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Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

23Na NMR microimaging: a tool for non-invasive monitoring of sodium distribution in living plants

Markus Rokitta A C , Danielle Medek A , James M. Pope B and Christa Critchley A
+ Author Affiliations
- Author Affiliations

A Department of Botany, The University of Queensland, St. Lucia, Qld 4072, Australia.

B School of Physical and Chemical Sciences, Queensland University of Technology, Gardens Point, Qld 4001, Australia.

C Corresponding author; email: rokitta@gmx.net

Functional Plant Biology 31(9) 879-887 https://doi.org/10.1071/FP04063
Submitted: 1 April 2004  Accepted: 5 July 2004   Published: 27 September 2004

Abstract

Detailed knowledge of the sodium (Na) distribution within the tissues of highly salt-tolerant Australian native species could help in understanding the physiological adaptations of salt-tolerance or salt-sensitive plants. 23Na nuclear magnetic resonance (NMR) microimaging is presented as a tool to achieve this goal. Maps of the Na distribution in stem tissue were obtained with an in-plane resolution of approximately125 µm and a slice thickness of 4 mm. Simultaneously recorded high resolution 1H NMR images showing water distribution in the same slice with 31 µm in-plane resolution and 1 mm slice thickness, were used as an anatomical reference together with optical micrographs that were taken immediately after the NMR experiments were completed. To quantify the Na concentration, reference capillaries with known NaCl concentrations were located in the NMR probe together with the plant sample. Average concentration values calculated from signal intensities in the tissue and the capillaries were compared with concentration values obtained from atomic emission photometry and optical microscopy performed on digested stem sections harvested immediately after NMR experiments. Results showed that 23Na NMR microimaging has great potential for physiological studies of salt stress at the macroscopic level, and may become a unique tool for diagnosing salt tolerance and sensitivity.

Keywords: Avicennia marina, Casuarina glauca, environmental stress, NMR microimaging, plant water relations, salinity, 23Na NMR.


Acknowledgments

The authors thank John Bertram, Lina Daddow and Lui Weber for their help with the optical microscopy, Patrick Stevens for his support with atomic emission photometry and Dr Rana Munns, Prof. Tim Flowers and Dr Roger Meder for their suggestions to improve the manuscript. This work was supported by a grant from the German Academic Exchange Service (DAAD), Gemeinsames Hochschulsonderprogramm III von Bund und Ländern and a University of Queensland Postdoctoral Research Fellowship to MR.


References


Aswathappa NA, Munns R, Bachelard EP, Tonnet ML (1990) Ion concentrations in the xylem sap of two Casuarina species differing in salt tolerance. ‘Proceedings of the 7th international workshop on membrane transport in plants and fungi’. (Ed.  MJ Beilby , NA Walker , JR Smith ) pp. 486–489. (University of Sydney: Australia)


Ball MC (1988) Salinity tolerance in the mangroves, Aegiceras corniculatum and Avicennia marina. I. Water use in relation to growth, carbon partitioning and salt balance. Australian Journal of Plant Physiology 15( ), 447–464. open url image1

Bental M, Degani H, Avron M (1988) 23Na-NMR studies of the intracellular sodium ion concentration in the halotolerant alga Dunaliella salina. Plant Physiology 87( ), 813–817. open url image1

Bernstein L, Brown JW, Hayward HE (1956) The influence of rootstock and salt accumulation in stone-fruit trees and almonds. Proceedings of the American Society for Horticultural Science 68( ), 86–95. open url image1

Carden DE, Walker DJ, Flowers TJ, Miller AJ (2003) Single-cell measurements of the contributions of cytosolic Na+ and K+ to salt tolerance. Plant Physiology 131( ), 676–683.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Clearwater MJ, Clarke CJ (2003) In vivo magnetic resonance imaging of xylem vessel contents in woody lianas. Plant, Cell and Environment 26( ), 1205–1214.
Crossref | GoogleScholarGoogle Scholar | open url image1

