Evidence map›Paper›PMID 30563922›Full record

ArticlePlant physiology2019

Analysis of OJIP Chlorophyll Fluorescence Kinetics and Q

Hendrik Küpper, Zuzana Benedikty, Filis Morina, Elisa Andresen, Archana Mishra, Martin Trtílek

Open access · bronzeAbstract read
In one paragraph

Article in Plant physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
10.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 112 citations in OpenAlex.

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  14. Photosynthetic Responses ofPlants (Basel, Switzerland) · 2024
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Hendrik KüpperBiology Center of the Czech Academy of Sciences, Institute of Plant Molecular Biology, Department of Plant Biophysics and Biochemistry, 370 05 České Budějovice, Czech Republic hendrik.kuepper@umbr.cas.cz.ORCID 0000-0003-0712-7023
Zuzana BenediktyPhoton Systems Instruments, 664 24 Drasov, Czech Republic.ORCID 0000-0002-0154-8225
Filis MorinaBiology Center of the Czech Academy of Sciences, Institute of Plant Molecular Biology, Department of Plant Biophysics and Biochemistry, 370 05 České Budějovice, Czech Republic.ORCID 0000-0003-1521-125X
Elisa AndresenBiology Center of the Czech Academy of Sciences, Institute of Plant Molecular Biology, Department of Plant Biophysics and Biochemistry, 370 05 České Budějovice, Czech Republic.ORCID 0000-0002-7201-2508
Archana MishraBiology Center of the Czech Academy of Sciences, Institute of Plant Molecular Biology, Department of Plant Biophysics and Biochemistry, 370 05 České Budějovice, Czech Republic.
Martin TrtílekPhoton Systems Instruments, 664 24 Drasov, Czech Republic.
Czech Academy of Sciences · CZPhoton Systems Instruments (Czechia) · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chlorophyll fluorescence kinetic analysis has become an important tool in basic and applied research on plant physiology and agronomy. While early systems recorded the integrated kinetics of a selected spot or plant, later systems enabled imaging of at least the slower parts of the kinetics (20-ms time resolution). For faster events, such as the rise from the basic dark-adapted fluorescence yield to the maximum (OJIP transient), or the fluorescence yield decrease during reoxidation of plastoquinone A after a saturating flash, integrative systems are used because of limiting speed of the available imaging systems. In our new macroscopic and microscopic systems, the OJIP or plastonique A reoxidation fluorescence transients are directly imaged using an ultrafast camera. The advantage of such systems compared to nonimaging measurements is the analysis of heterogeneity of measured parameters, for example between the photosynthetic tissue near the veins and the tissue further away from the veins. Further, in contrast to the pump-and-probe measurement, direct imaging allows for measuring the transition of the plant from the dark-acclimated to a light-acclimated state via a quenching analysis protocol in which every supersaturating flash is coupled to a measurement of the fast fluorescence rise. We show that pump-and-probe measurement of OJIP is prone to artifacts, which are eliminated with the direct measurement. The examples of applications shown here, zinc deficiency and cadmium toxicity, demonstrate that this novel imaging platform can be used for detection and analysis of a range of alterations of the electron flow around PSII.

Indexed as

ArabidopsisBrassicaceaeChlorophyllEquipment DesignFluorescenceGlycine maxKineticsMesophyll CellsMicroscopy, FluorescencePhotosynthesisPlant LeavesPlastoquinoneZincChlorophyllPlastoquinoneZinc

Identifiers

PMID30563922
PMCPMC6376856
OpenAlexW2905075678

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.