PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2019 | 41 | 05 |
Tytuł artykułu

Selection of plant physiological parameters to detect stress effects in pot experiments using principal component analysis

Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Appropriate selection and well-timed measurement of plant developmental, morphological and physiological parameters are essential to maximize efficacy and minimize time consumption of experiments. To select for the most sensitive indicators of drought or salt stress, three independent pot experiments with diverse setups were analysed with 20–20 measured parameters. Parameters of plant growth, phenology and symbiotic interactions, visual stress symptoms, photosynthetic activity, nutrient composition and vitality were studied and the result matrices were evaluated with principal component analysis (PCA). Stress effects manifested in PC1 of two experiments and in PC2 of the third one. Traits assumed to be adequate for stress indication were characterized by high PC1 or PC2 loading values. Beside parameters of biomass production, growth and visible stress symptoms, less evident traits e.g. root electrical capacitance, membrane stability index in roots and leaves, relative water content of leaves and SPAD units were identified.
Słowa kluczowe
Wydawca
-
Rocznik
Tom
41
Numer
05
Opis fizyczny
Article 56 [10p.], fig.,ref.
Twórcy
autor
  • Centre for Agricultural Research, Institute for Soil Sciences and Agricultural Chemistry, Hungarian Academy of Sciences, Herman Otto Ut 15, Budapest 1022, Hungary
autor
  • Centre for Agricultural Research, Institute for Soil Sciences and Agricultural Chemistry, Hungarian Academy of Sciences, Herman Otto Ut 15, Budapest 1022, Hungary
  • Centre for Agricultural Research, Institute for Soil Sciences and Agricultural Chemistry, Hungarian Academy of Sciences, Herman Otto Ut 15, Budapest 1022, Hungary
autor
  • Centre for Agricultural Research, Institute for Soil Sciences and Agricultural Chemistry, Hungarian Academy of Sciences, Herman Otto Ut 15, Budapest 1022, Hungary
  • Deptartment of Plant Physiology and Molecular Plant Biology, Eötvos Lorand University, Pazmany Peter setany 1/c, Budapest 1117, Hungary
  • Centre for Agricultural Research, Institute for Soil Sciences and Agricultural Chemistry, Hungarian Academy of Sciences, Herman Otto Ut 15, Budapest 1022, Hungary
autor
  • Centre for Agricultural Research, Institute for Soil Sciences and Agricultural Chemistry, Hungarian Academy of Sciences, Herman Otto Ut 15, Budapest 1022, Hungary
autor
  • Centre for Agricultural Research, Institute for Soil Sciences and Agricultural Chemistry, Hungarian Academy of Sciences, Herman Otto Ut 15, Budapest 1022, Hungary
autor
  • Centre for Agricultural Research, Institute for Soil Sciences and Agricultural Chemistry, Hungarian Academy of Sciences, Herman Otto Ut 15, Budapest 1022, Hungary
Bibliografia
  • Ahanger MA, Tyagi SR, Wani MR, Ahmad P (2014) Drought tolerance: role of organic osmolytes, growth regulators, and mineral nutrients. In: Ahmed P, Wani MR (eds) Physiological mechanisms and adaptation strategies in plants under changing environment. Springer, New York, pp 25–55
  • Al-Karaki GN (2000) Growth of mycorrhizal tomato and mineral acquisition under salt stress. Mycorrhiza 10:51–54
  • Al-Karaki G, McMichael B, Zak J (2004) Field response of wheat to arbuscular mycorrhizal fungi and drought stress. Mycorrhiza 14:263–269
  • Andersone U, Samsone I, Ievinsh G (2012) Protection of photosynthesis in coastal salt marsh plants Aster tripolium and Hydrocotyle vulgaris in conditions of increased soil salinity. Environ Exp Biol 10: 89–97
  • Bajji M, Kinet JM, Lutts S (2002) The use of the electrolyte leakage method for assessing cell membrane stability as a water stress tolerance test in durum wheat. Plant Growth Reg 36:61–70
  • Barea JM, Azcón R, Azcón-Aguilar C (2002) Mycorrhizosphere interactions to improve plant fitness and soil quality. A van Leeuw J Microb 81:343–351
