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Plant function and evolutionary biology
RESEARCH ARTICLE

Morpho-physiological responses to dehydration stress of perennial ryegrass and tall fescue genotypes

Reihaneh Shahidi A C , Junko Yoshida A B , Mathias Cougnon A , Dirk Reheul A and Marie-Christine Van Labeke A
+ Author Affiliations
- Author Affiliations

A Department of Plant Production, Ghent University, Coupure Links 653, 9000 Gent, Belgium.

B Department of Sustainable Resource Sciences, Graduate School of Bioresources, Mie University, 1577 Kurimamachiya-cho, Tsu city, Mie 514-8507, Japan.

C Corresponding author. Email: reihaneh.shahidi@ugent.be

Functional Plant Biology 44(6) 612-623 https://doi.org/10.1071/FP16365
Submitted: 22 October 2016  Accepted: 24 February 2017   Published: 10 April 2017

Abstract

Worldwide drought stress is the most important restriction factor on food and fodder productivity. In this study, morpho-physiological adaptations to dehydration stress were investigated in two tall fescue (Festuca arundinacea Schreb.) genotypes (Fa13 and Fa19 with a high and low sheep grazing preference respectively) and Lolium perenne L. Drought stress as evaluated by decreasing stomatal conductance and chlorophyll content, chlorophyll fluorescence parameters and fructan concentration were first observed in L. perenne (16 days after the start of the drought stress). Furthermore, after 20 days of drought stress the activities of ascorbate peroxide (APX), catalase (CAT), and superoxide dismutase (SOD) were reduced in stressed plants indicating that the capacity to scavenge ROS diminished under severe stress though no differences between genotypes were observed. Osmotic adjustment by carbohydrates did also not differ between the genotypes. Proline, however, reached its highest level in drought-stressed L. perenne followed by Fa13 and Fa19 respectively. The studied species showed a similar degree in response in the traits assessed when plants were exposed to dehydration stress; however changes were first observed in L. perenne.

Additional keywords: APX, biomass, carbohydrates, chlorophyll fluorescence, drought stress, Festuca arundinacea, Lolium perenne, POX, proline, SOD.


References

AbdElgawad H, Farfan-Vignolo ER, de Vos D, Asard H (2015) Elevated CO2 mitigates drought and temperature-induced oxidative stress differently in grasses and legumes. Plant Science 231, 1–10.
Elevated CO2 mitigates drought and temperature-induced oxidative stress differently in grasses and legumes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXitVWku73L&md5=86c14cf9bd9e90e4ca2eea702c9b2220CAS |

Aebi H (1984) Catalase in vitro. In ‘Method in enzymology’. pp. 121–126. (Academic Press: New York)

Ajithkumar IP, Panneerselvam R (2013) Osmolyte accumulation, photosynthetic pigment and growth of Setaria italica (L.) P. Beauv. under drought stress. Asian Pacific Journal of Reproduction 2, 220–224.
Osmolyte accumulation, photosynthetic pigment and growth of Setaria italica (L.) P. Beauv. under drought stress.Crossref | GoogleScholarGoogle Scholar |

Akmal M, Janssens MJJ (2004) Productivity and light use efficiency of perennial ryegrass with contrasting water and nitrogen supplies. Field Crops Research 88, 143–155.
Productivity and light use efficiency of perennial ryegrass with contrasting water and nitrogen supplies.Crossref | GoogleScholarGoogle Scholar |

Amiard V, Morvan-Bertrand A, Billard JP, Huault C, Keller F, Prud’homme MP (2003) Fructans, but not the sucrosyl-galactosides, raffinose and loliose, are affected by drought stress in perennial ryegrass. Plant Physiology 132, 2218–2229.
Fructans, but not the sucrosyl-galactosides, raffinose and loliose, are affected by drought stress in perennial ryegrass.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXmsVanuro%3D&md5=96dc8d228a4ecd6de428ddd983a1f3aeCAS |

Arnon DI (1949) Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiology 24, 1–15.
Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaH1MXhtFaqtg%3D%3D&md5=0e5c5473e5ff5a58bdf4f81e1c37612cCAS |

Ayala A, Muñoz MF, Argüelles S (2014) Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxidative Medicine and Cellular Longevity 2014, 360438
Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal.Crossref | GoogleScholarGoogle Scholar |

