K. Apel and H. Hirt, REACTIVE OXYGEN SPECIES: Metabolism, Oxidative Stress, and Signal Transduction, Annual Review of Plant Biology, vol.55, issue.1, pp.373-399, 2004.
DOI : 10.1146/annurev.arplant.55.031903.141701

A. Baxter, R. Mittler, and N. Suzuki, ROS as key players in plant stress signalling, Journal of Experimental Botany, vol.149, issue.3, pp.1229-1240, 2014.
DOI : 10.1104/pp.108.133884
URL : https://academic.oup.com/jxb/article-pdf/65/5/1229/9403252/ert375.pdf

@. Bienert, G. P. Schjoerring, J. K. Jahn, and T. P. , Membrane transport of hydrogen peroxide, Biochimica et Biophysica Acta (BBA) - Biomembranes, vol.1758, issue.8, pp.994-1003, 2006.
DOI : 10.1016/j.bbamem.2006.02.015

@. Birtic, S. Ksas, B. Genty, B. Mueller, M. J. Triantaphylides et al., Using spontaneous photon emission to image lipid oxidation patterns in plant tissues, The Plant Journal, vol.85, issue.6, pp.1103-1115, 2011.
DOI : 10.1111/j.1751-1097.2009.00537.x

@. Bisby, R. H. Morgan, C. G. Hamblett, I. Gorman, and A. A. , Quenching of Singlet Oxygen by Trolox C, Ascorbate, and Amino Acids:?? Effects of pH and Temperature, The Journal of Physical Chemistry A, vol.103, issue.37, pp.7454-7459, 1999.
DOI : 10.1021/jp990838c

@. Carol, R. J. Dolan, and L. , The role of reactive oxygen species in cell growth: lessons from root hairs, Journal of Experimental Botany, vol.57, issue.8, pp.1829-1834, 2006.
DOI : 10.1093/jxb/erj201

@. Dall-'osto, L. Cazzaniga, S. Havaux, M. Bassi, and R. , Enhanced Photoprotection by Protein-Bound vs Free Xanthophyll Pools: A Comparative Analysis of Chlorophyll b and Xanthophyll Biosynthesis Mutants, Molecular Plant, vol.3, issue.3, pp.576-593, 2010.
DOI : 10.1093/mp/ssp117

@. Demidchik, V. Shabala, S. N. Coutts, K. B. Tester, M. A. Davies et al., Free oxygen radicals regulate plasma membrane Ca2+- and K+-permeable channels in plant root cells, Journal of Cell Science, vol.116, issue.1, pp.81-88, 2003.
DOI : 10.1242/jcs.00201
URL : http://jcs.biologists.org/content/joces/116/1/81.full.pdf

@. Espineda, C. E. Linford, A. S. Devine, D. Brusslan, and J. A. , The AtCAO gene, encoding chlorophyll a oxygenase, is required for chlorophyll b synthesis in Arabidopsis thaliana, Proceedings National Academy of Sciences USA 96, pp.10507-10511, 1999.
DOI : 10.1038/22101

@. Farmer, E. E. Davoine, and C. , Reactive electrophile species, Current Opinion in Plant Biology, vol.10, issue.4, pp.380-386, 2007.
DOI : 10.1016/j.pbi.2007.04.019

@. Fischer, B. B. Ledford, H. K. Wakao, S. Huang, S. G. Casero et al., SINGLET OXYGEN RESISTANT 1 links reactive electrophile signaling to singlet oxygen acclimation in Chlamydomonas reinhardtii, Proceedings National Academy Sciences USA 109, 2012.
DOI : 10.1089/ars.2010.3222
URL : http://www.pnas.org/content/109/20/E1302.full.pdf

@. Foreman, J. Demidchik, V. Bothwell, J. H. Mylona, P. Miedema et al., Reactive oxygen species produced by NADPH oxidase regulate plant cell growth, Nature, vol.15, issue.6930, pp.442-446, 2003.
DOI : 10.1046/j.1365-313X.1998.00188.x

@. Gechev, T. S. Minkov, I. N. Hille, and J. , Hydrogen Peroxide-induced Cell Death in Arabidopsis: Transcriptional and Mutant Analysis Reveals a Role of an Oxoglutarate-dependent Dioxygenase Gene in the Cell Death Process, IUBMB Life (International Union of Biochemistry and Molecular Biology: Life), vol.57, issue.3, pp.181-188, 2005.
DOI : 10.1080/15216540500090793

