J Plant Ecol ›› 2019, Vol. 12 ›› Issue (3): 507-518.doi: 10.1093/jpe/rty043

• Research Articles • Previous Articles     Next Articles

Anthocyanin accumulation in juvenile Schima superba leaves is a growth trade-off by consuming energy for adaptation to high light during summer

Zhengchao Yu, Qilei Zhang, Xiaoting Zheng, Xuandong Huang and Changlian Peng*#br#   

  1. Guangdong Provincial Key Laboratory of Biotechnology for Plant Development, School of Life Sciences, South China Normal University, Guangzhou 510631, China
    *Correspondence address. Guangdong Provincial Key Laboratory of Biotechnology for Plant Development, Guangzhou Key Laboratory of Subtropical Biodiversity and Biomonitoring, School of Life Sciences, South China Normal University, No. 55 Zhongshan Avenue West, Tianhe District, Guangzhou 510631, Guangdong, China. Tel: +86-20-85217612; Fax: +86-20-85211372; E-mail: pengchl@scib.ac.cn
  • Received:2018-08-22 Revised:2018-10-16 Accepted:2018-10-24 Online:2019-05-15 Published:2019-07-01



Anthocyanin accumulation is the main factor underlying why young plant leaves turn red, and plant growth follows the principle of maximizing the economic efficiency of energy. There is a need to verify the role of young plant leaves turning red and confirm whether anthocyanin accumulation overconsumes the energy of the plant.


We compared the different pigment contents, antioxidant capacities, leaf mass per area, photosynthetic characteristics, dark respiration rates, light compensation points (LCPs) and electron flow distribution of young and mature Schima superba leaves grown under full sunlight and 30% full sunlight conditions. We then examined the correlations between anthocyanins and total antioxidant capacity, photosynthetic pigments, dark respiration rates, LCPs by using linear regression. Finally, we analyzed Pearson correlation coefficients and used principal component analysis to evaluate the interactions of these functional indicators.

Important Findings

The young leaves of S. superba accumulated anthocyanins in full sunlight but not in 30% full sunlight. Anthocyanins substantially contributed to the total antioxidant capacity (accounting for 33.29%) in juvenile S. superba leaves. Young leaves containing more anthocyanin accumulated less reactive oxygen species after high light (HL) treatment. However, juvenile leaves accumulating anthocyanins showed 56.97% higher dark respiration rates, 24.79% higher LCPs and 5.32% higher allocations of electron flow to photorespiration and lower organic substance accumulation than did those without anthocyanins. These results suggest that young S. superba leaves must consume more energy to accumulate anthocyanins to adapt to HL environments. Therefore, plants sacrifice growth rate to ensure survival, which is a trade-off for their ability to respond to external environments.

Key words: juvenile leaves, anthocyanin, high light environment, trade-off, photoprotection

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[1] Liu Ying-di. The Role of Ultrastructure in Algal Systematics[J]. Chin Bull Bot, 1990, 7(04): 18 -23 .
[2] Fan Guo-qiang and Jiang Jian-ping. Study on the Methods of Extraction of Protein from Paulownia Leaves[J]. Chin Bull Bot, 1997, 14(03): 61 -64 .
[3] Tong Zhe and Lian Han-ping. Cryptochrome[J]. Chin Bull Bot, 1985, 3(02): 6 -9 .
[4] Huang Ju-fu and Luo Ai-ling. The Advances of the Studies on Extraction of FeMoco from Nitrogenase Molybdenum-Iron Protein[J]. Chin Bull Bot, 1991, 8(03): 19 -25 .
[5] Hsu Rong-jiang Gu Wen-mao Gao Jing-cheng and Peng Chang-ming. Inhibitory Effect of High CO2 and Low O2 Tension on Ethylene Evolution in Apples[J]. Chin Bull Bot, 1984, 2(01): 29 -31 .
[6] Zou Shu-hua;Zhao Shu-wen and Xu Bao. Electropheresis Profiles of Esterase Isozymes in Different Types of Soybean[J]. Chin Bull Bot, 1985, 3(06): 18 -20 .
[7] . [J]. Chin Bull Bot, 1999, 16(增刊): 49 -52 .
[8] Chi Tingfei;Shi Xiaofang;Huang Ruzhu;Zheng Xiangyun;Yuan Xiangning and Wu Dangjian. A Preliminary Study on the Chemical Constituents of the Leave Oil in prunus zippeliana Mig[J]. Chin Bull Bot, 1986, 4(12): 44 -45 .
[9] Houqing Zeng, Yaxian Zhang, Shang Wang, Xiajun Zhang, Huizhong Wang, Liqun Du. Calcium/calmodulin-mediated Signal Transduction System in Plants[J]. Chin Bull Bot, 2016, 51(5): 705 -723 .
[10] Zhu Zhi-qing. Abbreviations for some Commonly Used Terms in Ultrastructures of Plant Cells[J]. Chin Bull Bot, 1984, 2(04): 57 -58 .