Bandurska H, Jozwiak W (2010) A comparison of the effects of drought on proline accumulation and peroxidases activity in leaves of Festuca rubra L. and Lolium perenne L. Acta Societatis Botanicorum Poloniae 79, 111–116.
A comparison of the effects of drought on proline accumulation and peroxidases activity in leaves of Festuca rubra L. and Lolium perenne L.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtVSlurfL&md5=b3df2e3db7fad9dfdc22a1ec8421ce2dCAS |

Bates LS, Waldren RP, Teare ID (1973) Rapid determination of free proline for water-stress studies. Plant and Soil 39, 205–207.
Rapid determination of free proline for water-stress studies.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE3sXlsVGitLk%3D&md5=7defff6fc79bf274d695d8ed5adb8abcCAS |

Ben Rejeb K, Abdelly C, Savouré A (2014) How reactive oxygen species and proline face stress together. Plant Physiology and Biochemistry 80, 278–284.
How reactive oxygen species and proline face stress together.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXpsl2mt70%3D&md5=a9be1f29db14a732d4b9b2bf46d8f2dcCAS |
      Bilger W, Björkman O (1990) Role of the xanthophyll cycle in photoprotection elucidated by measurements of light-induced absorbance changes, fluorescence and photosynthesis in leaves of Hedera canariensis. Photosynthesis Research 25, 173–185.
Role of the xanthophyll cycle in photoprotection elucidated by measurements of light-induced absorbance changes, fluorescence and photosynthesis in leaves of Hedera canariensis.Crossref | GoogleScholarGoogle Scholar |

Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72, 248–254.
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE28XksVehtrY%3D&md5=2821bcfbf01a16b0f1b14eb3a73c5812CAS |

Chai Q, Jin F, Merewitz E, Huang BR (2010) Growth and physiological traits associated with drought survival and post-drought recovery in perennial turfgrass species. Journal of the American Society for Horticultural Science 135, 125–133.

Chance B, Maehly AC (1955) Assay of catalases and peroxidases. Methods in Enzymology 2, 764–775.
Assay of catalases and peroxidases.Crossref | GoogleScholarGoogle Scholar |

Cougnon M (2013) Potential in mixed swards and breeding of tall fescue (Festuca arundinacea Schreb.). PhD thesis. Department of Plant Production, Ghent University, Ghent, Belgium.

Cougnon M, Baert J, Reheul D (2014) Dry matter yield and digestibility of five cool season forage grass species under contrasting N fertilizations. In ‘Grassland science in Europe. Vol. 19. IBER’. pp. 175–177. (Aberystwyth University: Aberystwyth, UK)

Cougnon M, De Swaef T, Lootens P, Baert J, De Frenne P, Roldan I, Shahidi R, Reheul D (2017) In situ quantification of forage grass root biomass, distribution and diameter classes under two N fertilisation rates. Plant and Soil 411, 409
In situ quantification of forage grass root biomass, distribution and diameter classes under two N fertilisation rates.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC28XhsVCmsbjO&md5=1e3de9e73aa9049490b72cd4082ceceaCAS |

Durand J-L, Bariac T, Ghesquiere M, Biron P, Richard P, Humphreys M, Zwierzykovski Z (2007) Ranking of the depth of water extraction by individual grass plants, using natural 18O isotope abundance. Environmental and Experimental Botany 60, 137–144.
Ranking of the depth of water extraction by individual grass plants, using natural 18O isotope abundance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtlShsb0%3D&md5=5cc04641dc8492a2d4a2e64c2bb63b5bCAS |

Esterbauer H, Cheeseman KH (1990) Determination of aldehydic lipid peroxidation products: malonaldehyde and 4-hydroxynonenal. Methods in Enzymology 186, 407–421.
Determination of aldehydic lipid peroxidation products: malonaldehyde and 4-hydroxynonenal.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXks1Olt7w%3D&md5=7eb3c03635ad164b6129d303d4734564CAS |

Farooq M, Basra S, Wahid A, Ahmad N, Saleem B (2009) Improving the drought tolerance in rice (Oryza sativa L.) by exogenous application of salicylic acid. Journal Agronomy & Crop Science 195, 237–246.
Improving the drought tolerance in rice (Oryza sativa L.) by exogenous application of salicylic acid.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhtVGit73I&md5=4187f491398f352f15d6f67aa46bfa86CAS |

