Please wait a minute...
Journal of Integrative Agriculture  2013, Vol. 12 Issue (12): 2172-2178    DOI: 10.1016/S2095-3119(13)60411-6
Physiology & Biochentry · Tillage · Cultivation Advanced Online Publication | Current Issue | Archive | Adv Search |
Regulation of Calcium on Peanut Photosynthesis Under Low Night Temperature Stress
 LIU Yi-fei, HAN Xiao-ri, ZHAN Xiu-mei, YANG Jin-feng, WANG Yu-zhi, SONG Qiao-bo , CHEN
National Engineering Laboratory for Eff?icient Utilization of Soil and Fertilizer Resources/Biochar Engineering Technology Research Center of Liaoning Province/College of Land and Environment, Shenyang Agricultural Universi ty, Shenyang 110866, P.R.China
Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
摘要  The effects of different levels of CaCl2 on photosynthesis under low night temperature (8°C) stress in peanuts were studied in order to find out the appropriate concentration of Ca2+ through the artificial climate chamber potted culture test. The results indicated that Ca2+, by means of improving the stomatal conductivity of peanut leaves under low night temperature stress, may mitigate the decline of photosynthetic rate in the peanut leaves. The regulation with 15 mmol L-1 CaCl2 (Ca15) was the most effective, compared with other treatments. Subsequently, the improvement of Ca2+ on peanut photosynthesis under low night temperature stress was validated further through spraying with Ca15, Ca2+ chelator (ethylene glycol bis(2-aminoethyl) tetraacetic acid; EGTA) and calmodulin antagonists (trifluonerazine; TFP). And CaM (Ca2+-modulin) played an important role in the nutritional signal transduction for Ca2+ mitigating photosynthesis limitations in peanuts under low night temperature stress.

Abstract  The effects of different levels of CaCl2 on photosynthesis under low night temperature (8°C) stress in peanuts were studied in order to find out the appropriate concentration of Ca2+ through the artificial climate chamber potted culture test. The results indicated that Ca2+, by means of improving the stomatal conductivity of peanut leaves under low night temperature stress, may mitigate the decline of photosynthetic rate in the peanut leaves. The regulation with 15 mmol L-1 CaCl2 (Ca15) was the most effective, compared with other treatments. Subsequently, the improvement of Ca2+ on peanut photosynthesis under low night temperature stress was validated further through spraying with Ca15, Ca2+ chelator (ethylene glycol bis(2-aminoethyl) tetraacetic acid; EGTA) and calmodulin antagonists (trifluonerazine; TFP). And CaM (Ca2+-modulin) played an important role in the nutritional signal transduction for Ca2+ mitigating photosynthesis limitations in peanuts under low night temperature stress.
Keywords:  peanut       Ca2+       low night temperature stress       photosynthesis  
Received: 24 October 2012   Accepted:
Fund: 

This work was Supported by the China Postdoctoral Science Foundation (2012M510839), Doctoral Fund of Ministry of Education of China (20122103120011), the National Natural Science Initial Foundation of Shenyang Agricultural University, China (20112013), the Postdoctoral Science Foundation of Shenyang Agricultural University, China (105110) and the Peanut Nutrition and Fertilizer Program for China Agriculture Research System, China (CARS-14).

Corresponding Authors:  HAN Xiao-ri, Tel/Fax: +86-24-88493097, E-mail: hanxiaori@163.com   
About author:  LIU Yi-fei, E-mail: feifan61@gmail.com

Cite this article: 

LIU Yi-fei, HAN Xiao-ri, ZHAN Xiu-mei, YANG Jin-feng, WANG Yu-zhi, SONG Qiao-bo , CHEN . 2013. Regulation of Calcium on Peanut Photosynthesis Under Low Night Temperature Stress. Journal of Integrative Agriculture, 12(12): 2172-2178.

