Chloroplast avoidance movement reduces photodamage in plants

THE WATER-WATER CYCLE IN CHLOROPLASTS: Scavenging of Active Oxygens and Dissipation of Excess Photons

Asada, K. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.601 · Cited by 4,038

Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins

Bj�rkman, O., & Demmig, B. (1987) · Planta · doi:10.1007/bf00402983 · Cited by 2,514

Photoprotection and Other Responses of Plants to High Light Stress

Demmig‐Adams, B., & Adams, W. W. (1992) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.pp.43.060192.003123 · Cited by 2,484

PHOTOPROTECTION REVISITED:Genetic and Molecular Approaches

Niyogi, K. (1999) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.50.1.333 · Cited by 1,937

Photoinhibition of Photosynthesis Induced by Visible Light

Powles, S. B. (1984) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.pp.35.060184.000311 · Cited by 1,876

Too much of a good thing: light can be bad for photosynthesis

Barber, J. P., & Andersson, B. (1992) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(92)90503-2 · Cited by 1,022

phot1 and phot2 mediate blue light regulation of stomatal opening

Kinoshita, T., Doi, M., Suetsugu, N., Kagawa, T., Wada, M., & Shimazaki, K.-I. (2001) · Nature · doi:10.1038/414656a · Cited by 899 · cited 1×

Arabidopsis nph1 and npl1: Blue light receptors that mediate both phototropism and chloroplast relocation

Sakai, T., Kagawa, T., Kasahara, M., Swartz, T. E., Christie, J. M., Briggs, W. R., Wada, M., & Okada, K. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.101137598 · Cited by 715

Light intensity regulation of cab gene transcription is signaled by the redox state of the plastoquinone pool.

Escoubas, J.-M., Lomas, M. W., LaRoche, J., & Falkowski, P. G. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.22.10237 · Cited by 662

Arabidopsis NPL1: A Phototropin Homolog Controlling the Chloroplast High-Light Avoidance Response

Kagawa, T., Sakai, T., Suetsugu, N., Oikawa, K., Ishiguro, S., Kato, T., Tabata, S., Okada, K., & Wada, M. (2001) · Science · doi:10.1126/science.291.5511.2138 · Cited by 651

Algae-mediated bioremediation of ciprofloxacin through a symbiotic microalgae-bacteria consortium

Wang, Y., Ning, W., Han, M., Gao, C., Guo, W., Chang, J., & Ho, S. (2023) · Algal Research · doi:10.1016/j.algal.2023.103062 · Cited by 41

Biomolecular motors

Hess, H., & Bachand, G. D. (2005) · Materials Today · doi:10.1016/s1369-7021(05)71286-4 · Cited by 41

Phosphoinositides Play Differential Roles in Regulating Phototropin1- and Phototropin2-Mediated Chloroplast Movements in Arabidopsis

Aggarwal, C., Łabuz, J., & Gabryś, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055393 · Cited by 40

CO2 Diffusion Inside Photosynthetic Organs

Flexas, J., Cano, F. J., Carriquí, M., Coopman, R. E., Mizokami, Y., Tholen, D., & Xiong, D. (2018) · Advances in photosynthesis and respiration · doi:10.1007/978-3-319-93594-2_7 · Cited by 40

Chloroplasts in plant cells show active glassy behavior under low-light conditions

Schramma, N., Israëls, C. P., & Jalaal, M. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2216497120 · Cited by 39

Influence of Synthetic and Natural Microfibers on the Growth, Substance Exchange, Energy Accumulation, and Oxidative Stress of Field-Collected Microalgae Compared with Microplastic Fragment

Cheng, S., Jessica, Yoshikawa, K., & Cross, J. S. (2024) · Science of The Total Environment · doi:10.1016/j.scitotenv.2023.167936 · Cited by 36

The impact of temperature on blue light induced chloroplast movements in Arabidopsis thaliana

Łabuz, J., Hermanowicz, P., & Gabryś, H. (2015) · Plant Science · doi:10.1016/j.plantsci.2015.07.013 · Cited by 40