  • Barrs HD, Weatherley PE (1962) A re-examination of the relative turgidity technique for estimating water deficits in leaves. Aust J Biol Sci 15:413–428
  • Bassi PK, Spencer MS (1989) Methods for the quantification of ethylene produced by plants. In: Linskens HF, Jacksons JF (eds) Gases in plant and microbial cells. Modern methods of plant analysis. Springer, Berlin, pp 309–321
  • Berger JD, Ludwig C (2014) Contrasting adaptive strategies to terminal drought-stress gradients in Mediterranean legumes: phenology, productivity, and water relations in wild and domesticated Lupinus luteus L. J Exp Bot 65:6219–6229
  • Berger B, Parent B, Tester M (2010) High-throughput shoot imaging to study drought responses. J Exp Bot 61:3519–3528
  • Blum A, Ebercon A (1981) Cell membrane stability as a measure of drought and heat tolerance in wheat 1. Crop Sci 21:43–47
  • Bouslama M, Schapaugh WT (1984) Stress tolerance in soybeans. I. Evaluation of three screening techniques for heat and drought tolerance 1. Crop Sci 24:933–937
  • 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
  • Carvalho LM, Cacador I, Martins-Loucao MA (2001) Temporal and spatial variation of arbuscular mycorrhizas in salt marsh plants of the Tagus estuary (Portugal). Mycorrhiza 11:303–309
  • Chaves MM, Flexas J, Pinheiro C (2009) Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot 103:551–560
  • Chen D, Neumann K, Friedel S, Kilian B, Chen M, Altmann T, Klukas C (2014) Dissecting the phenotypic components of crop plant growth and drought responses based on high-throughput image analysis. Plant Cell 26:4636–4655
  • Clemensson-Lindell A, Persson H (1995) Fine-root vitality in a Norway spruce stand subjected to various nutrient supplies. Plant Soil 168:167–172
  • Cristescu SM, Mandon J, Arslanov D, De Pessemier J, Hermans C, Harren FJ (2012) Current methods for detecting ethylene in plants. Ann Bot 111:347–360
  • Cseresnyés I, Rajkai K, Vozáry E (2013) Role of phase angle measurement in electrical impedance spectroscopy. Int Agrophys 27:377–383
  • Cseresnyés I, Rajkai K, Takács T (2016) Indirect monitoring of root activity in soybean cultivars under contrasting moisture regimes by measuring electrical capacitance. Acta Physiol Plant 38:121
  • Dresler S, Hanaka A, Bednarek W, Maksymiec W (2014) Accumulation of low-molecular-weight organic acids in roots and leaf segments of Zea mays plants treated with cadmium and copper. Acta Physiol Plant 36:1565–1575
  • Farooq M, Wahid A, Kobayashi N, Fujita D, Basra SMA (2009) Plant drought stress: effects, mechanisms and management. Agron Sustain Dev 29:185–212
  • Füzy A, Tóth T, Biró B (2008a) Mycorrhizal colonisation can be altered by the direct and indirect effect of drought and salt in a split root experiment. Cereal Res Commun 35:401–404
  • Füzy A, Biró B, Tóth T, Hildebrandt U, Bothe H (2008b) Drought, but not salinity determines the apparent effectiveness of halophytes colonized by arbuscular mycorrhizal fungi. J Plant Phsyol 165:1181–1192
  • Gaspar T, Franck T, Bisbis B, Kevers C, Jouve L, Hausman JF, Dommes J (2002) Concepts in plant stress physiology. Application to plant tissue cultures. Plant Growth Regul 37:263–285
  • González L, González-Vilar M (2007) Determination of relative water content. In: Reigosa MJR (ed) Handbook of plant ecophysiology techniques. Kluwer Academic Publishers, Dordrecht, pp 207–212
  • Gray AJ (1974) The genecology of salt marsh plants. Aquat Ecol 8:152–165
  • Grümberg BC, Urcelay C, Shroeder MA, Vargas-Gil S, Luna CM (2015) The role of inoculum identity in drought stress mitigation by arbuscular mycorrhizal fungi in soybean. Biol Fertil Soils 51:1–10
  • He M, Dijkstra FA (2014) Drought effect on plant nitrogen and phosphorus: a meta-analysis. New Phytol 204:924–931
  • Högberg P, Read DJ (2006) Towards a more plant physiological perspective on soil ecology. Trends Ecol Evol 2:548–554
