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Indian Journal of Science and Technology

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2018

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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All

Ometto, Jean P.

Interannual Variation in Temperature and Rainfall can Modulate the Physiological and Photoprotective Mechanisms of a Native Semiarid Plant Species

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Authors

Ana C. B. Pinho-Pessoa ¹, Keila R. Mendes ¹, Alfredo Jarma-Orozco ², Marcos P. S. Pereira ³, Marcos A. Santos ¹, Romulo S. C. Menezes ⁴, Jean P. Ometto ⁵, Eugenia C. Pereira ⁶, Marcelo F. Pompelli ¹

Affiliations
1 Department of Botany, Plant Physiology Laboratory, Federal University of Pernambuco, CB, Recife, PE, 50670901, BR
2 University of Cordoba, Monteria, CO
3 Federal University of Alagoas, Institute of Atmospheric Sciences, Maceió, Alagoas, BR
4 Department of Nuclear Energy, Federal University of Pernambuco, Recife, Pernambuco, BR
5 Brazilian Institute for Space Research, Earth System Science Centre, Sao Jose dos Campos, SP, BR
6 Department of Geographical Sciences, Federal University of Pernambuco, Recife, Pernambuco, BR

Source

Indian Journal of Science and Technology, Vol 11, No 41 (2018), Pagination: 1-17

Abstract

Climate change may affect ecosystems worldwide, but can be aggravated in arid environments, leading to decreased rainfall and a consequent increase in air temperature. Objective: The present investigation aimed to study the behavior of a native plant, adapted to seasonal dry conditions, when faced with different conditions in two years: one extremely dry and the other with rains within the expected range. Methods/Analysis: To study the effects of the seasonal water deficiency, we collected all data in two consecutive years: 2012 and 2013. Results: In both years, we obtained data in May (rainy season) and August (dry season). The predawn water potential ( Ψ_w) ranged from -5.6 to -4.2 MPa in 2012 and from-2.16 to -2.98 MPa in 2013. These patterns show that even in the rainy season of the dry year, the plants were subjected to a very high water deficit when compared to the wet year; this was due to the sparse rains of 2012, the driest year of the preceding decade in the study area. All gas exchange and carbon uptake tended to zero in 2012; however, all the parameters recovered when the rains returned in 2013. Considering the entire data set, the water use efficiency (WUE) data presented a positive and significant correlation with all the photosynthetic parameters. However, when we excluded the 2012 data, the WUE was negatively correlated with transpiration (E ), stomatal conductance ( g_s ) and leaf temperature ( T_leaf ). One average, the potential photosynthesis (P_N-pot), maximum carboxylation velocity of Rubisco ( V_c-max ) and the maximum electron transport rate ( J_max ) values were on average 62%, 50% and 63% lower in the dry season than in rainy season in 2013. Discussion/Conclusions: We argue that the increase of intercellular carbon caused the increase in photosynthesis to its limitation point of photosynthesis by J_max . Below the collimation point, the photosynthetic rates were limited by V_c-max . Thus, the prolongation of the dry season could have potential impacts on the electron transport rate and on Rubisco carboxylation efficiency, taking into account the current concentrations of atmospheric carbon dioxide. During a prolonged drought, the reduced Ψ_w , osmotic adjustment and efficient antioxidative system appear to be the main strategies that C. pyramidale uses to avoid fatal plant dehydration, maintaining basal rates of net photosynthesis. However, with the intensification of climate changes expected for the study area, the species may no longer be a symbol of the ecosystem but rather a symbol of environmental degradation.

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References

Living with climate change: Welcome to the new normal. Available from: https://www.newscientist.com/article/mg23431310-200-living-with-climate-change-welcome-to-the-new-normal/. Date accessed: 21/06/2017.

