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应用生态学报 ›› 2010, Vol. 21 ›› Issue (3): 675-682.

• 研究报告 • 上一篇    下一篇

A23187和EGTA对光周期诱导菊花成花及其过程中叶片Ca2+分布和碳水化合物的影响

王文莉1,2;王秀峰1,2;郑成淑1,2**;朱翠英1,2;林桂玉1,2   

  1. 1山东农业大学园艺科学与工程学院园艺作物生物学农业部重点开放实验室, 山东泰安 271018;2作物生物学国家重点实验室, 山东泰安 271018
  • 出版日期:2010-03-20 发布日期:2010-03-20

Effects of Ca2+ -carrier A23187 and Ca2+-chelator EGTA on the flower formation of chrysanthemum under photoperiodic induction and the Ca2+ distribution and carbohydrate contents in leaves during the flower formation.

WANG Wen-li1,2;WANG Xiu-feng1,2;ZHENG Cheng-shu1,2;ZHU Cui-ying1,2;LIN Gui-yu1,2   

  1. 1Ministry of Agriculture Key Laboratory of Horticultural Crop Biology, College of Horticulture Science and Engineering, Shandong Agricultural University
    , Tai’an 271018, Shandong, China;2State Key Laboratory of Crop Biology, Tai’an 271018, Shandong, China
  • Online:2010-03-20 Published:2010-03-20

摘要: 以切花菊品种‘神马’为试材,研究光周期诱导菊花成花过程中Ca2+载体A23187和Ca2+螯合剂EGTA处理对花芽分化及其过程中叶片Ca2+分布和蔗糖、可溶性糖及淀粉含量变化的影响.结果表明:对照叶片Ca2+含量在花芽未分化期(Ⅰ)处于较低水平,而在花芽分化启动期(Ⅱ)迅速增加并达到高峰,之后下降;Ca2+亚细胞定位表明,在未分化期(Ⅰ)Ca2+沉淀主要分布在液泡、细胞壁和细胞间隙中,细胞质内较少,而在花芽分化启动期(Ⅱ)细胞质内积累大量的Ca2+沉淀.A23187处理的菊花花芽分化开始和结束时间比对照分别提前2 d和3 d,叶片Ca2+含量比对照显著增加;EGTA处理的叶片Ca2+含量比对照显著减少,花芽分化开始和结束时间分别比对照推迟4 d和8 d;A23187和EGTA处理的叶片Ca2+在花芽分化启动期(Ⅱ)均向细胞质流入并密集.A23187处理的蔗糖和可溶性糖含量在处理2 d时达到峰值,比对照达到峰值的时间提前2 d,与Ca2+达到峰值的时间一致,而EGTA处理的蔗糖和可溶性糖含量在处理2 d时没有明显变化,8 d时才迅速增加达到峰值,即所有处理的蔗糖、可溶性总糖含量在花芽分化启动期(Ⅱ)均增加并达到高峰,之后有所减少,但其在整个花芽分化过程均高于光周期诱导前的含量;对照和A23187处理的淀粉含量在处理2 d时开始减少,而EGTA则在处理8 d后开始减少,至花芽分化结束所有处理的淀粉含量均保持较低水平(低于诱导前).表明Ca2+碳水化合物参与了光周期诱导的菊花成花过程.

关键词: 菊花, 花芽分化, A23187, EGTA, Ca2+, 碳水化合物, 海河流域, 水库, 沉积物, 重金属, 生态风险

Abstract: This paper studied the effects of Ca2+ -carrier A23187 and Ca2+ -chelator EGTA on the bud differentiation of cut flower chrysanthemum (Dendranthema grandiflorium ‘Shenma’) under photoperiodic induction, as well as the Ca2+ distribution and the sucrose, soluble sugar, and starch contents in ‘Shenma’ leaves during the differentiation. In the control, the leaf Ca2+ content was lower at the vegetative stage of apical bud (Ⅰ), increased rapidly and reached a peak at the stage of initial differentiation (Ⅱ), and decreased then. At stage Ⅰ, the Ca2+ was mainly allocated in vacuole, cell wall, and cell lacuna; while at stage Ⅱ, it was more in cytoplasm. Compared with the control, the leaf Ca2+ content of A23187-treated plants increased significantly, and the days of initiation and ending of bud differentiation were advanced by 2 days and 3 days, respectively. On the other hand, the leaf Ca2+ content of EGTA-treated plants decreased significantly, and the days of initiation and ending of bud differentiation were postponed by 4 days and 8 days, respectively. For both A23187- and EGTA-treated plants, their leaf Ca2+  at stage Ⅱ was more allocated in cytoplasm. The leaf sucrose and soluble sugar contents of A23187-treated plants reached a peak on the 2nd day after treatment, and the time to reach the peak was shortened by 2 days, compared with the control, which was consistent with the peak time of Ca2+ . The leaf sucrose and soluble sugar contents of EGTA-treated plants had no significant changes on the 2nd day of treatment, but increased rapidly and reached the peak on the 8th day of treatment (stage Ⅱ), and then decreased. However, the leaf sucrose and soluble sugar contents during the whole period of bud differentiation were higher than those before photoperiodic induction. The leaf starch content of A23187-treated plants and the control decreased 2 days after treatment, while that of EGTA-treated plants began to decrease 8 days after treatment, and maintained at a lower level by the end of bud differentiation. The results indicated that Ca2+ and carbohydrates participated in the flower formation of chrysanthemum under photoperiodic induction.

Key words: chrysanthemum, bud differentiation, A23187, EGTA, Ca2+ , carbohydrate, Haihe River, reservoir, sediment, heavy metal, ecological risk.