[1]Ai X Z, Wang X F, Cui Z F, Wang Z L. 2006. Effect of calcium on photosynthesis of cucumber under low light intensity and sub-optimal temperature. Scientia Agricultura Sinica, 39, 1865-1871 (in Chinese)

[2]Anireddy S N, Gul S A, Helena C, Irene S D. 2011. Coping with stresses: role of calcium- and calcium/calmodulin- regulated gene expression. The Plant Cell, 23, 2010- 2032.

[3]Bagnall D J, King R W, Farquhar G D. 1988. Temperature- dependent feedback inhibition of photosynthesis in peanut. Planta, 175, 348-354

[4]Berry J, Bjorkman O. 1980. Photosynthetic response and adaptation to temperature in higher plants. Annual Review of Plant Physiology, 31, 491-543

[5]Damian J A, Donald R O. 2001. Impact of chilling temperatures on photosynthesis in warm climate plants. Trends in Plant Science, 6, 36-42

[6]Demmig A B, Adams W W. 1996. The role of xanthophyll cycle carotenoids in the protection of photosynthesis. Trends in Plant Science, l, 21-26

[7]Hepler P K. 2005. Calcium: A cent ral regulator of plant growth and development. The Plant Cell, 17, 2142-2155

[8]Li T G, Wang K C, Luo Q Y. 2012. Effects of exogenous Ca2+ on physiological and photosynthesis of Fritillaria anhuiensis under high temperature stress. Plant Nutrition and Fertilizer Science, 18, 765-770 (in Chinese)

[9]Liang F. 2009. Studies on mechanism of responsing to stress of low temperature and poor light and alleviatory effects of ASA and Ca2+ in chrysanthemum. MSc thesis, Shandong Agricultural University, Shandong, China. (in Chinese)

[10]Liang Y, Wang S G. 2001. The protective function of Ca2+ on the membrane of rice seedling under low temperature stress. Acta Agronomica Sinica, 27, 59-64 (in Chinese)

[11]Lin L Q, Li L, Bi C, Zhang Y L, Wan S B, Meng J J, Meng Q W, Li X G. 2011. Damaging mechanisms of chilling- and salt stress to Arachis hypogaea L. leaves. Photosynthetica, 49, 37-42

[12]Liu Y F, Li T L, Qi H Y, Xu C Q, Li J Y, Yin X Y. 2010. Effects of grafting on carbohydrate accumulation and sugar-metabolic enzyme activities in muskmelon. African Journal of Biotechnology, 9, 25-35

[13]Liu Y F, Qi H Y, Bai C M, Qi M F, Chen W Z, Xu C Q, Li T L. 2011. Grafting helps improve photosynthesis and carbohydrate metabolism in leaves of muskmelon. International Journal of Biological Sciences, 7, 1161- 1170.

[14]Mukesh J, Bhuvan P P, Alice C H, Barry L T, Maria G. 2011. Calcium dependent protein kinase (CDPK) expression during fruit development in cultivated peanut (Arachis hypogaea) under Ca2+-sufficient and -deficient growth regimens. Journal of Plant Physiology, 168, 2272-2277

[15]Sun D Y. 1998. Cellular Signal Transduction. Science Press, Beijing, China. (in Chinese)

[16]Sun X Z, Guo X F, Zheng C S, Wang W L, Liang F. 2008. Effects of exogenous Ca2+ on leaf photosynthetic apparatus and active oxygen scavenging enzyme system of chrysanthemum under high temperature stress. Chinese Journal of Applied Ecology, 19, 1983-1988 (in Chinese)

[17]Townley H E, Knight M R. 2000. Calmodulin as a potential negative regulator of Arabidopsis COR gene expression. Plant Physiology, 128, 1169-1172.