Distefano T, Kelly S. Are we in deep water? Water scarcity and its limits to economic growth. Ecological Economics. 2017; 142(1):130-47. https://doi.org/10.1016/j.ecolecon. 2017.06.019

Schleuning M, Frund J, Schweiger O, Weld E, Albrecht J, Albrecht M, Beil M, Benadi G, Bluthgen N, Bruelheide H, Bohning-Gaese K, Dehling DM, Dormann CF, Exeler N, Farwig N, Harpke A, Hickler T, Kratochwil A, Kuhlmann M, Kuhn I, Michez D, Mudri-Stojnic S, Plein M, Rasmont P, Schwabe A, Settele J, Vujic A, Weiner CN, Wiemers M, Hof C. Ecological networks are more sensitive to plant than to animal extinction under climate change. Nature Communication. 2016; 7(1):1-9. https://doi.org/10.1038/ncomms13965

Glotfelty T, Zhang Y. Impact of future climate policy scenarios on air quality and aerosol-cloud interactions using an advanced version of CESM/CAM5: Part II. Future trend analysis and impacts of projected anthropogenic emissions. Atmospheric Environment. 2017; 152(1):531-52. https://doi.org/10.1016/j.atmosenv.2016.12.034

Ciancio A, Mukerji KG. Concept for plant protection in changing tropical environments. Ciancio A, Mukerji KG, editors. General Concepts in Integrated Pest and Disease Management. The Netherlands. Springer. 2007; p. 1-53. https://doi.org/10.1007/978-1-4020-6061-8_4 https://doi.org/10.1007/978-1-4020-6061-8

Antunes WC, Mendes KR, Chaves ARM, Ometto JP, Jarma- Orozco A, Pompelli MF. Spondia stuberosa trees grown in tropical, wet environments are more susceptible to drought than those grown in arid environments. Revista Colombiana de Ciencias Pecuarias. 2016; 10(1):9-27.

Gatti LV, Gloor M, Miller JB, Doughty CE, Malhi Y, D LG, B LS, M A, C CSC, Borges VF, Freitas S, Braz R, Anderson LO, Rocha H, Grace J, Phillips OL, Lloyd J. Drought sensitivity of Amazonian carbon balance revealed by atmospheric measurements. Nature. 2014; 506(7486):76-83. https://doi.org/10.1038/nature12957 PMid:24499918

Flood PJ, Hancock AM. The genomic basis of adaptation in plants. Current Opinion in Plant Biology. 2017; 36(1):88-94. https://doi.org/10.1016/j.pbi.2017.02.003 PMid:28242535

Giday H, Kjaer KH, Fanourakis D, Ottosen C-O. Smaller stomata require less severe leaf drying to close: A case study in Rosa hydrida. Journal of Plant Physiology. 2013; 170(15):1309-16. https://doi.org/10.1016/j.jplph.2013.04.007 PMid:23726470

Fanourakis D, Heuvelink E, Carvalho SMP. A comprehensive analysis of the physiological and anatomical components involved in higher water loss rates after leaf development at high humidity. Journal of Plant Physiology. 2013; 170(10):890-8. https://doi.org/10.1016/j.jplph.2013.01.013 PMid:23474196

Camargos Antunes W, Rego Mendes K, Rodrigues de Melo Chaves A, Ometto JP, Jarma-Orozco A, Pompelli MF. Spondias tuberosa trees grown in tropical, wet environments are more susceptible to drought than those grown in arid environments. Revista Colombiana de Ciencias Horticolas. 2016; 10(1).

Hsie BS, Mendes KR, Antunes WC, Endres L, Campos MLO, Souza FC, Santos ND, Singh B, Arruda ECP, Pompelli MF. Jatropha curcas L. (Euphorbiaceae) modulates stomatal traits in response to leaf-to-air vapor pressure deficit. Biomass Bioenergy. 2015; 81(1):273-81. https://doi.org/10.1016/j.biombioe.2015.07.014

Antunes WC, Daloso DM, Pinheiro DP, Williams TCR, Loureiro ME. Guard cell-specific down-regulation of the sucrose transporter SUT1 leads to improved water use efficiency and reveals the interplay between carbohydrate metabolism and K+accumulation in the regulation of stomatal opening. Environmental and Experimental Botany. 2017; 135(1):73-85. https://doi.org/10.1016/j.envexpbot. 2016.12.004

