Root Endodermis and Exodermis: Structure, Function, and Responses to the Environment

被引:459
作者
Daryl E. Enstone [1 ]
Carol A. Peterson [1 ]
Fengshan Ma [1 ]
机构
[1] University of Waterloo,Department of Biology
[2] Waterloo ON N2L 3G1,undefined
关键词
Endodermis; Exodermis; Structure; Drought; Mycorrhizae; Casparian bands; Suberin lamellae;
D O I
10.1007/s00344-003-0002-2
中图分类号
学科分类号
摘要
Roots of virtually all vascular plants have an endodermis with a Casparian band, and the majority of angiosperm rootstested also have an exodermis with a Casparian band. Both the endodermis and exodermis may develop suberin lamellae and thick, tertiary walls. Each of these wall modifications has its own function(s). The endodermal Casparian band prevents the unimpeded movement of apoplastic substances into the stele and also prevents the backflow of ions that have moved into the stele symplastically and then were released into its apoplast. In roots with a mature exodermis, the barrier to apoplastic inflow of ions occurs near the root surface, but prevention of backflow of ions from the stele remains a function of the endodermis. The suberin lamellae protect against pathogen invasion and possibly root drying during times of stress. Tertiary walls of the endodermis and exodermis are believed to function in mechanical support of the root, but this idea remains to be tested. During stress, root growth rates decline, and the endodermis and exodermis develop closer to the root tip. In two cases, stress is known to induce the formation of an exodermis, and in several other cases to accelerate the development of both the exodermis and endodermis. The responses of the endodermis and exodermis to drought, exposure to moist air, flooding, salinity, ion deficiency, acidity, and mechanical impedance are discussed.
引用
收藏
页码:335 / 351
页数:16
相关论文
共 288 条
[1]  
Aloni R(1998)Indirect evidence for bulk water flow in root cortical cell walls of three dicotyledonous species. Planta 207 1-7
[2]  
Enstone DE(2001)Rice and Am J Bot 88 1359-1370
[3]  
Peterson CA(2000): effects of organic acids on growth, root permeability, and radial oxygen loss to the rhizosphere. Ann Bot 86 687-703
[4]  
Armstrong J(1994)Oxygen distribution in wetland plant roots and permeability barriers to gas-exchange with the rhizosphere: a microelectrode and modelling study with Physiol Plant 92 343-349
[5]  
Armstrong W(2002)Effects of growing conditions and development of the underlying exodermis on the vitality of the onion root epidermis. Can J Bot 80 227-240
[6]  
Armstrong W(1968)Demystifying suberin. J Cell Biol 37 199-205
[7]  
Cousins D(1988)The root endodermis: fine structure and function. Protoplasma 146 133-142
[8]  
Armstrong J(1990)A berberine-aniline blue fluorescent staining procedure for suberin, lignin, and callose in plant tissue. Can J Bot 68 551-578
[9]  
Turner DW(2002)Comparative anatomy of roots and mycorrhizae of common Ontario trees. J Exp Bot 53 1659-1669
[10]  
Beckett PM(1981)The fungal sheath of ectomycorrhizal pine roots: an apoplastic barrier for the entry of calcium, magnesium, and potassium into the root cortex? Am J Bot 68 154-161