Comparative effects of salt and alkali stress on photosynthesis and root physiology of oat at anthesis

Authors

  • Yan Qin Institute of Grassland Research of Chinese Academy of Agricultural Sciences, Hohhot, 010010
  • Jianhui Bai Institute of Grassland Research of Chinese Academy of Agricultural Sciences, Hohhot, 010010
  • Yuqing Wang Institute of Grassland Research of Chinese Academy of Agricultural Sciences, Hohhot, 010010
  • Jinghui Liu Science Innovation Team of Oats, Inner Mongolia Agricultural University, Hohhot, 010019
  • Yongning Hu Monitoring and Planning Institute of Inner Mongolia Forestry Administration, 010020
  • Zhi Dong Shandong Provincial Key Laboratory of Soil Erosion and Ecological Restoration, Shandong Agricultural University, 271018
  • Lei Ji Institute of Grassland Research of Chinese Academy of Agricultural Sciences, Hohhot, 010010

Keywords:

oat, salt stress, alkali stress, photosynthesis, root physiology, anthesis

Abstract

The effects of different concentrations of salt and alkali on root physiology and photosynthesis in oat (Avena sativa L.) at anthesis were compared. Treatment with salt and particularly with alkali, decreased yield and grain weight. Both alkali and salt treatments decreased the photosynthetic rate (Pn), stomatal conductance and chlorophyll content, with the effect on Pn and the chlorophyll content more marked after treatment with alkali. The decrease in Pn induced by salt and mild alkali (50 mmol L-1) contributed to a decrease in stoma opening. Under moderate and severe concentrations of alkali (100 and 150 mmol L-1 respectively), other factors rather than stoma closure were responsible for limiting Pn. The transpiration rates (Tr) in alkali-treated plants were higher than in salt-treated plants. We also observed decreases in both root volume and root dry weight, and increases in root activity in alkali- and salt-treated plants. Severe alkali and salt concentrations (150 mmol L-1) decreased the root-shoot ratio. A positive correlation between yield and root dry weight and a negative correlation between root activity and Pn were observed. Alkali and salt treatments increased superoxide dismutase (SOD) and peroxidase (POD) activities and the malondialdehyde (MDA) content, but decreased catalase (CAT) activity. Yield was negatively correlated with MDA, and the MDA content was greater under alkali treatments than after salt treatment. We conclude that alkali treatments had more severe effects on oat plants at anthesis than salt treatments.

https://doi.org/10.2298/ABS171124050Q

Received: July 10, 2017; Revised: November 24, 2017; Accepted: November 25, 2017; Published online: November 29, 2017

How to cite this article: Qin Y, Bai J, Wang Y, Liu J, Hu Y, Dong Z, Ji L. Comparative effects of salt and alkali stress on photosynthesis and root physiology of oat at anthesis. Arch Biol Sci. 2018;70(2):329-38.

Downloads

Download data is not yet available.

References

Alasvandyari F, Mahdavi B, Hosseini SM. Glycine betaine affects the antioxidant system and ion accumulation and reduces salinity-induced damage in safflower seedlings. Arch Biol Sci. 2017;69(1):139-47.

Caruso G, Cavaliere C, Guarino C, Gubbiotti R, Foglia P, Laganà A. Identification of changes in Triticum durum L. leaf proteome in response to salt stress by two-dimensional electrophoresis and MALDI-TOF mass spectrometry. Anal Bioanal Chem. 2008;391(1):381-90.

Cheng YW, Qi YC, Zhu Q, Chen X, Wang N, Zhao X, Chen HY, Cui XJ, Xu LL, Zhang W. New changes in the plasma-membrane-associated proteome of rice roots under salt stress. Proteomics. 2009;9(11):3100-14.

Hartung W, Leport L, Ratcliffe RG, Sauter A, Duda R, Turner N. Abscisic acid concentration, root pH and anatomy do not explain growth differences of chickpea (Cicer arietinum L.) and lupin (Lupinus angustifolius L.) on acid and alkaline soils. Plant Soil. 2002;240(1):191-9.

