Dehydration-induced responses of primary photosynthetic processes and spectral reflectance indices in Antarctic Nostoc commune

Vol.6,No.1(2016)

Abstract

In this study, we investigated the relationship between relative water content (RWC) of N. commune colonies recorded during gradual dehydration and (i) normalized difference vegetation index (NDVI), (ii) photochemical reflectance index (PRI), and (iii) primary photochemical processes of photosynthesis, effective quantum yield of photosynthetic processes (FPSII) in photosystem II particular. PRI increased from -0.05 to 0.02 with RWC decrease from 100% (full hydration) to 0% (dry state). NDVI showed somewhat curvilinear relationship with desiccation with minimum value of 0.25 found at 10% RWC. Negative effect of suprasaturation of N. commune colony with water on effective quantum yield (FPSII) was found at RWC range 80-100%. At the RWC range, FPSII reached only 50 % of maximum found at RWC of 30%. In general, desiccation-response curve of showed polyphasic character with three main phases (phase I – constant FPSII values, phase II – an increase with desiccation at RWC 80-30%, and phase III – sigmoidal decrease with desiccation at RWC 0-30%). Non-photochemical quenching (qN) of absorbed light energy showed triphasic dependence on RWC as well. qN showed constant values in the phase I, an increase (phase II), and constant values at severe dehydration (phase III).


Keywords:
PRI; NDVI; Antarctic; James Ross Island; saturation effect; colony
References

Abed, R. M. M., Polerecky, L., Al-Habsi, A., Oetjen, J., Strous, M. and de Beer, D. (2014): Rapid recovery of cyanobacterial pigments in desiccated biological soil crusts following addition of water. PLoS ONE 9 (11): e112372. doi: 10.1371/journal.pone.0112372.

Barták, M., Hazdrová, J., Skácelová, K., Trnková, K., Váczi, P. and Hájek, J. (2015a): Resistance of Antarctic Nostoc sp. colonies to dehydration assessed by chlorophyll fluorescence parameters and spectral reflectance. In: Book of Abstract, 6th International Conference on Polar and Alpine Microbiology, České Budějovice.

Barták, M., Váczi, P. (2014): Long-term fluorometric measurements of photosynthetic processes in Antarctic moss Bryum sp. During austral summer season. Czech Polar Reports, 4: 63-72.

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.

Belnap J., Gardner J. S. (1993): Soil microstructure in soils of the Colorado Plateau: The role of the cyanobacterium Microcoleus vaginatus. Great Basin Naturalist, 53: 40-47.

Esseen, P-A., Olsson, T., Coxson, D. and Gauslaa, Y. (2015): Morphology influences water storage in hair lichens from boreal forest canopies. Fungal Ecology, 18: 26-35, http://dx.doi.org/10.1016/j.funeco.2015.07.008.

Estvāo, D. M. 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.

Fukuda, S., Yamakawa, R., Hirai, M., Kashino, Y. Koike, H. and Satoh, K. (2008): Mechanisms to avoid photoinhibition in a desiccation-tolerant cyanobacterium, Nostoc commune. Plant and Cell Physiology, 49 : 488-492.

Gao, K., Ai, H. (2004): Relationship of growth and photosynthesis with colony size in an edible cyanobacterium, Ge–Xian–Mi Nostoc (Cyanophyceae). Journal of Phycology, 40: 523-526.

Gupta, R. K., Kashyap, A. K. (1995): Water uptake and loss by Antarctic cyanobacterium Nostoc commune. Eleventh Indian Expedition to Antarctica, Scientific Report, Department of Ocean Development, Technical Publication No. 9, pp. 221-227.

Gypser, S., Veste, M.,Thomas, Fischer, T. and Lange, P. (2016): Infiltration and water retention of biological soil crusts on reclaimed soils of former open-cast lignite mining sites in Brandenburg, north-east Germany. Journal of Hydrology and Hydromechanics, 64: 1-11.