@. Gechev, T. S. Van-breusegem, F. Stone, J. M. Denev, I. Laloi et al., Reactive oxygen species as signals that modulate plant stress responses and programmed cell death, BioEssays, vol.11, issue.11, pp.1091-1101, 2006.
DOI : 10.1002/bies.20493

@. Gonzalez-perez, S. Gutierrez, J. Garcia-garcia, F. Osuna, D. Dopazo et al., Early Transcriptional Defense Responses in Arabidopsis Cell Suspension Culture under High-Light Conditions, PLANT PHYSIOLOGY, vol.156, issue.3, pp.1439-1456, 2011.
DOI : 10.1104/pp.111.177766
URL : http://www.plantphysiol.org/content/plantphysiol/156/3/1439.full.pdf

@. Henzler, T. Steudle, and E. , Transport and metabolic degradation of hydrogen peroxide in Chara corallina: model calculations and measurements with the pressure probe suggest transport of H2O2 across water channels, Journal of Experimental Botany, vol.51, issue.353, pp.2053-2066, 2000.
DOI : 10.1042/bj3220681

@. Kim, C. Meskauskiene, R. Zhang, S. Lee, K. P. Lakshmanan et al., Chloroplasts of Arabidopsis Are the Source and a Primary Target of a Plant-Specific Programmed Cell Death Signaling Pathway, The Plant Cell, vol.24, issue.7, pp.3026-3039, 2012.
DOI : 10.1105/tpc.112.100479

@. Krieger-liszkay, A. Trebst, and A. , Tocopherol is the scavenger of singlet oxygen produced by the triplet states of chlorophyll in the PSII reaction centre, Journal of Experimental Botany, vol.57, issue.8, pp.1677-1684, 2006.
DOI : 10.1093/jxb/erl002

@. Laloi, C. Havaux, and M. , Key players of singlet oxygen-induced cell death in plants, Frontiers in Plant Science, vol.160, issue.20130227, p.39, 2015.
DOI : 10.1104/pp.112.202846
URL : https://hal.archives-ouvertes.fr/hal-01222328

@. Lee, K. P. Kim, C. Landgraf, F. Apel, and K. , EXECUTER1- and EXECUTER2-dependent transfer of stress-related signals from the plastid to the nucleus of Arabidopsis thaliana, Proceedings of the National Academy of Sciences USA, pp.10270-10275, 2007.
DOI : 10.1073/pnas.0609063103

@. Levine, A. Tenhaken, R. Dixon, R. Lamb, and C. , H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response, Cell, vol.79, issue.4, pp.583-593, 1994.
DOI : 10.1016/0092-8674(94)90544-4

@. Li, H. Melo, T. B. Arellano, J. B. Razi, and N. K. , Temporal profile of the singlet oxygen emission endogenously produced by photosystem II reaction centre in an aqueous buffer, Photosynthesis Research, vol.92, issue.1, pp.75-79, 2012.
DOI : 10.1073/pnas.92.7.2929

@. Meskauskiene, R. Nater, M. Goslings, D. Kessler, F. Op-den-camp et al., FLU: A negative regulator of chlorophyll biosynthesis in Arabidopsis thaliana, Proceedings National Academy of Sciences USA98, pp.12826-12831, 2001.
DOI : 10.1104/pp.111.1.61

@. Montillet, J. L. Cacas, J. L. Garnier, L. Montane, M. H. Douki et al., The upstream oxylipin profile of Arabidopsis thaliana: a tool to scan for oxidative stresses, The Plant Journal, vol.10, issue.3, pp.439-451, 2004.
DOI : 10.17660/ActaHortic.1982.126.43

@. Op-den-camp, R. G. Przybyla, D. Ochsenbein, C. Laloi, C. Kim et al., Rapid Induction of Distinct Stress Responses after the Release of Singlet Oxygen in Arabidopsis, THE PLANT CELL ONLINE, vol.15, issue.10, pp.2320-2332, 2003.
DOI : 10.1105/tpc.014662

@. Pogson, B. J. Woo, N. S. Forster, B. Small, and I. D. , Plastid signalling to the nucleus and beyond, Trends in Plant Science, vol.13, issue.11, pp.602-609, 2008.
DOI : 10.1016/j.tplants.2008.08.008

