Abstract
The Núcleo de Estudos da Fotossíntese (NEF) of the Universidade Federal do Espirito Santo studied the regulation of photosynthesis in J. curcas accessions from different regions of Brazil and the world. The effects of environmental variations of stress factors, such as rainfall and temperature, on the kinetics of chlorophyll a fluorescence (CF) induction in leaves of three genotypes, Janaúba (NEF 01), CPATSA 1501 (NEF 02), and CPATSA C2/10 (NEF 03), were investigated for 4 years. High performance of photosystem II, transpiration rate, and rate of net CO2 assimilation were observed mainly in the NEF 02 accession. Since it was necessary to understand the dependence of tolerance mechanisms to diverse environmental stresses, the NEF team followed the development of these plants in several locations. The coastal region presents warm humid tropical climate, in contrast with an inland region where the temperature is very hot in the summer and cold in winter with extremes around 8 °C. The development of J. curcas plants was affected by the level of photosynthetically active radiation, seasonality of temperature and precipitation, casting doubt on the agroclimatic zoning, which meant that physiological variables needed to be considered. The plants with the best yield were those grown in the inland region, although the photochemical efficiency (PIABS and PITOTAL) and the net assimilation of CO 2 (A) of the plants in the coastal region were higher. The molecular mechanisms underlying the species adaptability may serve for modeling plant traits in order to maximize biofuel production and improve the agronomic features.
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References
Allen DJ, Ratner K, Giller YE et al (2000) An overnight chill induces a delayed inhibition of photosynthesis at midday in mango (Mangifera indica L.). J Exp Bot 51(352):1893–1902
Ao P-X, Li Z-G, Fan D-M et al (2013) Involvement of antioxidant defense system in chill hardening induced chilling tolerance in Jatropha curcas seedlings. Acta Physiol Plant 35:153–160
Brestic M, Zivcak M, Kalaji HM et al (2012) Photosystem II thermo stability in situ: environmentally induced acclimation and genotype-specific reactions in Triticum aestivum L. Plant Physiol Biochem 57:93–105
Chen Z, Higgins JD, Hui JTL et al (2011) Retinoblastoma protein is essential for early meiotic events in Arabidopsis. Eur Mol Biol Org J 30:744–755
Christen D, Schönmann S, Jermini M et al (2007) Characterization and early detection of grapevine (Vitis vinifera) stress responses to esca disease by in situ chlorophyll fluorescence and comparison with drought stress. Environ Exp Bot 60:504–514
Collares DG (2012) Empresa Brasileira de Pesquisa Agropecuária [Internet]. Espirito Santo: Incentivos para pinhão-manso apresentados em Fórum no Espírito Santo [cited 2018 May 01]. Available from: http://www.cnpa.embrapa.br/noticias/2012/noticia_20120718_1.html. (Portuguese)
Deng X, Hu Z, Wang H et al (2003) A comparison of photosynthetic apparatus of the detached leaves of the resurrection plant Boea hygrometrica with its non-tolerant relative Chirita heterotrichia in response to dehydration and rehydration. Plant Sci 165:851–861
Falqueto AR, Silva Júnior RA, Gomes MTG et al (2017) Effects of drought stress on chlorophyll a fluorescence in two rubber tree clones. Sci Hort 224:238–243
Feitosa N, Garcia LM, Zonetti PC et al (2009) Levantamento de espécies de plantas daninhas na cultura do pinhão manso (Jatropha curcas L., Euphorbiaceae): VI Encontro Internacional de Produção Cientifica Cesumar; Maringá, Paraná (Portuguese)
Flood PJ, Harbinson J, Aarts MG (2011) Natural genetic variation in plant photosynthesis. Trends Plant Sci 16:327–335
Galazzi EB (2011) Desempenho fotossintético de plantas de Jatropha curcas L. cultivadas no estado do Espirito Santo. Dissertation, Universidade Federal do Espírito Santo, Vitória (Portuguese)
Galazzi EB, Silva DM (2011) Eficiência fotossintética em plantas de pinhão manso cultivadas em distintas áreas no Estado do Espírito Santo. Anais do II Congresso Brasileiro de Pesquisas de Pinhão-Manso; Brasília, Distrito Federal (Portuguese)
Gama VN, Cunha JT, Lima IM et al (2013) Photosynthetic characteristics and quality of five passion fruit varieties under field conditions. Acta Physiol Plant 35:941–948
Gasparini XSS, Santos TA, Silva LF et al (2015) Phenotypic plasticity of Jatropha curcas L. and chlorophyll a fluorescence: Anais do XV Brazilian Congress of Plant Physiology, Campinas, São Paulo
