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

NaCl salinity affects lateral root development in Plantago maritima

Michael Rubinigg A , Julia Wenisch B , J. Theo M. Elzenga A and Ineke Stulen A C
+ Author Affiliations
- Author Affiliations

A University of Groningen, Laboratory of Plant Physiology, PO Box 14, 9750 AA Haren, The Netherlands.

B University of Nijmegen, Section of Experimental Plant Ecology, Department of Ecology, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands.

C Corresponding author; email: g.stulen@biol.rug.nl

Functional Plant Biology 31(8) 775-780 https://doi.org/10.1071/FP03222
Submitted: 9 November 2003  Accepted: 25 May 2004   Published: 23 August 2004

Abstract

Root growth and morphology were assessed weekly in hydroponically-grown seedlings of the halophyte Plantago maritima L. during exposure to 0, 50, 100 and 200 mm NaCl for 21 d. Relative growth rate was reduced by 25% at 200 mm NaCl. The lower NaCl treatments did not affect relative growth rates. Primary and lateral roots responded differently to NaCl. While primary-root length increased at all NaCl concentrations, total lateral-root length increased at 50 and was not affected at 100 mm but was considerably reduced at 200 mm NaCl. NaCl concentrations of 50 and 100 mm, which had no effect on relative growth rate or total lateral-root length, severely affected root branching pattern in that the number of first, second and third order laterals was reduced. At 200 mm NaCl third order laterals were not formed at all. However, mean lateral-root length was increased at all NaCl concentrations and was highest at 200 mm NaCl. We conclude that the increase in total lateral-root length in plants at 50 and 100 mm NaCl was mainly caused by increased length growth, while the decrease in total lateral-root length at 200 mm was the consequence of inhibition of lateral root primordia and / or the activation of apical meristems rather than reduced length growth.

Keywords: lateral roots, Plantago maritima, relative growth rate, root length, root morphology, salinity.


References


Bernstein N, Kafkafi U (2002) Root growth under salinity stress. ‘Plant roots: the hidden half’. 3rd edn(Eds Y Waisel, A Eshel, U Kafkafi) pp. 787–805. (Marcel Dekker: New York, NY)

Burssens S, Himanen K, van de Cotte B, Beeckman T, Van Montagu M, Inzé D, Verbruggen N (2000) Expression of cell cycle regulatory genes and morphological alterations in response to salt stress in Arabidopsis thaliana.  Planta 211, 632–640.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Charlton WA (1996) Lateral root initiation. ‘Plant roots: the hidden half’. 2nd edn(Eds Y Waisel, A Eshel, U Kafkafi) pp. 149–173. (Marcel Dekker: New York, NY)

Drew MC, Saker LR, Ashley TW (1973) Nutrient supply and the growth of the seminal root system in barley. Journal of Experimental Botany 24, 1189–1202. open url image1

Fitter A (2002) Characteristics and functions of root systems. ‘Plant roots: the hidden half’. 3rd edn(Eds Y Waisel, A Eshel, U Kafkafi) pp. 15–32. (Marcel Dekker: New York, NY)

Flanagan LB, Jefferies RL (1988) Stomatal limitation of photosynthesis and reduced growth of the halophyte, Plantago maritima L., at high salinity. Plant, Cell and Environment 11, 239–245. open url image1

Gersani M, Graham EA, Nobel PS (1993) Growth responses of individual roots of Opuntia ficus-indica to salinity. Plant, Cell and Environment 16, 827–834. open url image1

Hajibagheri MA, Yeo AR, Flowers TJ (1985) Salt tolerance in Suaeda maritima (L.) Dum. Fine structure and ion concentrations in the apical region of roots. New Phytologist 99, 331–343. open url image1

Hunt, R (1982). Plant growth curves. (Arnold: London, UK)

Lynch J (1995) Root architecture and plant productivity. Plant Physiology 109, 7–13.
PubMed |
open url image1

Malamy JE, Benfey PN (1997) Down and out in Arabidopsis: the formation of lateral roots. Trends in Plant Science 2, 390–396.
Crossref | GoogleScholarGoogle Scholar | open url image1

Maathuis F (1991) ‘Salt-tolerance of Plantago and application of the patch-clamp technique in plant cell membranes.’ PhD thesis. (University of Groningen:: Groningen, The Netherlands)

Paponov IA, Lebedinskai S, Koshkin EI (1999) Growth analysis of solution culture-grown winter rye, wheat and triticale at different rates or nutrient supply. Annals of Botany 84, 467–473.
Crossref | GoogleScholarGoogle Scholar | open url image1

Reinhardt DH, Rost TL (1995) Primary and lateral root development of dark- and light-grown cotton seedlings under salinity stress. Botanica Acta 108, 457–465. open url image1

Rengel Z (1992) The role of calcium in salt toxicity. Plant, Cell and Environment 15, 625–632. open url image1

Robertson GP, Klingensmith KM, Klug MJ, Paul EA, Crum JR, Ellis BG (1997) Soil resources, microbial activity and primary production across an agricultural ecosystem. Ecological Applications 71, 158–170. open url image1

Rubinigg M (2002) ‘Physiological aspects of N nutrition in saline and waterlogged soils.’ PhD thesis. (University of Groningen:: Groningen, The Netherlands)

Rubinigg M, Posthumus F, Ferschke M, Elzenga JTM, Stulen I (2003) Effects of NaCl salinity on 15N-nitrate fluxes and specific root length in the halophyte Plantago maritima L. Plant and Soil 250, 201–213.
Crossref |
open url image1

Smakman G, Hofstra JJ (1982) Energy metabolism of Plantago lanceolata as affected by change in root temperature. Physiologia Plantarum 56, 33–37. open url image1

Staal M, Maathuis JM, Elzenga JTM, Overbeek HM, Prins HBA (1991) Na+ antiport activity in tonoplast vesicles form roots of the salt-tolerant Plantago maritima and the salt-sensitive Plantago media  Physiologia Plantarum 82, 179–184.
Crossref | GoogleScholarGoogle Scholar | open url image1

Tennant D (1975) A test of a modified line intersect method of estimating root length. Journal of Ecology 63, 995–1001. open url image1

Volkmar KM, Hu Y, Steppuhn H (1998) Physiological responses of plants to salinity: a review. Canadian Journal of Plant Science 78, 19–27. open url image1

Waisel Y (1985) The stimulating effects of NaCl on root growth of Rhodes grass (Chloris gayana). Physiologia Plantarum 64, 519–522. open url image1

Waisel Y, Breckle SW (1987) Differences in responses of various radish roots to salinity. Plant and Soil 104, 191–194. open url image1

Zhang H, Forde BG (1998) An Arabidopsis MADS box gene that controls nutrient-induced changes in root architecture. Science 279, 407–409.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Zhang H, Jennings A, Barlow PW, Forde BG (1999) Dual pathways for regulation of root branching by nitrate. Proceedings of the National Academy of Science USA 96, 6529–6534.
Crossref | GoogleScholarGoogle Scholar | open url image1