© 1995 Oxford University Press
RESEARCH-ARTICLE |
Mineral nutrition and transport in xylem and phloem of Banksia prionotes (Proteaceae), a tree with dimorphic root morphology
1Botany Department, University of Western Australia Nedlands, WA 6009, Australia
2Julius-von-Sachs-lnstitut fur Biowissenschaften, Lehrstuhl für Botanik 1, Universität Würzburg D-97082 Würtzburg, Germany
3To whom correspondence should be addressed. Fax: +49 931 888 6158.
Xylem sap of proteoid roots, lateral roots, sinker root and age classes of trunk segments, and phloem sap of mid-trunks were collected from trees of Banksia prionotes (Proteaceae) in native habitat on highly impoverished sands in south-western Australia. Proteoid roots were major exporters of phosphate, K+ and amino acids during the wet winter season and showed in vitro nitrate reductase activity during periods of soil nitrification. Other parts of the root served as general sources of Na +, Cl, Mg2+, Ca2+, and SO24. Lateral root xylem sap was more concentrated in virtually all solutes than that of sinker roots, even during the dry summer following senescence of proteoid roots. Gradients in xylem sap concentration up the main trunks suggested lateral abstraction and storage of incoming phosphate in basal stem parts during winter and a subsequent release to the xylem in summer. Phloem sap was many times more concentrated in nutrient ions than xylem sap, and, like xylem sap, showed unusually low K+ and H2PO4 relative to Na+, Cl and SO24, suggesting a sparing role of the latter three ions in meeting ionic requirements of transport. Amino acid analyses showed higher overall concentrations in phloem than xylem sap, but much lower proportions of total amino N as glutamine and asparagine in the former sap. This suggested utilization of xylem-derived amide N by leaves for growth and synthesis of phloem-mobile amino acids.
Key words: Banksia prionotes, mineral transport, proteoid roots, xylem sap, phloem sap
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
F. Zeng, H. Yan, and S. K. Arndt Leaf and whole tree adaptations to mild salinity in field grown Populus euphratica Tree Physiol, October 1, 2009; 29(10): 1237 - 1246. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Abdolzadeh, K. Shima, H. Lambers, and K. Chiba Change in Uptake, Transport and Accumulation of Ions in Nerium oleander (Rosebay) as Affected by Different Nitrogen Sources and Salinity Ann. Bot., November 1, 2008; 102(5): 735 - 746. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. W. Shane and H. Lambers Systemic suppression of cluster-root formation and net P-uptake rates in Grevillea crithmifolia at elevated P supply: a proteacean with resistance for developing symptoms of 'P toxicity' J. Exp. Bot., January 1, 2006; 57(2): 413 - 423. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. W. Shane, M. E. McCully, and H. Lambers Tissue and cellular phosphorus storage during development of phosphorus toxicity in Hakea prostrata (Proteaceae) J. Exp. Bot., May 1, 2004; 55(399): 1033 - 1044. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. R. Warren and M. A. Adams Capillary electrophoresis for the determination of major amino acids and sugars in foliage: application to the nitrogen nutrition of sclerophyllous species J. Exp. Bot., June 1, 2000; 51(347): 1147 - 1157. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Watt and J. R. Evans Proteoid Roots. Physiology and Development Plant Physiology, October 1, 1999; 121(2): 317 - 324. [Full Text] |
||||
![]() |
M. Watt and J. R. Evans Linking Development and Determinacy with Organic Acid Efflux from Proteoid Roots of White Lupin Grown with Low Phosphorus and Ambient or Elevated Atmospheric CO2 Concentration Plant Physiology, July 1, 1999; 120(3): 705 - 716. [Abstract] [Full Text] |
||||



