Diurnal changes in photosynthetic activity of the biological soil crust and lichen: Effects of abiotic factors (Petuniabukta, Svalbard)

Vol.4,No.2(2014)

Abstract

In polar ecosystems, primary producers have to cope with a very harsh climate that limits the time available for growth and biomass production. In this study, diurnal measurement of photosynthetic processes in biological soil crust and a lichen were carried out in Petuniabukta, Spitsbergen. For field measurements, a method of induced fluorescence of chlorophyll was used. Measurements of photosynthetic activity were taken as repetitive measurements of effective quantum yield of photosystem II (ΦPSII). The short-term field measurements were carried out for 10 days in summer 2014. ΦPSII was recorded each 5 minutes as well as microclimatic data (air temperature, air humidi-ty, photosynthetically active radiation - PAR). The microclimatic parameters were recorded by a datalogger. In general, physiological activity of both biological soil crust and a lichen showed daily courses. Tested lichen was Cladonia rangiferina and the most dominant species in biological soil crust was Nostoc sp. Typically, most of ΦPSII values ranged 0.6 – 0.7 in both model organisms. The results have shown that photosynthetic activity was strongly correlated with all observed abiotic factors in both study objects. Particularly important was the relation found between PAR and ΦPSII in biological soil crust. When the biological soil crust was exposed to high PAR doses of irradiation (about 2300 µmol m-2 s-1) photoinhibition of primary processes of photosynthesis was observed as ΦPSII decrease, while photosynthetic activity of lichen remained at same level. Furthermore, it has been demonstrated increasing that in situ photosynthetic activity increased in both biological soil crust and lichen with a decrease in temperature.


Keywords:
Spitsbergen; lichen; biological soil crusts; photosynthesis; fluorescence; effective quantum yield; Cladonia rangiferina; Nostoc sp.
References

Allahverdiyeva, Y., Aro, E. (2012): Photosynthetic responses of plants to excess light: mechanisms and conditions for photoinhibition, excess energy dissipation and repair. Photosynthesis. 34: 275-297.

Barták, M. (2014). Lichen Photosynthesis. Scaling from the Cellular to the Organism Level. In: Hohmann-Marriott, M. F. (ed.): The Structural Basis of Biological Energy Generation. Advances in Photosynthesis and Respiration Volume 39, pp. 379-400. ISBN 978-94-017-8742-0.

Barták, M., Gloser, J. and Hájek, J. (2005): Visualized photosynthetic characteristics of the lichen Xanthoria elegans related to daily courses of light, temperature and hydration: a field study from Galindez Island, maritime Antarctica. The Lichenologist, 37: 433-443.

Barták, M., Váczi, P., Hájek, J. and Smykla, J. (2007): Low-temperature limitation of primary photosynthetic processes in Antarctic lichens Umbilicaria antarctica and Xanthoria elegans. Polar Biology, 31: 47–51.

Barták, M., Vráblíková, H. and Hájek, J. (2003): Sensitivity of photosystem 2 of antarctic lichens to high irradiance stress: Fluorometric study of fruticose (Usnea antarctica) and foliose (Umbilicaria decussata) species. Photosynthetica, 41: 497-504.

Belnap, J. (2006): The potential roles of biological soil crusts in dryland hydrologic cycles. Hydrological Processes, 20: 3159-3178.

Campbell, S. E. (1979): Soil stabilization by a prokaryotic desert crust: implications for Precambrian land biota. Origins of Life, 9: 335-348.

Chartres, C. J. (1992): Soil crusting in Australia. In: Sumner, M. E., Stewart, B. A. (eds.): Soil crusting: chemical and physical processes. Lewis, Boca Raton, Fla. pp. 339-365.

Danin, A. (1978): Plant species diversity and plant succession in a sandy area in the northern Negev. Flora, 167: 409-422.

Eldridge, D. J. (1993): Cryptogams, vascular plants, and soil hydro- logical relations: some preliminary results from the semiarid woodlands of eastern Australia. Great Basin Naturalist, 53: 48-58.

Eldridge, D. J., Greene, R. S. B. (1994): Microbiotic soil crusts: a review of their roles in soil and ecological processes in the rangelands of Australia. Australian Journal of Soil Research, 32: 389-415.

Hájek, J., Barták, M. and Gloser, J. (2001): Effects of thallus temperature and hydration on photosynthetic parameters of Cetraria islandica from contrasting habitats. Photosynthetica, 39: 427-435.

Hájek, J., Váczi, P., Barták, M. and Jahnová, L. (2012): Interspecific differences in cryoresistance of lichen symbiotic algae of genus Trebouxia assessed by cell viability and chlorophyll fluorescence. Cryobiology, 64: 215-222.

Harper, K. T., Marble, J. R. (1988): A role for nonvascular plants in management of arid and semiarid rangelands. In: Tueller, P. T (ed.): Vegetation Science Applications for Rangeland Analysis and Management. Kluwer Academic Press Dordrecht: Amsterdam, pp. 135-169.

