Abstract
The effect of four different NaCl concentrations (from 0 to 102 mM NaCl) on seedlings leaves of two corn (Zea mays L.) varieties (Aristo and Arper) was investigated through chlorophyll (Chl) a fluorescence parameters, photosynthesis, stomatal conductance, photosynthetic pigments concentration, tissue hydration and ionic accumulation. Salinity treatments showed a decrease in maximal efficiency of PSII photochemistry (Fv/Fm) in dark-adapted leaves. Moreover, the actual PSII efficiency (ϕPSII), photochemical quenching coefficient (qp), proportion of PSII centers effectively reoxidized, and the fraction of light used in PSII photochemistry (%P) were also dropped with increasing salinity in light-adapted leaves. Reductions in these parameters were greater in Aristo than in Arper. The tissue hydration decreased in salt-treated leaves as did the photosynthesis, stomatal conductance (g s) and photosynthetic pigments concentration essentially at 68 and 102 mM NaCl. In both varieties the reduction of photosynthesis was mainly due to stomatal closure and partially to PSII photoinhibition. The differences between the two varieties indicate that Aristo was more susceptible to salt-stress damage than Arper which revealed a moderate regulation of the leaf ionic accumulation.
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Abbreviations
- A N :
-
net assimilation rate
- Car:
-
carotenoid
- Chl a :
-
chlorophyll a
- Chl b :
-
chlorophyll b
- DM:
-
dry mass
- Fm :
-
maximal fluorescence of dark-adapted state
- Fm′:
-
maximal fluorescence of light-adapted state
- (Fm′-Fo)/Fm′:
-
proportion of PSII centers effectively re-oxidized
- Fo :
-
minimal fluorescence of dark-adapted state
- Fo′:
-
minimal fluorescence of light-adapted state
- Fs :
-
steady-state fluorescence of light-adapted leaves
- Fv :
-
variable fluorescence
- Fv/Fm :
-
maximal efficiency of PSII
- g s :
-
stomatal conductance
- LWC:
-
leaf water content
- NPQ:
-
non-photochemical quenching
- (1 − qp)/NPQ:
-
susceptibility of PSII to high irradiance
- PSII:
-
photosystem II
- QA :
-
primary quinone acceptor of PSII
- qp :
-
photochemical quenching
- %D:
-
thermal energy dissipation
- %P:
-
fraction of energy allocated to PSII photochemistry
- %X:
-
excess of energy excitation
- ϕPSII :
-
actual PSII efficiency
References
Akram, A.A., Hanaa, S.F., Fawzy, G.K., Regab, M.D.: Changes in growth, pigments and carbohydrates of Soybean and Rosemary Agroecosystem in response to soils treated with ceramic dust in Egypt. — J. Biol. Sci. 3: 802–823, 2003.
Aro, E.M., Suorsa, M., Rokka, A., Allahverdiyeva, Y., Paakkarinen, V., Saleem, A., Battchikova, N., Rintamaki, E.: Dynamics of photosystem II: a proteomic approach to thylakoid protein complexes. — J. Exp. Bot. 56: 347–356, 2005.
Baker, N.R.: A possible role for photosystem-II in environmental perturbations of photosynthesis. — Physiol. Plant. 81: 563–570, 1991.
Baker, N.R.: Chlorophyll fluorescence: a probe of photosynthesis in vivo. — Annu. Rev. Plant Biol. 59: 89–113, 2008.
Bilger, W., Björkman, O.: Temperature dependence of violaxanthin deepoxidation and non-photochemical fluorescence quenching in intact leaves of Gossypium hirsutum L. and Malva parviflora L. — Planta 184: 226–234, 1991.
Calatayud, A., Barreno, E.: Response to ozone in two lettuce varieties on chlorophyll a fluorescence, photosynthetic pigments and lipid peroxidation. — Plant Physiol. Biochem. 42: 549–555, 2004.
Cushman, J.C., Bohnert, H.J.: Crassulacean acid metabolism: Molecular genetics. — Annu. Rev. Plant Physiol. Plant Mol. Biol. 50: 305–332, 1999.
das Neves, J.P.C., Ferreira, L.F.P., Vaz, M.M., Gazarini, L.C.: Gas exchange in the salt marsh species Atriplex portulacoides L. and Limoniastrum monopetalum L. in Southern Portugal. — Acta Physiol. Plant. 30: 91–97, 2008.
