Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH FRONT

Cl uptake, transport and accumulation in grapevine rootstocks of differing capacity for Cl-exclusion

Joanna M. Tregeagle A B D E , Judy M. Tisdall B , Mark Tester C and Rob R. Walker A
+ Author Affiliations
- Author Affiliations

A CSIRO Plant Industry, PMB, Merbein, Vic. 3505, Australia.

B Department of Agricultural Sciences, La Trobe University, Vic. 3086, Australia.

C Australian Centre for Plant Functional Genomics and the University of Adelaide, Private Mail Bag 1, Glen Osmond, SA 5064, Australia.

D Present address: GHD Pty Ltd, 57 Orange Avenue, Mildura, Vic. 3500, Australia.

E Corresponding author. Email: rob.walker@csiro.au

Functional Plant Biology 37(7) 665-673 https://doi.org/10.1071/FP09300
Submitted: 16 December 2009  Accepted: 19 May 2010   Published: 2 July 2010

Abstract

Mechanisms of chloride (Cl) exclusion in rootstocks of grapevine (Vitis spp.) were studied using a strong Cl-excluding rootstock (140 Ruggeri) and a poor Cl-excluding rootstock (K51–40). Xylem Cl concentration in potted whole grapevines of 140 Ruggeri treated with 50 mM Cl was 6.8-fold lower than that in K51–40. Five-fold lower total shoot Cl in salt-treated 140 Ruggeri grapevines relative to that in K51–40 after 50 days, when shoots were of similar biomass, was unrelated to water use. Unidirectional influx of 36Cl into excised roots (up to 30 min), and uptake of 36Cl in roots of intact rooted-leaves (up to 180 min) in 10 mM Cl was similar between the genotypes. However, net accumulation of Cl by excised roots of K51–40 up to 180 min in 10 mM Cl was significantly higher than that of 140 Ruggeri. Intact rooted-leaves of 140 Ruggeri in 10 mM Cl accumulated higher Cl concentrations in roots, and had a lower percentage of total plant 36Cl accumulation in the shoot (petiole plus lamina) than those of K51–40. The greater Cl exclusion capacity of 140 Ruggeri appears to be associated with restricted entry of Cl to xylem and lower root to shoot Cl transport.

Additional keywords: 140 Ruggeri, anion, influx, K51–40, roots, salinity.


Acknowledgements

This research was supported by the Commonwealth Cooperative Research Centre Program and was conducted through the former Cooperative Research Centre for Viticulture with support from Australia’s grape growers and winemakers through the Grape and Wine Research and Development Corporation, with matching funds from the Federal Government. The authors also thank Deepa Jha (Australian Centre for Plant Functional Genomics) for her technical assistance with flux experiments and Deidre Blackmore for assistance during manuscript preparation.


References


Britto DT, Ruth TJ, Lapi S, Kronzucker HJ (2004) Cellular and whole-plant chloride dynamics in barley: insights into chloride–nitrogen interactions and salinity responses. Planta 218, 615–622.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | open url image1

Cram WJ (1968) Compartmentation and exchange of chloride in carrot root tissue. Biochimica et Biophysica Acta 163, 339–353.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | open url image1

Cram WJ (1973a) Chloride fluxes in cells of the isolated root cortex of Zea mays. Australian Journal of Biological Sciences 26, 757–779.
CAS |
open url image1

Cram WJ (1973b) Internal factors regulating nitrate and chloride influx in plant cells. Journal of Experimental Botany 24, 328–341.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Cram WJ (1975) Relationships between chloride transport and electrical potential differences in carrot root cells. Australian Journal of Plant Physiology 2, 301–310.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Cram WJ (1980) Chloride accumulation as a homeostatic system: negative feedback signals for concentration and turgor maintenance differ in a glycophyte and a halophyte. Australian Journal of Plant Physiology 7, 237–249.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Cram WJ (1983) Chloride accumulation as a homeostatic system. Set points and perturbations. Journal of Experimental Botany 34, 1484–1502.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Cram WJ, Laties GG (1971) The use of short-term and quasi-steady influx in estimating plasmalemma and tonoplast influx in barley root cells at various external and internal chloride concentrations. Australian Journal of Biological Sciences 24, 633–646.
CAS |
open url image1

Dunlop J, Bowling DJF (1971) The movement of ions to the xylem exudate of maize roots. III. The location of the electrical and electrochemical potential differences between the exudate and the medium. Journal of Experimental Botany 22, 453–464.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Gibberd MR, Walker RR, Condon AG (2003) Whole-plant transpiration efficiency of Sultana grapevine grown under saline conditions is increased through the use of a Cl– excluding rootstock. Functional Plant Biology 30, 643–652.
Crossref | GoogleScholarGoogle Scholar | open url image1

Greenway H, Thomas DA (1965) Plant response to saline substrate. V. Chloride regulation in the individual organs of Hordeum vulgare during treatment with sodium chloride. Australian Journal of Biological Sciences 18, 505–524.
CAS |
open url image1

