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Visible injury and growth inhibition of black pine in relation to oxidative stress in industrial areas

Journal of Ecology and Environment / Journal of Ecology and Environment, (P)2287-8327; (E)2288-1220
2010, v.33 no.4, pp.333-341





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Abstract

The objective of our study was to investigate the major reasons for the different growth and visible injury on the needles of black pine growing in Ulsan and Yeocheon industrial complex areas, South Korea. After 12 years of growth,we collected climatic and air pollutant data, and analyzed soil properties and the physiological characteristics of black pine needles. Annual and minimum temperatures in Ulsan were higher than those in Yeocheon from 1996 to 2008. Ozone (O₃) was the pollutant in greatest concentration in Yeocheon, and whereas the SO₂ concentration in most areas decreased gradually during the whole period of growth, SO₂ concentration in Yeocheon has increased continuously since 1999, where it was the highest out of four areas since 2005. Total nitrogen and cation exchange capacity in Yeocheon soil were significantly lower than those of Ulsan. The average growth of black pine in Yeocheon was significantly smaller than that in Ulsan, and the growth of damaged trees represented a significant difference between the two sites. Photosynthetic pigment and malondialdehyde content and antioxidative enzyme activity in the current needles of black pine in Yeocheon were not significantly different between damaged and healthy trees, but in 1-year-old needles, there were significant differences between damaged and healthy trees. In conclusion, needle damage in Yeocheon black pine can be considered the result of long-term exposure to oxidative stress by such as O₃ or SO₂ , rather than a difference in climatic condition or soil properties, and the additional expense of photosynthate needed to overcome damage or alleviate oxidative stress may cause growth retardation.

keywords
air pollutant, antioxidative enzyme activity, lipid peroxidation, ozone, photosynthetic pigment, SO₂

Reference

1.

Aarti PD, Tanaka R, Tanaka A. 2006. Effects of oxidative stress on chlorophyll biosynthesis in cucumber (Cucumis sativus) cotyledons. Physiol Plant 128: 186-197.

2.

Azevedo Neto AD, Prisco JT, Enéas-Filho J, Abreu CEB, Gomes-Filho E. 2006. Effect of salt stress on antioxidative enzymes and lipid peroxidation in leaves and roots of salt-tolerant and salt-sensitive maize genotypes. Environ Exp Bot 56: 87-94.

3.

Beauchamp C, Fridovich I. 1971. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal Biochem 44: 276-287.

4.

Becker K, Saurer M, Egger A, Fuhrer J. 1989. Sensitivity of white clover to ambient ozone in Switzerland. New Phytol 112: 235-243.

5.

Black VJ, Black CR, Roberts JA, Stewart CA. 2000. Impact of ozone on the reproductive development of plants. New Phytol 147: 421-447.

6.

Bungener P, Balls GR, Nussbaum S, Geissmann M, Grub A, Fuhrer J. 1999. Leaf injury characteristics of grassland species exposed to ozone in relation to soil moisture condition and vapour pressure deficit. New Phytol 142: 271-282.

7.

Burdon RD. 1977. Genetic correlation as a concept for studying genotype-environment interaction in forest tree breeding. Silvae Genet 26: 168-175.

8.

Bussotti F, Ferretti M. 2009. Visible injury, crown condition, and growth responses of selected Italian forests in relation to ozone exposure. Environ Pollut 157: 1427-1437.

9.

Bussotti F, Schaub M, Cozzi A, Kräuchi N, Ferretti M, Novak K, Skelly JM. 2003. Assessment of ozone visible symptoms in the field: perspectives of quality control. Environ Pollut 125: 81-89.

10.

Calatayud A, Pomares F, Barreno E. 2006. Interactions between nitrogen fertilization and ozone in watermelon cultivar Reina de Corazones in open-top chambers: effects on chlorophyll a fluorescence, lipid peroxidation and yield. Photosynthetica 44: 93-101.

11.

Carlberg I, Mannervik B. 1985. Glutathione reductase. Methods Enzymol 113: 484-490.

12.

Chandler JW, Dale JE. 1995. Nitrogen deficiency and fertilization effects on needle growth and photosynthesis in Sitka spruce (Picea sitchensis). Tree Physiol 15: 813-817.

13.

Chappelka AH, Samuelson LJ. 1998. Ambient ozone effects on forest trees of the eastern United States: a review. New Phytol 139: 91-108.

14.

Cornic G, Massacci A. 1996. Leaf photosynthesis under drought stress. In: Photosynthesis and the Environment (Baker NR, ed). Kluwer Academic Publishers, Dordrecht, pp 47-366.

15.

Davison AW, Barnes JD. 1998. Effects of ozone on wild plants. New Phytol 139: 135-151.

16.

Deepak SS, Agrawal M. 2001. Influence of elevated CO2 on the sensitivity of two soybean cultivars to sulphur dioxide. Environ Exp Bot 46: 81-91.

17.

Fares S, McKay M, Holzinger R, Goldstein AH. 2010. �Ozone fluxes in a Pinus ponderosa ecosystem are dominated by non-stomatal processes: evidence from long-term continuous measurements. Agric For Meteorol 150: 420-431.

18.

Flagler RB. 1998. Recognition of Air Pollution Injury to Vegetation: A Pictorial Atlas. 2nd ed. Air & Waste Management Association, Pittsburgh, PA.

19.

