Photosynthetica 2016, 54(3):478-480 | DOI: 10.1007/s11099-016-0184-z

Physiological and biochemical responses of roadside trees grown under different urban environmental conditions in Seoul

H. N. You1, S. Y. Woo1,*, C. R. Park2
1 Department of Environmental Horticulture, University of Seoul, Seoul, Republic of Korea
2 Division of Forest Ecology, National Institute of Forest Science, Seoul, Republic of Korea

The present study revealed that Ginkgo biloba and Platanus occidentalis, the most abundant roadside trees in Seoul, grown under polluted environmental conditions, displayed lower contents of total chlorophyll (Chl), carotenoids (Car), and ascorbic acid (AsA) compared to the trees grown under clean conditions. The reduction in Chl, Car, and AsA contents was 59, 53, and 50%, respectively, in G. biloba, contrary to 26, 23, and 24%, respectively, in P. occidentalis. Furthermore, relative ion leakage and leaf temperature was higher in the trees grown under polluted conditions than in those grown under clean conditions. The increase in relative ion leakage and leaf temperature was 58 and 3% for G. biloba and 17 and 4% for P. occidentalis, respectively. Our results, therefore, highlighted the negative impact of urban environmental pollution on the physiological and biochemical parameters in roadside trees.

Keywords: antioxidant; pigments; transpiration; urban air pollution; urban forest

Received: September 15, 2014; Accepted: October 30, 2015; Published: September 1, 2016Show citation

ACS AIP APA ASA Harvard Chicago IEEE ISO690 MLA NLM Turabian Vancouver
You, H.N., Woo, S.Y., & Park, C.R. (2016). Physiological and biochemical responses of roadside trees grown under different urban environmental conditions in Seoul. Photosynthetica54(3), 478-480. doi: 10.1007/s11099-016-0184-z.
Download citation

References

  1. Arnon D.I.: Copper enzymes in isolated chloroplasts. Polyphenol oxidase in Beta vulgaris.-Plant Physiol. 24: 1-15, 1949. Go to original source...
  2. Asada K.: The water-water cycle in chloroplast: Scavenging of active oxygens and dissipation of excess photons.-Annu. Rev. Plant Phys. 50: 601-639, 1999. Go to original source...
  3. Baek S.G., Woo S.Y.: Physiological and biochemical responses of two tree species in urban areas to different air pollution levels.-Photosynthetica 48: 23-29, 2010. Go to original source...
  4. Campos P.S., Quartin V., Ramalho J.C. et al.: Electrolyte leakage and lipid degradation account for cold sensitivity in leaves of Coffea sp. plants.-Plant Physiol. 160: 283-292, 2003. Go to original source...
  5. Demidchik V., Straltsova D., Medvedev S.S. et al.: Stress induced electrolyte leakage: the role of K+-permeable channels and involvement in programmed cell death and metabolic adjustment.-J. Exp. Bot. 65: 1259-1270, 2014. Go to original source...
  6. Fenger J.: Air pollution in the last 50 years-From local to global.-Atmos. Environ. 43: 13-22, 2009. Go to original source...
  7. Joshi P.C., Swami A.: Air pollution induced changes in the photosynthetic pigments of selected plant species.-J. Environ. Biol. 30: 295-298, 2009.
  8. Joshi P.C., Swami A.: Air pollution induced changes in the photosynthetic pigments of selected plant species.-J. Environ. Biol. 30: 295-298, 2009.
  9. Kampfenkel K., Van Montagu M., Inze D.: Extraction and determination of ascorbate and dehydroascrobate from plant tissue.-Anal. Biochem. 225:165-167, 1995. Go to original source...
  10. Melhorn H., Tabner J.M., Wellburn A.R.: Electron spin resonance evidence for deformation of free radicals in plants exposed to ozone.-Physiol. Plantarum 79: 377-383, 1990. Go to original source...
  11. NIER (National Institute of Environmental Research): Annual Report of Air Quality in Korea. Pp. 3-284. Ministry of Environment, Seoul 2013.
  12. Nowak D.J., Crane D.E., Stevens J.C.: Air pollution removal by urban trees and shrubs in the United States.-Urban For. Urban Gree. 4: 115-123, 2006. Go to original source...