Investigation of the salt tolerance of new Polish bread and durum wheat cultivars

• Autorzy: Plazek A. , Tatrzanska M. , Maciejewski M. , Koscielniak M. , Gondek K. , Bojarczuk J. , Dubert F.
• Języki publikacji: EN

Abstrakty

EN

In some regions of the world, low annual precipitation necessitates irrigation of crop plants which usually leads to soil salinity. Due to climatic changes this effect is also expected in the countries of Central Europe, and so in Poland. The aim of the study was (1) to compare tolerance to salt stress of Polish Triticum aestivum cvs. ‘Bogatka’ and ‘Banderola’ with T. durum cv. ‘Komnata’ and breeding line 121, and (2) to indicate the physiological parameter/parameters most suitable for such comparison. The investigation was performed in two experiments. In the first one, the germination ability of caryopses and coleoptiles’ growth were estimated at 0–250 mM of NaCl. The second experiment was conducted on plants grown in a glasshouse in saline soil at 0–150 mM of NaCl for 6 weeks. Salt tolerance was evaluated on the basis of following parameters: chlorophyll fluorescence, net photosynthesis rate (PN), transpiration rate (E), stomatal conductance (gs), cell membrane permeability (EL), proline content, fresh weight (FW), dry weight (DW), and relative water content (RWC). Highest germination of caryopses of durum cultivars was recorded at all the salinity levels; however, their coleoptiles were shorter than coleoptiles of bread wheat cultivars. Analysis of chlorophyll fluorescence showed that applied salt doses did not disturb the light phase of photosynthesis in all cultivars under study. Plants of durum wheat showed the higher dissipation of energy excess at the level of the antenna chlorophyll (DIo/CSm) under salinity as compared to plants of bread wheat. Both ‘Komnata’ and line 121 showed stronger PN reduction as an effect of salinity. A decline of PN was closely connected with a decrease in gs. The PN correlated with a decrease in DW in all studied cultivars except ‘Bogatka’. Control plants of ‘Komnata’ and line 121 were characterized by higher EL and proline level than bread wheat cultivars. An increasing cell membrane permeability correlated with a decrease of RWC in ‘Banderola’ and ‘Komnata’. The content of proline under the increasing salinity correlated with changes of RWC in ‘Banderola’, ‘Komnata’ and line 121, which indicate protectoral role of proline against dehydration of tissue. Dry weight and RWC seem to be the parameters most useful in the salt-tolerance estimation of wheat plants. Taking into account the studied parameters ‘Banderola’ could be recognized as more salt tolerant, the degree of salinity tolerance of ‘Bogatka’ is the same as line 121, while ‘Komnata’ seems to be the most salt sensitive. The salt tolerance of T. aestivum and T. durum depends on the cultivar rather than the wheat species.

• Wydawca: -
• Czasopismo: Acta Physiologiae Plantarum
• Rocznik: 2013
• Tom: 35
• Numer: 08
• Opis fizyczny: p.2513-2523,fig.,ref.

Twórcy

autor

Plazek A.

• Department of Plant Physiology, Faculty of Agriculture and Economics, University of Agriculture, Podłu_zna 3, 30-239 Krako´w, Poland

autor

Tatrzanska M.

• F. Go´rski Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, 30-239 Krako´w, Poland

autor

Maciejewski M.

• F. Go´rski Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, 30-239 Krako´w, Poland

autor

Koscielniak M.

• Department of Plant Physiology, Faculty of Agriculture and Economics, University of Agriculture, Podłu_zna 3, 30-239 Krako´w, Poland

autor

Gondek K.

• Department of Agricultural and Environmental Chemistry, Faculty of Agriculture and Economics, University of Agriculture, Mickiewicza 21, 31-120 Krako´w, Poland

autor

Bojarczuk J.

• Plant Breeding Smolice, Plant Breeding and Acclimatization Institute Group, 63-740 Kobylin, Smolice 146, Poland

autor

Dubert F.

• F. Go´rski Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, 30-239 Krako´w, Poland