Fossati P, Prencipe L, Berti G. 1980. Use of 3,5-dichloro-2-hydroxybenzenesulfonic acid/4-aminophenazone chromogenic system in direct enzymic assay of uric acid in serum and urine. Clin Chem 26: 227-231.

20.

Han SH, Kim DH, Lee JC, Kim PG. 2009. Effects of fertilization on physiological parameters in American sycamore (Platanus occidentalis) during ozone stress and recovery phase. J Ecol Field Biol 32: 149-158.

21.

Han SH, Kim DH, Lee KY, Ku JJ, Kim PG. 2007. Physiological damages and biochemical alleviation to ozone toxicity in five species of genus Acer. J Korean For Soc 96: 551-560.

22.

Heath RL. 1989. Alteration of chlorophyll in plants upon air pollutant exposure. In: Biologic Markers of Air-Pollution Stress and Damage in Forests (Committee on Biologic Markers of Air-Pollution Damage in Trees, National Research Council, eds). National Academy Press, Washington, DC.

23.

Heath RL, Packer L. 1968. Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125: 189-198.

24.

Hirano T, Morimoto K. 1999. Growth reduction of the Japanese black pine corresponding to an air pollution episode. Environ Pollut 106: 5-12.

25.

Innes JL, Skelly JM, Schaub M. 2001. Ozone and Broadleaved Species: A Guide to the Identification of Ozone-Induced Foliar Injury. Paul Haupt Publishing, Bern.

26.

Kunert KJ, Ederer M. 1985. Leaf aging and lipid peroxidation: the role of the antioxidants vitamin C and E. Physiol Plant 65: 85-88.

27.

Law RD, Crafts-Brandner SJ. 2001. High temperature stress increases the expression of wheat leaf ribulose-1,5-bisphosphate carboxylase/oxygenase activase protein. Arch Biochem Biophys 386: 261-267.

28.

Lichtenthaler HK. 1987. Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. Methods Enzymol 148: 350-382.

29.

Mehne-Jakobs B. 1996. Magnesium deficiency treatment causes reductions in photosynthesis of well-nourished Norway spruce. Trees Struct Funct 10: 293-300.

30.

Ministry of Environment. 2008. Annual Report of Ambient Air Quality in Korea. Ministry of Environment, Gwacheon.

31.

Mittler R. 2006. Abiotic stress, the field environment and stress combination. Trends Plant Sci 11: 15-19.

32.

Mwanamwenge J, Loss SP, Siddique KHM, Cocks PS. 1999. Effect of water stress during floral initiation, flowering and podding on the growth and yield of faba bean (Vicia faba L.). Eur J Agron 11: 1-11.

33.

Nakano Y, Asada K. 1981. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22: 867-880.

34.

Oren R, Werk KS, Buchmann N, Zimmermann R. 1993. Chlorophyll-nutrient relationships identify nutritionally caused decline in Picea abies stands. Can J For Res 23: 1187-1195.

35.

Osswald WF, Senger H, Elstner EF. 1987. Ascorbic acid and glutathione contents of spruce needles from different locations in Bavaria. Z Naturforsch 42: 879-884.

36.

Polle A, Chakrabarti K, Chakrabarti S, Seifert F, Schramel P, Rennenberg H. 1992. Antioxidants and manganese deficiency in needles of Norway spruce (Picea abies L.) trees. Plant Physiol 99: 1084-1089.

37.

Ranieri A, D'Urso G, Nali C, Lorenzini G, Soldatini GF. 1996. Ozone stimulates apoplastic antioxidant systems in pumpkin leaves. Physiol Plant 97: 381-387.

38.

Scholz F. 1989. Genetic research in forest decline implications for nongenetic investigations. In: Air Pollution and Forest Decline (Bucher JB, Bucher-Wallin I, eds). Proceeding 14th International Meeting for Specialists in Air Pollution Effects on Forest Ecosystems, IUFRO P2.05, 1988 Oct 2-8, Interlaken. Eidgennssische Anstalt fur das forstliche Versuchswesen, Birmensdorf, pp 325-328.

39.

Schwanz P, Polle A. 2001. Growth under elevated CO2 ameliorates defenses against photo-oxidative stress in poplar (Populus alba × tremula). Environ Exp Bot 45: 43-53.

40.

Shimazaki K, Sakaki T, Kondo N, Sugahara K. 1980. Active oxygen participation in chlorophyll destruction and lipid peroxidation in SO2-fumigated leaves of spinach. Plant Cell Physiol 21: 1193-1204.

41.

Skelly JM, Davis DD, Merrill W, Cameron EA, Brown HD, Drummond DB, Dochinger LS. 1987. Diagnosing Injury to Eastern Forest Trees: A Manual for Identifying Damage Caused by Air Pollution, Pathogens, Insects, and Abiotic Stresses. Pennsylvania State University, College of Agricultural Sciences, University Park, PA.

42.

Tausz M, Zellnig G, Bermadinger-Stabentheiner E, Grill D, Katzensteiner K, Glatzel G. 1996. Physiological, structural, and nutritional parameters of Norway spruce needles from declining forest stands in Austria. Can J For Res 26: 1769-1780.

43.

Turcsányi E, Lyons T, Plöchl M, Barnes J. 2000. Does ascorbate in the mesophyll cell walls form the first line of defence against ozone? Testing the concept using broad bean (Vicia faba L.). J Exp Bot 51: 901-910.

44.

Vollenweider P, Günthardt-Goerg MS. 2005. Diagnosis of abiotic and biotic stress factors using the visible symptoms in foliage. Environ Pollut 137: 455-465.

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