Barták, M.: Lichen photosynthesis. Scaling from the cellular to the organism level. — In: Hohmann-Marriott, M. (ed.): The Structural Basis of Biological Energy Generation. Advances in Photosynthesis and Respiration. Pp. 379–400. Springer, Dordrecht 2014.
Barták, M., Solhaug, K.-A., Vráblíková, H., Gauslaa, Y.: Curling during desiccation protects the foliose lichen Lobaria pulmonaria against photoinhibition. — Oecologia 149: 553–560, 2006.
Barták, M., Hájek, J., Očenášová, P.: Photoinhibition of photosynthesis in Antarctic lichen Usnea antarctica. I. Light intensity- and light duration-dependent changes in functioning of photosystem II. — Czech Polar Reports 2: 42–51, 2011.
Barták, M., Hájek, J., Vráblíková, H. et al.: High-light stress and photoprotection in Umbilicaria antarctica monitored by chlorophyll fluorescence imaging and changes in zeaxanthin and glutathione. — Plant Biol. 6: 333–341, 2004.
Barták, M., Vráblíková, H., Hájek, J.: 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 2003.
Barták, M., Vráblíková-Cempírková, H., Štepigová, J. et al.: Duration of irradiation rather than quantity and frequency of high irradiance inhibits photosynthetic processes in the lichen Lasallia pustulata. — Photosynthetica 46: 161–169, 2008.
Bilger, W., Rimke, S., Schreiber, U. et al.: Inhibition of energytransfer to photosystem II in lichens by dehydration. — J. Plant Physiol. 134: 261–268, 1989.
Bjerke, J.W., Joly, D., Nilsen, L. et al.: Spatial trends in usnic acid concentrations of the lichen Flavocetraria nivalis along local climatic gradients in the Arctic (Kongsfjorden, Svalbard). — Polar Biol. 27: 409–417, 2004.
Bohuslavová, O.: Ecology of lichens on deglaciated parts of James Ross Island, the Antarctic. Ph.D. Thesis. Pp. 1–73. Masaryk University, Brno 2012.
Burrit, D.J., MacKenzie, S.: Antioxidant metabolism during acclimation of Begonia × erythrophylla to high light levels. — Ann. Bot. 91: 783–794, 2003.
Carreras, H.A., Wannaz, E.D., Perez, C.A. et al.: The role of urban air pollutants on the performance of heavy metal accumulation in Usnea amblyoclada. — Environ. Pollut. 97: 50–57, 2005.
Colville, L., Kranner, I.: Desiccation tolerant plants as model systems to study redox regulation of protein thiols. — Plant Growth Regul. 62: 241–255, 2010.
Davies, B.J., Glasser, N.F., Carrivick, J.L. et al.: Landscape evolution and ice-sheet behaviour in a semi-arid polar environment: James Ross Island, NE Antarctic Peninsula. — In: Hambrey, M.H., Barker, P.F., Barrett, P.J. et al. (ed.): Antarctic Palaeoenvironments and Earth-Surface Processes. Pp. 353–395. Geological Society, London 2013.
Del Hoyo, A., Álvarez, R., Del Campo, E.M. et al.: Oxidative stress induces distinct physiological responses in the two Trebouxia phycobionts of the lichen Ramalina farinacea. — Ann. Bot. 107: 109–118, 2011.
Demmig-Adams, B., Maguas, C., Adams, W.W. et al.: Effect of high light on the efficiency of photochemical energyconversion in a variety of lichen species with green and bluegreen phycobionts. — Planta 180: 400–409, 1990.
Hauck, M., Dulamsuren, C., Mühlenberg, M.: Lichen diversity on steppe slopes in the northern Mongolian mountain taiga and its dependence on microclimate. — Flora 202: 530–546, 2007.
Heber, U., Azarkovich, M., Shuvalov, V.: Activation of mechanisms of photoprotection by desiccation and by light: poikilohydric photoautotrophs. — J. Exp. Bot. 58: 2745–2759, 2007.
Holm, G.: Chlorophyll mutations in barley. — Acta Agr. Scand. 4: 457–471, 1954.
Huneck, S.: Progress in the chemistry of lichen substances, 2000–2005. — J. Hattori Bot. Lab. 100: 671–694, 2006.
Kappen L., Breuer M., Bölter M.: Ecological and physiological investigations in continental antarctic cryptogams. 3. Photosynthetic production of Usnea sphacelata: diurnal courses, models, and the effect of photoinhibition. — Polar Biol. 11: 393–402, 1991.
Košler, J., Magna, T., Mlčoch, B. et al.: Combined Sr, Nd, Pb, and Li isotope geochemistry of alkaline lavas from northern James Ross Island (Antarctic Peninsula) and implications for back-arc magma formation. — Chem. Geol. 258: 207–218, 2009.
Krábková, G.: [Content of UV-absorbing compounds and pigments in extracts from lichens from different Earth regions.] Pp. 1–67. Diploma Thesis. Masaryk University, Brno 2013. [In Czech]
Kranner, I.: Determination of glutathione, glutathione disulphide and two related enzymes, glutathione reductase and glucose-6-phosphate dehydrogenase, in fungal and plant cells. — In: Varma, A. (ed.): Mycorrhiza Manual. Pp. 227–241. Springer, Berlin 1998.
Kranner, I.: Glutathione status correlates with different degrees of desiccation tolerance in three lichens. — New Phytol. 154: 451–460, 2002.
Kranner, I., Birtić, S.: A modulating role for antioxidants in desiccation tolerance. — Integr. Comp. Biol. 45: 734–740, 2005.