Clipson NJW, Flowers TJ (1987) Salt tolerance in the halophyte Suaeda maritima (L.) Dum. The effect of salinity on the concentration in the xylem. New Phytologist 105( ), 359–366. open url image1

Esau, K (1960). ‘Anatomy of seed plants.’ (Wiley International: New York)

Fan T-WM, Higashi RM, Norlyn J, Epstein E (1989) In vivo 23Na and 31P NMR measurement of a tonoplast Na/H exchange process and its characteristics in two barley cultivars. Proceedings of the National Academy of Sciences USA 86, 9856–9860. open url image1

Gerasimowicz WV, Tu SI, Pfeffer PE (1986) Energy facilitated Na+ uptake in excised corn roots via 31P and 23Na NMR. Plant Physiology 81, 925–928. open url image1

Gupta RK, Gupta P (1982) Direct observation of resolved resonances from intra cellular and extracellular sodium-23 ions in NMR studies of intact cells and tissues using dysprosium(III)tripolyphosphate as paramagnetic shift reagent. Journal of Magnetic Resonance 47, 344–350.
Crossref |
open url image1

Koizumi M, Ishida N, Takagishi H, Shirata K, Kano H (1992) Observation of water and Na+ in tissues of the Bruguiera gymnorrhiza by 1H- and 23Na-NMR imaging. Botanical Magazine Tokyo 105, 1–11. open url image1

Marshall A, Xu W (1998) Quantitative elemental x-ray imaging of frozen-hydrated biological samples. Journal of Microscopy 190, 305–316.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Munns R (1985) Na+, K+ and Cl− in xylem sap flowing to shoots of NaCl-treated barley. Journal of Experimental Botany 36, 1032–1042. open url image1

Munns R (2002) Comparative physiology of salt and water stress. Plant, Cell and Environment 25, 239–250.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Olt S, Krötz E, Komor E, Rokitta M, Haase A (2000) 23Na- and 1H-NMR-microimaging of intact plants. Journal of Magnetic Resonance 144, 297–304.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Packer L, Spath S, Martin JB, Roby C, Bligny R (1987) 23Na and 31P NMR studies of the effects of salt stress on the freshwater cyanobacterium synechococcus 6311. Archives of Biochemistry and Biophysics 256, 354–361.
PubMed |
open url image1

Pitman MG (1972) Uptake and transport of ions in barley seedlings. III. Correlation between transport to the shoot and relative growth rate. Australian Journal of Biological Sciences 25, 243–257. open url image1

Ratcliffe RG (1994) In vivo NMR studies of higher plants and algae. ‘Advances in botanical research. Vol. 20’. edn pp. 43–123. (Academic Press: London, UK)

Shapiro EM, Borthakur A, Gougoutas A, Reddy R (2002) 23Na MRI accurately measures fixed charge density in articular cartilage. Magnetic Resonance in Medicine 47, 284–291.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Sillerud LO, Heyser JW (1984) Use of 23Na-NMR to follow sodium uptake and efflux in NaCl-adapted and non-adapted millet (Panicum miliaceum) suspensions. Plant Physiology 75, 269–272. open url image1

Spickett CM, Smirnoff N, Ratcliffe RG (1993) An in vivo nuclear magnetic resonance investigation of ion transport in maize (Zea mays) and Spartina anglica roots during exposure to high salt concentrations. Plant Physiology 102, 629–638.
PubMed |
open url image1

Walker RR (1986) Sodium exclusion and potassium–sodium selectivity in salt-treated trifoliate orange (Poncirus trifoliata) and Cleopatra mandarin (Citrus reticulata) plants. Australian Journal of Plant Physiology 13, 293–303. open url image1

Walker RR, Törökfalvy E, Behboudian MH (1987) Uptake and distribution of chloride, sodium and potassium ions and growth of salt-treated pistachio plants. Australian Journal of Agricultural Research 38, 383–394. open url image1