Isoprenoid emissions, photosynthesis and mesophyll diffusion conductance in response to blue light

Pallozzi, E., Tsonev, T. D., Marino, G., Copolovici, L. O., Niinemets, Ü., Loreto, F., & Centritto, M. (2013) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2013.06.001 · Cited by 39

Toxicity of bisphenol A and its structural congeners to microalgae Chlorella vulgaris and Desmodesmus armatus

Czarny-Krzymińska, K., Krawczyk, B., & Szczukocki, D. (2022) · Journal of Applied Phycology · doi:10.1007/s10811-022-02704-3 · Cited by 38

The Evolution of Photosynthetic Anatomy inViburnum(Adoxaceae)

Chatelet, D. S., Clement, W. L., Sack, L., Donoghue, M. J., & Edwards, E. J. (2013) · International Journal of Plant Sciences · doi:10.1086/673241 · Cited by 38

Red Light, Phot1 and JAC1 Modulate Phot2-Dependent Reorganization of Chloroplast Actin Filaments and Chloroplast Avoidance Movement

Ichikawa, S., Yamada, N., Suetsugu, N., Wada, M., & Kadota, A. (2011) · Plant and Cell Physiology · doi:10.1093/pcp/pcr087 · Cited by 38

Toxicity and biotransformation of bisphenol S in freshwater green alga Chlorella vulgaris

Ding, T., Li, W., Yang, M., Yang, B., & Li, J. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.141144 · Cited by 38

The phototropin family as photoreceptors for blue light-induced chloroplast relocation

Kagawa, T. (2002) · Journal of Plant Research · doi:10.1007/s10265-002-0072-4 · Cited by 38

Non‐invasive, whole‐plant imaging of chloroplast movement and chlorophyll fluorescence reveals photosynthetic phenotypes independent of chloroplast photorelocation defects in chloroplast division mutants

Dutta, S., Cruz, J. A., Jiao, Y., Chen, J., Kramer, D., & Osteryoung, K. W. (2015) · The Plant Journal · doi:10.1111/tpj.13009 · Cited by 38

Distinct leaf developmental and gene expression responses to light quantity depend on blue-photoreceptor or plastid-derived signals, and can occur in the absence of phototropins

López‐Juez, E., Bowyer, J. R., & Sakai, T. (2007) · Planta · doi:10.1007/s00425-007-0599-7 · Cited by 37

Light environment within a leaf. II. Progress in the past one-third century

Terashima, I., Ooeda, H., Fujita, T., & Oguchi, R. (2016) · Journal of Plant Research · doi:10.1007/s10265-016-0808-1 · Cited by 37

Bundling actin filaments from membranes: some novel players

Thomas, C. (2012) · Frontiers in Plant Science · doi:10.3389/fpls.2012.00188 · Cited by 41

The leaf anatomy of a broad‐leaved evergreen allows an increase in leaf nitrogen content in winter

Muller, O., Oguchi, R., Hirose, T., Werger, M. J. A., & Hikosaka, K. (2009) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2009.01224.x · Cited by 37

The chloroplast division mutant caa33 of Arabidopsis thaliana reveals the crucial impact of chloroplast homeostasis on stress acclimation and retrograde plastid‐to‐nucleus signaling

Šimková, K., Kim, C., Gacek, K., Baruah, A., Laloi, C., & Apel, K. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04825.x · Cited by 37

Acclimatization of Photosynthetic Apparatus of Tor Grass (Brachypodium pinnatum) during Expansion

Bąba, W., Kalaji, H. M., Kompała‐Bąba, A., & Goltsev, V. N. (2016) · PLoS ONE · doi:10.1371/journal.pone.0156201 · Cited by 37

Blue Light-Induced Phototropism of Inflorescence Stems and Petioles is Mediated by Phototropin Family Members phot1 and phot2

Kagawa, T., Kimura, M., & Wada, M. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp119 · Cited by 37

The kinesin‐like proteins, KAC1/2, regulate actin dynamics underlying chloroplast light‐avoidance in Physcomitrella patens

