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Heidelberg: Springer-Verlag",{},false,{"id":495,"createTime":496,"updateTime":497,"relativeEntities":498,"slug":499,"properties":500,"entityType":274,"verifyStatus":275,"verifyTime":497,"verifyNote":277,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19,"primaryUrl":509,"fullTextUrl":18,"authors":510,"publicationType":322,"publisherRelationship":564,"citationCount":18,"citationInfo":18,"publishDate":597,"publishYear":598,"citationAnalyzeStatus":17,"lastCitationAnalyze":18,"indexDatabases":18,"openAccess":18,"references":18,"isForceReanalyzing":493},"d072b3c0-b2f1-4907-9f24-e0e3283b4a8b","2024-01-27T07:21:13.515+00:00","2025-01-20T23:59:21.799+00:00",[],"Hydrogen-peroxide-generation-and-antioxidant-enzyme-activities-in-the-leaves-and-roots-of-wheat-cultivars-subjected-to-long-term-soil-drought-stress",{"references":501,"abstract":503,"title":505,"doi":507},{"VOID":502},"Al-Ghamdi AA (2009) Evaluation of oxidative stress tolerance in two wheat (Triticim aestivum) cultivars in response to drought. Int J Agric Biol 11:7–12\nAliev JA (2001) Physiological bases of wheat breeding tolerant to water stress. Proceedings of the 6th international wheat conference, Budapest, Hungary, 2000. In: Bedo Z, Lang L (eds) Wheat in a global environment, Kluwer Academic Publishers, Dordrecht, Boston, London, 9:693–698\nAliyev JA (2012) Physiological and molecular bases of drought tolerance in wheat (Trticum L.) genotypes. In: Neves DF, Sanz JD (eds) Environmental science, engineering and technology. Drought: new research, vol 2. Nova Science Publishers, Inc., New York, pp 47–95\nAnderson M, Prasad T, Stewart C (1995) Changes in isozyme profiles of catalase, peroxidase, and glutathione reductase during acclimation to chilling in mesocotyls of maize seedlings. Plant Physiol 109(4):1247–1257\nAndreeva VA (1988) The enzyme peroxidase: involvement in the plant defense system. Nauka, Moscow\nAnjum SA, Xie X, Wang L, Saleem MF, Man C, Lei W (2011) Morphological, physiological and biochemical responses of plants to drought stress. Afr J Agric Res 6:2026–2032\nChugh V, Kaur N, Gupta K (2011) Evaluation of oxidative stress tolerance in maize (Zea mays L.) seedlings in response to drought. Indian J Biochem Biophys 48:47–53\nCia MC, Guimarães ACR, Medici LO, Chabregas SM, Azevedo RA (2012) Antioxidant responses to water deficit by drought-tolerant and-sensitive sugarcane varieties. Annals of Appl Biol 161(3):313–324\nCuypers A, Vangronsveld J, Ciijsters H (2002) Peroxidases in roots and primary leaves of Pharsalus vulgaris copper and zinc phytotoxcity: a comparison. J Plant Physiol 159:869–876\nDavis B (1964) Disc electrophoresis. I. Method and application to human serum proteins. Ann N Y Acad Sci 121:404–427\nDevi R, Kaur N, Gupta AK (2011) Potential of antioxidant enzymes in depicting drought tolerance of wheat (Triticum aestivum L.). Indian J Biochem Biophys 49:257–265\nEl-Fadly GAB, Menshawy AM, Farhat WZE (2007) Molecular and biochemical studies on some bread wheat genotypes in relation to water stress tolerance. Afr Crop Sci Conf Proc 8:605–612\nForeman J, Demidchik V, Bothwell JH (2003) Reactive oxygen species produced by NADPH oxidase regulates plant cell growth. Nature 27:442–446\nFoyer CH, Noctor G (2005) Oxidant and antioxidant signaling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant, Cell Environ 28:1056–1071\nFryer MJ, Ball L, Oxborough K, Karpinski S, Mullineaux PM, Baker NR (2003) Control of ascorbate peroxidase 2 expressions by hydrogen peroxide and leaf water status during excess light stress reveals a functional organization of Arabidopsis leaves. Plant J 33:691–705\nGajhede M (2001) Plant peroxidases: substrate complexes with mechanistic implications. Biochem Soc Trans 29:21–29\nGechev T, Gadjiev I, van Breusagem F, İnze D, Dukiandjiev S, Toneva V, Minkov I (2002) Hydrogen peroxide protects tobacco from oxidative stress by inducing a set of antioxidant enzymes. Cell Mol Life Sci 59:708–714\nHammond-Kosack KE, Jones JDG (1996) Resistance gene-dependent plant defense responses. Plant Cell 8(10):1773–1791\nHasheminasab H, Assad MT, Aliakbari A, Sahhafi R (2012) Influence of drought stress on oxidative damage and antioxidant defense systems in tolerant and susceptible wheat genotypes. J Agric Sci 4(8):20–30\nHirt H, Shinozaki K (2004) Plant responses to abiotic stress. Springer, Vienna\nHuseynova IM (2012) Photosynthetic characteristics and enzymatic antioxidant capacity of leaves from wheat cultivars exposed to drought. Biochim Biophys Acta 1817:1516–1523\nHuseynova IM, Suleymanov SY, Aliyev JA (2007) Structural-functional state of thylakoid membranes of wheat genotypes under water stress. Biochim Biophys Acta 1767:869–875\nJang IC, Park SY, Kwon SY, Kim GK, Kwak SS (2004) Differential expression of 10 sweet potato peroxidase genes in response to bacterial pathogen, Pectobacterium chrysanthemi. Plant Physiol Biochem 42:451–455\nJebali J (2007) Oxidative DNA damage levels and catalase activity in the clam Ruditapes decussatus as pollution biomarkers of Tunisian marine environment. Environ Monit Assess 124:195–200\nKachout SS, Mansoura AB, Leclerc JC, Mechergui R, Rejeb MN, Ouerghi Z (2009) Effects of heavy metals on antioxidant activities of A. hortensis and A. rosea. J Food Agric Environ 7(3–4):938–945\nKannan ND, Kulandaivelu G (2011) Drought induced changes in physiological, biochemical and phytochemical properties of Withania somnifera Dun. J Med Plants Res 5:3929–3935\nKariola T, Brader G, Helenius E, Li J, Heino P, Palva ET (2006) Early responsive to dehydration 15—a negative regulator of ABA-responses in Arabidopsis. Plant Physiol 142:1559–1573\nKlisurska B, Dencheva A (1980) Substrate specificity of peroxidase isoenzymes for hydrogen donors. Biol Plant 22(6):404–409\nKumar RR, Karajol K, Naik GR (2011) Effect of polyethylene glycol induced water stress on physiological and biochemical responses in pigeon pea (Cajanus cajan L. Mill sp.). Recent Res Sci Technol 3(1):148–152\nLum MS, Hanafi MM, Rafii YM, Akmar ASN (2014) Effect of drought stress on growth, proline and antioxidant enzyme activities of upland rice. J Anim Plant Sci 24(5):1487–1493\nMahalingam R, Shah A, Scrymgeour N (2005) Temporal evolution of the Arabidopsis oxidative stress response. Plant Mol Biol 57:709–730\nMaksimović JD, Maksimović V, Živanović B, Šukalović VHT, Vuletić M (2008) Peroxidase activity and phenolic compounds content in maize root and leaf apoplast and their association with growth. Plant Sci 175(5):656–662\nMedrano H, Escalona JM, Bota J, Gulias J, Flexas J (2002) Regulation of photosynthesis of C3 plants in response to progressive drought: the stomatal conductance as a reference parameter. Ann Bot 89:895–905\nMenvielle-Bourg FJ (2005) Superoxide dismutase (SOD), a powerful antioxidant, is now available orally. Phytothérapie 3:1–4\nMiller G, Suzuki N, Ciftci-Yilmaz S, Mittler R (2010) Reactive oxygen species homeostasis and signaling during drought and salinity stresses. Plant, Cell Environ 33:453–467\nMittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410\nMittler R, Zilinskas BA (1993) Detection of ascorbate peroxidase activity in native gels by inhibition of the ascorbate dependent reduction of nitroblue tetrazolium. Anal Biochem 212:540–546\nNakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. 