
   1. Turn on the halogen lamp as the external light source with the measuring light on after recording F_M (see 4.2.4). First, irradiate the leaf sample with the weakest light (30 μmol photons m^–2 s^–1).
   2. Turn on the spectral radiometer at the same time to monitor the leaf reflectance.
   3. Wait for 20 min or longer for the photosynthetic reaction to reach steady state under the light conditions. The fluorescence intensity of the steady state is called Fs.
   4. Supply a saturating pulse at intervals of 1 min during illumination with the actinic light. The maximum fluorescence value achieved under the pulsed light is called F_M′.
   5. Record the data of F_M′ at 20 min after turning on the actinic light.
   6. Take leaf reflectance data by averaging 10 scans at an optimized integration time, with a dark current subtraction.
4. Calculation of photosynthetic parameters at steady state.
   1. Calculate the quantum yields of PSII photochemistry (Φ_PSII), which can be estimated by irradiating with saturated pulses under actinic light, using the following equation.
      Φ_PSII = (F_M′- F_S) / F_M′
   2. Estimate the linear electron flux (LEF) from the PSII reaction center as follows ⁴.
      LEF = The irradiance intensity of the actinic light × Φ_PSII × 0.5 × 0.84
   3. Calculate the NPQ, which can be expressed the thermal dissipation, using the following equation.
      NPQ = (F_M - F_M′) / F_M′
      NOTE: Light energy is primarily consumed by photosynthesis reactions. However, when plants absorb more light energy than energy consumed by photosynthesis, the mechanisms for the thermal dissipation are induced to avoid the excess energy.
   4. Using the spectral data acquired with the radiometer under the same light conditions, calculate the leaf reflectance ratio as follows.
      Reflectance ratio = R_leaf / R_standard
   5. Calculate PRI from 531 nm and 570 nm as follows. These two wavelengths are extracted from the reflectance ratio.
      PRI = (R₅₃₁–R₅₇₀) / (R₅₃₁+R₅₇₀)
      NOTE: R is a reflectance.
5. Measuring of the relaxation kinetics of non-photochemical quenching.
   1. Turn off the actinic light after acquiring Fs and leaf reflectance.
   2. Monitor chlorophyll fluorescence by PAM for 10 min after turning off light.
   3. Provide a saturating pulse at intervals of 1 min during the dark relaxation. The maximum fluorescence value induced by the saturation pulse under the dark is called F_M′′. Obtain ten of F_M′′ in one test.
   4. Save the data of F_M′′ at 2 min and 10 min after turning off the actinic light.
   5. Turn the actinic light on set to the next irradiance intensity, 60 μ mol photons m^–2 s^–1.
   6. Repeat a light adaptation for 20 min and a dark relaxation for 10 min with pulsing saturation light at intervals of 1 min. Record all data as described above. Repeat all steps and measurements using irradiation at 120, 240, and 480 μ mol photons m^–2 s^–1.
6. Calculation of parameters of the non-photochemical quenching from the relaxation kinetics.
   NOTE: Light-dependent induction of NPQ is relaxed by turning off the light source¹³. It is possible to fractionate each NPQ function by adjusting the relaxation timescales.
   1. Estimate the qE (energy-dependent quenching) fraction using F_M′′ after 2-min dark adaptation.
      qE = (F_M2m′′–F_M′) / F_M′
      NOTE: The qE fraction is rapidly reversed within 1–2 min. This fraction includes mainly PsbS protonation and part of xanthophyll conversion, which depend on light-induced ΔpH across the thylakoid membrane¹³. Both are reversible on breakdown of the gradient.
   2. Calculate the qZ (zeaxanthin dependent quenching) fraction using F_M′′ after 10-min dark adaptation.
      qZ = (F_M10m′′–F_M′) / F_M′
      NOTE: A relaxation kinetics of NPQ at approximately 10 min after actinic light off reflects a xanthophyll cycle¹⁴. Most of the xanthophyll conversion is reversed at longer timescales of approximately 10 min (qZ) because the conversion requires a VDE (violaxanthin de-epoxidase) enzymatic reaction. The fraction is also relaxed by breakdown of the ΔpH across the thylakoid membrane.
   3. Calculate the qI (photoinhibitory state) as follows.
      qI = (F_M–F_M10m′′) / F_M′
      NOTE: The slowest recovery among NPQ fractions is thought to be photodamage of PSII (indicating D1 turnover). This fraction of the photoinhibitory state (qI), which does not recover by 10 min¹⁵.

Results

Figure 1 presents a schematic diagram of the experimental set up for simultaneously measuring chlorophyll fluorescence and leaf reflectance. The fiber probes of the PAM and spectral radiometer were set perpendicularly to the leaf surface at the leaf holder on the custom-made sample stage, and a halogen lamp was used for actinic light irradiation from both left and right directions without casting any shadows. The PAM and leaf reflectance signals were detected...

Discussion

In this study, we obtained additional evidence to show that PRI represents xanthophyll pigments by simultaneously measuring chlorophyll fluorescence and leaf reflectance.

A halogen light, which has wavelengths similar to sunlight, was adapted for use as an actinic light source to activate photosynthesis. We initially used a white LED light source to avoid thermal damage of the leaf surface, but this produced slow dark relaxation kinetics and exceptionally high qI (photoinhibitory quenching), p...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Halogen light source	OptoSigma	SHLA-150
Light quantum meter	LI-COR	LI-1000
PAM chlorophyll fluorometer	Walz	JUNIOR-PAM
PAM controliing software	Walz	WinControl-3.27
Reflectance standard	Labsphere, Inc.	SRT-99-050
Spectral radiometer	ADS Inc.	Field Spec3
Spectral radiometer controlling software	ADS Inc.	RS3