Location via proxy:   [ UP ]  
[Report a bug]   [Manage cookies]                
*
 

iForest - Biogeosciences and Forestry

*

Effect of drought stress on some growth, morphological, physiological, and biochemical parameters of two different populations of Quercus brantii

Shahram Jafarnia (1), Moslem Akbarinia (1)   , Batool Hosseinpour (2), Seyed Ali Mohammad Modarres Sanavi (3), Seyed A Salami (4)

iForest - Biogeosciences and Forestry, Volume 11, Issue 2, Pages 212-220 (2018)
doi: https://doi.org/10.3832/ifor2496-010
Published: Mar 01, 2018 - Copyright © 2018 SISEF

Research Articles


In recent years, drought-induced tree mortality has occurred in the oak forests of the Zagros Mountains (western Iran). The impacts of climate change induced by drought stress have been most acutely experienced by two populations of Persian oaks (Quercus brantii Lindl) grown in the western provinces (Ilam and Lorestan) of the Zagros region. We surveyed growth, physiological, and biochemical responses of one-year-old Persian oak seedlings from Melasyah (Ilam) and Chegeni (Lorestan) provenances, which were subjected to three watering regimes (100%, 40%, and 20% of field capacity) in a greenhouse. The severe drought stress decreased the diameter and height growth, total biomass, net photosynthesis, gas exchange, xylem water potential, maximum Rubisco activity (Vcmax) as well as the maximum PSII photochemical efficiency of the oak seedlings in both populations, but the rate of decrease was greater in Chegeni seedlings as compared to Melasyah seedlings. Although proline and soluble sugar contents significantly increased in response to drought in both populations under stress, the rate of increase was higher in Melasyah seedlings as compared to Chegeni seedlings. In addition, the activities of peroxidase, superoxide dismutase, catalase, and ascorbic peroxidase as well as that of phenylalanine ammonia lyase were promoted in both populations under drought stress. However, the incremental rate was higher in the Melasyah population than in the Chegeni population. Under severe drought stress, the MDA content, electrolyte leakage, the content of hydrogen peroxide, and superoxide radical significantly increased in both the populations. The rate of increase, however, was higher in the Chegeni population. Under drought stress, the total phenol and flavonoid contents of Melasyah seedlings were higher than those of Chegeni seedlings. The results showed that Chegeni seedlings are more sensitive than Melasyah seedlings when exposed to a water limitation stress. Our findings suggest that the climate conditions of the Persian oak stands should be considered by nursery managers while creating establishment and restoration programs.

  Keywords


Drought Stress, Persian Oak, Zagros Mountain, Provenance, Drought Resistance

Authors’ address

(1)
Shahram Jafarnia
Moslem Akbarinia
Department of Forestry, Faculty of Natural Resources, Tarbiat Modares University, P. O. Box 14115-111 (Iran)
(2)
Batool Hosseinpour
Department of Agriculture, Iranian Research Organization for Science and Technology (IROST), P. O. Box 3353-5111, Tehran (Iran)
(3)
Seyed Ali Mohammad Modarres Sanavi
Department of Agronomy, Faculty of Agriculture, Tarbiat Modares University, P. O. Box 14115-336, Tehran (Iran)
(4)
Seyed A Salami
Department of Horticultural Sciences, Faculty of Agriculture and Natural Resources, University of Tehran, P. O. Box 41111, Tehran (Iran)

Corresponding author

 
Moslem Akbarinia
akbarinia.m@gmail.com

Citation

Jafarnia S, Akbarinia M, Hosseinpour B, Modarres Sanavi SAM, Salami SA (2018). Effect of drought stress on some growth, morphological, physiological, and biochemical parameters of two different populations of Quercus brantii. iForest 11: 212-220. - doi: 10.3832/ifor2496-010

Academic Editor

Claudia Cocozza

Paper history

Received: May 19, 2017
Accepted: Nov 22, 2017

First online: Mar 01, 2018
Publication Date: Apr 30, 2018
Publication Time: 3.30 months

Breakdown by View Type

(Waiting for server response...)

