Suberin lamella development in maize seedling roots grown in aerated and stagnant conditions

被引:68
作者
Enstone, DE [1 ]
Peterson, CA [1 ]
机构
[1] Univ Waterloo, Dept Biol, Waterloo, ON N2L 3G1, Canada
关键词
Zea mays L; aerenchyma; Casparian bands; endodermis; exodermis; hypoxia; radial oxygen loss (ROL);
D O I
10.1111/j.1365-3040.2005.01286.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Hypoxia can stimulate the development of a suberized exodermis in aquatic plants; however, its influence on this aspect of terrestrial root development is sparsely documented. To determine the effects of hypoxia on maize (Zea mays cv. Seneca Horizon) roots, seedlings were grown in vermiculite (VERM), aerated hydroponics (AER), stagnant hydroponics with agar (STAG), or aerated hydroponics with agar (AERAG). The endo- and exodermis were examined for wall modifications. Lateral root emergence and aerenchyma formation were documented qualitatively. The endodermal Casparian band formation was unaffected by treatment. Endodermal and exodermal suberin lamella formation was earliest and most extensive in VERM. Suberization, especially in the exodermis of aerated treatments, was depressed in all hydroponic media. In comparison with AER, STAG exodermal lamellae were increased, but endodermal lamellae were decreased. Since the suberized exodermis forms a barrier to radial oxygen loss from roots to the medium, its stimulation in STAG roots (which also developed extensive aerenchyma) would help retain oxygen in the root. The reduction of endodermal lamellae should facilitate oxygen diffusion into the stele. Clearly, the response to environmental conditions is variable within individual cortical cell layers. Additionally, the observed patterns of lamellae, aerenchyma and lateral root development indicate a tight radial co-ordination of root development.
引用
收藏
页码:444 / 455
页数:12
相关论文
共 41 条
[1]   Rice and Phragmites: effects of organic acids on growth, root permeability, and radial oxygen loss to the rhizosphere [J].
Armstrong, J ;
Armstrong, W .
AMERICAN JOURNAL OF BOTANY, 2001, 88 (08) :1359-1370
[3]   Oxygen distribution in wetland plant roots and permeability barriers to gas-exchange with the rhizosphere:: a microelectrode and modelling study with Phragmites australis [J].
Armstrong, W ;
Cousins, D ;
Armstrong, J ;
Turner, DW ;
Beckett, PM .
ANNALS OF BOTANY, 2000, 86 (03) :687-703
[4]   USE OF POLAROGRAPHY IN ASSAY OF OXYGEN DIFFUSING FROM ROOTS IN ANAEROBIC MEDIA [J].
ARMSTRONG, W .
PHYSIOLOGIA PLANTARUM, 1967, 20 (03) :540-+
[5]  
Armstrong W., 2002, Plant Roots: The Hidden Half, P729, DOI DOI 10.1201/9780203909423
[6]  
ARMSTRONG W, 1978, ADV BOT RES, P225
[7]  
Armstrong W., 1991, Plant Life Under Oxygen Deprivation, P267
[8]   A HISTOLOGICAL STUDY OF LATERAL ROOT INITIATION AND DEVELOPMENT IN ZEA-MAYS [J].
BELL, JK ;
MCCULLY, ME .
PROTOPLASMA, 1970, 70 (02) :179-&
[9]  
BENFEY PN, 1993, DEVELOPMENT, V119, P57
[10]   EFFICIENT LIPID STAINING IN PLANT-MATERIAL WITH SUDAN RED-7B OR FLUORAL YELLOW-088 IN POLYETHYLENE GLYCOL-GLYCEROL [J].
BRUNDRETT, MC ;
KENDRICK, B ;
PETERSON, CA .
BIOTECHNIC & HISTOCHEMISTRY, 1991, 66 (03) :111-116