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Physiol Plant 104:747–752\nSedmak JJ, Grossberg SE (1977) A rapid, sensitive and versatile assay for protein using Coomassie brilliant blue G 250. Anal Biochem 79:544–552\nShetty NP, Kristensen BK, Newman MA et al (2003) Association of hydrogen peroxide with restriction of Septoria tritici in resistant wheat. Physiol Mol Plant Pathol 62(6):333–346\nTambussi EA, Nogues S, Araus JL (2005) Ear of durum wheat under water stress: water relations and photosynthetic metabolism. Planta 221:446–458\nUpadhyaya H, Khan MH, Panda SK (2007) Hydrogen peroxide induces oxidative stress in detached leaves of Oryza sativa L. Gen Appl Plant Physiol 33(1–2):83–95\nZhang JX, Kirkham MB (1994) Drought-stress induced changes in activities of superoxide dismutase, catalase and peroxidase in wheat species. Plant Cell Physiol 35:785–791\nZhang QH, Liu HS, Meng FT, Zhang ST, Zhang ZH, Kang GZ (2000) The effect of drought stress on physiological characters of leaves and seed-filling characteristics of the new wheat cultivar Yamai 36 during the late developmental stage. Sci Agric Sin 33(4):94–96\nZhu JK (2002) Salt and drought stress signal transduction in plants. Annu Rev Plant Physiol 53:243–273\nZhu Z, Wei G, Li J, Qian Q, Yu J (2004) Silicon alleviates salt stress and increases antioxidant enzymes activity in leaves of salt-stressed cucumber (Cucumis sativus L.). Plant Sci 167:527–533",{"EN":504},"The dynamics of the activity of catalase, ascorbate peroxidase, guaiacol peroxidase, and benzidine peroxidase, as well as the level of hydrogen peroxide in the vegetative organs of durum wheat (Triticum durum Desf.) cultivars was studied under long-term soil drought conditions. It was established that hydrogen peroxide generation occurred at early stages of stress in the tolerant variety Barakatli-95, whereas in the susceptible variety Garagylchyg-2 its significant amounts were accumulated only at later stages. Garagylchyg-2 shows a larger reduction of photochemical activity of PS II in both genotypes at all stages of ontogenesis under drought stress than Barakatli-95. The highest activity of catalase which plays a leading role in the neutralization of hydrogen peroxide was observed in the leaves and roots of the drought-tolerant variety Barakatli-95. Despite the fact that the protection system also includes peroxidases, the activity of these enzymes even after synthesis of their new portions is substantially lower compared with catalase. Native PAGE electrophoresis revealed the presence of one isoform of CAT, seven isoforms of APX, three isoforms of GPO, and three isoforms of BPO in the leaves, and also three isoforms of CAT, four isoforms of APX, two isoforms of GPO, and six isoforms of BPO in the roots of wheat. One isoform of CAT was found in the roots when water supply was normal and three isoforms were observed under drought conditions. Stress associated with long-term soil drought in the roots of wheat has led to an increase in the heterogeneity due to the formation of two new sedentary forms of catalase: CAT2 and CAT3.",{"EN":506},"Hydrogen peroxide generation and antioxidant enzyme activities in the leaves and roots of wheat cultivars subjected to long-term soil drought stress",{"VOID":508},"10.1007\u002Fs11120-015-0160-7","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs11120-015-0160-7",[511,527,539,551],{"id":512,"sortIndex":19,"researcher":18,"roles":513,"affiliations":515,"properties":524},"e773bf03-df38-4c42-9e28-4ea211f1f549",[514],"AUTHOR",[516],{"id":18,"sortIndex":19,"affiliation":517,"properties":18},{"id":518,"createTime":519,"updateTime":519,"relativeEntities":520,"slug":18,"properties":521,"entityType":63,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},"f75560a1-45de-4d59-9519-ba1a3f052429","2024-01-27T07:21:13.564+00:00",[],{"title":522},{"VI":523},"Department of Fundamental Problems of Biological Productivity, Institute of Molecular Biology and Biotechnology, Azerbaijan National Academy of Sciences, Baku, Azerbaijan",{"title":525},{"VI":526},"Irada M. Huseynova",{"id":528,"sortIndex":284,"researcher":18,"roles":529,"affiliations":530,"properties":536},"4412e3f1-1385-4e2d-877c-ee9da8430414",[514],[531],{"id":18,"sortIndex":19,"affiliation":532,"properties":18},{"id":518,"createTime":519,"updateTime":519,"relativeEntities":533,"slug":18,"properties":534,"entityType":63,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},[],{"title":535},{"VI":523},{"title":537},{"VI":538},"Durna R. 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I. Assimilation of nitrate nitrogen by Scenedesmus\n; citation_author=D I Arnon, P Ishioya, G Wessel, A Fujiwara, J T Woolley; citation_volume=8; citation_publication_date=1955; citation_pages=538-551; citation_id=CR1\ncitation_journal_title=Anal Biochem; citation_title=A rapid and sensitive method for the quantitation of microgram quanties of protein utilizing the principle of protein-dye binding; citation_author=M M Bradford; citation_volume=72; citation_publication_date=1976; citation_pages=248-256; citation_id=CR2\ncitation_journal_title=Plant Physiol; citation_title=Phosphofructokinase activities in photosynthetic organisms, the occurrence of pyrophosphate-dependent 6-phosphofructokinase in plants and algae; citation_author=N W Carnal, C C Black; citation_volume=71; citation_publication_date=1983; citation_pages=150-155; citation_id=CR3\ncitation_journal_title=Plant Physiol; citation_title=Modulation of chloroplast phosphofructokinase by NADPH; citation_author=C Cséke, A N Nishizawa, B B Buchanan; citation_volume=70; citation_publication_date=1982; citation_pages=658-661; citation_id=CR4\ncitation_journal_title=Proc Natl Acad Sci USA; citation_title=A special fructose bisphosphate functions as a cytoplasmic regulatory metabolite in green leaves; citation_author=C Cséke, N F Weeden, B B Buchanan, K Uyeda; citation_volume=79; citation_publication_date=1982; citation_pages=4322-4326; citation_id=CR5\ncitation_journal_title=Biochem Biophys Res Commun; citation_title=Phosphofructokinase: a regulatory enzyme in plants; citation_author=D T Dennis, T P Coultate; citation_volume=25; citation_publication_date=1966; citation_pages=187-191; citation_id=CR6\ncitation_journal_title=Biochim Biophys Acta; citation_title=The regulatory properties of a plant phosphofructokinase during leaf development; citation_author=D T Dennis, T P Coultate; citation_volume=146; citation_publication_date=1967; citation_pages=129-137; citation_id=CR7\ncitation_journal_title=Arch Biochem Biophys; citation_title=Plastid and cytosolic phosphofructokinases from the developing endosperm of Ricinus communis. I. Separation, purification, and initial characterization of the isozymes; citation_author=W J Garland, D T Dennis; citation_volume=204; citation_publication_date=1980; citation_pages=302-309; citation_id=CR8\ncitation_journal_title=Arch Biochem Biophys; citation_title=Plastid and cytosolic phosphofructokinases from the