Helm, R.F., Huang, Z., Edwards, D., Leeson, H., Peery, W. and Potts, M. (2000): Structural Characterization of the Released Polysaccharide of Desiccation-Tolerant Nostoc commune DRH-1. Journal of Bacteriology, 182: 974-982.

Hill, D. R., Keenan, T.W., Helm, R.F., Potts, M., Crowe, L.M. and Crowe, J.H. (1997): Extracellular polysaccharide of Nostoc commune (Cyanobacteria) inhibits fusion of membrane vesicles during desiccation. Journal of Applied Phycology, 9: 237-248.

Komárek, J., Genuário, G.B., Fiore, M. F. and Elster, J. (2015): Heterocytous cyanobacteria of the Ulu Peninsula, James Ross Island, Antarctica. Polar Biology, 38: 475-492.

Kosugi, M., Katashima, Y., Aikawa, S. and Satoh, K. (2010): Comparative study on the photosynthetic properties of Prasiola (Chlorophyceae) and Nostoc (Cyanophyceae) from Antarctic and non-antarctic sites. Journal of Phycology, 46: 466-476.

Kutser, T., Metsamaa, L., Strömbeck, N. and Vahtmäe, E. (2006): Monitoring cyanobacterial blooms by satellite remote sensing. Estuarine, Coastal and Shelf Science, 67: 303-312.

Kvíderová, J., Elster, J. and Šimek, M. (2011): In situ response of Nostoc commune s.l. colonies to desiccation in Central Svalbard, Norwegian High Arctic. Fottea, 11: 87-97.

Lakatos, M., Bilger, W. and Büdel, B. (2001): Carotenoid composition of terrestrial Cyanobacteria: response to natural light conditions in open rock habitats in Venezuela. European Journal of Phycology, 36: 367-375.

Lange, O.L., Green, T.G.A., Reichenberger, H. and Meyer, A. (1996): Photosynthetic depression at high thallus water contents in lichens: Concurrent use of gas exchange and fluorescence techniques with a cyanobacterial and a green algal Peltigera species. Botanica Acta, 109: 43-50.

Lange, O. L., Green, T. G. A. and Heber, U. (2001): Hydration-dependent photosynthetic production of lichens: what do laboratory studies tell us about field performance? Journal of Experimental Botany, 52: 2033-2042.

Láska, K., Barták, M., Hájek, J., Prošek, P. and Bohuslavová, O. (2011): Climatic and ecological characteristics of deglaciated area of James Ross Island, Antarctica, with a special respect to vegetation cover. Czech Polar Reports, 1: 49-62.

Li, L., Li, L. and Song, K. (2015): Remote sensing of freshwater cyanobacteria: An extended IOP Inversion Model of Inland Waters (IIMIW) for partitioning absorption coefficient and estimating phycocyanin. Remote Sensing of Environment, 157: 9-23.

Novis, P.M., Smissen, R.D. (2006): Two genetic and ecological groups of Nostoc commune in Victoria Land, Antarctica, revealed by AFLP analysis. Antarctic Science, 18: 573-581.

Novis, P. M., Whitebread, D., Gregorich, E. G., Hunt, J.E., Sparrow, A.D., Hopkins, D.W., Elberling, B. and Greenfield, L.G. (2007): Annual carbon fixation in terrestrial populations of Nostoc commune (Cyanobacteria) from an Antarctic dry valley is driven by temperature regime. Global Change Biology, 13: 1224-1237.

Pereira, S., Zille, A., Micheletti, E., Moradas-Ferreira, P., De Philippis, R. and Temagnini, P. (2009): Complexity of cyanobacterial exopolysaccharides: composition, structures, including factors of putative genes involved in their biosynthesis and assembly. FEMS Microbiology Reviews, 33: 917-941.

Potts, M., Olie, J. J., Nickels, J. S., Parsons, J. and White, D. C. (1987): Variation in phospholipid ester-linked fatty acids and carotenoids of desiccated Nostoc commune (cyanobacteria) from different geographic locations. Applied and Environmental Microbiology, 53: 4-9.