Genty B, Briantais JM, Baker NR (1989) The relationship between photosystem II efficiency and quantum of yield photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990:87–92
Guidi L, Calatayud A (2014) Non-invasive tools to estimate stress-induced changes in photosynthetic performance in plants inhabiting Mediterranean areas. Environ Exp Bot 103:42–52
Ilik P, Schansker G, Kotabova E et al (2006) A dip in the chlorophyll fluorescence induction at 0.2–2s in Trebouxia-possessing lichens reflects a fast reoxidation of photosystem I. A comparison with higher plants. Biochim Biophys Acta 1757:12–20
Kalaji HM, Jajoo A, Oukarroum A et al (2016) Chlorophyll a fluorescence as a tool to monitor physiological status of plants under abiotic stress conditions. Acta Physiol Plant 38:102. https://doi.org/10.1007/s11738-016-2113-y
Kelley LA, Gardner SP, Sutcliffe MJ (1996) An automated approach for clustering an ensemble of NMR-derived protein structures into conformationally related subfamilies. Protein Eng 9:1063–1065
Laviola BG, Rosado TB, Bhering LL et al (2010) Genetic parameters and variability in physic nut accessions during early developmental stages. Pesq Agropec Bras 45(10):1117–1123 (Portuguese)
Lazár D (2013) Simulations show that a small part of variable chlorophyll a fluorescence originates in photosystem I and contributes to overall fluorescence rise. J Theor Biol 335:249–264
Li Z-G, Yuan L-X, Wang Q-L et al (2013) Combined action of antioxidant defense system and osmolytes in chilling shock-induced chilling tolerance in Jatropha curcas seedlings. Acta Physiol Plant 35:2127–2136
Long SP, Humphries S, Falkowski PG (1994) Photoinhibition of photosynthesis in nature. Ann Rev Plant Physiol Plant Mol Biol 45:633–662
Machado MIP, Laviola BG (2011) Estudo bibliométrico da produção científica em pinhão manso no web of ciência no período de 1945 a 2011: II Congresso Brasileiro De Pesquisa De Pinhão-Manso; novembro de 2011; Brasília, Distrito Federal (Portuguese)
Maxwell K, Johnson GN (2000) Chlorophyll fluorescence: a practical guide. J Exp Bot 51:659–668
Morales-Flores F, Aguilar MI, King-Díaz B et al (2013) Derivatives of diterpen labdane-8a, 15-diol as photosynthetic inhibitors in spinach chloroplasts and growth plant inhibitors. J Photochem Photobiol 125:42–50
Neuner G, Larcher W (1991) The effect of light, during and subsequent to chilling, on the photosynthetic activity of two soybean cultivars, measured by in vivo chlorophyll fluorescence. Photosynthetica 25(2):257–266
Ohada I, Berg A, Berkowicz SM et al (2011) Photoinactivation of photosystem II: is there more than one way to skin a cat? Physiol Plant 142:79–86
Oliveira PS, Pereira LS, Silva DC et al (2018) Hydraulic conductivity in stem of young plants of Jatropha curcas L. cultivated under irrigated or water deficit conditions. Ind Crop Prod 116:15–23
Osmond B (2014) Our eclectic adventures in the slower eras of photosynthesis: from New England down under to biosphere 2 and beyond. Annu Rev Plant Biol 65:1–32
Parker WC, Mohammed GH (2000) Photosynthetic acclimation of shade-grown red pine (Pinus resinosa Ait.) seedlings to a high light environment. New For 19:1–11
Pezzopane JEM, Castro FS, Pezzopane JRM et al (2012) Agrometeoreologia: aplicações para o Espírito Santo. Alegre, Espirito Santo, Caufes (Portuguese)
Prado AKS (2007) Florescimento e frutificação em laranjeiras ‘Valência’ com diferentes cargas de frutos e submetidas ou não à irrigação. Brag Camp 66(2):173–182
Rungrat T, Awlia M, Brown T et al (2016) Using phenomic analysis of photosynthetic function for abiotic stress response gene discovery. In: The arabidopsis book. The American Society of Plant Biologists. https://doi.org/10.1199/tab.0185
Santos CM (2008) Fenologia e capacidade fotossintética do pinhão-manso (Jatropha curcas L.). Dissertation, Universidade Federal de Alagoas, Rio Largo (Portuguese)
Santos TA, Tessari LFA, Tonetti Júnior P et al (2012) Respostas fotossintéticas de três genótipos de pinhão manso analisados em condições de campo no município de Santa Teresa/ES: Anais do 5° Congresso da Rede Brasileira de Tecnologia de Biodiesel e 8° Congresso Brasileiro de Plantas Oleaginosas, Óleos, Gorduras e Biodiesel; Salvador, Bahia (Portuguese)
Santos TA, Gasparini XSS, Tessari LFA et al (2014) Photosynthetic efficiency and chlorophyll fluorescence of Jatropha curcas L. in greenhouse and field: 16th international congress on photobiology. Universidad Nacional de Córdoba, Argentina, Córdoba, p 56
Schansker G, Tóth SZ, Holzwarth AR et al (2013) Chlorophyll a fluorescence: beyond the limits of the QA model. Photosynth Res 5:1–7