Shen, Z., Liu, Y., Bibeau, J. P., Lemoi, K. P., Tüzel, E., & Vidali, L. (2015) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12303 · Cited by 36

Methylparaben toxicity and its removal by microalgae Chlorella vulgaris and Phaeodactylum tricornutum

Chang, X., He, Y., Song, L., Ding, J., Ren, S., Lv, M., & Chen, L. (2023) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2023.131528 · Cited by 36

Chloroplasts do not have a polarity for light-induced accumulation movement

Tsuboi, H., Yamashita, H., & Wada, M. (2008) · Journal of Plant Research · doi:10.1007/s10265-008-0199-z · Cited by 32

Impaired chloroplast positioning affects photosynthetic capacity and regulation of the central carbohydrate metabolism during cold acclimation

Kitashova, A., Schneider, K., Fürtauer, L., Schröder, L., Scheibenbogen, T., Fürtauer, S., & Nägele, T. (2020) · Photosynthesis Research · doi:10.1007/s11120-020-00795-y · Cited by 35

Context, Quantification, and Measurement Guide for Non-Photochemical Quenching of Chlorophyll Fluorescence

Logan, B. A., Demmig‐Adams, B., Adams, W. W., & Bilger, W. (2014) · Advances in photosynthesis and respiration · doi:10.1007/978-94-017-9032-1_7 · Cited by 36

Chloroplast anchoring: its implications for the regulation of intracellular chloroplast distribution

Takagi, S., Takamatsu, H., & Sakurai-Ozato, N. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp193 · Cited by 37

Regulatory Role of Components of Ascorbate–Glutathione Pathway in Plant Stress Tolerance

Latowski, D., Surówka, E., & Strzałka, K. (2010) · Springer eBooks · doi:10.1007/978-90-481-9404-9_1 · Cited by 36

Chloroplast Photorelocation Movement: A Sophisticated Strategy for Chloroplasts to Perform Efficient Photosynthesis

Suetsugu, N., & Wada, M. (2012) · InTech eBooks · doi:10.5772/26838 · Cited by 36

Acclimation of shade-tolerant and light-resistant Tradescantia species to growth light: chlorophyll a fluorescence, electron transport, and xanthophyll content

Mishanin, V. I., Trubitsin, B. V., Patsaeva, S. V., Ptushenko, V. V., Solovchenko, A. E., & Tikhonov, A. N. (2017) · Photosynthesis Research · doi:10.1007/s11120-017-0339-1 · Cited by 35

Effect of Supplementary Lighting Duration on Growth and Activity of Antioxidant Enzymes in Grafted Watermelon Seedlings

Wei, H., Wang, M., & Jeong, B. R. (2020) · Agronomy · doi:10.3390/agronomy10030337 · Cited by 35

Simultaneously measuring pulse-amplitude-modulated (PAM) chlorophyll fluorescence of leaves at wavelengths shorter and longer than 700 nm

Pfündel, E. E. (2021) · Photosynthesis Research · doi:10.1007/s11120-021-00821-7 · Cited by 35

Comparative analysis of light-stimulated motility responses in three diatom species

Cohn, S. A., Halpin, D., Hawley, N., Ismail, A., Kaplan, Z., Kordes, T., Kuhn, J., Macke, W. J., Marhaver, K., Ness, B., et al. (2015) · Diatom Research · doi:10.1080/0269249x.2015.1058295 · Cited by 38

Two patterns of leaf photosynthetic response to irradiance transition from saturating to limiting one in some plant species

Chen, Y., & Xu, D. (2005) · New Phytologist · doi:10.1111/j.1469-8137.2005.01624.x · Cited by 35

Speed of signal transfer in the chloroplast accumulation response

Tsuboi, H., & Wada, M. (2009) · Journal of Plant Research · doi:10.1007/s10265-009-0284-y · Cited by 33

Rethinking the Influence of Chloroplast Movements on Non-photochemical Quenching and Photoprotection

Wilson, S., & Ruban, A. V. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.20.00549 · Cited by 34