Farooq M, Hussain M, Wahid A, Siddique KHM (2012) Drought stress in plants: an overview. In ‘Plant responses to drought stress’. (Ed. R Aroca) pp. 1–33. (Springer: Berlin)

Fu J, Huang B (2001) Involvement of antioxidants and lipid peroxidation in the adaptation of two cool-season grasses to localized drought stress. Environmental and Experimental Botany 45, 105–114.
Involvement of antioxidants and lipid peroxidation in the adaptation of two cool-season grasses to localized drought stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXitF2msrg%3D&md5=0cc0a7e6bc06925e00934d852465aa40CAS |

Fu JM, Huang BR, Fry J (2010) Osmotic potential, sucrose level, and activity of sucrose metabolic enzymes in tall fescue in response to deficit irrigation. Journal of the American Society for Horticultural Science 135, 506–510.

Genty B, Briantais JM, Baker NR (1989) The relationship between the quantum yield of photosynthetic electron-transport and quenching of chlorophyll fluorescence. Biochimica et Biophysica Acta 990, 87–92.
The relationship between the quantum yield of photosynthetic electron-transport and quenching of chlorophyll fluorescence.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1MXhsFWntL4%3D&md5=ca3f55cdd9fa28062542f823d0b95a3aCAS |

Golding AJ, Johnson GN (2003) Down-regulation of linear and activation of cyclic electron transport during drought. Planta 218, 107–114.
Down-regulation of linear and activation of cyclic electron transport during drought.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXovV2ltL4%3D&md5=1641c384cd30413b46800708431bf206CAS |

Hodges DM, DeLong JM, Forney CF, Prange RK (1999) Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta 207, 604–611.
Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXhslKisLw%3D&md5=19c2c9677886e16fb031144ada6dc4d9CAS |

Hsiao TC (1973) Plant responses to water stress. Annual Review of Plant Physiology 24, 519–570.
Plant responses to water stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE3sXlt1emurY%3D&md5=18ad5c6ad0c43fae913622ba58f48ef1CAS |

Huang BR, Fry J, Wang B (1998) Water relations and canopy characteristics of tall fescue cultivars during and after drought stress. HortScience 33, 837–840.

Humphreys MW, Yadav R, Cairns AJ, Turner L, Humphreys J, Skøt L (2006) A changing climate for grassland research. New Phytologist 169, 9–26.
A changing climate for grassland research.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtVygt7k%3D&md5=3b5415b14a0d5415499a32c883c3029cCAS |

Jiang YW, Yao Y, Wang Y (2012) Physiological response, cell wall components, and gene expression of switchgrass under short-term drought stress and recovery. Crop Science 52, 2718–2727.
Physiological response, cell wall components, and gene expression of switchgrass under short-term drought stress and recovery.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhvVelur%2FI&md5=60dbbcaa7fb9e2963831b7d6533f93b7CAS |

Jones M (1997) The impacts of global climate change on grassland ecosystems. In ‘Proceedings of the 18th International Grasslands Congress, Winnipeg, Manitoba and Saskatoon, Saskatchewan, Canada’. pp. 8–19. Department of Agriculture and Agri-food Canada, Canadian Society of Agronomy.

Joudi M, Ahmadi A, Mohamadi V, Abbasi A, Vergauwen R, Mohammadi H, Van den Ende W (2012) Comparison of fructan dynamics in two wheat cultivars with different capacities of accumulation and remobilization under drought stress. Physiologia Plantarum 144, 1–12.
Comparison of fructan dynamics in two wheat cultivars with different capacities of accumulation and remobilization under drought stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhtFSqtw%3D%3D&md5=080497af90cf07a5a9edfe0d8e1b6a06CAS |

Kościelniak J, Filek W, Biesaga-Kościelniak J (2006) The effect of drought stress on chlorophyll fluorescence in Lolium-Festuca hybrids. Acta Physiologiae Plantarum 28, 149–158.
The effect of drought stress on chlorophyll fluorescence in Lolium-Festuca hybrids.Crossref | GoogleScholarGoogle Scholar |

Lee BR, Muneer S, Jung WJ, Avice JC, Ourry A, Kim TH (2012) Mycorrhizal colonization alleviates drought‐induced oxidative damage and lignification in the leaves of drought‐stressed perennial ryegrass (Lolium perenne). Physiologia Plantarum 145, 440–449.
Mycorrhizal colonization alleviates drought‐induced oxidative damage and lignification in the leaves of drought‐stressed perennial ryegrass (Lolium perenne).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhtVOqsb7P&md5=ccb2899359cc998e81503d94a5e32786CAS |