[18]Wan S B. 2007. Peanut Quality Sciences. Chinese Agricultural Science and Technology Press, Beijing, China. (in Chinese)

[19]Wayne A S, Hillel F. 1998. Calmodulin, calmodulin-related proteins and plant responses to the environment. Trends in Plant Science, 3, 299-304

[20]Yang T B, Poovaiah B W. 2003. Calcium/calmodulin- mediated signal network in plants. Trends in Plant Science, 8, 505-512

[21]Yi J H, Sun Z J. 2004. Responses of photosynthesis to different low temperatures in tobacco seedlings leaves. Acta Agronomica Sinica, 30, 582-588 (in Chinese)

[22]You J H, Lu J M, Yang W J. 2002. Effects of Ca2+ on photosynthesis and related physiological indexes of wheat seedlings under low temperature stress. Acta Agronomica Sinica, 28, 693-696. (in Chinese)

[23]Yu C W, Murphy T M, Sung W W, Lin C H. 2002. H2O2 treatment induces glutathione accumulation and chilling tolerance in mung bean. Functional Plant Biology, 29, 1081-1087.

[24]Yu S L. 2008. Peanut Varieties and Their Pedigree in China. Shanghai Science and Technology Press, Shanghai, China. (in Chinese)

[25]Zhang H C, Yin W L, Xia X L. 2007. The Mechanism of Ca2+ signal transduction under abiotic stresses in plants. Chinese Bulletin of Botany, 24, 114-122.

[26]Zhu X J, Yand J S, Liang Y C, Lou Y S, Yang X Y. 2004. Effects of exogenous calcium on photosynthesis and its related physiological characteristics of rice seedlings under salt stress. Scientia Agricultura Sinica, 37, 1497- 1503. (in Chinese)
[1] Shengzhong Zhang, Xiaohui Hu, Feifei Wang, Huarong Miao, Chu Ye, Weiqiang Yang, Wen Zhong, Jing Chen. Identification of QTLs for plant height and branching-related traits in cultivated peanut[J]. >Journal of Integrative Agriculture, 2025, 24(7): 2511-2524.
[2] Bingyan Huang, Hua Liu, Yuanjin Fang, Lijuan Miao, Li Qin, Ziqi Sun, Feiyan Qi, Lei Chen, Fengye Zhang, Shuanzhu Li, Qinghuan Zheng, Lei Shi, Jihua Wu, Wenzhao Dong, Xinyou Zhang. Identification of oil content QTLs on Arahy12 and Arahy16, and development of KASP markers in cultivated peanut (Arachis hypogaea L.)[J]. >Journal of Integrative Agriculture, 2025, 24(6): 2096-2105.
[3] Shumin Wang, Tao Guo, Shaolin Zhang, Hong Yang, Li Li, Qingchuan Yang, Junping Quan, Ruicai Long. Functional identification of Medicago truncatula MtRAV1 in regulating growth and development[J]. >Journal of Integrative Agriculture, 2025, 24(5): 1944-1957.
[4] Fei Jin, Lei Xu, Zhihu Lü, Yuchuan Zhang, Qinghua Yang, Qingfang Han, Baili Feng. Combined physiological and pathway analysis revealed the effect of Sporisorium destruens on photosynthesis in broomcorn millet (Panicum miliaceum L.) [J]. >Journal of Integrative Agriculture, 2025, 24(3): 1065-1079.
[5] Jiamao Gu, Pengkun Liu, Wenting Nie, Zhijun Wang, Xiaoyu Cui, Hongdan Fu, Feng Wang, Mingfang Qi, Zhouping Sun, Tianlai Li, Yufeng Liu. Abscisic acid alleviates photosynthetic damage in the tomato ABA-deficient mutant sitiens and protects photosystem II from damage via the WRKY22–PsbA complex under low-temperature stress[J]. >Journal of Integrative Agriculture, 2025, 24(2): 546-563.
[6] Yulong Wang, Aizhong Yu, Pengfei Wang, Yongpan Shang, Feng Wang, Hanqiang Lü, Xiaoneng Pang, Yue Li, Yalong Liu, Bo Yin, Dongling Zhang, Jianzhe Huo, Keqiang Jiang, Qiang Chai. No-tillage with total green manure mulching increases maize yield through improved soil moisture and temperature environment and enhanced maize root structure and photosynthetic capacity[J]. >Journal of Integrative Agriculture, 2025, 24(11): 4211-4224.
[7] Kai Zhao, Yanzhe Li, Zhan Li, Zenghui Cao, Xingli Ma, Rui Ren, Kuopeng Wang, Lin Meng, Yang Yang, Miaomiao Yao, Yang Yang, Xiaoxuan Wang, Jinzhi Wang, Sasa Hu, Yaoyao Li, Qian Ma, Di Cao, Kunkun Zhao, Ding Qiu, Fangping Gong, Zhongfeng Li, Xingguo Zhang, Dongmei Yin. Genome-wide analysis of AhCN genes reveals that AhCN34 is involved in bacterial wilt resistance in peanut[J]. >Journal of Integrative Agriculture, 2025, 24(10): 3757-3771.
[8] Xinyu Man, Sha Tang, Yu Meng, Yanjia Gong, Yanqing Chen, Meng Wu, Guanqing Jia, Jun Liu, Xianmin Diao, Xiliu Cheng. Convergent and divergent signaling pathways in C3 rice and C4 foxtail millet crops in response to salt stress[J]. >Journal of Integrative Agriculture, 2025, 24(10): 3719-3738.
[9] Fei Xiang, Zhenyuan Li, Yichen Zheng, Caixia Ding, Benu Adhikari, Xiaojie Ma, Xuebing Xu, Jinjin Zhu, Bello Zaki Abubakar, Aimin Shi, Hui Hu, Qiang Wang. Characterization and correlation of engineering properties with microstructure in peanuts: A microscopic to macroscopic analysis[J]. >Journal of Integrative Agriculture, 2025, 24(1): 339-352.
[10] Bo Jiao, Xin Guo, Yiying Chen, Shah Faisal, Wenchao Liu, Xiaojie Ma, Bicong Wu, Guangyue Ren, Qiang Wang. Low-fat microwaved peanut snacks production: Effect of defatting treatment on structural characteristics, texture, color, and nutrition[J]. >Journal of Integrative Agriculture, 2024, 23(7): 2491-2502.
[11] Song Wan, Yongxin Lin, Hangwei Hu, Milin Deng, Jianbo Fan, Jizheng He. Excessive manure application stimulates nitrogen cycling but only weakly promotes crop yields in an acidic Ultisol: Results from a 20-year field experiment[J]. >Journal of Integrative Agriculture, 2024, 23(7): 2434-2445.
[12] Xiaohui Wu, Mengyuan Zhang, Zheng Zheng, Ziqi Sun, Feiyan Qi, Hua Liu, Juan Wang, Mengmeng Wang, Ruifang Zhao, Yue Wu, Xiao Wang, Hongfei Liu, Wenzhao Dong, Xinyou Zhang.