Diurnal movements of chloroplasts in Halophila stipulacea and their effect on PAM fluorometric measurements of photosynthetic rates

Sharon, Y., & Beer, S. (2007) · Aquatic Botany · doi:10.1016/j.aquabot.2007.11.006 · Cited by 34

Primary Processes During the Light‐signal Transduction of Phototropin

Matsuoka, D., Iwata, T., Zikihara, K., Kandori, H., & Tokutomi, S. (2006) · Photochemistry and Photobiology · doi:10.1562/2006-03-29-ra-861 · Cited by 34

Phototropin2 Contributes to the Chloroplast Avoidance Response at the Chloroplast-Plasma Membrane Interface

Ishishita, K., Higa, T., Tanaka, H., Inoue, S.-I., Chung, A., Ushijima, T., Matsushita, T., Kinoshita, T., Nakai, M., Wada, M., et al. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.20.00059 · Cited by 34

Strigolactones Stimulate High Light Stress Adaptation by Modulating Photosynthesis Rate in Arabidopsis

Thula, S., Moturu, T. R., Salava, H., Balakhonova, V., Berka, M., Kerchev, P., Mishra, K. B., Nodzyński, T., & Simon, S. (2022) · Journal of Plant Growth Regulation · doi:10.1007/s00344-022-10764-5 · Cited by 33

Multigenerational effects of microplastic fragments derived from polyethylene terephthalate bottles on duckweed Lemna minor: Size-dependent effects of microplastics on photosynthesis

Cui, R., Kwak, J. I., & An, Y. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.162159 · Cited by 34

Light signaling in photosynthetic eukaryotes with ‘green’ and ‘red’ chloroplasts

Lepetit, B., & Dietzel, L. (2014) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2014.07.007 · Cited by 34

Photo-Protection in the Centric Diatom Coscinodiscus granii is Not Controlled by Chloroplast High-Light Avoidance Movement

Goessling, J. W., Cartaxana, P., & Kühl, M. (2016) · Frontiers in Marine Science · doi:10.3389/fmars.2015.00115 · Cited by 31

Enhancement of non-photochemical quenching as an adaptive strategy under phosphorus deprivation in the dinoflagellate Karlodinium veneficum.

Cui, Y., Zhang, H., & Lin, S. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00404 · Cited by 32

Costs and benefits of photosynthetic light acclimation by tree seedlings in response to gap formation

Oguchi, R., Hikosaka, K., Hiura, T., & Hirose, T. (2008) · Oecologia · doi:10.1007/s00442-007-0951-4 · Cited by 32

Light acclimation of shade-tolerant and light-resistant Tradescantia species: induction of chlorophyll a fluorescence and P700 photooxidation, expression of PsbS and Lhcb1 proteins

Mishanin, V. I., Trubitsin, B. V., Benkov, M. A., Minin, A. A., & Tikhonov, A. N. (2016) · Photosynthesis Research · doi:10.1007/s11120-016-0252-z · Cited by 32

CHUP1 mediates actin-based light-induced chloroplast avoidance movement in the moss Physcomitrella patens

Usami, H., Maeda, T., Fujii, Y., Oikawa, K., Takahashi, F., Kagawa, T., Wada, M., & Kasahara, M. (2012) · Planta · doi:10.1007/s00425-012-1735-6 · Cited by 31

Effect of the Enhanced Production of Chlorophyll b on the Light Acclimation of Tomato

Khan, I. A., Zada, A., Jia, T., & Hu, X. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043377 · Cited by 31

Transitions of gene expression induced by short‐term blue light

Lehmann, P., Nöthen, J., von Braun, S. S., Bohnsack, M. T., Mirus, O., & Schleiff, E. (2010) · Plant Biology · doi:10.1111/j.1438-8677.2010.00377.x · Cited by 31

Chlorophyll fluorescence in the leaves of Tradescantia species of different ecological groups: Induction events at different intensities of actinic light

