Quang hợp của hai lớp địa y rêu từ sa mạc Tengger với độ nhạy khác nhau đối với bức xạ UV-B bổ sung

Albert, K.R., Mikkelsen, T.N., Ro-Poulsen, H. et al.: Ambient UV-B radiation reduces PSII performance and net photosynthesis in high Arctic Salix arctica. — Environ. Exp. Bot. 73: 10–18, 2011. Allen, J.F., de Paula, W.B.M., Puthiyaveetil, S., Nield, J.: A structural phylogenetic map for chloroplast photosynthesis. — Trends Plant Sci. 16: 645–655, 2011. Aráoz, R., Häder, D.P.: Ultraviolet radiation induces both degradation and synthesis of phycobilisomes in Nostoc sp.: a spectroscopic and biochemical approach. — FEMS Microbiol. Ecol. 23: 301–313, 1997. Atanassova, M., Georgieva, S., Ivancheva, K.: Total phenolic and total flavonoid contents, antioxidant capacity and biological contaminants in medicinal herbs. — J. Univ. Chem. Technol. Metallurgy 46: 81–88, 2011. Bashandy, T., Taconnat, L., Renou, J.P. et al.: Accumulation of flavonoids in an ntra ntrb mutant leads to tolerance to UV-C. — Mol. Plant 2: 249–258, 2009. Bassman, J.H., Edwards, G.E., Robberecht, R.: Photosynthesis and growth in seedlings of five forest tree species with contrasting leaf anatomy subjected to supplemental UV-B radiation. — Forest Sci. 49: 176–187, 2003. Bassman, J.H., Robberecht, R.: Growth and gas exchange in field-grown and greenhouse-grown Quercus rubra following three years of exposure to enhanced UV-B radiation. — Tree Physiol. 26: 1153–1163, 2006. Belnap, J., Lange, O.L.: Biological Soil Crusts: Structure, Function and Management. — Springer, Berlin 2003. Belnap, J., Phillips, S.L., Smith, S.D.: Dynamics of cover, UVprotective pigments, and quantum yield in biological soil crust communities of an undisturbed Mojave Desert shrubland. — Flora 202: 674–686, 2007. Bieza, K., Lois, R.: An Arabidopsis mutant tolerant to lethal ultraviolet-B levels shows constitutively elevated accumulation of flavonoids and other phenolics. — Plant Physiol. 126: 1105–1115, 2001. Bischof, K., Hanelt, D., Wiencke, C.: Effect of ultraviolet radiation on photosynthesis and related enzyme reactions of marine macroalgae. — Planta 211: 555–562, 2000. Bornman, J.F.: New trends in photobiology: Target sites of UV-B radiation in photosynthesis of higher plants. — J. Photoch. Photobiol. B 4: 145–158, 1989. Bowker, M.A., Reed, S.C., Belnap, J., Phillips, S.L.: Temporal variation in community composition, pigmentation, and Fv/Fm of desert cyanobacterial soil crusts. — Microbial Ecol. 43: 13–25, 2002. Bowker, M.A., Belnap, J., Davidson, D.W., Phillips, S.L.: Evidence for micronutrient limitation of biological soil crusts: importance to arid-lands restoration. — Ecol. Appl. 15: 1941–1951, 2005. Bowker, M.A., Belnap, J., Davidson, D.W., Goldstein, H.: Correlates of biological soil crust abundance across a continuum of spatial scales: support for a hierarchical conceptual model. — J. Appl. Ecol. 43: 152–163, 2006. Bowker, M.A.: Biological soil crust rehabilitation in theory and practice: an underexploited opportunity. — Restor. Ecol. 15: 13–23, 2007. Bradford, M.M.: A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. — Anal. Biochem. 