Rossi, F., de Philippis, R. (2015): Role of Cyanobacterial Exopolysaccharides in Phototrophic Biofilms and in Complex Microbial Mats. Life, 5: 1218-1238.

Satoh, K., Hirai, M., Nishio, J., Yamaji, T., Kashino, Y. and Koike, H. (2002): Recovery of photosynthetic systems during rewetting is quite rapid in a terrestrial cyanobacterium, Nostoc commune. Plant and Cell Physiology, 43:170-176.

Sand-Jensen, K. (2014): Ecophysiology of gelatinous Nostoc colonies: unprecedented slow growth and survival in resource-poor and harsh environments. Annals of Botany, 114: 17-33.

Schagerl, M., Müller, B. (2006): Acclimation of chlorophyll a and carotenoid levels to different irradiances in four freshwater cyanobacteria. Journal of Plant Physiology, 163: 709-716.

Shirkey, B., Kovarcik, D. P., Wright, D. J., Wilmoth, G., Prickett, T. F., Helm, R. F., Gregory, E. M. and Potts, M. (2000): Active Fe-containing superoxide dismutase and abundant sodF mRNA in Nostoc commune (Cyanobacteria) after years of desiccation. Journal of Bacteriology, 182:189-197.

Singh, N. K., Sonani, R. R., Rastogi, R. P. and Madamwar, D. (2015): The Phycobilisomes: An Early Requisite for Efficient Photosynthesis in Cyanobacteria. EXCLI Journal, 14: 268-89.

Skácelová, K., Barták, M., Coufalík, P., Nývlt, D. and Trnková, K. (2013): Biodiversity of freshwater algae and cyanobacteria on deglaciated northern part of James Ross Island, Antarctica. A preliminary study. Czech Polar Reports, 3: 93-106.

Tamaru, Y., Takani, Y., Yoshida, T. and Sakamoto, T. (2005): Crucial role of extracellular polysaccharides in desiccation and freezing tolerance in the terrestrial cyanobacterium Nostoc commune. Applied and Environmental Microbiology (AEM), 71: 7327-7333.

Taranto, P. A., Keenan, T. W. and Potts, M. (1993): Rehydration induces rapid onset of lipid biosynthesis in desiccated Nostoc commune (Cyanobacteria). Biochimica et Biophysics Acta, 1168: 228-237.

Trnková, K., Barták, M. (2016): Desiccation-induced changes in photochemical processes of photosynthesis and spectral reflectance in Nostoc commune (Cyanobacteria, Nostocales) colonies from polar regions. Phycological Research, accepted.

Victoria, de F. C., Albuquerque, de M. P., Pereira, A. B. , Simas, F. N. B., Spielmann, A. A. and Schaefer, C.E.G.R. (2013): Characterization and mapping of plant communities at Hennequin Point, King George Island, Antarctica. Polar Research, 32, 19261,

http://dx.doi.org/10.3402/polar.v32i0.19261.

Vincent, W., Downes, M.T., Castenholz, R.W. and Howard-Williams, C. (1993): Community structure and pigment organisation of cyanobacteria-dominated microbial mats in Antarctica. European Journal of Phycology, 28: 213-221.

Walker, D. A., Timling, I., Frost, S. M., Matyshak, G. V., Frost, G. V., Epstein, H. E., Zhurbenko, M. and Afonina, O. (2012): High cover, biomass and NDVI of biological soil crusts on Hayes Island, Franz Josef Land, Russia. Book of Abstracts, the 10th International Conference on Permafrost, Salekhard, Russia, 25-29 June 2012.

Yamano, H., Chen, J., Zhang, Y. and Tamura, M. (2006): Relating photosynthesis of biological soil crusts with reflectance: preliminary assessment based on a hydration experiment. International Journal of Remote Sensing , 27 : 5393-5399.,

Metrics

219

Views

24

PDF views