Ptushenko, V. V., Ptushenko, E. A., Samoilova, O. P., & Tikhonov, A. N. (2013) · Biosystems · doi:10.1016/j.biosystems.2013.08.001 · Cited by 31

Differential Positioning of C4 Mesophyll and Bundle Sheath Chloroplasts: Recovery of Chloroplast Positioning Requires the Actomyosin System

Kobayashi, H., Yamada, M., Taniguchi, M., Kawasaki, M., Sugiyama, T., & Miyake, H. (2008) · Plant and Cell Physiology · doi:10.1093/pcp/pcn177 · Cited by 31

Spatiotemporal Heterogeneity of Chlorophyll Content and Fluorescence Response Within Rice (Oryza sativa L.) Canopies Under Different Nitrogen Treatments

Zhang, J., Wan, L., Igathinathane, C., Zhang, Z., Guo, Y., Sun, D., & Cen, H. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.645977 · Cited by 31

Detecting short-term stress and recovery events in a vineyard using tower-based remote sensing of photochemical reflectance index (PRI)

Wong, C. Y. S., Bambach, N. E., Alsina, M. M., McElrone, A. J., Jones, T., Buckley, T. N., Kustas, W. P., & Magney, T. S. (2022) · Irrigation Science · doi:10.1007/s00271-022-00777-z · Cited by 31

Dynamic Behavior of Double-Membrane-Bounded Organelles in Plant Cells

Takagi, S., Islam, M. S., & Iwabuchi, K. (2011) · International review of cytology · doi:10.1016/b978-0-12-385859-7.00004-5 · Cited by 29

Blue-light-induced reorganization of the actin cytoskeleton and the avoidance response of chloroplasts in epidermal cells of Vallisneria gigantea

Sakurai, N., Domoto, K., & Takagi, S. (2004) · Planta · doi:10.1007/s00425-004-1416-1 · Cited by 31

Do plants and animals differ in phenotypic plasticity?

Borges, R. M. (2005) · Journal of Biosciences · doi:10.1007/bf02705149 · Cited by 31

Phototropin 1 and 2 Influence Photosynthesis, UV-C Induced Photooxidative Stress Responses, and Cell Death

Rusaczonek, A., Czarnocka, W., Willems, P., Sujkowska‐Rybkowska, M., Breusegem, F. V., & Karpiński, S. M. (2021) · Cells · doi:10.3390/cells10020200 · Cited by 32

Molecular insights into the phototropin control of chloroplast movements

Łabuz, J., Sztatelman, O., & Hermanowicz, P. (2022) · Journal of Experimental Botany · doi:10.1093/jxb/erac271 · Cited by 30

Progress in Coupling Plant Form and Photosynthetic Function

Smith, W. K., & Hughes, N. M. (2009) · Castanea · doi:10.2179/08-009r5.1 · Cited by 30

Chloroplast aggregation during the cold-positioning response in the liverwort Marchantia polymorpha

Tanaka, H., Sato, M., Ogasawara, Y., Hamashima, N., Buchner, O., Holzinger, A., Toyooka, K., & Kodama, Y. (2017) · Journal of Plant Research · doi:10.1007/s10265-017-0958-9 · Cited by 30

Fluorescent Protein Aided Insights on Plastids and their Extensions: A Critical Appraisal

Delfosse, K., Wozny, M. R., Jaipargas, E.-A., Barton, K. A., Anderson, C., & Mathur, J. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2015.01253 · Cited by 31

CHLOROPLAST UNUSUAL POSITIONING 1 is a plant-specific actin polymerization factor regulating chloroplast movement

Kong, S., Yamazaki, Y., Shimada, A., Kijima, S. T., Hirose, K., Katoh, K., Ahn, J., Song, H., Han, J., Higa, T., et al. (2023) · The Plant Cell · doi:10.1093/plcell/koad320 · Cited by 29

Identification of major QTLs and epistatic interactions for seed protein concentration in soybean under multiple environments based on a high-density map