72: 248–254, 1976. Bray, E.A., Baily-Serres, J., Weretilnyk, E.: Responses to abiotic stresses. — In: Buchanan, B., Gruissem, W., Jones, R. (ed.): Biochemistry and Molecular Biology of Plants. Pp. 1158–1203. Wiley, USA 2000. Çakirlar, H., Çiçek, N., Fedina, I. et al.: NaCl induced crossacclimation to UV-B radiation in four Barley (Hordeum vulgare L.) cultivars. — Acta Physiol. Plant. 30: 561–567, 2008. Caldwell, M.M., Bornman, J.F., Ballaré, C.L. et al.: Terrestrial ecosystems, increased solar ultraviolet radiation, and interactions with other climate change factors. — Photochem. Photobiol. Sci. 6: 252–266, 2007. Cerovic, Z.G., Ounis, A., Cartelat, A. et al.: The use of chlorophyll fluorescence excitation spectra for the nondestructive in situ assessment of UV-absorbing compounds in leaves. — Plant Cell Environ. 25: 1663–1676, 2002. Chen, L.-Z., Wang, G.-H., Hong, S. et al.: UV-B-induced oxidative damage and protective role of exopolysaccharides in desert cyanobacterium Microcoleus vaginatus. — J. Integr. Plant Biol. 51: 194–200, 2009. Chimphango, S.B.M., Musil, C.F., Dakora, F.D.: Effects of UVB radiation on plant growth, symbiotic function and concentration of metabolites in three tropical grain legumes. — Funct. Plant Biol. 30: 309–318, 2003. Choi, B.Y., Roh, K.S.: UV-B radiation affects chlorophyll and activation of Rubisco by Rubisco activase in Canavalia ensiformis L. leaves. — J. Plant Biol. 46: 117–121, 2003. Csintalan, Z., Tuba, Z., Takács, Z., Laitat, E.: Responses of nine bryophyte and one lichen species from different microhabitats to elevated UV-B radiation. — Photosynthetica 39: 317–320, 2001. Darby, B.J., Neher, D.A., Belnap, J.: Soil nematode commu nities are ecologically more mature beneath late-than earlysuccessional stage biological soil crusts. — Appl. Soil Ecol. 35: 203–212, 2007. Deckmyn, G., Martens, C., Impens, I.: The importance of the ratio UV-B/photosynthetic active radiation (PAR) during leaf development as determining factor of plant sensitivity to increased UV-B irradiance: effects on growth, gas exchange and pigmentation of bean plants (Phaseolus vulgaris cv. Label). — Plant Cell Environ. 17: 295–301, 1994. Eichholz, I., Rohn, S., Gamm, A. et al.: UV-B-mediated flavonoid synthesis in white asparagus (Asparagus officinalis L.). — Food Res. Int. 48: 196–201, 2012. Fagerberg, W.R., Bornman, J.F.: Ultraviolet-B radiation causes shade-type ultrastructural changes in Brassica napus. — Physiol. Plantarum 101: 833–844, 1997. Fagerberg, W.R., Bornman, J.F.: Modification of leaf cytology and anatomy in Brassica napus grown under above ambient levels of supplemental UV-B radiation. — Photochem. Photobiol. Sci. 4: 275–279, 2005. Flint, S.D., Searles, P.S., Caldwell, M.M.: Field testing of biological spectral weighting functions for induction of UVabsorbing compounds in higher plants. — Photochem. Photobiol. 79: 399–403, 2004. Gehrke, C.: Impacts of enhanced ultraviolet-B radiation on mosses in a subarctic heath ecosystem. — Ecology 80: 1844–1851, 1999. Germ, M., Kreft, I., Osvald, J.: Influence of UV-B exclusion and selenium treatment on photochemical efficiency of photosystem II, yield and respiratory potential in pumpkins (Cucurbita pepo L.). — Plant Physiol. Biochem. 43: 445–448, 2005. Guidi, L., Mori, S., Degl’Innocenti, E., Pecchia, S.: Effects of ozone exposure or fungal pathogen on white lupin leaves as determined by imaging of chlorophyll a fluorescence. — Plant Physiol. Biochem. 