UV-B effects on filamentous alga Zygnema strain (EEL201) from Antarctica

Vol.6,No.1(2016)

Abstract

Filamentous alga Zygnema sp. is frequently found in extreme polar environments with freshwater availability for at least part of summer season. In such habitats, Zygnema might be exposed to several stress factors, like freeze, desiccation and high irradiation levels. This study investigated the effect of UV-B on primary photosynthetic processes in Zygnema sp. (EEL201 strain) from Antarctica. Samples were cultivated in liquid medium and exposed to supplemental UV-B (1.4 W m-2) for 6 h. During the UV-B treatment and following recovery, the changes in chlorophyll fluorescence paramaters caused UV-B were measured. Negative effects on FV/FM and FPSII were found after 6 h treatment with only limited recovery in dark. The only parameter that recovered was photochemical quenching (qP) indicating a potential to restore photosynthesis in the reaction centres that were not damaged by UV-B treatment. However, the share on damaged RC PS II was much higher compared to those showing the recovery. Thus, the effect of short-term supplemental 1.4 W m-2 UV-B light was considered heavy causing substantial damages to PS II. These results provide insights on the effects of UV-B light onZygnemasp. that can help in the interpretation of response mechanisms of Arctic algae to radiation.


Keywords:
James Ross Island; chlorophyll fluorescence parameters; photosystem II; photoinhibition; absorption spectrum
References

Barták, M., Hazdrová, J., Jáchymová, G., Pláteníková, E., Monteiro Estevao, D. M., Hájek, J., Skácelová, K., Váczi, P. and Balarinová, K. (2015a): Photosynthetic parameters and synthesis of UV-B absorbing compounds is species-specific in Antarctic lichens exposed to supplemental UV-B radiation. Bulletin ČSEBR, 69 p.

Barták, M., Váczi, P., Stachoň, Z. and Kubešová, S. (2015b): Vegetation mapping of moss-dominated areas of northern part of James Ross Island (Antarctica) and a suggestion of protective measures. Czech Polar Reports, 5: 75-87.

Berteotti, S., Ballottari, M., and Bassi, R. (2016): Increased biomass productivity in green algae by tuning non-photochemical quenching. Scientific Reports, 6: 21339.

Conti, S., Hazdrová, J., Hájek, J., Očenášová, P., Barták, M., Skácelová, K. and Adamo, P. (2014): Comparative analysis of heterogeneity of primary photosynthetic processes within fruticose lichen thalli: Preliminary study of interspecific differences. Czech Polar Reports, 4: 149-157.

Choi, J-I., Yoon, M., Lim, S., Kim, G. H. and Park, H. (2014): Effect of gamma irradiation on physiological and proteomic changes of Arctic Zygnema sp. (Chlorophyta, Zygnematales). Phycologia, 54: 333-341.

Dring, M. J., Wagner, A., Boeskov, J. and Luning, K. (1996): Sensitivity of intertidal and subtidal red algae to UVA and UVB radiation, as monitored by chlorophyll fluorescence measurements: influence of collection depth and season and length of irradiation.European Journal of Phycology, 31:293-302.

Erickson, E., Wakao, S., and Niyogi, K.K. (2015): Light stress and photoprotection in Chlamydomonas reinhardtii. The Plant Journal, 82: 449-465.

Estevez, M. S., Malanga, G. and Puntarulo, S. (2001). UV-B effects on Antarctic Chlorella sp cells. Journal of Photochemistry and Photobiology B: Biology, 62: 19-25.

Germ, M., Kreft, I. and Gaberščik, A. (2009): UV-B radiation and selenium affected energy availability in green alga Zygnema. Biologia, 64: 676-679.

Häder, D.-P., Kumar, H. D., Smith, R. C. and Worrest, R. C. (2003): Aquatic ecosystems: effects of solar ultraviolet radiation and interactions with other climatic change factors. Photochemical and Photobiological Sciences, 2: 39-50.

Häder, D.-P., Kumar, H. D., Smith, R. C. and Worrest, R. C. (2007): Effects of solar UV radiation on aquatic ecosystems and interactions with climate change. Photochemical and Photobiological Sciences, 6: 267-285.

Herburger, K., Lewis, L. A. and Holzinger, A. (2015): Photosynthetic efficiency, desiccation tolerance and ultrastructure in two phylogenetically distinct strains of alpine Zygnema sp. (Zygnematophyceae, Streptophyta): role of pre-akinete formation. Protoplasma, 252: 571-589.

Holzinger, A., Roleda, M. Y. and Lütz, C. (2009): The vegetative arctic fresh water green alga Zygnema is insensitive to experimental UV exposure. Micron, 40: 831-838.

Kaplan, F., Lewis, L. A., Herburger, K. and Holzinger, A. (2013): Osmotic stress in Arctic and Antarctic strains of the green alga Zygnema (Zygnematales, Streptophyta): Effects on photosynthesis and ultrastructure. Micron, 44: 317-330.