Santos CM, Verissimo V, Wanderley-Filho HCL, Ferreira VM, Cavalcante PGS, Rolim EV, Endres L. Seasonal variations of photosynthesis, gas exchange, quantum efficiency of photosystem II and biochemical responses of Jatropha curcas L. grown in semi-humid and semi-arid areas subjeted to water stress. Industrial Crops and Products. 2013; 41(1):203-13. https://doi.org/10.1016/j.indcrop.2012.04.003

Drake PL, Froend RH, Franks PJ. Smaller, faster stomata: scaling of stomatal size, rate of response, and stomatal conductance. Journal of Experimental Botany. 2013; 64(2):495-505. https://doi.org/10.1093/jxb/ers347 PMid:23264516 PMCid:PMC3542046

Mate CJ, Hudson GS, von Caemmerer S, Evans JR, Andrews TJ. Reduction of ribulose bisphosphate carboxylase activase levels in tobacco (Nicotiana tabacum) by antisense RNA reduces ribulose bisphosphate carboxylase carbamylation and impairs photosynthesis. Plant Physiology. 1993; 102(4):1119-28. https://doi.org/10.1104/pp.102.4.1119 PMid:8278543 PMCid:PMC158896

Basher L, Elliot SAH, Tait A, Page M, Rosser B, McIvor I, Douglas G, Jones H. Impacts of climate change on erosion and erosion control methods - A critical review. Wellington, New Zealand: Ministry for Primary Industries. 2012.

Sohngen B, Tian X. Global climate change impacts on forests and markets. Policy Economics. 2016; 72(1):18-26. https://doi.org/10.1016/j.forpol.2016.06.011

Kirilenko AP, Sedjo RA. Climate change impacts on forestry. Proceedings of the National Academy of Sciences of the United States of America. 2007; 104(50):19697-702. https://doi.org/10.1073/pnas.0701424104 PMid:18077403 PMCid:PMC2148360

O’Neill BC, Oppenheimer M, Warren R, Hallegatte S, Kopp RE, Porter HO, Scholes R, Birkmann J, Foden W, Licker R, Mach KJ, Marbaix P, Mastrandrea MD, Price J, Takahashi K, van Ypwesele J-P, Yoke G. IPCC reasons for concern regarding climate change risks. Nature Clim Change. 2017; 7(1):28-37. https://doi.org/10.1038/nclimate3179

Santos MG, Oliveira MT, Figueiredo KV, Falcao HM, Arruda ECP, Almeida-Cortez JS, Sampaio EVSB, Ometto JPHB, Menezes RSC, Oliveira AFM, Pompelli MF, Antonino ACD. Caatinga, the Brazilian dry tropical forest: can it tolerate climate changes? Theoretical and Experimental Plant Physiology. 2014; 26(1):83-99. https://doi.org/10.1007/s40626-014-0008-0

Pereira MPS, Justino F, Malhado ACM, Barbosa H, Marengo JA. The influence of oceanic basins on drought and ecosystem dynamics in northeast Brazil. Environment Research Letter. 2014; 9(1):1-9. https://doi.org/10.1088/17489326/9/12/124013

Scholander PF, Bradstreet ED, Hemmingsen EA, Hammel HT. Sap pressure in vascular plants negative hydrostatic pressure can be measures in plants. Science. 1965; 148(1):339-46. https://doi.org/10.1126/science.148.3668.339 PMid:17832103

Mendes KR, Granja JAA, Ometto JP, Antonino ACD, Menezes RSC, Pereira EC, Pompelli MF. Croton blanchetianus modulates its morphophysiological responses to tolerate drought in a tropical dry forest. Functional Plant Biology. 2017; 44(10):1039-51. https://doi.org/10.1071/FP17098