Henri D. Ch. (2011): Durham E-Theses: The physiological response of sub-Arctic lichens to their abiotic environment. Thesis (Masters), 127 p. (http://etheses.dur.ac.uk/623/1/All_together-_w_corrections.pdf?DDD1+)

Jupa, R., Hájek, J., Hazdrová, J. and Barták, M. (2012): Interspecific differences in photosynthetic efficiency and spectral reflectance in two Umbilicaria species from Svalbard during controlled desiccation. Czech Polar Reports, 2: 31-41.

Kappen, L. (1993): Plant activity under snow and ice, with particular reference to lichens. Arctic, 46: 297-302.

Kappen, L., Schroeter, B., Scheidegger, C., Sommerkorn, M. and Hestmark, G. (1996): Cold resistance and metabolic activity of lichens below 0°C. Advances in Space Research, 18: 119-128.

Kappen, L., Sommerkorn, M. and Schroeter, B. (1995): Carbon acquisition and water relations of lichens in polar regions–potentials and limitations. Lichenologist, 27: 531-545.

Karsten, U., Holzinger, A. (2012): Effects on photosynthetic activity, and drought-induced ultrastructural changes in the green alga Klebsormidium dissectum (Streptophyta) from a high alpine soil crust. Microbial Ecology, 63: 51-63.

Karsten, U., Lütz, C. and Holzinger, A. (2010): Ecophysiological performance of the aeroterrestrial green alga Klebsormidium crenulatum (Charophyceae, Streptophyta) isolated from an Alpine soil crust with an emphasis on desiccation stress. Journal of Phycology, 46: 1187-1197.

Kitzing, C., Pröschold, T. and Karsten, U. (2014): Growth, photosynthetic performance and sunscreen contents in different populations of the green alga Klebsormidium fluitans (Streptophyta) from Alpine soil crusts. Microbial Ecology, 67: 327-340.

Li, X.-R., Wang, X.-P., Li, T. and Zhang, J.-G. (2002): Microbiotic soil crust and its effect on vegetation and habitat on artificially stabilized desert dunes in Tengger Desert, North China. Biology and Fertility of Soils, 35: 147-154.

Lukeš, M., Procházková, L., Shmidt, V., Nedbalová, L. and Kaftan, D. (2014): Temperature dependence of photosynthesis and thylakoid lipid composition in the red snow alga Chlamydomonas cf. nivalis (Chlorophyceae). FEMS MicrobiologyEcology. Special Issue: Polar and Alpine Microbiology. 89: 303-315.

Pannewitz, S., Green, T. G. A., Maysek, K., Schlensog, M., Seppelt, R., Sancho, L. G., Türk, R. and Schroeter, B. (2005): Photosynthetic responses of three common mosses from continental Antarctica. Antarctic Science, 17: 341-352.

Schulten, J. A. (1985): Soil aggregation by cryptogams of a sand prairie. American Journal of Botany, 72: 1657-1661.

Schlensog, M., Schroeter, B. (2001): A new method for the accurate in situ monitoring of chlorophyll a fluorescence in lichens and bryophytes. The Lichenologist, 33: 443-452.

St. Clair, L. L., Johansen, J. R. and Rushforth, S. R. (1993): Lichens of soil crust communities in the intermountain area of the western United States. Great Basin Naturalist, 53: 5-12.

Tsoar, H., Moller, J. T. (1986): The role of vegetation in the formation of linear sand dunes. In: Nickling, W. G. (ed.): Aeolian geo- morphology. Proceedings of the 17th Annual Binghamton geomorphology symposium. Allen and Unwin, Boston, Mass. pp 74-95.

West, N. E. (1990): Structure and function of microphytic soil crusts in wildland ecosystem of arid and semi-arid regions. Advances in Ecological Research, 20: 179-223.

Wiencke, C., Clayton, M. N., Gómez, I., Iken, K., Lüder, U. H., Amsler, C. D., Karsten, U., Hanelt, D., Bischof, K. and Dunton, K. (2006): Life strategy, ecophysiology and ecology of seaweeds in polar waters. Reviews in Environmental Science and Bio/Technology, 6: 95-126.

Wu, L., Lan, S., Zhang, D. and Hu, C. (2012). Functional reactivation of photosystem II in lichen soil crusts after long-term desiccation. Plant and Soil, 369: 177-186.

Wu, L., Zhang, G., Lan, S., Zhang, D. and Hu, C. (2013): Microstructures and photosynthetic diurnal changes in the different types of lichen soil crusts. European Journal of Soil Biology, 59: 48-53.

Yair, A. (1990): Runoff generation in a sandy area – the Nizzana sands, western Negev, Israel. Earth Surface Processes Landforms, 15: 597-609.,

Metrics

218

Views

34

PDF views