45: 851–857, 2007. Guo, D.P., Guo, Y.P., Zhao, J.P. et al.: Photosynthetic rate and chlorophyll fluorescence in leaves of stem mustard (Brassica juncea var. tsatsai) after turnip mosaic virus infection. — Plant Sci. 168: 57–63, 2005. Haapala, J.K., Mörsky, S.K., Saarnio, S. et al.: Long-term effects of elevated UV-B radiation on photosynthesis and ultrastructure of Eriophorum russeolum and Warnstorfia exannulata. — Sci. Total Environ. 409: 370–377, 2010. Havaux, M., Kloppstech, K.: The protective functions of carotenoid and flavonoid pigments against excess visible radiation at chilling temperature investigated in Arabidopsis npq and tt mutants. — Planta 213: 953–966, 2001. Hectors, K., Jacques, E., Prinsen, E. et al.: UV radiation reduces epidermal cell expansion in leaves of Arabidopsis thaliana. — J. Exp. Bot. 61: 4339–4349, 2010. Helliot, B., Swennen, R., Poumay, Y. et al.: Ultrastructural changes associated with cryopreservation of banana (Musa spp.) highly proliferating meristems. — Plant Cell Rep. 21: 690–698, 2003. Holzinger, A., Lütz, C., Karsten, U., Wiencke, C.: The effect of ultraviolet radiation on ultrastructure and photosynthesis in the red macroalgae Palmaria palmata and Odonthalia dentata from Arctic waters. — Plant Biol. 6: 568–577, 2004. Holzinger, A., Karsten, U., Lütz, C., Wiencke, C.: Ultrastructure and photosynthesis in the supralittoral green macroalga Prasiola crispa from Spitsbergen (Norway) under UV exposure. — Phycologia 45: 168–177, 2006. Jia, R.L., Li, X.R., Liu, L.C. et al.: Differential wind tolerance of soil crust mosses explains their micro-distribution in nature. — Soil Biol. Biochem. 45: 31–39, 2012. Joshi, P., Gartia, S., Pradhan, M.K., Biswal, B.: Photosynthetic response of clusterbean chloroplasts to UV-B radiation: Energy imbalance and loss in redox homeostasis between QA and QB of photosystem II. — Plant Sci. 181: 90–95, 2011. Kadur, G., Swapan, B., Sunita, K. et al.: Growth enhancement of soybean (Glycine max) upon exclusion of UV-B and UVB/A components of solar radiation: characterization of photosynthetic parameters in leaves. — Photosynth. Res. 94: 299–306, 2007. Kakani, V.G., Reddy, K.R., Zhao, D., Sailaja, K.: Field crop responses to ultraviolet-B radiation: a review. — Agr. Forest Meteorol. 120: 191–218, 2003. Keiller, D.R., Holmes, M.G.: Effects of long-term exposure to elevated UV-B radiation on the photosynthetic performance of five broad-leaves tree species. — Photosynth. Res. 67: 229–240, 2001. Kumari, R., Agrawal, S.B.: Supplemental UV-B induced changes in leaf morphology, physiology and secondary metabolites of an Indian aromatic plant Cymbopogon citratus (D.C.) Staph under natural field conditions. — Int. J. Environ. Stud. 67: 655–675, 2010. Kummerová, M., Krulová, J., Zezulka, Š., Tříska, J.: Evaluation of fluoranthene phytotoxicity in pea plants by Hill reaction and chlorophyll fluorescence. — Chemosphere 65: 489–496, 2006. Lan, S.B., Wu, L., Zhang, D.L., Hu, C.X., Liu, Y.D.: Ethanol outperforms multiple solvents in the extraction of chlorophylla from Biological soil crusts. — Soil Biol. Biochem. 43: 857–861, 2011. Lee, J.J., Correia, M.: Endosymbiotic diatoms from previously unsample habitats. — Symbiosis 38: 251–260, 2005. Li, X.-R., Wang, X.-P., Li, T., Zhang, J.