@. Ramel, F. Birtic, S. Ginies, C. Soubigou-taconnat, L. Triantaphylides et al., Carotenoid oxidation products are stress signals that mediate gene responses to singlet oxygen in plants, Proceedings National Academy of Sciences USA, pp.5535-5540, 2012.
DOI : 10.1038/sj.emboj.7601750
URL : https://hal.archives-ouvertes.fr/hal-01335774

@. Ramel, F. Ksas, B. Akkari, E. Mialoundama, A. S. Monnet et al., Light-Induced Acclimation of the Arabidopsis chlorina1 Mutant to Singlet Oxygen, The Plant Cell, vol.25, issue.4, pp.1445-1462, 2013.
DOI : 10.1105/tpc.113.109827
URL : https://hal.archives-ouvertes.fr/hal-00914997

@. Ramel, F. Ksas, B. Havaux, and M. , Jasmonate, Plant Signaling & Behavior, vol.8, issue.12, 2013.
DOI : 10.1186/1471-2229-9-12

@. Rastogi, A. Yadav, D. K. Szymanska, R. Kruk, J. Sedlarova et al., : relevance to photooxidative stress, Plant, Cell & Environment, vol.425, issue.2, pp.392-401, 2014.
DOI : 10.1042/BJ20090704

@. Rijgersberg, C. P. Amesz, J. Thielen, A. P. Swager, and J. A. , Fluorescence emission spectra of chloroplasts and subchloroplast preparations at low temperature, Biochimica et Biophysica Acta (BBA) - Bioenergetics, vol.545, issue.3, pp.473-482, 1979.
DOI : 10.1016/0005-2728(79)90156-7

@. Shao, N. Duan, G. Y. Bock, and R. , A Mediator of Singlet Oxygen Responses in Chlamydomonas reinhardtii and Arabidopsis Identified by a Luciferase-Based Genetic Screen in Algal Cells, The Plant Cell, vol.25, issue.10, pp.4209-4226, 2013.
DOI : 10.1105/tpc.113.117390

@. Shao, N. Krieger-liszkay, A. Schroda, M. Beck, and C. F. , A reporter system for the individual detection of hydrogen peroxide and singlet oxygen: its use for the assay of reactive oxygen species pr (2014) Dihydroactinidiolide, a high light-induced beta-carotene derivative that can regulate gene expression and photoacclimation in Arabidopsis, Molecular Plant, vol.7, pp.1248-1251, 2007.

@. Shumbe, L. Chevalier, A. Legeret, B. Taconnat, L. Monnet et al., Singlet oxygeninduced cell death in Arabidopsis under high-light stress is controlled by OXI1 kinase, Plant Physiology, vol.170, pp.1757-1771, 2016.

@. Simkova, K. Moreau, F. Pawlak, P. Vriet, C. Baruah et al., Integration of stress-related and reactive oxygen species-mediated signals by Topoisomerase VI in Arabidopsis thaliana, Proceedings National Academy of Sciences USA, pp.16360-16365, 2012.
DOI : 10.1111/j.1365-313X.2004.02169.x
URL : https://hal.archives-ouvertes.fr/hal-01626289

@. Telfer and A. , Singlet Oxygen Production by PSII Under Light Stress: Mechanism, Detection and the Protective role of ??-Carotene, Plant and Cell Physiology, vol.7, issue.7, pp.1216-1223, 2014.
DOI : 10.1371/journal.pone.0045883

@. Triantaphylides, C. Havaux, and M. , Singlet oxygen in plants: production, detoxification and signaling, Trends in Plant Science, vol.14, issue.4, pp.219-228, 2009.
DOI : 10.1016/j.tplants.2009.01.008

@. Triantaphylides, C. Krischke, M. Hoeberichts, F. A. Ksas, B. Gresser et al., Singlet Oxygen Is the Major Reactive Oxygen Species Involved in Photooxidative Damage to Plants, PLANT PHYSIOLOGY, vol.148, issue.2, pp.960-968, 2008.
DOI : 10.1104/pp.108.125690

@. Vanderauwera, S. Zimmermann, P. Rombauts, S. Vandenabeele, S. Langebartels et al., Genome-Wide Analysis of Hydrogen Peroxide-Regulated Gene Expression in Arabidopsis Reveals a High Light-Induced Transcriptional Cluster Involved in Anthocyanin Biosynthesis, PLANT PHYSIOLOGY, vol.139, issue.2, pp.806-821, 2005.
DOI : 10.1104/pp.105.065896