Demiral, T., Türkan, I.: Exogenous glycinebetaine affects growth and proline accumulation and retards senescence in two rice cultivars under NaCl stress. — Environ. Exp. Bot. 56: 72–79, 2006.
Demmig, B., Winter, K.: Characterization of 3 components of non photochemical fluorescence quenching and their response to photoinhibition. — Aust. J. Plant Physiol. 15: 163–177, 1988.
Demmig-Adams, B., Adams, W.W.III, Barker, D.H., Logan, B.A., Bowling, D.R., Verhoeven, A.S.: Using chlorophyll fluorescence to assess the fraction of absorbed light allocated to thermal dissipation of excess excitation. — Physiol. Plant. 98: 253–264, 1996.
Flowers, T.J., Hajibagheri, M.A., Yeo, A.R.: Ion accumulation in the cell-walls of rice plants growing under saline condition — evidence for the Oertli hypothesis. — Plant Cell Environ. 14: 319–325, 1991.
Genty, B., Briantais, J.M., Baker, N.R.: The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. — Acta Biochem. Biophys. Sin. 990: 87–92, 1989.
Hajlaoui, H., Denden, M., Bouslama, M.: Effet du chlorure de sodium sur les critères morpho-physiologiques et productifs du pois chiche (Cicer arietinum L.). — Ann. INRGREF 8: 171–187, 2006. [In French.]
Hajlaoui, H., Denden, M., El Ayeb, N.: Differential responses of two maize (Zea mays L.) varieties to salt stress: Changes on polyphenols composition of foliage and oxidative damages. — Indust. Crops Prod. 30: 144–151, 2009.
Hasan, R., Kawasaki, M., Taniguichi, M., Miyake, H.: Salinity stress induces granal development in bundle sheath chloroplasts of maize, an NADP-malic enzyme-type C4 plant. — Plant Prod. Sci. 9: 256–265, 2006.
Hasegawa, P.M., Bressan, R.A., Zhu, J., Bohnert, H.J.: Plant cellular and molecular responses to high salinity. — Ann. Rev. Plant Physiol. Plant Mol. Biol. 51: 463–499, 2000.
Jiang, Q., Roche, D., Monaco, T.A., Durham, S.: Gas exchange, chlorophyll fluorescence parameters and carbon isotope discrimination of 14 barley genetic lines in response to salinity. — Field Crops Res. 96: 269–278, 2006.
Juan, M., Rivero, R.M., Romero, L., Ruiz, J.M.: Evaluation of some nutritional and biochemical indicators in selecting salt-resistant tomato cultivars. — Environ. Exp. Bot. 54: 193–201, 2005.
Kaya, C., Higgs, D., Kirnak, H., Tas, I.: Ameliorative effects of calcium nitrate on cucumber and melon plants drip irrigated with saline water. — J. Plant Nutr. 26: 1665–1681, 2003.
Krause, G.H.: Photoinhibition of photosynthesis — an evaluation of damaging and protective mechanisms. — Physiol. Plant. 74: 566–574, 1988.
Lawlor, D.W.:Limitation to photosynthesis in water stressed leaves: stomata vs. metabolism and the role of ATP. — Ann. Bot. 89: 871–885, 2002.
Lichtenthaler, H.K., Burkart, S.: Photosynthesis and high light stress. — Bulg. J. Plant Physiol. 25: 3–16, 1999.
Long, S.P., Bernacchi, C.J.: Gas exchange measurements, what can they tell us about the underlying limitations to photosynthesis? Procedures and sources of error. — J. Exp. Bot. 54: 2393–2401, 2003.
Lu, C., Jiang, G., Wang, B., Kuang, T.: Photosystem II photochemistry and photosynthetic pigment composition in salt-adapted halophyte Artimisia anethifolia grown under outdoor conditions. — J. Plant Physiol. 160: 403–408, 2003.
Lu, Q. T., Lu, C.M.: Photosynthetic pigment composition and photosystem II photochemistry of wheat ears. — Plant Physiol. Biochem. 42: 395–402, 2004.
