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pH dependent chlorophyll fluorescence quenching in spinach thylakoids from light treated or dark adapted leaves
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00033160openalex-snapshot
The carotenoid zeaxanthin and ‘high-energy-state quenching’ of chlorophyll fluorescence
inferredcites →https://doi.org/10.1007/bf00033161openalex-snapshot
The effect of high-energy-state excitation quenching on maximum and dark level chlorophyll fluorescence yield
inferredcites →https://doi.org/10.1016/0003-9861(75)90122-8openalex-snapshot
Energy-dependent cation-induced control of chlorophyll a fluorescence in isolated intact chloroplasts
inferredcites →https://doi.org/10.1016/0005-2728(72)90242-3openalex-snapshot
The pH dependence of delayed and prompt fluorescence in uncoupled chloroplasts
inferredcites →https://doi.org/10.1016/0005-2728(79)90156-7openalex-snapshot
Fluorescence emission spectra of chloroplasts and subchloroplast preparations at low temperature
inferredcites →https://doi.org/10.1016/0005-2728(79)90160-9openalex-snapshot
Quenching of the System II chlorophyll fluorescence by the plastoquinone pool
inferredcites →https://doi.org/10.1016/0005-2728(79)90193-2openalex-snapshot
A quantitative study of the slow decline of chlorophyll a fluorescence in isolated chloroplasts
inferredcites →https://doi.org/10.1016/0005-2728(82)90262-6openalex-snapshot
Photoinduced quenching of chlorophyll fluorescence in intact chloroplasts and algae. Resolution into two components
inferredcites →https://doi.org/10.1016/0005-2728(83)90117-2openalex-snapshot
Characterization of chlorophyll fluorescence quenching in chloroplasts by fluorescence spectroscopy at 77 K II. ATP-dependent quenching
inferredcites →https://doi.org/10.1016/0005-2728(87)90190-3openalex-snapshot
Quantum efficiency of Photosystem II in relation to ‘energy’-dependent quenching of chlorophyll fluorescence
inferredcites →https://doi.org/10.1016/0005-2728(88)90128-4openalex-snapshot
A study of the regulation and function of energy-dependent quenching in pea chloroplasts
inferredcites →https://doi.org/10.1016/0005-2728(88)90144-2openalex-snapshot
Studies on the induction of chlorophyll fluorescence in isolated barley protoplasts. IV. Resolution of non-photochemical quenching
inferredcites →https://doi.org/10.1016/0005-2728(90)90088-lopenalex-snapshot
Carotenoids and photoprotection in plants: A role for the xanthophyll zeaxanthin
inferredcites →https://doi.org/10.1016/0014-5793(89)81688-6openalex-snapshot
Correlation between dissipative fluorescence quenching at photosystem II and 50 μs recombination luminescence
inferredcites →https://doi.org/10.1016/0014-5793(89)81723-5openalex-snapshot
Enhancement of the ΔpH‐dependent dissipation of excitation energy in spinach chloroplasts by light‐activation: correlation with the synthesis of zeaxanthin
inferredcites →https://doi.org/10.1016/0014-5793(91)80819-oopenalex-snapshot
Control of the light‐harvesting function of chloroplast membranes by aggregation of the LHCII chlorophyll—protein complex
inferredcites →https://doi.org/10.1016/0031-9422(91)83768-gopenalex-snapshot
Perspectives in Biochemical and Genetic Regulation of Photosynthesis:
inferredcites →https://doi.org/10.1016/s0005-2728(05)80143-4openalex-snapshot
The relationship between zeaxanthin, energy-dependent quenching of chlorophyll fluorescence, and trans-thylakoid pH gradient in isolated chloroplasts
inferredcites →https://doi.org/10.1016/s0005-2728(05)80221-xopenalex-snapshot
Long-wavelength chlorophyll species are associated with amplification of high-energy-state excitation quenching in higher plants
inferredcites →https://doi.org/10.1016/s0005-2728(05)80236-1openalex-snapshot
Dissipation of excitation energy by Photosystem II particles at low pH
inferredcites →https://doi.org/10.1016/s0304-4165(89)80016-9openalex-snapshot
The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence
inferredcites →https://doi.org/10.1093/jxb/41.2.123openalex-snapshot
Photodestruction of Pigments in Higher Plants by Herbicide Action
inferredcites →https://doi.org/10.1098/rspb.1984.0007openalex-snapshot
Studies on the induction of chlorophyll fluorescence in barley protoplasts. II. Resolution of fluorescence quenching by redox state and the transthylakoid pH gradient
inferredcites →https://doi.org/10.1104/pp.84.2.218openalex-snapshot
Photoinhibition and Zeaxanthin Formation in Intact Leaves