  • Howeler RH, Sieverding E, Saif S (1987) Practical aspects of mycorrhizal technology in some tropical crops and pastures. Plant Soil 100:249–283
  • Hu Y, Schmidhalter U (2005) Drought and salinity: a comparison of their effects on mineral nutrition of plants. J Plant Nutr Soil Sc 168:541–549
  • James JJ, Tiller RL, Richards JH (2005) Multiple resources limit plant growth and function in a saline-alkaline desert community. J Ecol 93:113–126
  • James RA, von Caemmerer S, Condon AT, Zwart AB, Munns R (2008) Genetic variation in tolerance to the osmotic stress component of salinity stress in durum wheat. Funct Plant Biol 35:111–123
  • Jedmowski C, Ashoub A, Brüggemann W (2013) Reactions of Egyptian landraces of Hordeum vulgare and Sorghum bicolor to drought stress, evaluated by the OJIP fluorescence transient analysis. Acta Physiol Plant 35:345–354
  • Kalaji HM, Jajoo A, Oukarroum A, Brestic M, Zivcak M, Samborska IA, Cetner MD, Łukasik I, Goltsev V, Ladle RJ (2016) Chlorophyll a fluorescence as a tool to monitor physiological status of plants under abiotic stress conditions. Acta Physiol Plant 38:102
  • Kaya C, Ashraf M, Sonmez O, Aydemir S, Tuna AL, Cullu MA (2009) The influence of arbuscular mycorrhizal colonisation on key growth parameters and fruit yield of pepper plants grown at high salinity. Sci Hortic 121:1–6
  • Kjeldahl JZ (1883) A new method for the determination of nitrogen in organic bodies. Z Anal Chem 22:366–383
  • Krause GH, Weis E (1984) Chlorophyll fluorescence as a tool in plant physiology. Photosynth Res 5:139–157
  • Ku YS, Au-Yeung WK, Yung YL, Li MW, Wen CQ, Liu X, Lam HM (2013) Drought stress and tolerance in soybean. In A comprehensive survey of international soybean research-genetics, physiology, agronomy and nitrogen relationships. InTech New York
  • Latef AAHA, Chaoxing H (2014) Does inoculation with Glomus mosseae improve salt tolerance in pepper plants? J Plant Growth Regul 33:644–653
  • Li RH, Guo PG, Michael B, Stefania G, Salvatore C (2006) Evaluation of chlorophyll content and fluorescence parameters as indicators of drought tolerance in barley. Agric Sci China 5:751–757
  • Li L, Zhang Q, Huang D (2014) A review of imaging techniques for plant phenotyping. Sensors 14:20078–20111
  • Maruyama K, Urano K, Yoshiwara K, Morishita Y, Sakurai N, Suzuki H, Kojima M, Sakakibara H, Shibata D, Saito K, Shinozaki K (2014) Integrated analysis of the effects of cold and dehydration on rice metabolites, phytohormones, and gene transcripts. Plant Physiol 164:1759–1771
  • Mehta P, Jajoo A, Mathur S, Bharti S (2010) Chlorophyll a fluorescence study revealing effects of high salt stress on photosystem II in wheat leaves. Plant Physiol Bioch 48:16–20
  • Munns R (2002) Comparative physiology of salt and water stress. Plant Cell Environ 25:239–250
  • Nakayama N, Saneoka H, Moghaieb RE, Premachandra GS, Fujita K (2007) Response of growth, photosynthetic gas exchange, translocation of 13C-labelled photosynthate and N accumulation in two soybean (Glycine max L. Merrill) cultivars to drought stress. Int J Agr Biol 9:669–674
  • Ohashi Y, Nakayama N, Saneoka H, Fujita K (2006) Effects of drought stress on photosynthetic gas exchange, chlorophyll fluorescence and stem diameter of soybean plants. Biol Plant 50:138–141
  • Phillips JM, Hayman DS (1970) Improved procedures for clearing roots and staining parasitic and VAM fungi for rapid assessment of infection. Trans Br Mycol Soc 55:158–161
  • Porra RJ, Thompson WA, Kreidemann PE (1989) Determination of accurate extinction coefficients and simultaneous equations for assaying chlorophylls a and b extracted with four different solvents: verification of the concentration of chlorophyll standards by atomic absorption spectroscopy. BBA Bioenerg 975:384–394
  • Rahnama A, James RA, Poustini K, Munns R (2010) Stomatal conductance as a screen for osmotic stress tolerance in durum wheat growing in saline soil. Funct Plant Biol 37:255–263