Kranner, I., Cram, W.J., Zorn, M. et al.: Antioxidants and photoprotection in a lichen as compared with its isolated symbiotic partners. — P. Natl. Acad. Sci. USA 102: 3141–3146, 2005.
Láska, K., Barták, M., Hájek, J. et al.: 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, 2011.
Manrique, E., Balaguer, L., Barnes, J. et al.: Photoinhibition studies in lichens using chlorophyll fluorescence analysis. — Bryologist 96: 443–449, 1993.
May, M.J., Vernoux, T., Leaver, C. et al.: Glutathione homeostasis in plants: implications for environmental sensing and plant development. — J. Exp. Bot. 49: 649–667, 1998.
Mrak, T., Jeran, Z., Batič, F. et al.: Arsenic accumulation and thiol status in lichens exposed to As(V) in controlled conditions. — Biometals 23: 207–219, 2010.
Müller, M., Zechmann, B., Zellnig, G.: Ultrastructural localization of glutathione in Cucurbita pepo plants. — Protoplasma 223: 213–219, 2004.
Noctor, G., Foyer, C.H.: Ascorbate and glutathione: Keeping active oxygen under control. — Annu. Rev. Plant Phys. 49: 249–279, 1998.
Noctor, G., Gomez, L., Vanacker, H. et al.: Interactions between biosynthesis, compartmentation and transport in the control of glutathione homeostasis and signalling. — J. Exp. Bot. 53: 1283–1304, 2002.
Onofri, S., Fenice, M., Cicalini, A.R. et al.: Ecology and biology of microfungi from Antarctic rocks and soils. — Ital. J. Zool. 67: 163–167, 2000.
Palmqvist, K., Dahlman, L., Valladares, F. et al.: CO2 exchange and thallus nitrogen across 75 contrasting lichen associations from different climate zones. — Oecologia 133: 295–306, 2002.
Rausch, T., Wachter, A.: Sulfur metabolism: a versatile platform for launching defence operations. — Trends Plant Sci. 10: 503–509, 2005.
Riddell, J., Padgett, P.E., Nash III, T.H.: Physiological responses of lichens to factorial fumigations with nitric acid and ozone. — Environ. Pollut. 170: 202–210, 2012.
Rikkinen, J.: What’s Behind the Pretty Colours. A Study on the Photobiology of Lichens. Edition 4: Bryobrothera. Pp. 239, The Finnish Bryological Society, Helsinki 1995.
Singh, J., Dubey, A.K., Singh, R.P.: Antarctic terrestrial ecosystem and role of pigments in enhanced UV-B radiations. — Rev. Environ. Sci. Biotechnol. 10: 63–77, 2011.
Singh, R., Ranjan, S., Nayaka, S. et al.: Functional characteristics of a fruticose type of lichen, Stereocaulon foliolosum Nyl., in response to light and water stress. — Acta Physiol. Plant. 35: 1605–1615, 2013.
Smellie, J.L., Johnson, J.S., McIntosh, W.C. et al.: Six million years of glacial history recorded in volcanic lithofacies of the James Ross Island Volcanic Group, Antarctic Peninsula. — Palaeogeogr. Palaeoclimatol. Palaeoecol. 260: 122–148, 2008.
Štepigová, J., Vráblíková, H., Lang, J. et al.: Glutathione and zeaxanthin formation during high light stress in foliose lichens. — Plant Soil Environ. 53: 340–344, 2007.
Stirbet, A.: Excitonic connectivity between photosystem II units: what is it, and how to measure it? — Photosynth. Res. 116: 189–214, 2013.
Strasser, R.J., Shrivastava, A., Tsimilli-Michael, M.: The fluorescence transient as a tool to characterize and screen photosynthetic samples. — In: Yunus, M., Pathre, U., Mohanty, P. (ed): Probing Photosynthesis: Mechanisms, Regulation and Adaptation. Pp. 445–483. Taylor and Francis, London 2000.
Szalai, G., Kellös, T., Galiba, G. et al.: Glutathione as an antioxidant and regulatory molecule in plants under abiotic stress conditions. — Plant Growth Regul. 28: 66–80, 2009.
Tausz, M.: The role of glutathione in plant response and adaptation to natural stress. — In: Grill, D., Tausz, M., De Kok, L.J.: Significance of Glutathione to Plant Adaptation to the Environment. Pp. 101–122. Springer, Dordrecht 2001.
Terauds, A., Chown, S.L., Morgan, F. et al.: Conservation biogeography of the Antarctic. — Diversity Distrib. 18: 726–741, 2012.
Tretiach, M., Baruffo, L., Piccotto, M.: Effects of Mediterranean summer conditions on chlorophyll a fluorescence emission in the epiphytic lichen Flavoparmelia soredians: a field study. — Plant Biosyst. 146: 171–180, 2012.
Veerman, J., Vasil’ev, S., Paton, G.D. et al.: Photoprotection in the lichen Parmelia sulcata: The origins of desiccation-induced fluorescence quenching. — Plant Physiol. 145: 997–1005, 2007.
Vráblíková, H., Barták, M., Wönisch, A.: Changes in glutathione and xanthophyll cycle pigments in the high light-stressed lichens Umbilicaria antarctica and Lassalia pustulata. — J. Photoch. Photobiol. B 79: 35–41, 2005.
Wendler, J., Holzwarth, A.R.: State transitions in the green alga Scenedesmus obliquus probed by time-resolved chlorophyll fluorescence spectroscopy and global data analysis. — Biophys. J. 52: 717–728, 1987.