Meloni, D.A., Oliva, M.A., Martinez, C.A., Cambraia, J.: Photosynthesis and activity of superoxide dismutase, peroxidase and glutathione reductase in cotton under salt stress. — Environ. Exp. Bot. 49: 69–76, 2003.
Mishra, S.K., Subrahmanyam, D., Singhal, G.S.: Interactionship between salt and light stress on the primary process of photosynthesis. — J. Plant Physiol. 138: 92–96, 1991.
Munns, R., Termaat, A.: Whole-plant responses to salinity. — Aust. J. Plant Physiol. 13: 143–160, 1986.
Netondo, G.W., Onyango, J.C., Beck, E.: Sorghum and salinity: II. Gas exchange and chlorophyll fluorescence of sorghum under salt stress. — Crop Sci. 44: 806–811, 2004.
Ort, D.R.: When there is too much light. — Plant Physiol. 125: 29–32, 2001.
Oxborough, K., Baker, N.R.: Resolving chlorophyll a fluorescence images of photosynthetic efficiency into photochemical and non-photochemical components-calculation of qp and Fv′/Fm′ without measuring Fo′. — Photosynth. Res. 54: 135–142, 1997.
Park, Y.I., Chow, W.S., Anderson, J.M.: The quantum yield of photoinactivation of photosystem II in pea leaves is grater at low than at high photon exposure. — Plant Cell Physiol. 36: 1163–1167, 1995.
Pasternak, D., Sagih, N., DeMalach, Y., Keren, Y., Shaffer, A.: Irrigation with brackish water under desert conditions. 9. Salt tolerance in sweet-corn cultivars. — Agri. Water Manag. 28: 325–334, 1995.
Qiujie, D., Bin, Y., Shaobai, H.: Response of oxidative stress defense systems in rice (Oryza sativa) leaves with supplemental UV B radiation. — Physiol. Plant. 101: 301–308, 1997.
Romero, L., Belakbir, A., Ragala, L., Ruiz, J.M.: Response of plant yield and leaf pigments to saline conditions: effectiveness of different rootstocks in melon plants (Cucumis melo L.). — Soil Sci. Plant Nutr. 43: 855–862, 1997.
Santos, C.V.: Regulation of chlorophyll biosynthesis and degradation by salt stress in sunflower leaves. — Sci. Hort. 103: 93–99, 2004.
Schreiber, U., Schliwa, U., Bilger, W.: Continuous recording of photochemical and non-photochemical fluorescence quenching with a new type of modulation fluorometer. — Photosynth. Res. 10: 51–62, 1986.
Shabala, S.N., Shabala, S.I., Martynenko, A.I., Babourina, O., Newman, I.A.: Salinity effect on bioelectric activity, growth, Na+ accumulation and chlorophyll fluorescence of maize leaves: a comparative survey and prospects for screening. — Aust. J. Plant Physiol. 25: 609–616, 1998.
Sonneveld, C., Voogt, W.: Response of tomatoes (Lycopersicum esculentum) to an unequal distribution of salts in the root environment. — Plant Soil 124: 251–256, 1990.
Steduto, P., Albrizio, R., Giorio, P., Sorrentino, G.: Gasexchange response and stomatal and nonstomatal limitations to carbon assimilation of sunflower under salinity. — Environ. Exp. Bot. 44: 243–255, 2000.
van Kooten, O., Snel, J.F.H.: The use of chlorophyll fluorescence nomenclature in plant stress physiology. — Photosynth. Res. 25: 147–150, 1990.
Yang, X.H., Lu, C.M.: Photosynthesis is improved by exogenous glycinebetaine in salt-stressed maize plants. — Physiol. Plant. 124: 343–352, 2005.
Yang, C.W., Wang, P., Li, C.Y., Shi, D.C., Wang, D.L.: Comparison of effects of salt and alkali stresses on the growth and photosynthesis of wheat. — Photosynthetica 46: 107–114, 2008.
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Hichem, H., El Naceur, A. & Mounir, D. Effects of salt stress on photosynthesis, PSII photochemistry and thermal energy dissipation in leaves of two corn (Zea mays L.) varieties. Photosynthetica 47, 517–526 (2009). https://doi.org/10.1007/s11099-009-0077-5
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DOI: https://doi.org/10.1007/s11099-009-0077-5