Farquhar GD, von Caemmerer S, Berry JA. A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta. 1980; 149(1):78-90. https://doi.org/10.1007/ BF00386231 PMid:24306196

Medlyn BE, Badeck F-W, De Pury DGG, Barton CVM, Broadmeadow M, Ceulemans R, De Angelis P, Forstreuter M, Jach ME, Kellomaki S, Laitat E, Marek M, Philippot S, Rey A, Strassemeyer J, Laitinen K, Liozon R, Portier B, Roberntz P, Wang K, Jarvis PG. Effects of elevated [CO2] on photosynthesis in European forest species: a metaanalysis of model parameters. Plant Cell Environment.1999; 22(12):1475-95. https://doi.org/10.1046/j.1365-3040.1999.00523.x

Pompelli MF, Antunes WC, Ferreira DTRG, Cavalcante PPGS, Wanderley-Filho HCL, Endres L. Allometric models for non-destructive leaf area estimation of the Jatropha curcas. Biomass Bioenergy. 2012; 36(1):77-85. https://doi.org/10.1016/j.biombioe.2011.10.010

Dubois M, Gilles KA, Hamilton JK, Reders PA, Smith F. Colorimetric method for determination of sugars and related substances. Analytical Chemistry. 1956; 28(3):3506. https://doi.org/10.1021/ac60111a017

Moore S, Stein WH. A modified ninhydrin reagent for the photometric determination of amino acids and related compounds. Journal of Biology Chemistry. 1954; 221(2):907-13.

Pompelli MF,Franca SCS, Tigre RC, Oliveira MT, Sacilot M, Pereira ECG. Spectrophotometric determinations of chloroplastidic pigments in acetone, ethanol and dimethylsulphoxide. Brazilian Journal of Biological Sciences. 2013; 11(1):52-8.

Bates LS, Waldren RP, Teare ID. Rapid determination of free proline for water-stress studies. Plant Soil. 1973; 39(1):2057. https://doi.org/10.1007/BF00018060

Campos MLO, Hsie BS, Granja JAA, Correia RM, Silva SRS, Almeida-Cortez JS, Pompelli MF. Photosynthesis and antioxidant activity mechanisms in Jatropha curcas L.under salt stress. Brazilian Journal of Biological Sciences. 2012; 24(1):55-67.

Ggplot2: Create elegant data visualisations using the grammar of graphics. Available from: https://CRAN.R-project.org/package=ggplot2. Date accessed: 03/07/2018.

Klein RW. Private protection and housing property insurers in the United States. International Encyclopedia of Housing and Home. 2012; 1(1):372-80. https://doi.org/10.1016/ B978-0-08-047163-1.00497-5

Klemes JJ, Varbanov PS, Lam HL, Yusup S. Energy, water and environmental footprint interactions: implications for the major economy sectors of Europe, South East Asia and Worldwide. Procedia Engineering. 2016; 148(1):1199-205. https://doi.org/10.1016/j.proeng.2016.06.630

Torga R, Mander U, Soosaar K, Kupper P, Tullus A, Rosenvald K, Ostonen I, Kutti S, Jaagus J, Sober J, Maddison M, Kaasik A, Lohmus K. Weather extremes and tree species shape soil greenhouse gas fluxes in an experimental fast-growing deciduous forest of air humidity manipulation. Ecological Engineering. 2017; 106:369-77. https://doi.org/10.1016/j.ecoleng.2017.05.025

Pussinen A, Nabuurs GJ, Wieggers HJJ, Reinds GJ, Wamelink GWW, Kros J, Mol-Dijkstra JP, de Vries W. Modelling long-term impacts of environmental change on mid- and high-latitude European forests and options for adaptive forest management. Forest Ecology and Management. 2009; 258(8):1806-13. https://doi.org/10.1016/j.foreco.2009.04.007

Dombroski JLD, Praxedes SC, de Freitas RMO, Pontes FM. Water relations of Caatinga trees in the dry season. South African Journal of Botany. 2011; 77(2):430-4. https://doi.org/10.1016/j.sajb.2010.11.001