Article Usage

Total Article Views: 47322
(from publication date up to now)

Breakdown by View Type
HTML Page Views: 39269
Abstract Page Views: 3010
PDF Downloads: 4024
Citation/Reference Downloads: 32
XML Downloads: 987

Web Metrics
Days since publication: 2437
Overall contacts: 47322
Avg. contacts per week: 135.93

Article Citations

Article citations are based on data periodically collected from the Clarivate Web of Science web site
(last update: Feb 2023)

Total number of cites (since 2018): 33
Average cites per year: 5.50

 

Publication Metrics

by Dimensions ©

Articles citing this article

List of the papers citing this article based on CrossRef Cited-by.

 
(1)
Ahmadi R, Kiadaliri H, Mataji A, Kafaki S (2014)
Oak forest decline zonation using AHP model and GIS technique in Zagros Forests of Ilam Province. Journal of Biodiversity and Environmental Sciences 4: 141-150. -
Online | Gscholar
(2)
Ahmed C, Ben F, Rouina B, Sensoy S, Boukhris M, Abdallah F (2009)
Changes in gas exchange, proline accumulation and antioxidative enzyme activities in three olive cultivars under contrasting water availability regimes. Environment and Experimental Botany 67: 345-352.
CrossRef | Gscholar
(3)
Arnon DI (1949)
Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiology 24: 1-15.
CrossRef | Gscholar
(4)
Bai T, Li C, Ma F, Feng F, Shu H (2010)
Responses of growth and antioxidant system to root-zone hypoxia stress in two Malus species. Plant Soil 327: 95-105.
CrossRef | Gscholar
(5)
Bates LS, Waldren RP, Teare ID (1973)
Rapid determination of free proline for water-stress studies. Plant Soil 39: 205-207.
CrossRef | Gscholar
(6)
Beauchamp C, Fridovich I (1971)
Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Analytical Biochemistry 44: 276-287.
CrossRef | Gscholar
(7)
Bergmeyer HU (1972)
Methoden der enzymatischen Analyse, 2. Auflage [Methods of enzymatic analysis, 2nd edition]. Akademie-Verlag, Berlin, Germany, pp. 318. [in German]
Gscholar
(8)
Boussadia O, Mariem F, Ben Mechri B, Boussetta W, Braham M, Ben El Hadj S (2008)
Response to drought of two olive tree cultivars (cv. Koroneki and Meski). Scientia Horticulturae 116: 388-393.
CrossRef | Gscholar
(9)
Cotrozzi L, Remorini D, Pellegrini E, Landi M, Massai R, Nali C, Guidi L, Lorenzini G (2016)
Variations in physiological and biochemical traits of oak seedlings grown under drought and ozone stress. Physiologia Plantarum 157: 69-84.
CrossRef | Gscholar
(10)
Disante KB, Fuentes D, Cortina J (2011)
Response to drought of Zn-stressed Quercus suber L. seedlings. Environmental and Experimental Botany 70: 96-103.
CrossRef | Gscholar
(11)
Ebadzad G, Medeira C, Maia I, Martins J, Cravador A (2015)
Induction of defense responses by cinnamomins against Phytophthora cinnamomi in Quercus suber and Quercus ilex subs. rotundifolia. European Journal of Plant Pathology 143: 705-723.
CrossRef | Gscholar
(12)
Fassnacht FE, Stenzel S, Gitelson AA (2015)
Non-destructive estimation of foliar carotenoid content of tree species using merged vegetation indices. Journal of Plant Physiology 176: 210-217.
CrossRef | Gscholar
(13)
Fini A, Bellasio C, Pollastri S, Tattini M, Ferrini F (2013)
Water relations, growth, and leaf gas exchange as affected by water stress in Jatropha curcas. Journal of Arid Environments 89: 21-29.
CrossRef | Gscholar
(14)
Flexas J, Diaz-Espejo A, Gago J, Gallé A, Galmés J, Gulías J, Medrano H (2014)
Photosynthetic limitations in Mediterranean plants: a review. Environmental and Experimental Botany 103: 12-23.
CrossRef | Gscholar
(15)
Ghanbary E, Tabari Kouchaksaraei M, Mirabolfathy M, Modarres Sanavi SAM, Rahaei M (2017)
Growth and physiological responses of Quercus brantii seedlings inoculated with Biscogniauxia mediterranea and Obolarina persica under drought stress. Forest Pathology 47 (5): e12353.