developing endosperm of Ricinus communis. II. Comparison of the kinetic and regulatory properties of the enzymes; citation_author=W J Garland, D T Dennis; citation_volume=204; citation_publication_date=1980; citation_pages=310-317; citation_id=CR9\ncitation_journal_title=Phytochemistry (Oxf.); citation_title=Phosphofructokinase from Lycopersicon esculentum. I. Kinetic properties in relation to its substrates; citation_author=J E Isaac, M J C Rhodes; citation_volume=15; citation_publication_date=1986; citation_pages=339-343; citation_id=CR10\ncitation_journal_title=Plant Cell Physiol; citation_title=Contrasting sensitivities of Chlorella and higher plant phosphofructokinases to dilution; citation_author=G J Kelly, E Latzko; citation_volume=2292; citation_publication_date=1981; citation_pages=291-296; citation_id=CR11\ncitation_journal_title=Plant Physiol; citation_title=Chloroplast phosphofruc-tokinase I. Proof of phosphofructokinase activity in chloroplasts; citation_author=G J Kelly, E Latzko; citation_volume=60; citation_publication_date=1977; citation_pages=290-294; citation_id=CR12\ncitation_journal_title=Plant Physiol; citation_title=Chloroplast phosphofruc-tokinase II. Partial purification, kinetic and regulatory properties; citation_author=G J Kelly, E Latzko; citation_volume=60; citation_publication_date=1977; citation_pages=295-299; citation_id=CR13\ncitation_journal_title=Plant Cell Physiol; citation_title=Purification, kinetic and regulatory properties of phosphofructokinases from Chlorella pyrenoidosa\n; citation_author=G J Kelly, U Mukherjee, J A M Holtum, E Latzko; citation_volume=26; citation_issue=2; citation_publication_date=1985; citation_pages=301-307; citation_id=CR14\ncitation_journal_title=Arch Biochem Biophys; citation_title=Chloroplast phosphofruc-tokinase in the green alga, Dunaliella marina: partial purification and kinetic and regulatory properties; citation_author=E Kombrink, G Wöber; citation_volume=213; citation_publication_date=1982; citation_pages=602-619; citation_id=CR15\ncitation_inbook_title=The regulation of glycolysis and the pentose phosphate pathway. The Biochemistry of Plants; citation_publication_date=1980; citation_pages=279-316; citation_id=CR16; citation_author=J F Turner; citation_author=D H Turner; citation_publisher=Academic Press\ncitation_journal_title=J Biol Chem; citation_title=A novel type of phosphofructokinase from plants; citation_author=J Wong, B C Yee, B B Buchanan; citation_volume=262; citation_publication_date=1987; citation_pages=3185-3191; citation_id=CR17\ncitation_journal_title=FEBS Lett; citation_title=A novel PFP (pyrophosphate fructose-6-phosphate fructose-6-phosphate 1-phosphotransferase) from carrot roots. Relation to PFK from the same source; citation_author=J H Wong, T Kang, B B Buchanan; citation_volume=238; citation_publication_date=1988; citation_pages=405-410; citation_id=CR18",{"EN":609},"Cell-free preparations from the green alga, Chlorella pyrenoidosa, contained two forms of phosphofructokinase (PFK), designated PFK I and PFK II. This represents the first evidence for a second form of PFK in green algae. A pyrophosphate D-fructose-6-phosphate, 1-phosphotransferase (PFP) activity, that was unaffected by the regulatory metabolite, fructose-2,6-bisphosphate, co-purified with PFK II through several steps. The data suggest that Chlorella pyrenoidosa resembles higher plants in containing two forms of PFK, but differs in containing an atypical form of PFP.",{"EN":611},"Identification of two forms of PFK and a fructose-2,6-bisphosphate independent form of PFP in a green alga",{"VOID":613},"10.1007\u002FBF00033366","2025-02-06T23:59:02.250+00:00","Author affiliation is blank","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF00033366","https:\u002F\u002Flink.springer.com\u002Fcontent\u002Fpdf\u002F10.1007\u002FBF00033366.pdf",[619,626,651,663,676,688],{"id":620,"sortIndex":360,"researcher":18,"roles":621,"affiliations":622,"properties":623},"c7ab5278-8f34-49d5-977c-eb05c3e17bd3",[514],[],{"title":624},{"VI":625},"Balogh, A.",{"id":627,"sortIndex":209,"researcher":18,"roles":628,"affiliations":629,"properties":648},"be26002f-7eb7-4ecc-ace4-8744acf97b5a",[514],[630,640],{"id":631,"sortIndex":284,"affiliation":632,"properties":639},"6b9e7148-30e6-488a-89ff-2c6766fa2a98",{"id":633,"createTime":634,"updateTime":634,"relativeEntities":635,"slug":18,"properties":636,"entityType":63,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},"d998c627-e70c-400d-94a3-03c1ace38edf","2024-01-28T05:25:41.054+00:00",[],{"title":637},{"VI":638},"Division of Molecular Plant Biology, University of California, Berkeley, USA",{},{"id":18,"sortIndex":19,"affiliation":641,"properties":18},{"id":642,"createTime":643,"updateTime":643,"relativeEntities":644,"slug":18,"properties":645,"entityType":63,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},"dca84c7c-ff9b-473a-901c-7b01cb6bd4dd","2024-01-28T05:25:41.049+00:00",[],{"title":646},{"VI":647},"Department of Biology and Chemistry, György Bessenyei College, Nyiregyháza, Hungary",{"title":649},{"VI":650},"Klecan, A. 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Annu Rev Plant Physiol 31:491–543\nBrown WV (1975) Variations in anatomy, associations and origins of kranz tissue. Am J Bot 62:395–402\nBrown RH, Byrd GT (1993) Estimation of bundle sheath cell conductance in C4 species and O2 insensitivity of photosynthesis. Plant Physiol 103:1183–1188\nvon Caemmerer S, Furbank RT (1999) Modelling C4 photosynthesis. In: Sage RF, Monson RK (eds) C4 plants biology. Academic Press, London, pp 173–211\nvon Caemmerer S, Furbank RT (2003) The C4 pathway: an efficient CO2 pump. Photosynth Res 77:191–207\nvon Caemmerer S, Millgate A, Farquhar GD, Furbank RT (1997) Reduction of Rubisco by antisense RNA in C4 plant Flaveria bidentis leads to reduced assimilation rates and increased carbon isotope discrimination. Plant Physiol 113:469–477\nCousins AB, Badger MR, von Caemmerer S (2006) Carbonic anhydrase and its influence on carbon isotope discrimination during C4 photosynthesis. Insight from antisense RNA in Flaveria bidentis. Plant Physiol 141:232–242\nDai Z, Ku MSB, Edwards GE (1995) C4 photosynthesis – the effects of leaf development on CO2 concentrating mechanism and photorespiration in maize. Plant Physiol 107:815–825\nDengler NG, Nelson T (1999) Leaf structure and development in C4 plants. In: Sage RF, Monson RK (eds) C4 plants biology. Academic Press, London, pp 133–172\nDwyer SA, Ghannoum O, Nicotra A, von Caemmerer S (2007) High temperature acclimation of C4 photosynthesis is linked to changes in photosynthetic biochemistry. Plant Cell Env 30:53–66\nEspelie KE, Kolattukudy PE (1979) Composition of aliphatic components of suberin from the bundle sheaths of Zea mays leaves. Plant Sci Lett 15:225–230\nEhleringer J, Pearcy RW (1983) Variation in quantum yield for CO2 uptake among C3 and C4 plants. Plant Physiol 73:555–559\nEvans RJ, Sharkey TD, Berry JA, Farquhar GD (1986) Carbon isotope discrimination measured concurrently with gas exchange to investigate CO2 diffusion in leaves of higher plants. Aust J Plant Physiol 13:281–292\nFarquhar GD (1983) On the nature of carbon