Falcao HM, Medeiros CD, Silva BLR, Sampaio EVSB, Almeida-Cortez JS, Santos MS. Phenotypic plasticity and ecophysiological strategies in a tropical dry forest chronosequence: A study case with Poincianella pyramidalis. Forest Ecology and Management. 2015; 340(1):62-9. https://doi.org/10.1016/j.foreco.2014.12.029

Shao HB, Chu L-Y, Jaleel CA, Zhao D. Water-deficit stressinduced anatomical changes in higher plants. Comptes Rendus Biologies. 2008; 331(3):215-25. https://doi.org/10.1016/j.crvi.2008.01.002 PMid:18280987

Liu F, Stutzel H. Biomass partitioning, specific leaf area, and water use efficiency of vegetable amaranth (Amaranthus spp.) in response to drought stress. B.Sc. Horticulture. 2004; 102(1):15-27. https://doi.org/10.1016/j.scienta.2003.11.014

Trentacoste ER, Contreras-Zanessi O, Beya-Marshall V, Puertas CM. Genotypic variation of physiological and morphological traits of seven olive cultivars under sustained and cyclic drought in Mendoza, Argentina. Agricultural Water Management. 2018; 196:48-56. https://doi.org/10.1016/j.agwat.2017.10.018

Pagotto MA, Roig FA, Ribeiro AS, Lisi CS. Influence of regional rainfall and Atlantic sea surface temperature on tree-ring growth of Poincianella pyramidalis, semiarid forest from Brazil. Dendrochronologia. 2018; 35(1):14-23.

Barros V, Frosi G, Santos M, Ramos DG, Falcao HM, Santos MG. Arbuscular mycorrhizal fungi improve photosynthetic energy use efficiency and decrease foliar construction cost under recurrent water deficit in woody evergreen species. Plant Physiology and Biochemistry. 2018; 127(1):46977. https://doi.org/10.1016/j.plaphy.2018.04.016 PMid:29689510

Franc J-P, Michel JM. Fundamentals of cavitation. New York: Kluwer Academic Publishers. 2005. PMCid:PMC2362019

Pompelli MF, Barata-Luis RM, Vitorino HS, Goncalves ER, Rolim EV, Santos MG, Almeida-Cortez JS, Ferreira VM, Lemos EE, Endres L. Photosynthesis, photoprotection and antioxidant activity of purging nut under drought deficit and recovery. Biomass Bioenergy. 2010; 34(1):1207-15. https://doi.org/10.1016/j.biombioe.2010.03.011

Rivas R, Frosi G, Ramos DG, Pereira S, Benko-Iseppon NA, Santos MG. Photosynthetic limitation and mechanisms of photoprotection under drought and recovery of Calotropis procera, an evergreen C3 from arid regions. Plant Physiology and Biochemistry. 2017; 118(1):589-99. https://doi.org/10.1016/j.plaphy.2017.07.026 PMid:28793281

Fuchs R, Dupouy C, Douillet P, Caillaud M, Mangin A, Pinazo C. Modelling the impact of a La Niña event on a South West Pacific Lagoon. Marine Pollution Bulletin. 2012; 64(8):1596-613. https://doi.org/10.1016/j.marpolbul. 2012.05.016 PMid:22721694

Flexas J, Medrano H. Drought-inhibition of photosynthesis in C3 plants: stomatal and non-stomatal limitations revisited. Annals of Botany. 2002; 89(2):183-9. https://doi.org/10.1093/aob/mcf027 PMCid:PMC4233792

Galmes J, Abadia A, Cifre J, Medrano H, Flexas J.mPhotoprotection processes under water stress and recovery in Mediterranean plants with different growth forms and leaf habits. Physiology Plant. 2007; 130(4):495-510. https:// doi.org/10.1111/j.1399-3054.2007.00919.x

