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. 1981 Jul;68(1):74–81. doi: 10.1104/pp.68.1.74

Inhibition of Seagrass Photosynthesis by Ultraviolet-B Radiation 1

Robert P Trocine 1,2, John D Rice 1,3, Gary N Wells 1,4
PMCID: PMC425892  PMID: 16661893

Abstract

Effects of ultraviolet-B radiation on the photosynthesis of seagrasses (Halophila engelmanni Aschers, Halodule wrightii Aschers, and Syringodium filiforme Kütz) were examined. The intrinsic tolerance of each seagrass to ultraviolet-B, the presence and effectiveness of photorepair mechanisms to ultraviolet-B-induced photosynthetic inhibition, and the role of epiphytic growth as a shield from ultraviolet-B were investigated.

Halodule was found to possess the greatest photosynthetic tolerance for ultraviolet-B. Photosynthesis in Syringodium was slightly more sensitive to ultraviolet-B while Halophila showed relatively little photosynthetic tolerance. Evidence for a photorepair mechanism was found only in Halodule. This mechanism effectively attenuated photosynthetic inhibition induced by ultraviolet-B dose rates and dosages in excess of natural conditions. Syringodium appeared to rely primarily on a thick epidermal cell layer to reduce photosynthetic damage. Halophila seemed to have no morphological or photorepair capabilities to deal with ultraviolet-B. This species appeared to rely on epiphytic and detrital shielding and the shade provided by other seagrasses to reduce ultraviolet-B irradiation to tolerable levels. The presence of epiphytes on leaf surfaces was found to reduce the extent of photosynthetic inhibition from ultraviolet-B exposure in all species.

Observations obtained in this study seem to suggest the possibility of anthocyanin and/or other flavonoid synthesis as an adaptation to long term ultraviolet-B irradiation by these species. In addition, Halophila appears to obtain an increased photosynthetic tolerance to ultraviolet-B as an indirect benefit of chloroplast clumping to avoid photo-oxidation by intense levels of photosynthetically active radiation.

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Selected References

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  1. Brandle J. R., Campbell W. F., Sisson W. B., Caldwell M. M. Net Photosynthesis, Electron Transport Capacity, and Ultrastructure of Pisum sativum L. Exposed to Ultraviolet-B Radiation. Plant Physiol. 1977 Jul;60(1):165–169. doi: 10.1104/pp.60.1.165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cicerone R. J., Stolarski R. S., Walters S. Stratospheric ozone destruction by man-made chlorofluoromethanes. Science. 1974 Sep 27;185(4157):1165–1167. doi: 10.1126/science.185.4157.1165. [DOI] [PubMed] [Google Scholar]
  3. Cutchis P. Stratospheric ozone depletion and solar ultraviolet radiation on Earth. Science. 1974 Apr 5;184(4132):13–19. doi: 10.1126/science.184.4132.13. [DOI] [PubMed] [Google Scholar]
  4. Hammond A. L., Maugh T. H., 2nd Stratospheric Pollution: Multiple Threats to Earth's Ozone. Science. 1974 Oct 25;186(4161):335–338. doi: 10.1126/science.186.4161.335. [DOI] [PubMed] [Google Scholar]
  5. Johnston H. Reduction of stratospheric ozone by nitrogen oxide catalysts from supersonic transport exhaust. Science. 1971 Aug 6;173(3996):517–522. doi: 10.1126/science.173.3996.517. [DOI] [PubMed] [Google Scholar]
  6. Jones L. W., Kok B. Photoinhibition of chloroplast reactions. I. Kinetics and action spectra. Plant Physiol. 1966 Jun;41(6):1037–1043. doi: 10.1104/pp.41.6.1037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lindoo S. J., Caldwell M. M. Ultraviolet-B Radiation-induced Inhibition of Leaf Expansion and Promotion of Anthocyanin Production: Lack of Involvement of the Low Irradiance Phytochrome System. Plant Physiol. 1978 Feb;61(2):278–282. doi: 10.1104/pp.61.2.278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Mantai K. E., Wong J., Bishop N. I. Comparison studies on the effects of ultraviolet irradiation on photosynthesis. Biochim Biophys Acta. 1970 Mar 3;197(2):257–266. doi: 10.1016/0005-2728(70)90036-8. [DOI] [PubMed] [Google Scholar]
  9. Sisson W. B., Caldwell M. M. Photosynthesis, Dark Respiration, and Growth of Rumex patientia L. Exposed to Ultraviolet Irradiance (288 to 315 Nanometers) Simulating a Reduced Atmospheric Ozone Column. Plant Physiol. 1976 Oct;58(4):563–568. doi: 10.1104/pp.58.4.563. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Van Baalen C. The effects of ultraviolet irradiation on a coccoid blue-green alga: survival, photosynthesis, and photoreactivation. Plant Physiol. 1968 Oct;43(10):1689–1695. doi: 10.1104/pp.43.10.1689. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Wellmann E. UV dose-dependent induction of enzymes related to flavonoid biosynthesis in cell suspension cultures of parsley. FEBS Lett. 1975 Mar 1;51(1):105–107. doi: 10.1016/0014-5793(75)80863-5. [DOI] [PubMed] [Google Scholar]

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