isotope discrimination in C4 species. Aust J Plant Physiol 10:205–226\nFravolini A, Williams DG, Thompson TL (2002) Carbon isotope discrimination and bundle sheath leakiness in three C4 subtypes grown under variable nitrogen, water and atmospheric CO2 supply. J Exp Bot 53:2261–2269\nFurbank RT, Hatch MD (1987) Mechanism of C4 photosynthesis: the size and composition of the inorganic carbon pool in bundle sheath cells. Plant Physiol 85:958–964\nFurbank RT, Jenkins CLD, Hatch MD (1989) CO2 concentrating mechanism of C4 photosynthesis – permeability of isolated bundle sheath cells to inorganic carbon. Plant Physiol 91:1364–1371\nFurbank RT, Jenkins CLD, Hatch MD (1990) C4 photosynthesis: quantum requirement, C4 acid overcycling and Q-cycle involvement. Aust J Plant Physiol 17:553–558\nFurbank RT, Hatch MD, Jenkins CLD (2000) C4 photosynthesis: mechanism and regulation. In: Leegood RC, Sharkey TD, von Caemmerer S (eds) Photosynthesis: physiology and metabolism. Kluwer Academic Publishers, The Netherlands, pp 435–457\nGhannoum O, Siebke K, von Caemmerer S, Conroy JP (1998) The photosynthesis of young Panicum C4 leaves is not C3-like. Plant Cell Env 21:1123–1131\nGhannoum O, Evans JR, Chow WS, Andrews TJ, Conroy JP, von Caemmerer S (2005) Faster Rubisco is the key to superior nitrogen use efficiency in NADP-ME relative to NAD-ME C4 grasses. Plant Physiol 137:638–650\nGhashghaie J, Badeck FW, Lanigan G, Nogués S, Tcherkez G, Deléens E, Cornic G, Griffiths H (2003) Carbon isotope fractionation during dark respiration and photorespiration in C3 plants. Phytochem Rev 2:145–161\nGillon J, Yakir D (2001) Influence of carbonic anhydrase activity in terrestrial vegetation on the 18O content of atmospheric CO2. Science 291:2584–2587\nGutierrez M, Gracen VE, Edwards GE (1974) Biochemical and cytological relationships in C4 plants. Planta 119:279–300\nHatch MD (1987) C4 photosynthesis: a unique blend of modified biochemistry, anatomy and ultra structure. Biochim Biophys Acta 895:81–106\nHatch MD, Agostino A, Jenkins CLD (1995) Measurement of the leakage of CO2 from bundle sheath cells of leaves during C4 photosynthesis. Plant Physiol 108:173–181\nHatch MD, Slack CD, Johnson HS (1967) Further studies on a new pathway of photosynthetic carbon dioxide fixation in sugarcane and its occurrence in other plant species. Biochem J 102:417–422\nHatch MD, Kagawa T, Craig S (1975) Subdivision of C4 pathway species based on different C4 acid decarboxylating systems and ultrastructural features. Aust J Plant Physiol 2:111–128\nHattersley PW, Browning AJ (1981) Occurence of suberized lamella in leaves of grasses of different photosyntetic types. I. In parenchymatous bundle sheaths and PCR (“kranz”) sheaths. Protoplasma 109:371–401\nHe D, Edwards GE (1996) Estimation of diffusive resistance of bundle sheath cells to CO2 from modelling of C4 photosynthesis. Photosynth Res 49:195–208\nHenderson SA, von Caemmerer S, Farquhar GD (1992) Short term measurements of carbon isotope discrimination in several C4 species. Aust J Plant Physiol 19:263–285\nHobbie EA, Werner RA (2003) Intramolecular, compound-specific, and bulk carbon isotope patterns in C3 and C4 plants: a review and synthesis. New Phytol 161:371–385\nJenkins CLD, Furbank RT, Hatch MD (1989) Inorganic carbon diffusion between C4 mesophyll and bundle sheath cells – direct bundle sheath CO2 assimilation in intact leaves in the presence of an inhibitor of the C4 pathway. Plant Physiol 91:1356–1363\nKanai R, Edwards G (1999) The biochemistry of C4 photosynthesis. In: Sage RF, Monson RK (eds) C4 plant biology. Academic Press, London, pp 49–87\nKiirats O, Lea PJ, Franceschi VR, Edwards GE (2002) Bundle sheath diffusive resistance to CO2 and effectiveness of C4 photosynthesis and refixation of photorespired CO2 in C4 cycle mutant and wild-type Amaranthus edulis. Plant Physiol 130:964–976\nKubásek J (2002) Diskriminace uhlíku 13C při fotosyntéze vyšších rostlin.(13C discrimination in higher-plants photosynthesis). Bachelor thesis in Czech, Faculty of Biology, University of South Bohemia, České Budějovice\nKubásek J (2004) C4 rostliny a stabilní izotopy. (C4 pants and stable isotopes). Diploma thesis in Czech, Faculty of Biology, University of South Bohemia, České Budějovice\nKubien DS, von Caemmerer S, Furbank RT, Sage F (2003) C4 photosynthesis at low temperature. A study using transgenic plants with reduced amounts of Rubisco. Plant Physiol 132:1577–1585\nLewis NG, Yamamoto E (1990) Lignin: occurrence, biogenesis and degradation. Ann Rev Plant Physiol Plant Mol Biol 41:455–496\nLong SP (1999) Environmental responses. In: Sage RF, Monson RK (eds) C4 plants biology. Academic Press, London, pp 215–249\nLudwig M, von Caemmerer S, Price GD, Badger MR, Furbank RT (1998) Expression of tobacco carbonic anhydrase in the C4 dicot Flaveria bidentis leads to increase leakiness of the bundle sheath and a defective CO2 concentrating mechanism. Plant Physiol 117:1071–1081\nMeinzer FC, Saliedra NZ (1997) Spatial patterns of carbon isotope discrimination and allocation of photosynthetic activity in sugarcane leaves. Aust J Plant Physiol 24:769–775\nMook WG, Bommerson JC, Staverman WH (1974) Carbon isotope fractionation between dissolved bicarbonate and gaseous carbon dioxide. Earth Planet Sci Lett 22:169–176\nO’ Brien TP, Carr DJ (1970) A suberized layer in the cell walls of the bundle sheath of grasses. Aust J Biol Sci 23:275–287\nOberhuber W, Edwards GE (1993) Temperature dependence of the linkage of quantum yield of photosystem II to CO2 fixation in C4 and C3 plants. Plant Physiol 101:507–512\nPeisker M, Henderson SA (1992) Carbon – terrestrial C4 plants. Plant Cell Env 15:987–1004\nPospíšilová J, Šantrůček J (1994) Stomatal patchiness. Biol Plant 36(4):481–510\nSage RF (2001) C4 Plants. In: Levin SA (ed) Encyclopedia of biodiversity. Academic Press, pp 575–598\nTazoe Y, Noguchi K, Terashima I (2006) Effects of growth light and nitrogen nutrition on the organisation of the photosynthetic apparatus in leaves of a C4 plant, Amaranthus cruentus. Plant Cell Env 29(4):691–700\nWang SY, Lin H (2006) Effect of plant growth temperature on membrane lipids in strawberry (Fragaria x ananassa Duch.). Sci Horticult 108(2006):35–42\nWilliams DG, Gempko V, Fravolini A, Leavitt SW, Wall GW, Kimball PJ, Pinter PJ Jr, LaMorte R, Ottman M (2001) Carbon isotope discrimination by Sorghum bicolor under CO2 enrichment and drought. New Phytol 150:285–293",{"EN":752},"We combined measurements of short-term (during gas exchange) and long-term (from plant dry matter) carbon isotope discrimination to estimate CO2 leakiness from bundle sheath cells in six C4 species (three grasses and three dicots) as a function of leaf insertion level, growth temperature and short-term irradiance. The two methods for determining leakiness yielded similar results (P > 0.05) for all species except Setaria macrostachya, which may be explained by the leaf of this species not being accommodating to gas exchange. Leaf insertion level had no effect on leakiness. At the highest growth temperature (36°C) leakiness was lower than at the two lower growth temperatures (16°C and 26°C), between which no differences