Qi, Z., Pan, J.-B., Han, X., Qi, H., Xin, D., Li, W., Mao, X., Wang, Z., Jiang, H., Liu, C., et al. (2016) · Molecular Breeding · doi:10.1007/s11032-016-0475-x · Cited by 30

Using remotely sensed spectral reflectance to indicate leaf photosynthetic efficiency derived from active fluorescence measurements

Peng, Y., Zeng, A., Zhu, T., Fang, S., Gong, Y., Tao, Y., Zhou, Y., & Liu, K. (2017) · Journal of Applied Remote Sensing · doi:10.1117/1.jrs.11.026034 · Cited by 29

Electron transfer through the acceptor side of photosystem I: Interaction with exogenous acceptors and molecular oxygen

Cherepanov, D. A., Milanovsky, G. E., Petrova, A. A., Tikhonov, A. N., & Semenov, A. Y. (2017) · Biochemistry (Moscow) · doi:10.1134/s0006297917110037 · Cited by 29

Functional characterization of GhPHOT2 in chloroplast avoidance of Gossypium hirsutum

Shang, B., Zang, Y., Zhao, X., Zhu, J., Fan, C., Guo, X., & Zhang, X. (2018) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2018.11.027 · Cited by 30

Plant Nuclei Move to Escape Ultraviolet-Induced DNA Damage and Cell Death

Iwabuchi, K., Hidema, J., Tamura, K., Takagi, S., & Hara‐Nishimura, I. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.01400 · Cited by 29

Novel protein-protein interaction family proteins involved in chloroplast movement response

Kodama, Y., Suetsugu, N., & Wada, M. (2011) · Plant Signaling & Behavior · doi:10.4161/psb.6.4.14784 · Cited by 27

Light acclimation of shade-tolerant and sun-resistant Tradescantia species: photochemical activity of PSII and its sensitivity to heat treatment

Benkov, M. A., Yatsenko, A. M., & Tikhonov, A. N. (2018) · Photosynthesis Research · doi:10.1007/s11120-018-0535-7 · Cited by 28

Rapid Chlorophyll a Fluorescence Light Response Curves Mechanistically Inform Photosynthesis Modeling

Pleban, J. R., Guadagno, C. R., Mackay, D. S., Weinig, C., & Ewers, B. E. (2020) · PLANT PHYSIOLOGY · doi:10.1104/pp.19.00375 · Cited by 28

Involvement of oxidative stress in the sensitivity of two algal species exposed to roxithromycin

Han, Q., Zheng, Y., Qi, Q., Peng, J., Song, J., Guo, J., & Guo, J. (2020) · Ecotoxicology · doi:10.1007/s10646-020-02192-6 · Cited by 28

Transcriptomics unveiled metabolic perturbations in Desmodesmus quadricauda by sulfacetamide: Key functional genes involved in the tolerance and biodegradation process

Xiong, J.-Q., Qi, X., & Qin, J. (2022) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2022.154436 · Cited by 28

Investigations on the Photoregulation of Chloroplast Movement and Leaf Positioning in Arabidopsis

Han, I., Cho, H., Moni, A., Lee, A., & Briggs, W. R. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs098 · Cited by 28

Reorganized actin filaments anchor chloroplasts along the anticlinal walls of Vallisneria epidermal cells under high-intensity blue light

Sakai, Y., & Takagi, S. (2005) · Planta · doi:10.1007/s00425-005-1493-9 · Cited by 28

Photobiology of the symbiotic acoel flatwormSymsagittifera roscoffensis: algal symbiont photoacclimation and host photobehaviour

Serôdio, J., Silva, R., Ezequiel, J., & Calado, R. (2010) · Journal of the Marine Biological Association of the United Kingdom · doi:10.1017/s0025315410001001 · Cited by 27

Transcriptomic insights into the blue light-induced female floral sex expression in cucumber (Cucumis sativus L.)

