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Solute patterns of four halophytic plant species at Suncheon Bay in Korea

Journal of Ecology and Environment / Journal of Ecology and Environment, (P)2287-8327; (E)2288-1220
2014, v.37 no.3, pp.131-137
https://doi.org/10.5141/ecoenv.2014.016





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Abstract

To investigate the solute pattern of salt marsh plants in Suncheon Bay in Korea, plants and soil samples were collected at three sites (Carex scabrifolia and Phragmites communis, site 1; Suaeda malacosperma, site 2; Suaeda japonica, site 3) once a month from July to September. The soil pH around the investigated species was weakly alkaline, 6.9–8.1. The total ion and Cl- content of site 1 gradually increased, while those of site 2 and site 3 were lowest in August and highest in September. The exchangeable Ca2+, Mg2+ and K+ in the soil was relatively constant during the study period, but the soil exchangeable Na+ content was variable. Leaves of the investigated plant species were collected once a month in their natural habitats from July to September. Carex scabrifolia and Pharagmites communis had constant leaf water content during the period. Suaeda malacosperma and Suaeda japonica had high leaf water content, but this decreased after August. C. scabrifolia and P. communis had very high concentrations of soluble carbohydrates. However, S. malacosperma and S. japonica had very low, but constant soluble carbohydrate concentrations. C. scabrifolia accumulated similar amounts of Na+ and K+ ions in its leaves. P. communis contained a high concentration of K+ ions. S. japonica and S. malacosperma had more Na+ and Cl- ions than K+ ions in their leaves. S. japonica had higher levels of glycine betaine in its leaves under saline conditions than Carex scabrifolia and Phragmites communis. According to these results, it can be concluded that the physiological characteristics of salt marsh chenopodiaceous plants (S. japonica and S. malacosperma) are the high storage capacity for inorganic ions (especially alkali cations and chloride) and accumulation of glycine betaine, but monocotyledonous plant species (C. scabrifolia and P. communis) show high K+ concentrations, efficient regulation of ionic uptake (exclusion of Na+ and Cl-), and accumulation of soluble carbohydrates. These characteristics enable salt marsh plants to grow in saline habitats.

keywords
inorganic solutes, organic solutes, halophyte, salt marsh

Reference

1.

Chaplin MF, Kennedy JF. 1994. Carbohydrate Analysis: A Practical Approach. 2nd ed. Oxford University Press, New York, NY, pp 2-3.

2.

Chinnusamy V, Jagendorf A, Zhu JK. 2005. Understanding and improving salt tolerance in plants. Crop Sci 45: 437-448.

3.

Choi SC, Bae JJ, Choo YS. 2004. Inorganic and organic solute pattern of costal plant, korea. Korean J Ecol 27: 355-361.

4.

Choi SC, Lim SH, Kim SH, Choi DG, Kim JG, Choo YS. 2012. Growth and solute pattern of Suaeda maritima and Suaeda asparagoides in an abandoned salt field. J Ecol Field Biol 35: 351-358.

5.

Choo YS, Albert R. 1997. The physiotype concept: an approach integrating plant ecophysiology and systematics. Phyton 37: 93-106.

6.

Choo YS, Albert R. 1999. Mineral ion, nitrogen and organic solute pattern in sedges (Carex spp.) – a contribution to the physiotype concept. II. Culture experiments. Flora 194: 75-87.

7.

Choo YS, Do JW, Song SD. 1999. Free amino acid and nitrogen contents of the coastal plants in Korea. Korean J Ecol 22: 109-117.

8.

Cramer GR, Lauchli A, Polito VS. 1985. Displacement of Ca2+ by Na+ from the plasmalemma or root cells: a primary response to salt stress. Plant Physiol 79: 207-211.

9.

Di Martino C, Delfine S, Pizzuto R, Loreto F, Fuggi A. 2003. Free amino acids and glycine betaine in leaf osmoregulation of spinach responding to increasing salt stress. New Phytol 158: 455-463.

10.

Flores HE, Galston AW. 1984. Osmotic stress-induced polyamine accumulation in cereal leaves. II. Relation to amino acid pools. Plant Physiol 75: 110-113.

11.