Hoagland DR , Arnon DI (1938) ‘The water-culture method for growing plants without soil.’ (The College of Agriculture University of California: Berkeley)

Lessani H, Marschner H (1978) Relation between salt tolerance and long-distance transport of sodium and chloride in various crop species. Australian Journal of Plant Physiology 5, 27–37.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Moya JL, Primo-Millo E, Talon M (1999) Morphological factors determining salt tolerance in citrus seedlings: the shoot to root ratio modulates root uptake of chloride ions and their accumulation in leaves. Plant, Cell & Environment 22, 1425–1433.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Moya JL, Gomez-Cadenas A, Primo-Millo E, Talon M (2003) Chloride absorption in salt-sensitive Carrizo citrange and salt-tolerant Cleopatra mandarin citrus rootstocks is linked to water use. Journal of Experimental Botany 54, 825–833.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | open url image1

Munns R, Passioura JB (1984) Effect of prolonged exposure to NaCl on the osmotic pressure of leaf xylem sap from intact, transpiring barley plants. Australian Journal of Plant Physiology 11, 497–507.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Passioura JB (1980) The transport of water from soil to shoot in wheat seedlings. Journal of Experimental Botany 31, 333–345.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Passioura JB, Munns R (1984) Hydraulic resistance of plants. II. Effects of rooting medium, and time of day, in barley and lupin. Australian Journal of Plant Physiology 11, 341–350.
Crossref | GoogleScholarGoogle Scholar | open url image1

Pitman MG (1971) Uptake and transport of ions in barely seedlings I. Estimation of chloride fluxes in cells of excised roots. Australian Journal of Biological Sciences 24, 407–421.
CAS |
open url image1

Rohlf FJ , Sokal RS (1981) ‘Statistical tables.’ (W.H. Freeman: San Francisco)

Sauer MR (1968) Effects of vine rootstocks on chloride concentration in Sultana scions. Vitis 7, 223–226. open url image1

Schachtman DP, Thomas MR (2003) A rapid method for generating sufficient amounts of uniform genotype-specific material from the woody perennial grapevine for ion transport studies. Plant and Soil 253, 195–199.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Soar CJ, Speirs J, Maffei SM, Loveys BR (2004) Gradients in stomatal conductance, xylem sap ABA and bulk leaf ABA along canes of Vitis vinifera cv. Shiraz; molecular and physiological studies investigating their source. Functional Plant Biology 31, 659–669.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Storey R (1995) Salt tolerance, ion relations and the effect of root medium on the response of citrus to salinity. Australian Journal of Plant Physiology 22, 101–114.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Storey R, Schachtman DP, Thomas MR (2003) Root structure and cellular chloride, sodium and potassium distribution in salinised grapevines. Plant, Cell & Environment 26, 789–800.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | open url image1

Sykes SR (1985) Chloride uptake and distribution by grapevines with established and developing root systems in relation to variations in rootzone salinity. American Journal of Enology and Viticulture 36, 222–229. open url image1

Sykes SR (1987) Variation in chloride accumulation in hybrids and backcrosses of Vitis berlandieri and Vitis vinifera under glasshouse conditions. American Journal of Enology and Viticulture 38, 313–320.
CAS |
open url image1

Teakle NL, Tyerman SD (2010) Mechanisms of Cl– transport contributing to salt tolerance. Plant, Cell & Environment 33, 566–589.
Crossref | GoogleScholarGoogle Scholar | CAS | PubMed | open url image1

Tregeagle JM, Tisdall JM, Blackmore DH, Walker RR (2006) A diminished capacity for chloride exclusion by grapevine rootstocks following long-term saline irrigation in an inland versus coastal region of Australia. Australian Journal of Grape and Wine Research 12, 178–191.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Walker NA , Pitman MG (1976) Measurement of fluxes across membranes. In ‘Encyclopedia of plant physiology, Vol. 2 (a)’. (Eds E Luttge, M Pitman) pp. 93–126. (Springer-Verlag: Berlin)

Walker RR, Torokfalvy E, Scott NS, Kriedemann PE (1981) An analysis of photosynthetic response to salt treatment in Vitis vinifera. Australian Journal of Plant Physiology 8, 359–374.
Crossref | GoogleScholarGoogle Scholar | open url image1

Walker RR, Blackmore DH, Clingeleffer PR (2010) Impact of rootstock on yield and ion concentrations in petioles, juice and wine of Shiraz and Chardonnay in different viticultural environments with different irrigation water salinity. Australian Journal of Grape and Wine Research 16, 243–257.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1

Watson BJ , Lewis WJ , Maggs DH , Page PE (1984) Austrofruit 1. Checklist of tropical and subtropical horicultural crops – botanical and common names (standard nomenclature for Australia). (Queensland Department of Primary Industries: Brisbane)

White PJ, Broadley MR (2001) Chloride in soils and its uptake and movement within the plant. Annals of Botany 88, 967–988.
Crossref | GoogleScholarGoogle Scholar | CAS | open url image1