Karentz, D., Cleaver, J. E. and Mitchell, D. L. (1991): Cell survival characteristics and molecular responses of Antarctic phytoplankton to ultraviolet-B radiation. Journal of Phycology, 27: 326-341.

Leya, T., Rahn, A., Lütz, C. and Remias, D. (2009): Response of arctic snow and permafrost algae to high light and nitrogen stress by changes in pigment composition and applied aspects for biotechnology. FEMS Microbiology ecology, 67: 432-443.

Maxwell, K., Johnson, G.N. (2000): Chlorophyll fluorescence - a practical guide. Journal of Experimental Botany, 51: 659-668.

Medina, M. G., Avalos-Chacon, R. (2015): Physiological performance of a foliose macrolichen Umbilicaria antarctica as affected by supplemental UV-B treatment. Czech Polar Reports, 5: 222-229.

Monteiro Estvāo, D. M. (2015): Production of UV-B screens and changes in photosynthetic efficiency in Antarctic Nostoc commune colonies and a lichen Xanthoria elegans depend on a dose and duration of UV-B stress. Czech Polar Reports, 5: 55-68.

Pichrtová, M. (2014): Stress resistance of polar hydro-terrestrial algae Zygnema sp. (Zygnematophyceae, Streptophyta). Ph.D. Thesis, Charles University, Prague, 146 p.

Pichrtová, M., Remias, D., Lewis, L. A. and Holzinger, A. (2013): Changes in phenolic compounds and cellular ultra structure of arctic and antarctic strains of Zygnema (Zygnema-tophyceae, Streptophyta) after exposure to experimentally enhanced UV to PAR ratio. Microbial Ecology, 65: 68-83.

Pichrtová, M., Hájek, T. and Elster, J. (2014a): Osmotic stress and recovery in field populations of Zygnema sp. (Zygnematophyceae, Streptophyta) on Svalbard (High Arctic) subjected to natural desiccation. FEMS Microbiology ecology, 89: 270-280.

Pichrtová, M., Kulichová, A. and Holzinger, A. (2014b): Nitrogen limitation and slow drying induce desiccation tolerance in conjugating green algae (Zygnematophyceae, Streptophyta) from Polar Habitats. PlosOne, Volume: 9, Issue: 11, Article Number: e113137.

Rivas, C., Navarro, N., Huovinen, P. and Gómez, I. (2016): Photosynthetic UV stress tolerance of the Antarctic snow alga Chlorella sp. modified by enhanced temperature? Revista Chilena de Historia Natural, 89 (7), doi: 10.1186/s40693-016-0050-1.

Rodrigues, L. H. R., Arenzon, A., Raya-Rodriguez, M. T. and Fontoura, N. F. (2011): Algal density assessed by spectrophotometry: A calibration curve for the unicellular algae Pseudokirchneriella subcapitata. Journal of Environmental Chemistry and Ecotoxicology, 3: 225-228.

Stamenković, M., Hanelt, D. (2014): Sensitivity of photosynthesis to UV radiation in several Cosmarium strains (Zygnematophyceae, Streptophyta) is related to their geographical distribution. Photochemical & photobiological sciences, 13: 1066-108.

Stamenković, M., Bischov, K. and Hanelt, D. (2014): Xanthophyll cycle pool size and composition in several Cosmarium strains (Zygnematophyceae, Streptophyta) are related to their geographic distribution patterns. Protist, 165: 14-30.

Thangaraj, G. (2015): Antarctic strain of green filamentous alga Zygnema sp. shows a high resistance to photonhibition under simulated polar conditions. Czech Polar Reports, 5: 176-184.

Tian, J., Yu, J. (2009): Changes in ultrastructure and responses of antioxidant systems of algae (Dunaliella salina) during acclimation to enhanced ultraviolet-B radiation. Journal of Photochemistry and Photobiology B: Biology, 97: 152-160.

Tilbrook, K. Dubois, M., Crocco, C. D., Yin, R., Chappuis, R., Allorent, G., Schmid-Siegert, E., Goldschmidt-Clermont, M. and Ulm, R. (2016): UV-B Perception and Acclimation in Chlamydomonas reinhardtii. Plant Cell, 28: 966-983.

White, A. L., Jahnke, L. S. (2002): Contrasting Effects of UV-A and UV-B on Photosynthesis and Photoprotection of β-carotene in two Dunaliella spp. Plant and Cell Physiology, 43: 877-884.

Wong, C. Y., Chu, W. L., Marchant, H. and Phang, S. M. (2007): Comparing the response of Antarctic, tropical and temperate microalgae to ultraviolet radiation (UVR) stress. Journal of Applied Phycology, 19: 689-699. doi:10.1007/s10811-007-9214-3.

Xiong, F., Komenda, J., Kopecký, J. and Nedbal, L. (1997): Strategies of ultraviolet-B protection in microscopic algae. Physiologia Plantarum, 100: 378-388.

Xue, L. Zhang, Y., Zhang, T., An, L. and Wang, X. (2005): Effects of enhanced ultraviolet-b radiation on algae and cyanobacteria. Critical Reviews in Microbiology, 31: 79-89.,

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