Lichtenthaler HK (1987) Chlorophylls and carotenoids – pigments of photosynthetic biomembranes. Methods in Enzymology 148, 350–382.
Chlorophylls and carotenoids – pigments of photosynthetic biomembranes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1cXhs1Cgu78%3D&md5=39725a9fd4bc49e607b3b2823cadd6baCAS |

Man D, Bao YX, Han LB, Zhang XZ (2011) Drought tolerance associated with proline and hormone metabolism in two tall fescue cultivars. HortScience 46, 1027–1032.

Manuchehri R, Salehi H (2015) Morphophysiological and biochemical changes in tall fescue (Festuca arundinacea Schreb.) under combined salinity and deficit irrigation stresses. Desert 20, 29–38.

Maxwell K, Johnson GN (2000) Chlorophyll fluorescence – a practical guide. Journal of Experimental Botany 51, 659–668.

McElroy JS, Kopsell DA (2009) Physiological role of carotenoids and other antioxidants in plants and application to turfgrass stress management. New Zealand Journal of Crop and Horticultural Science 37, 327–333.
Physiological role of carotenoids and other antioxidants in plants and application to turfgrass stress management.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhvFagtbo%3D&md5=d3f9d0e8a97f4157761dd400d957ee8dCAS |

Merewitz EB, Gianfagna T, Huang BR (2011) Photosynthesis, water use, and root viability under water stress as affected by expression of SAG12-ipt controlling cytokinin synthesis in Agrostis stolonifera. Journal of Experimental Botany 62, 383–395.
Photosynthesis, water use, and root viability under water stress as affected by expression of SAG12-ipt controlling cytokinin synthesis in Agrostis stolonifera.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhsFamurfN&md5=35db5f9546d94434adbc2134d193fed1CAS |

Nakano Y, Asada K (1981) Hydrogen-peroxide is scavenged by ascorbate-specific peroxidase in spinach-chloroplasts. Plant & Cell Physiology 22, 867–880.

Nelson CJ, Asay KH, Sleper DA (1977) Mechanisms of canopy development of tall fescue genotypes. Crop Science 17, 449–452.
Mechanisms of canopy development of tall fescue genotypes.Crossref | GoogleScholarGoogle Scholar |

Panunzi E (2008) Are grasslands under threat? Brief analysis of FAO statistical data on pasture and fodder crops. Available at http://www.fao.org/ag/agp/agpc/doc/grass_stats/grass-stats.htm [Verified 3 March 2017].

Pérez-Ramos IM, Volaire F, Fattet M, Blanchard A, Roumet C (2013) Tradeoffs between functional strategies for resource-use and drought-survival in Mediterranean rangeland species. Environmental and Experimental Botany 87, 126–136.
Tradeoffs between functional strategies for resource-use and drought-survival in Mediterranean rangeland species.Crossref | GoogleScholarGoogle Scholar |

Pryor WA (1989) On the detection of lipid hydroperoxides in biological samples. Free Radical Biology & Medicine 7, 177–178.
On the detection of lipid hydroperoxides in biological samples.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK3c%2FjsValtg%3D%3D&md5=77e03e78489649914a945dfced243628CAS |

Shahidi R, Cougnon M, Struyf E, Van Waes C, Van Labeke M, Reheul D (2016) Parameters influencing preference by sheep in soft leaved tall fescue genotypes. In ‘Breeding in a World of Scarcity’. (Eds I Roldán-Ruiz, J Baert, D Reheul) pp. 283–287. (Springer: Switzerland)

Siddiqui MH, Al-Khaishany MY, Al-Qutami MA, Al-Whaibi MH, Grover A, Ali HM, Al-Wahibi MS, Bukhari NA (2015) Response of different genotypes of faba bean plant to drought stress. International Journal of Molecular Sciences 16, 10214–10227.
Response of different genotypes of faba bean plant to drought stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2MXptlCnt74%3D&md5=487191f1ff2e603b7ce820b9d47f51c0CAS |

Slavik B (1974) ‘Methods of studying plant water relations.’ (Springer-Verlag: Berlin)