inferredcites →https://doi.org/10.1104/pp.87.1.17openalex-snapshot
Zeaxanthin and the Heat Dissipation of Excess Light Energy in Nerium oleander Exposed to a Combination of High Light and Water Stress
inferredcites →https://doi.org/10.1104/pp.90.3.887openalex-snapshot
Zeaxanthin and the Induction and Relaxation Kinetics of the Dissipation of Excess Excitation Energy in Leaves in 2% O2, 0% CO2
inferredcites →https://doi.org/10.1104/pp.91.2.542openalex-snapshot
Light-Induced Spectral Absorbance Changes in Relation to Photosynthesis and the Epoxidation State of Xanthophyll Cycle Components in Cotton Leaves
inferredcites →https://doi.org/10.1104/pp.92.2.293openalex-snapshot
Inhibition of Zeaxanthin Formation and of Rapid Changes in Radiationless Energy Dissipation by Dithiothreitol in Spinach Leaves and Chloroplasts
inferredcites →https://doi.org/10.1104/pp.92.2.302openalex-snapshot
Relative Contributions of Zeaxanthin-Related and Zeaxanthin-Unrelated Types of `High-Energy-State' Quenching of Chlorophyll Fluorescence in Spinach Leaves Exposed to Various Environmental Conditions
inferredcites →https://doi.org/10.1515/znc-1987-0514openalex-snapshot
Energy-Dependent Chlorophyll Fluorescence Quenching in Chloroplasts Correlated with Quantum Yield of Photosynthesis
inferredcites →https://doi.org/10.1515/znc-1987-11-1217openalex-snapshot
The Polyphasic Rise of Chlorophyll Fluorescence upon Onset of Strong Continuous Illumination: I. Saturation Characteristics and Partial Control by the Photosystem II Acceptor Side
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Mathematical Model to Simulate Dynamics of Photosynthetic Light Reactions in an Oscillating Light
inferred← citeshttps://doi.org/10.1002/bbpc.19961001214openalex-snapshot
The pH‐dependence of the photosystem II fluorescence: Cooperative transition to a quenching state
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Photosystem II Heterogeneity
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Carotenoids: Localization and Function
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Regulation of Light Utilization for Photosynthetic Electron Transport
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Leaf C3 Photosynthesis in silico: Integrated Carbon/Nitrogen Metabolism
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inferred← citeshttps://doi.org/10.1007/978-94-017-2087-8_15openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00016277openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00034778openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00042966openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf00714469openalex-snapshot
Activation of non-photochemical quenching in thylakoids and leaves
inferred← citeshttps://doi.org/10.1007/bf02183039openalex-snapshot
Thermoluminescence as a probe of Photosystem II in intact leaves: Non-photochemical fluorescence quenching in peas grown in an intermittent light regime
inferred← citeshttps://doi.org/10.1007/bf02187121openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/bf02187470openalex-snapshot
The role of calcium in the pH-dependent control of Photosystem II
inferred← citeshttps://doi.org/10.1007/s004250050629openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10265-025-01627-7openalex-snapshot
Abscisic acid enhances non-photochemical quenching through SnRK2 and ABI3 in Physcomitrium patens
inferred← citeshttps://doi.org/10.1007/s11120-006-9109-1openalex-snapshot
C3 photosynthesis in silico
inferred← citeshttps://doi.org/10.1007/s11120-013-9857-7openalex-snapshot
Models and measurements of energy-dependent quenching
inferred← citeshttps://doi.org/10.1007/s11120-015-0094-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11120-019-00663-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11120-020-00767-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11120-022-00934-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0005-2728(92)90061-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0005-2728(92)90062-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0005-2728(93)90036-fopenalex-snapshot
LHCII, the major light-harvesting pigment-protein complex is a zeaxanthin epoxidase
inferred← citeshttps://doi.org/10.1016/0005-2728(93)90103-mopenalex-snapshot
ΔpH-dependent quenching of the Fo level of chlorophyll fluorescence in spinach leaves