Goyal M, Asthir B. Polyamine catabolism influences antioxidative defense mechanism in shoots and roots of five wheat genotypes under high temperature stress. Plant Growth Regul. 2010;60(1):13-25.

Campestrea MP, Bordenavea CD, Origonea AC, Menendeza AB, Ruiza OA, Rodrigueza AA, Maialea SJ. Polyamine catabolism is involved in response to salt stress in soybean hypocotyls. J Plant Physiol. 2011;168(11):1234-40.

Prasad S, Shamala T, Frans JMM. Long term salinity stress reveals variety specific differences in root oxidative stress response. Rice Sci. 2012;19(1):36-43.

Yang K, Zhang BJ, Hu YG, Wang SH, Xue XF. Effects of complex saline-alkaline stress on seeds germination and physiological and biochemical parameters of oats seedlings. Agric Res Arid Areas. 2009;27:188-92.

Wang B, Song FB, Ren CZ, Liu SQ, Han XY. Effects of Saline-Alkali Stress on ultrastructure in chloroplast and some physiological indexes of oats. J Jilin Agr U. 2005;27(5):473-7.

Wang XP, Geng SJ, Ri YJ, Cao DH, Liu J, Shi DC, Yang CW. Physiological responses and adaptive strategies of tomato plants to salt and alkali stresses. SCI Hortic-Amsterdam. 2011;130(1):248-55.

Yang CW, Shi DC, Wang DL. Comparative effects of salt and alkali stresses on growth, osmotic adjustment and ionic balance of an alkali-resistant halophyte Suaeda glauca (Bge.). Plant Growth Regul. 2008;56(2):179-90.

Li RL, Shi FC, Fukuda K, Yang YL. Effects of salt and alkali stresses on germination, growth, photosynthesis and ion accumulation in alfalfa (Medicago sativa L.). Soil Sci Plant Nutr. 2010;56(5):725-33.

Zhao GQ, Ma BL, Ren CZ. Growth, Gas Exchange, Chlorophyll Fluorescence, and Ion Content of Naked Oat in Response to Salinity. Crop Sci. 2007;47:123-31.

Chen WC, Cui PJ, Sun HY, Guo WQ, Yang CW, Jin H, Fang B, Shi DC. Comparative effects of salt and alkali stresses on organic acid accumulation and ionic balance of seabuckthorn (Hippophae rhamnoides L.). Ind Crop Prod. 2009;30(3):351-8.

Doganlar ZB, Demi̇R K, Basak H, Gul I. Effects of salt stress on pigment and total soluble protein contents of three different tomato cultivars. Afr J Agr Res. 2010;15(15):2056-65.

Arnon DI, Hoagland DR. A comparison of water culture and soil as media for crop production. Science. 1939;89(2318):512-4.

Qin JQ, Xia BC, Zhao P. Photosynthetic physiological response of two Miscanthus floridulus populations to Cd stress. Acta Ecologica Sinica. 2010;30(2):288-99.

Li ZJ, Xie XY, Zhang SQ, Liang YC. Negative Effects of Oxytetracycline on Wheat (Triticum aestivum L.) Growth, Root Activity, Photosynthesis, and Chlorophyll Contents. J Integr Agr. 2011;10(10):1545-53.

Musick GJ, Fairchild ML, Fergason VL, Zuber MS. A method of measuring root volume in corn (Zeamays L.). Crop Sci. 1965; 5(6): 601-2.

Bai BZ, Shi AG, Zhang JY. Plant Physiology. 1st ed. China: Beijing Agricultural Press; 2001. 23p.

Zhang GW, Liu ZL, Zhou JG, Zhu YL. Effects of Ca(NO3)2 stress on oxidative damage, antioxidant enzymes activities and polyamine contents in roots of grafted and non-grafted tomato plants. Plant Growth Regul. 2008;56(1):7-19.