Flowers TJ, Colmer TD. 2008. Salinity tolerance in halophytes. New Phytol 179: 945-963.

12.

Hartzendor T, Rolletschek H. 2001. Effects of NaCl-salinity on amino acid and carbohydrate contents of Phragmites australis. Aquat Bot 69: 195-208.

13.

Kefu Z, Hai F, Ungar IA. 2002. Survey of halophyte species in china. Plant Science 163: 491-498.

14.

Khan MA, Ungar IA, Showalter AM. 2000. Effects of salinity on growth, water relations and Ion accumulation of the subtropical perennial halophyte, Atriplex griffithii var. stocksii. Ann Bot 85: 225-232.

15.

Kim JH, Cho KJ, Mun HT, Min BM. 1986. Production dynamics of Phragmites longivalvis, Carex scabrifolia and Zoysia sinica stand of sand bar at the Nagdong river estuary. Korean J Ecol 9: 59-71.

16.

Koyro HW, Zoerb C, Debez A, Huchzermeyer B. 2013. The effect of hyperosmotic salinity on protein pattern and enzyme activities of halophytes. Plant Biol 40: 787-804.

17.

Lee JS. 1988. Studies on the distribution of vegetation in the salt marsh of the Mankyung River estuary. Korean J Environ Biol 6: 1-10.

18.

Lee SH, Ji KJ, An Y, Ro HM. 2003. Soil salinity and vegetation distribution at four tidal reclamation project areas. Korean J Environ Agric 22: 79-86. (in Korean with English abstract)

19.

McCue KF, Hanson AD. 1990. Drought and salt tolerance: towards understanding and application. Trends Biotechnol 8: 358-362.

20.

Min BM and Kim JH. 1999. Plant community structure in reclaaimed land on the West Coast of Korea. J Plant Biol 42: 287-293.

21.

Moghaieb REA, Saneoka H, Fujita K. 2004. Effect of salinity on osmotic adjustment, glycinebetaine accumulation and the betaine aldehyde dehydrogenase gene expression in two halophytic plants, Salicornia europaea and Suaeda maritima. Plant Sci 166: 1345-1349.

22.

Munns R. 2002. Comparative physiology of salt and water stress. Plant Cell Environ 25: 239-250.

23.

Parida AK, Das AB. 2005. Salt tolerance and salinity effects on plants: a review. Ecotoxicol Environ Saf 60: 324-349.

24.

Parks GE, Dietrich MA, Schumaker KS. 2002. Increased vacuolar Na+/H+ exchange activity in Salicornia bigelovii Torr. in response to NaCl. J Exp Bot 53: 1055-1065.

25.

Pulich WM. 1986. Variations in leaf soluble amino acids and ammonium content in subtropical seagrasses related to salinity stress. Plant Physiol 80: 283-286.

26.

Qi CH, Chen M, Song J, Wang BS. 2009. Increase in aquaporin activity is involved in leaf succulence of the euhalophyte Suaeda salsa, under salinity. Plant Sci 179: 200-205.

27.

Rhodes D, Hanson AD. 1993. Quaternary ammonium and tertiary sulfonium compounds in higher plants. Annu Rev Plant Physiol Plant Mol Biol 44: 357-384.

28.

Rozema J, Flowers T. 2008. Crops for a salinized world. Science 322: 1478-1480.

29.

Shen YG, Du BX, Zhang WK, Zhang JS, Chen SY. 2002. Ah- CMO, regulated by stresses in Atriplex hortensis, can improve drought tolerance in transgenic tobacco. Theor Appl Genet 105: 815-821.

30.

Voetberg GS, Sharp RE. 1991. Growth of the maize primary root at low water potentials. III. Role of increased proline deposition in osmotic adjustment. Plant Physiol 96: 1125-1130.

31.

Wang LW, Showalter AM. 2004. Cloning and salt-induced, ABA-independent expression of choline mono-oxygenase in Atriplex prostrata. Physiol Plant 120: 405-412.

32.

Yang HS. 1999. A syntaxonomical study on the vegetation of ruined salt field in Chonnam province. Korean J Ecol 22: 265-270.

33.

Zhu JK. 2001. Plant salt tolerance. Trends Plant Sci 6: 66-71.

Journal of Ecology and Environment