Fine-mapping of a candidate gene for web blotch resistance in Arachis hypogaea L. [J]. >Journal of Integrative Agriculture, 2024, 23(5): 1494-1506.

[13] Xinlong Gao, Fan Li, Yikun Sun, Jiaqi Jiang, Xiaolin Tian, Qingwen Li, Kaili Duan, Jie Lin, Huiquan Liu, Qinhu Wang.

Basal defense is enhanced in a wheat cultivar resistant to Fusarium head blight [J]. >Journal of Integrative Agriculture, 2024, 23(4): 1238-1258.

[14] WANG Kang-kang, JIN Meng-jiao, LI Jing-jing, REN Ye-song, LI Zai-yuan, REN Xing-hai, HUANG Cong, WAN Fang-hao, QIAN Wan-qiang, LIU Bo.

The evolution and diurnal expression patterns of photosynthetic pathway genes of the invasive alien weed, Mikania micrantha [J]. >Journal of Integrative Agriculture, 2024, 23(2): 590-604.

[15] XU Yan-xia, ZHANG Jing, WAN Zi-yun, HUANG Shan-xia, DI Hao-chen, HE Ying, JIN Song-heng. Physiological and transcriptome analyses provide new insights into the mechanism mediating the enhanced tolerance of melatonin-treated rhododendron plants to heat stress[J]. >Journal of Integrative Agriculture, 2023, 22(8): 2397-2411.
No Suggested Reading articles found!