inferred← citeshttps://doi.org/10.1016/0005-2728(94)90143-0openalex-snapshot
Modulation of chlorophyll fluorescence quenching in isolated light harvesting complex of Photosystem II
inferred← citeshttps://doi.org/10.1016/0005-2728(94)90202-xopenalex-snapshot
Prompt heat release associated with ΔpH-dependent quenching in spinach thylakoid membranes
inferred← citeshttps://doi.org/10.1016/0014-5793(92)81089-5openalex-snapshot
The molecular mechanism of the control of excitation energy dissipation in chloroplast membranes Inhibition of ΔpH‐dependent quenching of chlorophyll fluorescence by dicyclohexylcarbodiimide
inferred← citeshttps://doi.org/10.1016/0168-9452(96)04395-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/1011-1344(93)87087-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/1011-1344(94)07067-xopenalex-snapshot
Role of ΔpH in the mechanism of zeaxanthin-dependent amplification of qE
inferred← citeshttps://doi.org/10.1016/1011-1344(94)85032-1openalex-snapshot
New trends in photobiology
inferred← citeshttps://doi.org/10.1016/j.bbabio.2011.04.007openalex-snapshot
The photoprotective molecular switch in the photosystem II antenna
inferred← citeshttps://doi.org/10.1016/j.bbabio.2012.01.007openalex-snapshot
Polyamines induce aggregation of LHC II and quenching of fluorescence in vitro
inferred← citeshttps://doi.org/10.1016/j.bbabio.2013.11.018openalex-snapshot
pH sensitivity of chlorophyll fluorescence quenching is determined by the detergent/protein ratio and the state of LHCII aggregation
inferred← citeshttps://doi.org/10.1016/j.bbabio.2014.02.014openalex-snapshot
Disentangling the low-energy states of the major light-harvesting complex of plants and their role in photoprotection
inferred← citeshttps://doi.org/10.1016/j.bbabio.2016.09.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbabio.2018.03.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbabio.2019.05.002openalex-snapshot
Single-molecule microscopy studies of LHCII enriched in Vio or Zea
inferred← citeshttps://doi.org/10.1016/j.biosystems.2013.08.001openalex-snapshot
Chlorophyll fluorescence in the leaves of Tradescantia species of different ecological groups: Induction events at different intensities of actinic light
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2015.07.015openalex-snapshot
Short-term regulation and alternative pathways of photosynthetic electron transport in Hibiscus rosa-sinensis leaves
inferred← citeshttps://doi.org/10.1016/j.jplph.2015.06.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1104/pp.106.4.1647openalex-snapshot
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inferred← citeshttps://doi.org/10.1104/pp.108.4.1479openalex-snapshot
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Non-Photochemical Quenching. A Response to Excess Light Energy
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Higher Plant Light‐Harvesting Complexes LHCIIa and LHCIIc are Bound by Dicyclohexylcarbodiimide During Inhibition of Energy Dissipation
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inferred← citeshttps://doi.org/10.1111/pce.13107openalex-snapshot
Dynamic interplay between photodamage and photoprotection in photosystem II
inferred← citeshttps://doi.org/10.1111/pce.13566openalex-snapshot
In vitro and in vivo investigation of chlorophyll binding sites involved in non‐photochemical quenching in Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1134/s0006350911030055openalex-snapshot
A model of photosystem II for the analysis of fast fluorescence rise in plant leaves
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inferred← citeshttps://doi.org/10.30546/2709-0752.6.1.2022.45openalex-snapshot
Existing understanding of the parameters controlling energy-dependent quenching of chlorophyll fluorescence in plants
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Special issue in honour of Prof. Reto J. Strasser - Probing the photosynthetic apparatus noninvasively in the laboratory of Reto Strasser in the countryside of Geneva between 2001 and 2009
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Light acclimation and pH perturbations affect photosynthetic performance in Chlorella mass culture
inferred← citeshttps://doi.org/10.3389/fpls.2016.00841openalex-snapshot
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Measurement of photosynthetic linear and cyclic electron flows, CO2 capture in green microalgae
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