in leakiness were apparent. Higher irradiance decreased leakiness in three species, while it had no significant effect on the others (there was an opposite trend in two species). The inverse response to increasing irradiance was most marked in the two NAD-ME dicots (both Amaranthus species), which both showed almost 50% leakiness at low light (300 μmol quanta m−2 s−1) compared to about 30% at high light (1,600 μmol quanta m−2 s−1). NADP-ME subtype grasses had lower leakiness than NAD-ME dicots. Although there were exceptions, particularly in the effect of irradiance on leakiness in Sorghum and Boerhavia, we conclude that conditions favourable to C4 photosynthesis (high temperature and high light) lead to a reduction in leakiness.",{"EN":754},"Light and growth temperature alter carbon isotope discrimination and estimated bundle sheath leakiness in C4 grasses and 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G, Cerovic ZG, Moya I (2000) The effect of decreasing temperature up to chilling values on the in vivo F685\u002FF735 chlorophyll fluorescence ratio in phaseolus vulgaris and pisum sativum: the role of the photosystem I contribution to the 735 nm fluorescence band. Photochem Photobiol 72(1):75–84\nBannari A, Morin D, Bonn F, Huete AR (1995) A review of vegetation indices. Remote Sens Rev 13:95–120. https:\u002F\u002Fdoi.org\u002F10.1080\u002F02757259509532298\nCerovic ZG, Goulas Y, Gorbunov M, Briantais JM, Camenen L, Moya I (1996) Fluorosensing of water stress in plants: Diurnal changes of the mean lifetime and yield of chlorophyll fluorescence, measured simultaneously and at a distance with a τ-LIDAR and a modified PAM-fluorimeter, in maize, sugar beet, and kalanchoë. Remote Sens Environ 58(3):311–321. https:\u002F\u002Fdoi.org\u002F10.1016\u002FS0034-4257(96)00076-4\nCogliati S, Celesti M, Cesana I, Miglietta F, Genesio L, Julitta T, Schuettemeyer D, Drusch M, Rascher U, Jurado P, Colombo R (2019) A spectral fitting algorithm to retrieve the fluorescence spectrum from canopy radiance. Remote Sensing 11:1840. https:\u002F\u002Fdoi.org\u002F10.3390\u002Frs11161840\nDau H (1994) Molecular mechanisms and quantitative models of variable photosystem II fluorescence. Photochem Photobiol 60:1–23. https:\u002F\u002Fdoi.org\u002F10.1111\u002Fj.1751-1097.1994.tb03937.x\nDaumard F, Champagne S, Fournier A, Goulas Y, Ounis A, Hanocq JF, Moya I (2010) A field platform for long-term measurement of canopy fluorescence. IEEE Trans Geosci Remote Sens 48(9):3358–3368. https:\u002F\u002Fdoi.org\u002F10.1109\u002FTGRS.2010.2046420\nDaumard F, Goulas Y, Champagne S, Fournier A, Ounis A, Olioso A, Moya I (2012) Canopy level chlorophyll fluorescence at 760 nm better tracks in-field sorghum growth. IEEE Trans Geosci Remote Sens 50(11):4292–4300\nDaumard F, Goulas Y, Ounis A, Pedrós R, Moya I (2015) Measurement and correction of atmospheric effects at different altitudes for remote sensing of sun-induced fluorescence in oxygen absorption bands. IEEE Trans Geosci Remote Sens 53(9):5180–5196. https:\u002F\u002Fdoi.org\u002F10.1109\u002FTGRS.2015.2418992\nDaumard F, Goulas Y, Ounis A, Pedros R, Moya I (2007). Atmospheric correction of airborne passive measurements of fluorescence. in Proc. ISPMSRS, Davos, Switzerland.\nDrusch M, Moreno J, Del Bello U, Franco R, Goulas Y, Huth A, Kraft S, Middleton EM, Miglietta F, Mohammed G, Nedbal L, Rascher U, Schüttemeyer D, Verhoef W (2017) The fluorescence explorer mission concept-ESA’s Earth Explorer 8. IEEE Trans Geosci Remote Sens 55:1273–1284. https:\u002F\u002Fdoi.org\u002F10.1109\u002Ftgrs.2016.2621820\nFlexas J-M, Briantais ZC, Medrano H, Moya I (2000) Steady-state and maximum chlorophyll fluorescence responses to water stress in grapevine leaves: a new remote sensing system. Remote Sens Environ 73:283–297\nFournier A, Daumard F, Champagne S, Ounis A, Goulas Y, Moya I (2012) Effect of canopy structure on sun-induced chlorophyll fluorescence. ISPRS J Photogrametry Remote Sensing 68:112–120. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.isprsjprs.2012.01.003\nFranck F, Juneau P, Popovic R (2002) Resolution of the Photosystem I and Photosystem II contributions tochlorophyll fluorescence of intact leaves at room temperature. Biochem Biophys Acta 1556:239–246. https:\u002F\u002Fdoi.org\u002F10.1016\u002FS0005-2728(02)00366-3\nLaisk A, Oja V, Eichelmanna H (1837) Dall’Osto L (2014) Action spectra of photosystems II and I and quantum yield of photosynthesis in leaves in State1. Biochem Biophys Acta 2:315–325. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.bbabio.2013.12.001\nLopez M.Ll. (2015) Seguimiento del estrés hidrico de la vid mediante tecnicas de fluorescencia de la clorophila y otros métodos ópticos. PhD thesis. Universidad de Castilla La Mancha. Albacete-España.\nLouis J, Cerovic ZG, Moya I (2006) Quantitative study of fluorescence excitation and emission spectra of bean leaves. J Photochem Photobiol b: Biol 85:65–67. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.jphotobiol.2006.03.009\nMoya I, Loayza H, López ML, Quiroz R, Ounis A, Goulas Y (2019) Canopy chlorophyll fluorescence applied to stress detection using an easy-to-build micro-lidar. Photosynth Res 142:1–15. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs11120-019-00642-9\nMoya I, Daumard F, Moise N, Ounis A, Goulas Y (2006) First airborne multi-wavelength passive chlorophyll fluorescence measurements over La Mancha (Spain) fields. In: 2nd International Symposium on Recent Advances in Quantitative Remote Sensing: RAQRS'II, 25–29th September 2006, Torrent (Valencia)-Spain.\nNiclòs R, Valiente JA, Barberá MJ, Coll C (2015) An autonomous system to take angular thermal-infrared measurements for validating satellite products. Remote Sensing 7:15269–15294. https:\u002F\u002Fdoi.org\u002F10.3390\u002Frs71115269\nPfündel E (1998) Estimating the contribution of photosystem I to total leaf chlorophyll fluorescence. Photosynth Res 56:185–195. https:\u002F\u002Fdoi.org\u002F10.1023\u002FA:1006032804606\nQuick WP, Horton P (1984) Studies on the induction of chlorophyll fluorescence in barley protoplasts. I. Factors affecting the observation of oscillations in the yield of chlorophyll fluorescence and the rate of oxygen evolution. Proceedings Royal Society London B 220:361–370. https:\u002F\u002Fdoi.org\u002F10.1098\u002Frspb.1984.0006\nRascher U, Agati G, Alonso L, Cecchi G, Champagne S, Colombo R, Damm A, Daumard F, De Miguel E, Fernandez G, Franch B, Franke J, Gerbig C, Gioli B, Gomez JA, Goulas Y, Guanter L, Gutierrez-de-la-Camara O, Hamdi K, Hostert P, Jimenez M, Kosvancova M, Lognoli D, Meroni M, Miglietta F, Moersch A, Moreno J, Moya I, Neininger B, Okujeni A, Ounis A, Palombi L, Raimondi V, Schickling A, Sobrino JA, Stellmes M, Toci G, Toscano P, Udelhoven T, Van der Linden S (2009) Zaldei A (2009) CEFLES2: the remote sensing component to quantify photosynthetic efficiency from the leaf to the region by measuring sun-induced fluorescence in the oxygen absorption bands. Biogeosciences 6:1181–1198. https:\u002F\u002Fdoi.org\u002F10.5194\u002Fbg-6-1181-2009\nSánchez JM, Kustas WP, Caselles V, Anderson M (2008) Modelling surface energy fluxes over maize using a two-source patch model and radiometric soil and canopy temperature observations. Remote Sens Environ 112:1130–1143. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.rse.2007.07.018\nSánchez JM, López-Urrea R, Rubio E, Caselles V (2011) Determining water use of sorghum from two-source energy balance and radiometric temperatures. Hydrol Earth Syst Sci 15:3061–3070. https:\u002F\u002Fdoi.org\u002F10.5194\u002Fhess-15-3061-2011\nSánchez JM, López-Urrea R, Rubio E, González-Piqueras J, Caselles V (2014) Assessing crop coefficients of sunflower and canola using two-source energy balance and thermal radiometry. Agric Water Manag 137:23–29. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.agwat.2014.02.002\nSánchez JM, López-Urrea R, Doña C, Caselles V, González-Piqueras J, Niclós R (2015) Modeling evapotranspiration in spring wheat from thermal radiometry: crop coefficients and E\u002FT partitioning. Irrig Sci 33(6):399–410. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs00271-015-0476-2\nSánchez JM, López-Urrea R, Valentín F, Caselles V, Galve JM (2019) Lysimeter assessment of the Simplified Two-Source Energy Balance model and eddy covariance system to estimate vineyard evapotranspiration. Agric Meteorol 274:172–183. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.agrformet.2019.05.006\nSánchez JM, Galve JM, González J, López-Urrea R, Niclòs R, Calera A (2020) Monitoring 10-m LST from the Combination MODIS\u002FSentinel-2, validation in a high contrast semi-arid agroecosystem. Remote Sensing 12(9):1453. https:\u002F\u002Fdoi.org\u002F10.3390\u002Frs12091453\nSchreiber U, Schliwa U, Bilger W (1986) Continuous recording of photochemical and non-photochemical chlorophyll fluorescence quenching with a new type of modulation fluorometer. Photosynth Res 10:51–62. https:\u002F\u002Fdoi.org\u002F10.1007\u002FBF00024185\nSobrino JA, Skoković D (2016) Permanent stations for calibration\u002Fvalidation of thermal sensors over Spain. Data 1(2):10. https:\u002F\u002Fdoi.org\u002F10.3390\u002Fdata1020010\nTrissl HW (1997) Determination of the quenching efficiency of the oxidized primary donor of Photosystem I, P700: implications for the trapping mechanism. Photosynth Res 54:237–240. https:\u002F\u002Fdoi.org\u002F10.1023\u002FA:1005981016835",{"EN":875},"Ledflex is a fluorometer adapted to measure chlorophyll fluorescence at the canopy level. It has been described in detail by Moya et al. (2019), Photosynthesis Research. \n                https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs11120-019-00642-9\n                \n              . We used this instrument to determine the effect of water stress on the fluorescence of a fescue field under extreme temperature and light conditions through a 12 days campaign during summer in a Mediterranean area. The fescue field formed part of a lysimeter station in \"las Tiesas,\" near Albacete-Spain. In addition to the fluorescence data, the surface temperature was measured using infrared radiometers. Furthermore, \"Airflex,\" a passive fluorometer measuring the filling-in of the atmospheric oxygen absorption band at 760 nm, was installed in an ultralight plane and flown during the most critical days of the campaign. We observed with the Ledflex fluorometer a considerable decrease of about 53% of the stationary chlorophyll fluorescence level at noon under water stress, which was well correlated with the surface temperature difference between the stressed and control plots. Airflex data also showed a decrease in far-red solar-induced fluorescence upon water stress in agreement with surface temperature data and active fluorescence measurements after correction for PS I contribution. 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MN, Sun J-D, Byrd GT, Brown H and Black CC (1993) Novel characteristics of cassava, Manihot esculenta Crantz, a reputed C3-C4 intermediate photosynthesis species. Photosynth Res 38: 61–72\nAono M, Kubo A, Saji H, Natori T, Tanaka K and Kondo N (1991) Resistance to oxygen toxicity of transgenic Nicotiana tabacum that expresses the gene for glutathione reductase from Escherichia coli. Plant Cell Physiol 32: 691–697\nArnon DI (1949) Copper enzymes in chloroplasts. Polyphenoloxidases in Beta vulgaris. Plant Physiol 24: 1–14\nBarber J and Andersson B (1992) Too much of a good thing: Light can be bad for photosynthesis. Trends Biochem Sci 17: 61–66\nBlack CC (1966) Chloroplast reactions with dipyridyl salts. Biochim Biophys Acta 120: 332–340\nBlack CC (1980) Sunbeams, pathways, and plants. Antioch Review 38: 436–448\nBowler C, VanMontagu M and Inzé D (1992) Superoxide dismutase and stress tolerance. Annu Rev Plant Physiol Plant Mol Biol 43: 83–116\nDemmig-Adams B and Adams WWIII (1992) Photoprotection and other responses of plants to high light stress. Annu Rev Plant Physiol Plant Mol Biol 43: 599–626\nDemmig B, Winter K, Kruger A and Czygan F-C (1987) Photoinhibition and zeaxanthin formation in intact leaves. A possible role of the xanthophyll cycle in the dissipation of excess light energy. Plant Physiol 84: 218–224\nDonald CM (1962) In search of yield. J Aust Inst Agric Sci 28: 171–178\nEvans LT (1975) The physiological basis of crop yield. In: Evans LT (ed) Crop Physiology, pp 327–355. Cambridge University Press, Cambridge, UK\nFoyer C, Lelandais M, Galap C and Kunert K (1991) Effects of elevated cytosolic glutathione reductase activity on the cellular pool and photosynthesis in leaves under normal and stress conditions. Plant Physiol 97: 862–872\nGilmore AM and Yamamoto HY (1991) Resolution of lutein and zeaxanthin using a non-endcapped, light carbon-loaded C18 high-performance liquid chromatography column. J Chromatog 543: 137–145\nGilmore AM and Yamamoto HY (1992) Dark induction of zeaxanthin-dependent non-photochemical quenching measured by ATP. Proc Natl Acad Sci USA 89: 1899–1903\nHallauer ARJr and Miranda Fo JB (1981) Quantitative Genetics in Maize Breeding. Iowa State University Press, Ames, IA\nKrause GH (1988) Photoinhibition of photosynthesis. An evaluation of damaging and protective processes. Plant Physiol 74: 566–574\nMelis A (1991) Dynamics of photosynthetic membrane composition and function. Biochim Biophys Acta 1105: 87–106\nMoss DN (1976) Studies on increasing photosynthesis in crop plants. In: Burris RH and Black CC (eds) CO2 Metabolism and Plant Productivity, pp 31–41. University Park Press, Baltimore\nMurata Y and Matsushima S (1976) Rice. In: Evans LT (ed) Crop Physiology, pp 73–99, Cambridge University Press, Cambridge, UK\nÖquist G, Anderson JM, McCaffery S and Chow WS (1992) Mechanistic differences in photoinhibition of sun and shade plants. Planta 188: 422–431\nRabinowitch EI (1951) Midday depression and adaptation phenomena. In: Photosynthesis, Vol II, Part 1, pp 873–876. Interscience Publishers Inc. New York\nRaven JA (1989) Fight or flight: the economics of repair and avoidance of photoinhibition of photosynthesis. Funct Ecol 3: 5–19\nRuban AV, Young AJ and Horton P (1993) Induction of nonphotochemical energy dissipation and absorbance changes in leaves. Plant Physiol 102: 741–750\nSen Gupta A, Heinen JL, Holaday AS, Burke JJ and Allen RD (1993) Increased