Zhou, Y., Ahammed, G. J., Wang, Q., Wu, C., Wan, C. C., & Yang, Y. (2018) · Scientific Reports · doi:10.1038/s41598-018-32632-7 · Cited by 27

Light-harvesting regulation from leaf to molecule with the emphasis on rapid changes in antenna size

Xu, D.-Q., Chen, Y., & Chen, G. (2015) · Photosynthesis Research · doi:10.1007/s11120-015-0115-z · Cited by 26

Distinct Responses of Chloroplasts to Blue and Green Laser Microbeam Irradiations in the Centric Diatom Pleurosira laevis

Shihira‐Ishikawa, I., Nakamura, T., Higashi, S., & Watanabe, M. (2007) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2007.00167.x · Cited by 26

Analysis of light quality and assemblage composition on diatom motility and accumulation rate

Cohn, S. A., Dunbar, S., Ragland, R., Schulze, J., Suchar, A., Weiss, J., & Wolske, A. L. (2016) · Diatom Research · doi:10.1080/0269249x.2016.1193058 · Cited by 28

Steady‐state stomatal responses of C3 and C4 species to blue light fraction: Interactions with CO2 concentration

Zhen, S., & Bugbee, B. G. (2020) · Plant Cell & Environment · doi:10.1111/pce.13888 · Cited by 25

High-Light versus Low-Light: Effects on Paired Photosystem II Supercomplex Structural Rearrangement in Pea Plants

Grinzato, A., Albanese, P., Marotta, R., Swuec, P., Saracco, G., Bolognesi, M., Zanotti, G., & Pagliano, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228643 · Cited by 25

Acclimating Cucumber Plants to Blue Supplemental Light Promotes Growth in Full Sunlight

Kang, C., Zhang, Y., Cheng, R., Kaiser, E., Yang, Q., & Li, T. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.782465 · Cited by 25

Fluorescence ratio and photochemical reflectance index as a proxy for photosynthetic quantum efficiency of photosystem II along a phosphorus gradient

Wieneke, S., Balzarolo, M., Asard, H., AbdElgawad, H., Peñuelas, J., Rascher, U., Ven, A., Verlinden, M. S., Janssens, I. A., & Vicca, S. (2022) · Agricultural and Forest Meteorology · doi:10.1016/j.agrformet.2022.109019 · Cited by 25

Ferns, mosses and liverworts as model systems for light‐mediated chloroplast movements

Suetsugu, N., Higa, T., & Wada, M. (2016) · Plant Cell & Environment · doi:10.1111/pce.12867 · Cited by 22

UV-B Induces Chloroplast Movements in a Phototropin-Dependent Manner

Hermanowicz, P., Banaś, A. K., Sztatelman, O., Gabryś, H., & Łabuz, J. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01279 · Cited by 24

Chloroplast Photorelocation Movement

Suetsugu, N., & Wada, M. (2008) · Plant cell monographs · doi:10.1007/7089_2008_34 · Cited by 28

Pb-Induced Avoidance-Like Chloroplast Movements in Fronds of Lemna trisulca L.

Samardakiewicz, S., Krzeszowiec, W., Bednarski, W., Jankowski, A., Suski, S., Gabryś, H., & Woźny, A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0116757 · Cited by 26

Light regulation and differential tissue-specific expression of phototropin homologues from rice (Oryza sativa ssp. indica)

Jain, M., Sharma, P., Tyagi, S. B., Tyagi, A. K., & Khurana, J. P. (2006) · Plant Science · doi:10.1016/j.plantsci.2006.08.003 · Cited by 24

Blue light-induced orientation movements of chloroplasts in higher plants: Recent progress in the study of their mechanisms

Gabryś, H. (2004) · Acta Physiologiae Plantarum · doi:10.1007/s11738-004-0038-3 · Cited by 24

Modulation of Phototropin Signalosome with Artificial Illumination Holds Great Potential in the Development of Climate-Smart Crops

Sharma, S., Sanyal, S. K., Sushmita, K., Chauhan, M., Sharma, A. S., Anirudhan, G., Veetil, S. K., & Kateriya, S. (2021) · Current Genomics · doi:10.2174/1389202922666210412104817 · Cited by 22

