• 中文核心期刊
  • CSCD来源期刊
  • 中国科技核心期刊
  • CA、CABI、ZR收录期刊

镁营养对西瓜叶绿素荧光特性及生理代谢的影响

Effects of Magnesium on Chlorophyll Fluorescence and Metabolism of Citrullus lanatus

  • 摘要:
      目的  探讨镁营养对西瓜(Citrullus lanatus)生长发育和生理代谢的影响,明确西瓜生长的适宜镁浓度范围。
      方法  采用砂培法,对西瓜进行5个施镁质量浓度(0 、24 、48、96 和192 mg·L−1)处理,并测定西瓜在不同施镁浓度下的生长特性(叶片和根系形态、生物量积累)、果实品质(维生素C、可溶性固形物、可溶性蛋白和可溶性糖含量)、叶绿素荧光特性和生理响应(渗透调节、膜伤害和抗氧化酶系统)。
      结果  用24 ~96 mg·L−1的镁素可以降低西瓜叶片膜伤害,提高光系统Ⅱ(PSII)活性,增加叶片抗氧化物质谷胱甘肽(glutathione, GSH)和还原型抗坏血酸(reduced ascorbic acid, AsA)含量,增强叶片抗氧化酶活性,包括过氧化物酶(peroxidase, POD)、超氧化物歧化酶(superoxide dismutase, SOD)、过氧化氢酶(catalase, CAT)和单脱氢抗坏血酸还原酶(monodehydroascorbate reductase, DHAR),降低叶片丙二醛(malondialdehyde, MDA)和脯氨酸(proline, Pro)含量以及细胞膜透性,促进AsA-GSH循环,增强光合作用,提高生物量积累,增加果实中维生素C、可溶性固形物、可溶性蛋白和可溶性糖含量。其中,48 mg·L−1镁处理对西瓜的生长发育增效最明显,而缺镁(0 mg·L−1)和镁过量(192 mg·L−1)胁迫下,西瓜叶片产生膜脂过氧化伤害,根系变短,叶绿素荧光参数放氧复合体(OEC)、电子传递量子产额(φEo) 、受体库容量(Sm)和单位面积反应中心数量(RC/CSo)降低,单位反应中心光能的吸收(ABS/RC)、耗散(DI0/RC) 、捕获(TR0/RC)及QA还原速率(Mo)增加,叶片光合机构完整性被破坏,光合作用减弱,西瓜生长受到明显抑制,其中缺镁影响最严重。
      结论  缺镁和镁过量处理降低西瓜PSII活性,抑制西瓜生长,而适量增施镁可有效提高西瓜的生理活性,PSII的结构和功能稳定,光合作用强,西瓜生长好,果实品质高,48 mg·L−1为西瓜栽培最适宜施镁质量浓度。

     

    Abstract:
      Objective   Effects of magnesium on the growth, development, and metabolism of Citrullus lanatus were studied to determine the appropriate nutrient supply for the melon cultivation.
      Method   At the concentrations of 0, 24, 48, 96, and 192 mg·L−1 on magnesium in sand culture, the growth characteristics (i.e., leaf and root morphology, chlorophyll fluorescence, and biomass accumulation), fruit quality (i.e., vitamin C, soluble solids, soluble protein, and soluble sugar), and physiological responses (i.e., osmoregulation, membrane damage, and antioxidases) of various C. lanatus varieties were compared.
      Result   In the range of 24-96 mg·L−1, the application of magnesium reduced the vulnerability of leaf membrane to damages, increased the contents of antioxidant glutathione (GSH) and ascorbic acid (AsA) as well as the activities of photosystemⅡ (PSII), peroxidase (POD), superoxide dismutase (SOD), catalase (CAT), and monodehydroascorbate reductase (DHAR), while decreased the contents of malondialdehyde (MDA) and proline (Pro), and reduced the cell membrane permeability of the leaves. The addition also promoted the AsA-GSH cycle, photosynthesis, and the biomass accumulations on vitamin C, soluble solids, soluble protein, and soluble sugar. Among the treatments, the 48 mg·L−1 magnesium addition in the culture substrate rendered the most significant improvements on the growth and development of C. lanatus. Whereas, either a deficiency (at 0 mg·L−1) or an excess (e.g., at 192 mg·L−1) on the nutrient ill-affected the membrane lipid peroxidation and shortened the plant roots. Furthermore, the chlorophyll fluorescence declined as indicated by the lower oxygen evolution complex (OEC), quantum yield for electron transport (φEo), and receptor library capacity (Sm), the density of reaction centers (RC/CSo) decreased, the light energy absorption per unit reaction center (ABS/RC) lowered, and the dissipative (DI0/RC), capture (TR0/RC), and QA reduction rate (Mo) increased. Thus, either deprivation or over-supply of magnesium could significantly disrupt the normal photosynthetic function inhibiting the growth of C. lanatus.
      Conclusion  Particularly in deficiency, but also in excess, magnesium in soil could diminish the PSII activity and retard the growth of C. lanatus. Appropriate application of the nutrient, such as at 48 mg·L−1 concentration in soil, could effectively improve the physiological activity, stabilize the structure and function of PSII, strengthen the leaf photosynthesis to result in healthy growth and high quality fruit production of C. lanatus.

     

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