resistance to oxidative stress in transgenic plants that over-express chloroplastic Cu\u002FZn superoxide dismutase. Proc Natl Acad Sci USA 90: 1629–1633\nSiefermann-Harms D (1984) Evidence for a heterogenous organization of violaxanthin in thylakoid membranes. Photochem Photobiol 40: 507–512\nThayer SS and Björkman (1990) Leaf xanthophyll content and composition in sun and shade determined by HPLC. Photosynth Res 23: 331–343\nTu ZP, Cai WJ, Lin XZ, Huang QM, Lu B and Ye LY (1990) Photoinhibition and rice productivity. Jiangsu J of Agr Sci 6: 1–15\nTu ZP, Yu ZY, Huang QM, Lin XZ, Cai WJ and Lu B (1989) Heterosis, photosynthetic efficiency and rice breeding for both high yield and good quality. Proc 6th Intl Cong of SABRAO, pp 725–726. TsuKuba, Japan\nWise RR, Frederick JR, Alm DM, Kramer DM, Hesketh JD, Crofts AR and Ort DR (1990) Investigations of limitations to photosynthesis induced by leaf water deficit in field-grown sunflower (Helianthus annuus L.). Plant Cell Environ 13: 923–931",{"EN":1040},"The hypothesis we propose is that during photosynthesis the balance between potentially detrimental and beneficial photochemically induced events can be tipped beneficially toward increased photosynthesis and toward increased crop yield. To test this hypothesis a procedure has been devised with the rice plant, Oryza sativa, that has resulted in increasing both canopy photosynthesis and rice grain yield. Two elite rice varieties selected independently in the contrasting environments of either South China or Texas, each with distinct photosynthetic traits, were crossed to produce a hybrid with an increased canopy photosynthesis and grain yield that is regularly 20 to 22% higher than the mid-yields of the parents. The photosynthetic and mechanisms which may contribute to these beneficial results in the hybrid rice are: a reduction of the midday depression of photosynthesis; a rapid development of the canopy for photosynthetic light interception and an increased canopy photosynthesis; increased amounts of carotenoids for the xanthophyll cycle; an increased protection against free radicals induced by paraquat treatment; a 6 to 12 day shorter plant reproductive life cycle; and a 8 to 10 day increase in the longevity of the flag leaf over the parents. While the hybrid rice has successfully integrated these and likely other unknown characteristics to increase both crop photosynthesis and grain yield, we propose that understanding the underlying beneficial photosynthetic mechanisms supporting these crop plant traits is worthy of thorough investigation and application in crop production.",{"EN":1042},"An integration of photosynthetic traits and mechanisms that can increase crop photosynthesis and grain production",{"VOID":1044},"10.1007\u002FBF00020427","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002FBF00020427",[1047,1062,1084,1096,1111],{"id":1048,"sortIndex":665,"researcher":18,"roles":1049,"affiliations":1050,"properties":1059},"0e2b1e52-c14f-4adc-a33b-c1cacf214610",[514],[1051],{"id":18,"sortIndex":19,"affiliation":1052,"properties":18},{"id":1053,"createTime":1054,"updateTime":1054,"relativeEntities":1055,"slug":18,"properties":1056,"entityType":63,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},"c218247f-a0cd-47a0-80cf-a3c99fb3c5f4","2023-12-30T20:47:32.125+00:00",[],{"title":1057},{"VI":1058},"University of Georgia, Biochemistry and Molecular Biology, Athens, USA",{"title":1060},{"VI":1061},"M. 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CRC Press, Boca Raton. USA\nAmbasht NK, Agrawal M (1998) Physiological and biochemical responses of Sorghum vulgare plants to supplemental ultraviolet UV-B radiation. Can J Bot 76:1–5\nAmudha P, Jayakumar M, Kulandaivelu G (2005) Impacts of ambient solar UV (280–400 nm) radiation on three tropical legumes. J Plant Biol 48:284–291\nArnon DI (1949) Copper enzyme in isolated chloroplasts polyphenoloxidase in Beta vulgaris. Plant Physiol 24:1–15\nBeinert H, Kok B, Hoch G (1962) The light induced electron paramagnetic resonance signal of photocatalyst P700. Biochem Biophys Res Comm 7:209–212\nBornman JF (1989) Target sites of UV-B radiation in photosynthesis of higher plants. J Photochem Photobiol B: Biol 4:145–158\nBrandell JR, Campbell WF, Sisson WB, Caldwell MM (1977) Net photosynthesis, electron transport capacity and ultra structure of Pisum sativum L. exposed to ultraviolet-B radiation. Plant Physiol 60:165–169\nCaldwell MM (1971) Solar ultraviolet irradiation and the growth and development of higher plants. In: Giese AC (ed) Photophysiology. Academic Press, New York, pp 131–177\nCaldwell MM, Ballare CL, Bornman JF, Flint SD, Bjorn LO, Tramura AH, Kulandaivelu G, Tevini M (2003) Terrestrial ecosystem, increased solar ultraviolet radiation and interactions with other climatic change factors. Photochem Photobiol Sci 2:29–38\nCommoner B, Townsend J, Pake G (1954) Free radicals in biological materials. Nature 174:689–691\nFrisco G, Spetea C, Giacometti GM, Vass I, Barato R (1994) Degradation photosystem II reaction center D1 polypeptide induced by UV-B radiation in isolated thylakoids. Identification and characterization of C- and N- terminal breakdown products. Biochem Biophys Acta 1184:78–84\nFrisco G, Vass I, Spetea C, Barber J, Barbarto R (1995) UV-B induced degradation of the D1 protein in isolated reaction centers of photosystem II. Biochem Biophys Acta 1231:41–46\nGovindjee (1995) Sixty three years since Kautsky. Chlorophyll a fluorescence. Aus J Plant Physiol 22:131–160\nGovindjee (2000) Milestones in photosynthesis. In: Yunus M, Pathre U, Mohanty P (eds) Probing photosynthesis. Taylor and Fransis, London, pp 9–39\nHideg E, Barbato R, Vass I (1993) In activation of photosynthetic oxygen evolution by UV-B irradiation. A thermoluminescence study. Photosynth Res 38:455–462\nIwanzik W, Tevini M, Dohnt G, Voss M, Weiss W (1983) Action of UV-B radiation on photosynthetic primary reactions in spinach chloroplasts (Spinacia oleracea). Physiol Plant 58:401–407\nJajoo A, Bharti S, Govindjee (1998) Inorganic anions induce state changes in spinach thylakoid membranes. FEBS Lett 434:193–196\nKulandaivelu G, Neduchezhian N, Annamalainathan K (1991) Ultraviolet-B (280–320 nm) radiation induced changes in photochemical activities and polypeptide components of C3 and C4 chloroplasts. Photosynthetica 25:333–339\nLowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with folin phenol reagent. Biol Chem 193:265–275\nMohanty P (1985) Dynamics of electron flow between two photosystems. Effect of light intensity on steady state signal I in spinach choloroplasts. In: Srivastava SL (ed) Interface in physical and biological sciences symposium volume, Proc Natl Acad Sci India, 55A, pp 135–145\nNiyogi KK (1999) Photoprotection revisited: genetics and molecular approaches. Ann Rev Plant Physiol 50:333–359\nNoorudeen AM, Kulandaivelu G (1982) On the possible site of inhibition of photosynthetic electron transport by ultraviolet-B radiation. Physiol Plant 55:161–166\nRajagopal S, Jha IB, Murthy SD, Mohanty P (1998) Ultraviolet- B effects on Spirulina platensis cells: modification of chromophore–protein interaction and energy