Schock AA, Ramm A, Martinazzo EG et al (2014) Crescimento e fotossíntese de plantas de pinhão-manso cultivadas em diferentes condições de luminosidade. Rev Bras Engenharia Agrícola Ambient Campina Grande 18:3–9 (Portuguese)
Schreiber U, Schliwa U, Bilger W (1986) Continuous recording of photochemical and non-photochemical chlorophyll fluorescence quenching with a new type of modulated fluorometer. Photosynth Res 10:51–62
SEAG (2009) Secretaria de Estado da Agricultura, Abastecimento, Aquicultura e Pesca. Aspectos fitofisionômicos [Internet]. 2009 June [cited 2009 Jun 20]. Available from: www.seag.es.gov.br/setores/silvicultura. (Portuguese)
Singh P, Singh S, Mishra SP et al (2010) Molecular characterization of genetic diversity in Jatropha curcas L. Genes Genomes Genomics 4:1–8
Souza A, Wang J-Z, Dehesh K (2017) Retrograde signals: integrators of interorganellar communication and orchestrators of plant development. Annu Rev Plant Biol 68:85–108
Stirbet A (2013) Excitonic connectivity between photosystem II units: what is it, and how to measure it? Photosynth Res 116:189–214
Stirbet A, Govindjee (2012) Chlorophyll a fluorescence induction: a personal perspective of the thermal phase, the J-I-P rise. Photosynth Res 113:15–61
Stirbet A, Riznichenko GY, Rubin AB et al (2014) Modeling chlorophyll a fluorescence transient: relation to photosynthesis. Biochemistry 79(4):291–323
Stirbet A, Lazár D, Kromdijk J et al (2018) Chlorophyll a fluorescence induction: can just a one-second measurement be used to quantify abiotic stress responses? Photosynthetica 56:86–104
Strasser RJ, Govindjee (1991) The F0 and the O-J-I-P fluorescence rise in higher plants and algae. In: Argyroudi-Akoyunoglou JH (ed) Regulation of chloroplast biogenesis. Plenum Press, New York, pp 423–426
Strasser RJ, Strasser BJ (1995) Measuring fast fluorescence transients to address environmental questions: the JIP test. In: Mathis P (ed) Photosynthesis: from light to biosphere, V. Kluwer Academic Publishers, Dordrecht, pp 977–980
Strasser RJ, Srivastava A, Tsimilli-Michael M (1999) Screening the vitality and photosynthetic activity of plants by fluorescence transient. In: Behl RK, Punia MS, Lather BPS (eds) Crop improvement for food security. SSARM, Hisar, pp 79–126
Strasser RJ, Srivastava A, Tsimilli-Michael M (2000) The fluorescent transient as a tool to characterise and screen photosynthesic samples. In: Yunus M, Pathre U, Mohanty P (eds) Probing photosynthesis: mechanisms, regulation and adaptation. Taylor and Francis, London, pp 445–483
Strasser RJ, Tsimilli-Michael M, Srivastava A (2004) Analysis of the chlorophyll a fluorescence transient. In: Papageorgiou GC (ed) Chlorophyll a fluorescence: a signature of photosynthesis-advances in photosynthesis and respiration. Springer, Rotterdam, pp 321–362
Strasser RJ, Tsimilli-Michael M, Qiang S et al (2010) Simultaneous in vivo recording of prompt and delayed fluorescence and 820-nm reflection changes during drying and after rehydration of the resurrection plant Haberlea rhodopensis. Biochim Biophys Acta 1797:1313–1326
Tanya P, Taeprayoon P, Hadkam Y et al (2011) Genetic diversity among Jatropha and Jatropha-related species based on ISSR markers. Plant Mol Biol Rep 29:252–264
Tessari LFA, Santos TA, Sabino DSG et al (2012) Plasticidade fenotípica de três genótipos de pinhão manso em resposta à temperatura: Anais do 5° Congresso da Rede Brasileira de Tecnologia de Biodiesel e 8° Congresso Brasileiro de Plantas Oleaginosas, Óleos, Gorduras e Biodiesel; Salvador, Bahia (Portuguese)
Toledo JV, Martins LD, Klippel VH et al (2009) Zoneamento agroclimático para a cultura do pinhão manso (Jatropha curcas L.) e da mamona (Ricinus communis L.) no estado do Espírito Santo. ACSA – Agrop Cient Semi-Árido 5:41–51 (Portuguese)
Tsimilli-Michael M, Strasser RJ (2008) Experimental resolution and theoretical complexity determine the amount of information extractable from the chlorophyll fluorescence transient OJIP. In: Allen JF, Gantt E, Golbeck JH, Osmond B (eds) Photosynthesis. Energy from the sun: 14th international congress on photosynthesis. Springer, Dordrecht, pp 697–701
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Silva, D.M., Santos, R.N., Damasceno, P.C. (2019). Can One Use Chlorophyll A Fluorescence as a Physiological Marker of Jatropha curcas L.?. In: Mulpuri, S., Carels, N., Bahadur, B. (eds) Jatropha, Challenges for a New Energy Crop. Springer, Singapore. https://doi.org/10.1007/978-981-13-3104-6_15
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