Spollen WG, Nelson CJ (1994) Response of fructan to water-deficit in growing leaves of tall fescue. Plant Physiology 106, 329–336.
Response of fructan to water-deficit in growing leaves of tall fescue.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2cXmtVSqu78%3D&md5=56afe02c84aaacb1f42d220e2dc8d399CAS |

Stewart CR, Boggess SF (1978) Metabolism of [5-3H] proline by barley leaves and its use in measuring the effects of water stress on proline oxidation. Plant Physiology 61, 654–657.
Metabolism of [5-3H] proline by barley leaves and its use in measuring the effects of water stress on proline oxidation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE1cXkt1SgtLg%3D&md5=04962d669c583c5c77d6535b77b964cfCAS |

Turner LR, Holloway-Phillips MM, Rawnsley RP, Donaghy DJ, Pembleton KG (2012) The morphological and physiological responses of perennial ryegrass (Lolium perenne L.), cocksfoot (Dactylis glomerata L.) and tall fescue (Festuca arundinacea Schreb.; syn. Schedonorus phoenix Scop.) to variable water availability. Grass and Forage Science 67, 507–518.
The morphological and physiological responses of perennial ryegrass (Lolium perenne L.), cocksfoot (Dactylis glomerata L.) and tall fescue (Festuca arundinacea Schreb.; syn. Schedonorus phoenix Scop.) to variable water availability.Crossref | GoogleScholarGoogle Scholar |

van Kooten O, Snel JH (1990) The use of chlorophyll fluorescence nomenclature in plant stress physiology. Photosynthesis Research 25, 147–150.
The use of chlorophyll fluorescence nomenclature in plant stress physiology.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC2czkvF2qtw%3D%3D&md5=bcde6a36279a3ccb18d830214f19ce12CAS |

Verslues PE, Kim Y-S, Zhu J-K (2007) Altered ABA, proline and hydrogen peroxide in an Arabidopsis glutamate: glyoxylate aminotransferase mutant. Plant Molecular Biology 64, 205–217.
Altered ABA, proline and hydrogen peroxide in an Arabidopsis glutamate: glyoxylate aminotransferase mutant.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXktFagu7k%3D&md5=32bdce9da4c78c5fa23de15560c65ebeCAS |

Wang JPP, Bughrara SS (2008) Morpho-physiological responses of several fescue grasses to drought stress. HortScience 43, 776–783.

White RH, Engelke MC, Morton SJ, Ruemmele BA (1992) Competitive turgor maintenance in tall fescue. Crop Science 32, 251–256.
Competitive turgor maintenance in tall fescue.Crossref | GoogleScholarGoogle Scholar |

Wilman D, Gao Y, Leitch M (1998) Some differences between eight grasses within the Lolium‐Festuca complex when grown in conditions of severe water shortage. Grass and Forage Science 53, 57–65.
Some differences between eight grasses within the Lolium‐Festuca complex when grown in conditions of severe water shortage.Crossref | GoogleScholarGoogle Scholar |

Xu ZZ, Zhou GS (2006) Combined effects of water stress and high temperature on photosynthesis, nitrogen metabolism and lipid peroxidation of a perennial grass Leymus chinensis. Planta 224, 1080–1090.
Combined effects of water stress and high temperature on photosynthesis, nitrogen metabolism and lipid peroxidation of a perennial grass Leymus chinensis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XpvVart7c%3D&md5=e177867d38a666555dd9cdc11b74ad00CAS |

Xu L, Han L, Huang B (2011) Antioxidant enzyme activities and gene expression patterns in leaves of Kentucky bluegrass in response to drought and post-drought recovery. Journal of the American Society for Horticultural Science 136, 247–255.

Young A, Frank H (1996) Energy transfer reactions involving carotenoids: quenching of chlorophyll fluorescence. Journal of Photochemistry and Photobiology. B, Biology 36, 3–15.
Energy transfer reactions involving carotenoids: quenching of chlorophyll fluorescence.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XntlOnt7k%3D&md5=d738c208116d903e8d5e306f95c31886CAS |

Zwicke M, Picon-Cochard C, Morvan-Bertrand A, Prud’homme M-P, Volaire F (2015) What functional strategies drive drought survival and recovery of perennial species from upland grassland? Annals of Botany 116, 1001–1015.
What functional strategies drive drought survival and recovery of perennial species from upland grassland?Crossref | GoogleScholarGoogle Scholar |