Parry MAJ, Andralojc PJ, Khan S, Lea PJ, Keys AJ. Rubisco activity: Effects of drought stress. Annals of Botany.2002; 89(1):833-9. https://doi.org/10.1093/aob/mcf103 PMCid:PMC4233807

Wullschleger SD. Biochemical limitations to carbon assimilation in C3 plants - a retrospective analysis of the A/Ci curves from 109 species. Journal of Experimental Botany.m1993; 44(5):907-20. https://doi.org/10.1093/jxb/44.5.907

Manter DK, Kerrigan J. A/Ci curve analysis across a range of woody plant species: influence of regression analysis parameters and mesophyll conductance. Journal of Experimental Botany. 2004; 55(408):2581-8. https://doi.org/10.1093/jxb/erh260 PMid:15501912

Lloyd J, Farquhar GD. Effects of rising temperatures and [CO2] on the physiological of tropical forest trees. Home | Philosophical Transactions of the Royal Society B: Biological. 2008; 363(1498):1811-7.

Sage RF, Way DA, Kubien DS. Rubisco, Rubisco activase, and global climate change. Journal of Experimental Botany.m2008; 5(7):1581-95. https://doi.org/10.1093/jxb/ern053 PMid:18436544

Dunford S. Translocation in the Phloem. Taiz L, Zeiger E, editors. Plant Physiology 5th edition. Sunderland, MA, USA. Sinauer Associates Inc.; 2010; p. 1-782.

Apel J, Hirt H. Reactive Oxygen Species: Metabolism, Oxidative Stress, and Signal Transduction. Annual Review of Plant Biology. 2004; 55(1):373-99. https://doi.org/10.1146/annurev.arplant.55.031903.141701 PMid:15377225

Pompelli MF, Barata-Luis R, Vitorino HS, Goncalves ER, Rolim EV, Santos MS, Almeida-Cortez JS, Ferreira VM.mPhotosynthesis, photoprotection and antioxidant activity of purging nut under drought and recovery. Biomass Bioenergy. 2010; 34(8):1207-15. https://doi.org/10.1016/j.biombioe.2010.03.011

Shrestha P, Yun J-H, Ko Y-J, KIm M, Bae YS, Lee W.mC-terminal tail of NADPH oxidase organizer 1 (Noxo1) mediates interaction with NADPH oxidase activator (Noxa1) in the NOX1 complex. Biochemical and Biophysical Research Communications. 2017; 490(3):594600. https://doi.org/10.1016/j.bbrc.2017.06.083 PMid:28625920

Pompelli MF, Barata-Luis RM, Vitorino HS, Goncalves ER, Rolim EV, Santos MG, Almeida-Cortez JS, Endres L.Photosynthesis, photoprotection and antioxidant activity of purging nut under drought deficit and recovery. Biomass Bioenergy. 2010; 34(8):1207-15. https://doi.org/10.1016/j.biombioe.2010.03.011

Pompelli MF, Martins SCV, Antunes WC, Chaves ARM, DaMatta FM. Photosynthesis and photoprotection in coffee leaves is affected by nitrogen and light availabilities in winter conditions. Journal of Plant Physiology. 2010; 167(13):1052-60. https://doi.org/10.1016/j.jplph.2010.03.001 PMid:20381192

Niyogi KK. Photoprotection revisited: genetic and molecular approaches. Annual review of plant physiology and plant molecular biology. 1999; 50(1):333-59. https://doi.org/10.1146/annurev.arplant.50.1.333 PMid:15012213

Demmig-Adams B, Adams III WW. The role of xanthophyll cycle carotenoids in the protection of photosynthesis. Trends in Plant Science. 1996; 1(1):21-6. https://doi.org/10.1016/S1360-1385(96)80019-7

Schindler C, Lichtenthaler HK. Photosynthetic CO2assimilation, chlorophyll fluorescence and zeaxanthin accumulation in field grown mapletreesin the course of a sunny and a cloudy day. Journal of Plant Physiology. 1996; 148(1):399-412. https://doi.org/10.1016/S01761617(96)80272-0

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