transfer characteristics of phycobilisomes. Biochem Biophys Res Com 249:172–177\nStrid A, Chow WS, Anderson JM (1994) UV-B damage and protection at the molecular level in plants. Photosynth Res 39:475–489\nStrasser RJ, Srivastava A, Tsimilli-Michael M (2000) The fluorescence transient as a tool to characterize and screen photosynthetic samples. In: Yunus M, Pathre U, Mohanty P (eds) Probing photosynthesis: mechanism regulation and adaptation. Taylor and Francis, London, pp 445–483\nTeramura AH (1983) Effects of ultraviolet radiation on the growth and yield of crop plants. Physiol Plant 58:415–427\nTeramura AH, Sullivan JH (1994) Effects of UV-B radiation on photosynthesis and growth of terrestrial plants. Photosynth Res 39:463–473\nTeramura AH, Ziska LH (1996) Ultraviolet-B radiation and photosynthesis. In: Baker NR (ed) Photosynthesis and the environment. Kluwer Academic Publisher, Dordrecht, the Netherlands, pp 435–450\nTevini M (2004) Plant responses to ultraviolet radiation stress. In: Papageorgiou GC, Govindjee (eds) Chlorophyll a fluorescence a signature of photosynthesis. Springer, The Netherlands, pp 605–621\nTevini M, Teramura AH (1989) UV-B effects on terrestrial plants. Photochem Photobiol 50:479–487\nTrebst A, Depka B (1990) Degradation of D1 protein subunit of photosystem II in isolated thylakoids by UV light. Z Naturforsch 45:765–771\nVaralakshmi D, Lakshmi N, Guruprasad KN (2003) Physiological changes in soybean Cv. JS 71-05 after the exclusion of UV-A and UV-B from the solar radiation. Indian J Plant Physiol (Special Issue):602–606\nXiong FS, Day TA (2001) Effect of solar ultraviolet-B radiation during spring time ozone depletion on photosynthesis and biomass production of Antarctic vascular plants. Plant Physiol 125:738–751\nZiska L H, Teramura AH, Sullivan JH, McCoy A (1993) Influence of ultraviolet –B radiation on photosynthetic and growth characteristics in field grown cassava (Manihot esculentum Crantz). Plant Cell Environ 16:73–79",{"EN":1168},"Exclusion of UV (280–380 nm) radiation from the solar spectrum can be an important tool to assess the impact of ambient UV radiation on plant growth and performance of crop plants. The effect of exclusion of UV-B and UV-A from solar radiation on the growth and photosynthetic components in soybean (Glycine max) leaves were investigated. Exclusion of solar UV-B and UV-B\u002FA radiation, enhanced the fresh weight, dry weight, leaf area as well as induced a dramatic increase in plant height, which reflected a net increase in biomass. Dry weight increase per unit leaf area was quite significant upon both UV-B and UV-B\u002FA exclusion from the solar spectrum. However, no changes in chlorophyll a and b contents were observed by exclusion of solar UV radiation but the content of carotenoids was significantly (34–46%) lowered. Analysis of chlorophyll (Chl) fluorescence transient parameters of leaf segments suggested no change in the F\n                        v\u002FF\n                        m value due to UV-B or UV-B\u002FA exclusion. Only a small reduction in photo-oxidized signal I (P700+)\u002Funit Chl was noted. Interestingly the total soluble protein content per unit leaf area increased by 18% in UV-B\u002FA and 40% in UV-B excluded samples, suggesting a unique upregulation of biosynthesis and accumulation of biomass. Solar UV radiation thus seems to primarily affect the photomorphogenic regulatory system that leads to an enhanced growth of leaves and an enhanced rate of net photosynthesis in soybean, a crop plant of economic importance. 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Furthermore, Fe(II) cations can substitute for 1 or 2Mn cations (pH dependent) in Ca-depleted PSII membranes (Semin et al. in Journal of Bioenergetics and Biomembranes 48:227, 2016; Semin et al. in Journal of Photochemistry and Photobiology B 178:192, 2018). In the current study, we examined the effect of Ca2+ cations on the interaction of Fe(II) ions with Mn-depleted [PSII(-Mn)] and Ca-depleted [PSII(-Ca)] photosystem II membranes. We found that Ca2+ cations (about 50 mM) inhibit the light-dependent oxidation of Fe(II) (5 µM) by about 25% in PSII(-Mn) membranes, whereas inhibition of the blocking process is greater at about 40%. Blocking of the HA site by Fe cations also decreases the rate of charge recombination between QA− and YZ•+ from t1\u002F2 = 30 ms to 46 ms. However, Ca2+ does not affect the rate during the blocking process. An Fe(II) cation (20 µM) replaces 1Mn cation in the Mn4CaO5 catalytic cluster of PSII(-Ca) membranes at pH 5.7 but 2 Mn cations at pH 6.5. In the presence of Ca2+ (10 mM) during the substitution process, Fe(II) is not able to extract Mn at pH 5.7 and extracts only 1Mn at pH 6.5 (instead of two without Ca2+). Measurements of fluorescence induction kinetics support these observations. Inhibition of Mn substitution with Fe(II) cations in the OEC only occurs with Ca2+ and Sr2+ cations, which are also able to restore oxygen evolution in PSII(-Ca) samples. Nonactive cations like La3+, Ni2+, Cd2+, and Mg2+ have no influence on the replacement of Mn with Fe. These results show that the location and\u002For ligand composition of one Mn cation in the Mn4CaO5 cluster is strongly affected by calcium depletion or rebinding and that bound calcium affects the redox potential of the extractable Mn4 cation in the OEC, making it resistant to reduction.",{"EN":1787},"Ca2+ effects on Fe(II) interactions with Mn-binding sites in Mn-depleted oxygen-evolving complexes of photosystem II and on Fe replacement of Mn in Mn-containing, Ca-depleted complexes",{"VOID":1789},"10.1007\u002Fs11120-020-00813-z","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs11120-020-00813-z","https:\u002F\u002Flink.springer.com\u002Fcontent\u002Fpdf\u002F10.1007\u002Fs11120-020-00813-z.pdf",[1793,1808,1823,1835],{"id":1794,"sortIndex":553,"researcher":18,"roles":1795,"affiliations":1796,"properties":1805},"5cd50aa0-899d-4c9b-86d2-9d139a08052c",[514],[1797],{"id":18,"sortIndex":19,"affiliation":1798,"properties":18},{"id":1799,"createTime":1800,"updateTime":1800,"relativeEntities":1801,"slug":18,"properties":1802,"entityType":63,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},"ccca4ad0-64f8-42cb-a51e-9d92e739a0b2","2024-01-20T23:54:11.886+00:00",[],{"title":1803},{"VI":1804},"Laboratory, BioEnergy Sciences and Technology Directorate, National Renewable Energy, Golden, USA",{"title":1806},{"VI":1807},"Seibert, M.",{"id":1809,"sortIndex":284,"researcher":18,"roles":1810,"affiliations":1811,"properties":1820},"58868e9c-3a33-4e08-9594-1d2ca7bf059a",[514],[1812],{"id":18,"sortIndex":19,"affiliation":1813,"properties":18},{"id":1814,"createTime":1815,"updateTime":1815,"relativeEntities":1816,"slug":18,"properties":1817,"entityType":63,"verifyStatus":17,"verifyTime":18,"verifyNote":18,"syncStatus":17,"languages":18,"translateLanguages":18,"viewCount":19},"7f4e939f-b2bb-40b0-a677-857975d05d18","2024-01-08T16:30:49.004+00:00",[],{"title":1818},{"VI":1819},"Department of Biophysics, Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia",{"title":1821},{"VI":1822},"Davletshina, L. 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