The Effect of Diffuse Film Covers on Microclimate and Growth and Production of Tomato (Solanum lycopersicum L.) in a Mediterranean Greenhouse

Moreno-Teruel, M. A., Molina-Aiz, F. D., Peña-Fernández, A., López, A., & Martínez, D. L. V. (2021) · Agronomy · doi:10.3390/agronomy11050860 · Cited by 23

The functional domains of the chloroplast unusual positioning protein 1

Lehmann, P., Bohnsack, M. T., & Schleiff, E. (2011) · Plant Science · doi:10.1016/j.plantsci.2011.01.006 · Cited by 23

Investigate the Effect of Nd-Yag Laser Beam on Soybean (Glycin max) Leaves at the Protein Level

Khalifa, N. S., & Ghandoor, H. E. (2011) · International Journal of Biology · doi:10.5539/ijb.v3n2p135 · Cited by 23

Diverse Responses to Blue Light via LOV Photoreceptors

Shimazaki, K.-I., & Tokutomi, S. (2013) · Plant and Cell Physiology · doi:10.1093/pcp/pcs172 · Cited by 23

Salt crystal deposition as a reversible mechanism to enhance photoprotection in black mangrove

Esteban, R., Fernández‐Marín, B., Hernández, A., Jiménez, E. T., León, A., García‐Mauriño, S., Silva, C. D., Dolmus, J. R., Dolmus, C., Molina, M. J., et al. (2012) · Trees · doi:10.1007/s00468-012-0790-8 · Cited by 23

Linking chloroplast relocation to different responses of photosynthesis to blue and red radiation in low and high light-acclimated leaves of Arabidopsis thaliana (L.)

Pfündel, E. E., Latouche, G., Meister, A., & Cerović, Z. G. (2018) · Photosynthesis Research · doi:10.1007/s11120-018-0482-3 · Cited by 23

Rice phot1a mutation reduces plant growth by affecting photosynthetic responses to light during early seedling growth

Goh, C., Jang, S., Jung, S., Kim, H.-S., Kang, H., Park, Y., Bae, H., Lee, C.-H., & An, G. (2008) · Plant Molecular Biology · doi:10.1007/s11103-008-9442-1 · Cited by 24

Pennate diatoms make non-photochemical quenching as simple as possible but not simpler

Croteau, D., Jaubert, M. J., Falciatore, A., & Bailleul, B. (2025) · Nature Communications · doi:10.1038/s41467-025-57298-4 · Cited by 22

Transcriptome Analysis Reveals Roles of Anthocyanin- and Jasmonic Acid-Biosynthetic Pathways in Rapeseed in Response to High Light Stress

Luo, Y., Teng, S., Yin, H., Zhang, S., Tuo, X., & Tran, L. P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222313027 · Cited by 22

Leaf microscopy applications in photosynthesis research: identifying the gaps

Khoshravesh, R., Hoffmann, N., & Hanson, D. T. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab548 · Cited by 22

Velocity of chloroplast avoidance movement is fluence rate dependent

Kagawa, T., & Wada, M. (2004) · Photochemical & Photobiological Sciences · doi:10.1039/b316285k · Cited by 65

Green light attenuates blue‐light‐induced chloroplast avoidance movement in Arabidopsis and Landoltia punctata

Schmalstig, J. G., & Jainandan, K. (2021) · American Journal of Botany · doi:10.1002/ajb2.1717 · Cited by 7

Chloroplast photoprotection: face the light or run and hide?

Kirschner, G. K. (2023) · The Plant Journal · doi:10.1111/tpj.16340 · Cited by 2

Photoprotective function of chloroplast avoidance movement: In vivo chlorophyll fluorescence study

Sztatelman, O., Waloszek, A., Katarzyna Banaś, A., & Gabryś, H. (2010) · Journal of Plant Physiology · doi:10.1016/j.jplph.2009.12.015 · Cited by 59

Chloroplasts can move in any direction to avoid strong light

Tsuboi, H., & Wada, M. (2010) · Journal of Plant Research · doi:10.1007/s10265-010-0364-z · Cited by 52