Yang CW, Shi DC, Wang DL. Comparative effects of salt and alkali stresses on growth, osmotic adjustment and ionic balance of an alkali-resistant halophyte Suaeda glauca (Bge.). Plant Growth Regul. 2008;56(2):179-90.

Wang XP, Jiang P, Ma Y, Geng S, Wang S, Shi DC. Physiological strategies of sunflower exposed to salt or alkali stresses: restriction of ion transport in the cotyledon node zone and solute accumulation. Agron J. 2015;107(6):2181-92.

Guo R, Yang Z, Li F, Yan C, Zhong X, Liu Q, Xia X, Li H, Zhao L. Comparative metabolic responses and adaptive strategies of wheat (Triticum aestivum) to salt and alkali stress. BMC Plant Biol. 2015;15(1):170.

Campbell SA, Nishio JN. Iron deficiency studies of sugar beet using an improved sodium bicarbonate-buffered hydroponics growth system. J Plant Nutr. 2000;23(6): 741-57.

Saeedipour S, Moradi F. Effect of drought at the post-anthesis stage on remobilization of carbon reserves and some physiological changes in the flag leaf of two wheat cultivars differing in drought resistance. J Agr Sci. 2011;3(3):3425-29.

Yang CW, Xu HH, Wang LL, Liu J, Shi DC, Wang DL. Comparative effects of salt-stress and alkali-stress on the growth, photosynthesis, solute accumulation, and ion balance of barley plants. Photosynthetica. 2009;47(1):70-86.

Zheng YH, Xu XB, Wang MY, Zheng XH, Li ZJ, Jiang GM. Responses of salt-tolerant and intolerant wheat genotypes to sodium chloride: photosynthesis, antioxidants activities, and yield. Photosynthetica. 2009;47(1):87-94.

Yang JY, Zheng W, Tian Y, Wu Y, Zhou DW. Effects of various mixed salt-alkaline stresses on growth, photosynthesis, and photosynthetic pigment concentrations of Medicago ruthenica seedlings. Photosynthetica. 2011;49(2):275-84.

Komatsu Y. Some observations on the root development as related to the growth of the aerial part of rice plant treated with shading and nitrogen application into lower part of furrow slice. Jpn J Crop Sci. 2008;29(2):199-201.

Tang WB, Deng HB, Xiao YH, Zhang GL, Fan K, Mo H, Chen LY. Root characteristics of high-yield c liangyou rice combinations of two-line hybrid rice. Sci Agri Sinica. 2010;43(14):2859-68.

Seckin B, Sekmen AH, Türkan İ. An enhancing effect of exogenous mannitol on the antioxidant enzyme activities in roots of wheat under salt stress. J Plant Growth Regul. 2009;28(1):12-20.

Yang JC. Relationships of rice root morphology and physiology with the formation of grain yield and quality and the nutrient absorption and utilization. Sci Agri Sinica. 2011;44:36-46.

Xu J, Duan XG, Yang J, Beeching JR, Zhang P. Enhanced reactive oxygen species scavenging by overproduction of superoxide dismutase and catalase delays postharvest physiological deterioration of cassava storage roots. Plant Physiol. 2013;161(3):1517-28.

Erdei L, Trivedi S, Takeda K, Matsumot H. Effects of osmotic and salt stresses on the accumulation of polyamines in leaf segments from wheat varieties differing in salt and drought tolerance. J Plant Physiol. 1990;137(2):165-8.

Liu J, Jiang MY, Zhou YF, Liu YL. Production of polyamines is enhanced by endogenous abscisic acid in maize seedlings subjected to salt stress. J Integr Plant Biol. 2005;47(11):1326-34.

Downloads

Published

2018-05-30

How to Cite

1.
Qin Y, Bai J, Wang Y, Liu J, Hu Y, Dong Z, Ji L. Comparative effects of salt and alkali stress on photosynthesis and root physiology of oat at anthesis. Arch Biol Sci [Internet]. 2018May30 [cited 2024Nov.22];70(2):329-38. Available from: https://serbiosoc.org.rs/arch/index.php/abs/article/view/1939

Issue

Section

Articles