Bibliografia

• Ashraf M, Ali Q (2008) Relative membrane permeability and activities of some antioxidant enzymes as the key determinants of salt tolerance in canola (Brassica napus L.). Environ Exp Bot 63:266–273
• Ashraf M, Harris PJC (2004) Potential biochemical indicators of salinity tolerance in plants. Plant Sci 166:3–16
• Bates LE, Waldren RP, Teare ID (1973) Rapid determination of free proline for water stress studies. Plant Soil 39:205–207
• Brini F, Amara I, Feki K, Hanin M, Khoudi H, Masmoudi K (2009) Physiological and molecular analyses of seedlings of two Tunisian durum wheat (Triticum turgidum L. subsp. Durum [Desf.] varieties showing contrasting tolerance to salt stress. Acta Physiol Plant 31:145–154
• Filek M, Walas S, Mrowiec H, Rudolphy-Skórska E, Sieprawska A, Biesaga-Kościelniak J (2012) Membrane permeability and micro- and macroelement accumulation in spring wheat cultivars during the short-term effect of salinity- and PEG-induced water stress. Acta Physiol Plant 34:985–995
• Flowers TJ, Troke PF, Yeo AR (1977) The mechanism of salt tolerance in halophytes. Annu Rev Plant Physiol 28:89–121
• Greenway H, Munns R (1980) Mechanism of salt tolerance in non halophytes. Annu Rev Plant Physiol 31:149–190
• Hoagland DR, Arnon DI (1938) The water-culture method for plants without soil. University of California Agricultural Experiment Station Circular 347:29–32
• Hu M, Shi Z, Zhang Z (2012) Effects of exogenous glucose on seed germination and antioxidant capacity in wheat seedlings under salt stress. Plant Growth Regul 68:177–188
• Hura T, Hura K, Grzesiak M (2007) Effect of long-term drought stress on leaf gas exchange and fluorescence parameters in C3 and C4 plants. Acta Physiol Plant 29:103–113
• Kalaji HM, Govindjee, Bosa K, Kościelniak J, Żuk-Gołaszewska K (2011) Effects of salt stress on photosystem II efficiency and CO2 assimilation of two Syrian barley landraces. Environ Exp Bot 73:64–72
• Khan MA, Shirazi MU, Khan MA, Mujtaba SM, Islam E, Mumtaz S, Shereen AR, Ansari U, Ashraf MY (2009) Role of proline, K/Na ratio and chlorophyll content in salt tolerance of wheat (Triticum aestivum L.). Pak J Bot 41:633–638
• Khatkar D, Kuhad MS (2000) Short-term salinity induced changes in two wheat cultivars at different growth stages. Biol Plant 43:629–632
• Lazár D (1999) Chlorophyll a fluorescence induction. BBA 1412:1–28
• Mansour MMF (1998) Protection of plasma membrane of onion epidermal cells by glycinebataine and proline against NaCl stress. Plant Physiol Biochem 36:767–772
• Martyniak L, Dąbrowska-Zielińska K, Szymczyk R, Gruszczyńska M (2007) Validation of satellite-derived soil-vegetation indices for prognosis of spring cereals yield reduction under drought conditions—case study from central-western Poland. Adv Space Res 39:67–72
• Mitsuya S, Kawasaki M, Taniguchi M, Miyake H (2003) Light dependency of salinity-induced chloroplast degradation. Plant Prod Sci 6:219–223
• Moradi F, Ismail AM (2007) Responses of photosynthesis, chlorophyll fluorescence and ROS-Scavenging system to salt stress during seedling and reproductive stages in rice. Ann Bot 99:1161–1173
• Munns R, James R (2003) Screening methods for salinity tolerance: a case study with tetraploid wheat. Plant Soil 253:201–218
• Munns R, Tester M (2008) Mechanism of salinity tolerance. Annu Rev Plant Biol 59:651–681
• Munns R, Guo J, Passioura JB, Cramer GR (2000) Leaf water status controls daytime but not daily rates of leaf expansion in salttreated barley. Aust J Plant Physiol 27:949–957
• Muranaka S, Shimizu K, Kato M (2002) Ionic and osmotic effects of salinity on single-leaf photosynthesis in tow wheat cultivars with different drought tolerance. Photosynthetica 40:201–207
• Noori SAS, McNeilly T (2000) Assessment of variability in salt tolerance based on seedling growth in Triticum durum Desf. Genet Res Crop Evol 47:285–291
• Paul MJ, Foyer CH (2001) Sink regulation of photosynthesis. J Exp Bot 52:1383–1400
• Rawat L, Singh Y, Shukla N, Kumar J (2011) Alleviation of the adverse effects of salinity stress in wheat (Triticum aestivum L.) by seed biopriming with salinity tolerant isolates of Trichoderma harzianum. Plant Soil 347:387–400
• Romero-Aranda R, Soria T, Cuartero J (2001) Tomato plant-water uptake and plant-water relationships under saline growth conditions. Plant Sci 160:265–272
• Sairam RK, Tyagi A (2004) Physiology and molecular biology of salinity stres tolerance in plants. Curr Sci 86:407–421
• Schar C, Vidale PL, Luthi D, Frei C, Haberli C, Liniger MA, Appenenzeller C (2004) The role of increasing temperature variability in European summer heatwaves. Nature 427:332–336
• Sharma N, Gupta NK, Gupta S, Hasegawa H (2005) Effect of NaCl salinity on photosynthesis rate, transpiration rate, and oxidative stress tolerance in contrasting wheat genotypes. Photosynthetica 43:609–613
• Strasser RJ, Srivatava A, Tsimilli-Michael M (2000) The fluorescence transient as a tool to characterize and screen photosynthetics samples. In: Yunus M, Pathre U, Mohanty P (eds) Probing photosynthesis: mechanism, regulation and adaptation. Taylor and Francis, Bristol, pp 45–483
• Walter J, Nagy L, Hein R, Rascher U, Beierkuhnlein C, Willner E, Jentsch A (2011) Do plants remember drought? Hints towards a drought-memory in grasses. Environ Exp Bot 71:34–40
• Yasar F, Ellialtioglu S, Kusvuran S (2006) Ion and lipid peroxide content in sensitive and tolerant eggplant callus cultured under salt stress. Eur J Hortic Sci 71:169–172

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