  • Roger MJR (2001) Handbook of plant ecophysiology techniques. Kluwer Academic Publishers, Dordrecht
  • Sairam RK, Deshmukh PS, Shukla DS (1997) Tolerance to drought and temperature stress in relation to increased antioxidant enzyme activity in wheat. J Agron Crop Sci 178:171–177
  • Salvatori E, Fusaro L, Gottardini E, Pollastrini M, Goltsev V, Strasser RJ, Bussotti F (2014) Plant stress analysis: application of prompt, delayed chlorophyll fluorescence and 820 nm modulated reflectance. Insights from independent experiments. Plant Physiol Bioch 85:105–113
  • Schauer N, Fernie AR (2006) Plant metabolomics: towards biological function and mechanism. Trends Plant Sci 11:508–516
  • Serraj R, Sinclair TR, Purcell LC (1990) Symbiotic N2 fixation response to drought. J Exp Bot 50:143–155
  • Shennan C, Hunt R, Macrobbie EAC (1987) Salt tolerance in Aster tripolium L. I. The effect of salinity on growth. Plant Cell Environ 10:59–65
  • Shulaev V, Cortes D, Miller G, Mittler R (2008) Metabolomics for plant stress response. Physiol Plant 132:199–208
  • Sinclair TR, Zimet AR, Muchow RC (1988) Changes in soybean nodule number and dry weight in response to drought. Field Crop Res 18:197–202
  • Smith DL, Dijak M, Hume DJ (1988) The effect of water deficit on N₂ (C₂H₂) fixation by white bean and soybean. Can J Plant Sci 68:957–967
  • Strasser RJ (1988) A concept for stress and its application in remote sensing. Applications of chlorophyll fluorescene. In: Photosynthesis research, stress physiology, hydrobiology and remote sensing. Springer, Dordrecht, pp 333–337
  • Sutka M, Li G, Boudet J, Boursiac Y, Doumas P, Maurel (2011) Natural variation of root hydraulics in Arabidopsis grown in normal and salt-stressed conditions. Plant Physiol 155:1264–1276
  • Talaat NB, Shawky BT, Ibrahim AS (2015) Alleviation of drought-induced oxidative stress in maize (Zea mays L.) plants by dual application of 24-epibrassinolide and spermine. Environ Exp Bot 113:47–58
  • Tripathy JN, Zhang J, Robin S, Nguyen TT, Nguyen HT (2000) QTLs for cell-membrane stability mapped in rice (Oryza sativa L.) under drought stress. Theoretical Appl Gen 100:1197–1202
  • Trouvelot A, Kough JL, Gianinazzi-Pearson V (1989) Mesure du taux de mycorhization VA d’un systeme radiculaire. Recherche de methodes d’estimation ayant une significantion fonctionnelle. In: Gianinazzi-Pearson V, Gianinazzi S (eds) Physiological and genetic aspects of mycorrhizae. INRA, Paris, pp 217–221
  • Tsimilli-Michael M, Strasser RJ (2008) In vivo assessment of stress impact on plant’s vitality: applications in detecting and evaluating the beneficial role of mycorrhization on host plants. In Mycorrhiza (ed). pp 679–703. Springer Berlin Heidelberg
  • Ueda A, Kanechi M, Uno Y, Inagaki N (2003) Photosynthetic limitations of a halophyte sea aster (Aster tripolium L) under water stress and NaCl stress. J Plant Res 116:63–68
  • Verslues PE, Agarwal M, Katiyar-Agarwal S, Zhu J, Zhu JK (2006) Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status. Plant J 45:523–539
  • Vollenweider P, Günthardt-Goerg MS (2005) Diagnosis of abiotic and biotic stress factors using the visible symptoms in foliage. Environ Pollut 137:455–465
  • Wehner G, Balko C, Enders M, Humbeck K, Ordon F (2015) Identification of genomic regions involved in tolerance to drought stress and drought stress induced leaf senescence in juvenile barley. BMC Plant Biol 15:125
  • Wu QS, Zou YN, He XH (2010) Contributions of arbuscular mycorrhizal fungi to growth, photosynthesis, root morphology and ionic balance of citrus seedlings under salt stress. Acta Physiol Plant 32:297–304
  • Zhang M, Jin ZQ, Zhao J, Zhang G, Wu F (2015) Physiological and biochemical responses to drought stress in cultivated and Tibetan wild barley. Plant Growth Regul 75:567–574
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.agro-3f014062-a641-47a2-a4ba-035de28a6bb7
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.