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不同浓度盐胁迫下盐穗木叶片结构的比较观察

王虹;齐政;张富春   

  1. 新疆生物资源与基因工程重点实验室/新疆大学生命科学与技术学院,乌鲁木齐,830046
  • 收稿日期:2016-11-25 修回日期:2016-11-25 出版日期:2016-11-25 发布日期:2016-11-25

Leaf Anatomical Structure of Halostachys caspica under Different Concentrations of Salt Stress

WANG Hong;QI Zheng;ZHANG Fu-chun   

  • Received:2016-11-25 Revised:2016-11-25 Online:2016-11-25 Published:2016-11-25

摘要: 【目的】盐穗木叶片退化成鳞片状,在植株的光合作用中不是起主要作用,但其对逆境的变化很敏感,研究盐胁迫下盐穗木叶片结构变化,找出其最佳盐浓度范围。【方法】可用不同盐浓度胁迫下,切片后显微镜观察盐穗木叶片细胞结构的变化。【结果】随着盐浓度的增加,盐穗木叶片逐渐变厚,细胞排列由疏松到紧密,含晶细胞和储水细胞大而多,表皮细胞壁向外呈乳突状凸起逐渐增多,可以充分的吸收水分,而叶片表皮细胞壁外凸又由乳突状到毛状,细胞中水分的减少。叶表皮和气孔中有较多晶体,盐穗木叶片上的气孔器与表皮细胞的角质层均可以向外泌盐。【结论】盐穗木是一种聚盐和泌盐混合形式的盐生植物。在盐浓度在300~500 mmol/L下,盐穗木叶片细胞结构较正常,是其生长的最佳盐浓度范围。

Abstract: Objective]Although leaves of Halostachys caspica degenerate into a scaly shape and don't play a major role in plant photosynthesis,but they are very sensitive to the changes of environment.[Method]As an important organ,the leaf cell structure was observed under different salt concentration stresses by micro-scopes.[Result]With the increase of salt concentration,the leaves of H.caspica were getting thicker progres-sively,cells arrangement from loose to tight,and crystal and storage cells became larger and more.Papillary-like bulge of epidermal cell wall showed a gradual increase in the outward convex shape,which could fully absorb the water.The variation in papillary-like to hair-like bulge of leaf epidermal cell wall indicated that water content in cells was decreased.More crystal in the leaf epidermal and stomata showed that the cuticle of epidermal cells and stomata of H.caspica could secrete salt.[Conclusion]H.caspica is an excessive mixed halophyte plant both aggregating salt and salt secreting.300 mmol/L-500 mmol/L salt concentrations are the best salt concentrations for the growing of H.caspica,and leaf cell structure is normal under those salt concen-trations.


ISSN 1001-4330 CN 65-1097/S
邮发代号:58-18
国外代号:BM3342
主管:新疆农业科学院
主办:新疆农业科学院 新疆农业大学 新疆农学会

出版单位:《新疆农业科学》编辑部
地址:乌鲁木齐市南昌路403号新疆农业科学院
邮编:830091
电话:0991-4502046
E-mail:xjnykx-h@xaas.ac.cn


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