CrossRef | Gscholar
(16)
He F, Sheng M, Tang M (2017)
Effects of Rhizophagus irregularis on photosynthesis and antioxidative enzymatic system in Robinia pseudoacacia L. under drought stress. Frontiers in Plant Science 8: 183.
CrossRef | Gscholar
(17)
Hessini K, Martínez JP, Gandour M, Albouchi A, Soltani A, Abdelly C (2009)
Effect of water stress on growth, osmotic adjustment, cell wall elasticity and water-use efficiency in Spartina alterniflora. Environmental and Experimental Botany 67: 312-319.
CrossRef | Gscholar
(18)
Holland V, Koller S, Lukas S, Brüggemann W (2016)
Drought-and frost-induced accumulation of soluble carbohydrates during accelerated senescence in Quercus pubescens. Trees 30: 215-226.
CrossRef | Gscholar
(19)
Hoshika Y, Omasa K, Paoletti E (2013)
Both ozone exposure and soil water stress are able to induce stomatal sluggishness. Environmental and Experimental Botany 88: 19-23.
CrossRef | Gscholar
(20)
Hu L, Wang Z, Huang B (2010)
Diffusion limitations and metabolic factors associated with inhibition and recovery of photosynthesis from drought stress in a C3 perennial grass species. Physiologia Plantarum 139: 93-106.
CrossRef | Gscholar
(21)
Jin R, Shi H, Han C, Zhong B, Wang Q, Chan Z (2015)
Physiological changes of purslane (Portulaca oleracea L.) after progressive drought stress and rehydration. Scientia Horticulturae 194: 215-221.
CrossRef | Gscholar
(22)
Kocheva K, Lambrev P, Georgiev G, Goltsev V, Karabaliev M (2004)
Evaluation of chlorophyll fluorescence and membrane injury in the leaves of barley cultivars under osmotic stress. Bioelectrochemistry 63: 121-124.
CrossRef | Gscholar
(23)
La Porta N, Capretti P, Thomsen IM, Kasanen R, Hietala AM, Von Weissenberg K (2008)
Forest pathogens with higher damage potential due to climate change in Europe. Canadian Journal of Plant Pathology 30: 177-195.
CrossRef | Gscholar
(24)
Lima ALS, DaMatta FM, Pinheiro HA, Totola MR, Loureiro ME (2002)
Photochemical responses and oxidative stress in two clones of Coffea canephora under water deficit conditions. Environmental and Experimental Botany 47: 239-247.
CrossRef | Gscholar
(25)
Liu C, Liu Y, Guo K, Fan D, Li G, Zheng Y, Yu L, Yang R (2011)
Effect of drought on pigments, osmotic adjustment and antioxidant enzymes in six woody plant species in karst habitats of southwestern China. Environmental and Experimental Botany 71: 174-183.
CrossRef | Gscholar
(26)
Manes F, Vitale M, Donato E, Giannini M, Puppi G (2006)
Different ability of three Mediterranean oak species to tolerate progressive water stress. Photosynthetica 44: 387-393.
CrossRef | Gscholar
(27)
Mansori M, Chernane H, Latique S, Benaliat A, Hsissou D, El Kaoua M (2015)
Seaweed extract effect on water deficit and antioxidative mechanisms in bean plants (Phaseolus vulgaris L.). Journal of Applied Phycology 27: 1689-1698.
CrossRef | Gscholar
(28)
Mittler R (2002)
Oxidative stress, antioxidants and stress tolerance. Trends in Plant Science 7: 405-410.
CrossRef | Gscholar
(29)
Nakano Y, Asada K (1981)
Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant and Cell Physiology 22: 867-880.
CrossRef | Gscholar
(30)
Nayyar H (2003)
Accumulation of osmolytes and osmotic adjustment in water-stressed wheat (Triticum aestivum) and maize (Zea mays) as affected by calcium and its antagonists. Environmental and Experimental Botany 50: 253-264.
CrossRef | Gscholar
(31)
Oguchi R, Hikosaka K, Hiura T, Hirose T (2006)
Leaf anatomy and light acclimation in woody seedlings after gap formation in a cool-temperate deciduous forest. Oecologia 149: 571-582.
CrossRef | Gscholar
(32)
Ozkur O, Ozdemir F, Bor M, Turkan I (2009)
Physiochemical and antioxidant responses of the perennial xerophyte Capparis ovata Desf. to drought. Environmental and Experimental Botany 66: 487-492.
CrossRef | Gscholar
(33)
Porth I, Scotti-Saintagne C, Barreneche T, Kremer A, Burg K (2005)
Linkage mapping of osmotic stress induced genes of oak. Tree Genetics and Genomes 1: 31-40.
CrossRef | Gscholar
(34)
Santos C, Fragoeiro S, Phillips A (2005)
Physiological response of grapevine cultivars and a rootstock to infection with Phaeoacremonium and Phaeomoniella isolates: an in vitro approach using plants and calluses. Scientia Horticulturae 103: 187-198.
CrossRef | Gscholar
(35)
Sharkey TD, Bernacchi CJ, Farquhar GD, Singsaas EL (2007)
Fitting photosynthetic carbon dioxide response curves for C3 leaves. Plant, Cell and Environment 30: 1035-1040.
CrossRef | Gscholar
(36)
Shi H, Ye T, Song B, Qi X, Chan Z (2015)
Comparative physiological and metabolomic responses of four Brachypodium distachyon varieties contrasting in drought stress resistance. Acta Physiologiae Plantarum 37: 1-12.
CrossRef | Gscholar
(37)
Shukla N, Awasthi RP, Rawat L, Kumar J (2012)
Biochemical and physiological responses of rice (Oryza sativa L.) as influenced by Trichoderma harzianum under drought stress. Plant Physiology and Biochemistry 54: 78-88.
CrossRef | Gscholar
(38)
Singleton VL, Rossi JA (1965)
Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagents. American Journal of Enology and Viticulture 16: 144-158.
Online | Gscholar
(39)
Smirnoff N (1993)
The role of active oxygen in the response of plants to water deficit and desiccation. New Phytologist 125: 27-58.
CrossRef | Gscholar
(40)
Sturrock RN, Frankel SJ, Brown AV, Hennon PE, Kliejunas JT, Lewis KJ, Worrall JJ, Woods AJ (2011)
Climate change and forest diseases. Plant Pathology 60: 133-149.
CrossRef | Gscholar
(41)
Szabados L, Savoure A (2010)
Proline: a multifunctional amino acid. Trends in Plant Science 15: 89-97.
CrossRef | Gscholar
(42)
Talbi S, Romero-Puertas MC, Hernández A, Terrón L, Ferchichi A, Sandalio LM (2015)
Drought tolerance in a Saharian plant Oudneya africana: role of antioxidant defences. Environmental and Experimental Botany 111: 114-126.
CrossRef | Gscholar
(43)
Valentovic P, Luxova M, Kolarovic L, Gasparikova O (2006)
Effect of osmotic stress on compatible solutes content, membrane stability and water relations in two maize cultivars. Plant Soil and Environment 52: 186-191.
CrossRef | Gscholar
(44)
Velikova V, Yordanov I, Edreva A (2000)
Oxidative stress and some antioxidant systems in acid rain-treated bean plants: protective role of exogenous polyamines. Plant Science 151: 59-66.
CrossRef | Gscholar
(45)
Wanjiku JG, Bohne H (2017)
Growth and drought responses of three Prunus spinosa L. ecotypes. African Journal of Horticulture Science 12: 40-50.
Online | Gscholar
(46)
Wang JW, Zheng LP, Wu JY, Tan RX (2006)
Involvement of nitric oxide in oxidative burst, phenylalanine ammonia-lyase activation and Taxol production induced by low-energy ultrasound in Taxus yunnanensis cell suspension cultures. Nitric Oxide 15: 351-358.
CrossRef | Gscholar
(47)
Xiaoling L, Ning L, Jin Y, Fuzhou Y, Faju C, Fangqing C (2011)
Morphological and photosynthetic responses of riparian plant Distylium chinense seedlings to simulated autumn and winter flooding in Three Gorges Reservoir region of the Yangtze River, China. Acta Ecologica Sinica 31: 31-39.
CrossRef | Gscholar
(48)
Zarafshar M, Akbarinia M, Askari H, Hosseini SM, Rahaie M, Struve D, Striker GG (2014)
Morphological, physiological and biochemical responses to soil water deficit in seedlings of three populations of wild pear (Pyrus boisseriana). Biotechnology, Agronomy, Society and Environment 18: 353-366.
Online | Gscholar
(49)
Zhishen J, Mengcheng T, Jianming W (1999)
The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals. Food Chemistry 64: 555-559.
CrossRef | Gscholar
 

This website uses cookies to ensure you get the best experience on our website. More info