-G.: Microbiotic soil crust and its effect on vegetation and habitat on artificially stabilized desert dunes in Tengger Desert, North China. — Biol. Fertil. Soils 35: 147–154, 2002. Li, X.-R., Zhou, H.-Y., Wang, X.-P. et al.: The effects of sand stabilization and revegetation on cryptogam species diversity and soil fertility in Tengger Desert, Northern China. — Plant Soil 251: 237–245, 2003. Li, X.R., Chen, Y.W., Su, Y.G., Tan, H.J.: Effects of biological soil crust on desert insect diversity: Evidence from the Tengger Desert of Northern China. — Arid Land Res. Manag. 20: 263–280, 2006a. Li, X.R., Xiao, H.L., He, M.Z., Zhang, J.G.: Sand barriers of straw checkerboards for habitat restoration in extremely arid desert regions. — Ecol. Eng. 28: 149–157, 2006b. Li, X.R., He, M.Z., Zerbe, S. et al.: Micro-geomorphology determines community structure of biological soil crusts at small scales. — Earth Surf. Processes 35: 932–940, 2010a. Li, X.R., Tian, F., Jia, R.L. et al.: Do biological soil crusts determine vegetation changes in sandy deserts? Implications for managing artificial vegetation. — Hydrol. Process. 24: 3621–3630, 2010b. Li, X.R., Jia, R.L., Chen, Y.W. et al.: Association of ant nests with successional stages of biological soil crusts in the Tengger Desert, Northern China. — Appl. Soil Ecol. 47: 59–66, 2011. Liu, L.-X., Xu, S.-M., Woo, K.C.: Solar UV-B radiation on growth, photosynthesis and the xanthophyll cycle in tropical acacias and eucalyptus. — Environ. Exp. Bot. 54: 121–130, 2005. Liu, M.L., Cao, B., Zhou, S.H., Liu, Y.B.: Responses of the flavonoid pathway to UV-B radiation stress and the correlation with the lipid antioxidant characteristics in the desert plant Caryopteris mongolica. — Acta Ecol. Sin. 32: 150–155, 2012. Lud, D., Moerdijk, T.C.W., Van de Poll, W.H., Buma, A.G.J., Huiskes, A.H.L.: DNA damage and photosynthesis in Antarctic and Arctic Sanionia uncinata (Hedw.) Loeske under ambient and enhanced levels of UV-B radiation. — Plant Cell Environ. 25: 1579–1589, 2002. Lud, D., Schlensog, M., Schroeter, B., Huiskes, A.H.L.: The influence of UV-B radiation on light-dependent photosynthetic performance in Sanionia uncinata (Hedw.) Loeske in Antarctica. — Polar Biol. 26: 225–232, 2003. Mackerness, S.A.H., John, C.F., Jordan, B., Thomas, B.: Early signaling components in ultraviolet-B responses: distinct roles for different reactive oxygen species and nitric oxide. — FEBS Lett. 489: 237–242, 2001. Manukyan, A.: Effects of PAR and UV-B radiation on herbal yield, bioactive compounds and their antioxidant capacity of some medicinal plants under controlled environmental conditions. — Photochem. Photobiol. 89: 406–414, 2013. Marshall, T., Williams, K.M.: Total protein determination in urine: Elimination of a differential response between the Coomassie Blue and Pyrogallol Red protein dye-binding assays. — Clin. Chem. 46: 392–398, 2000. Martínez-Abaigar, J., Núñez-Olivera, E., Beaucourt, N. et al.: Different physiological responses of two aquatic bryophytes to enhanced ultraviolet-B radiation. — J. Bryol. 25: 17–30, 2003. McKenzie, R.L., Björn, L.O., Bais, A., Ilyasd, M.: Changes in biologically active ultraviolet radiation reaching the Earth’s surface. — Photochem. Photobiol. Sci. 2: 5–15, 2003. Medina, C.D., Tracanna, B.C., Hilal, M. et al.: Effect of solar UV-B exclusion on the phytoplankton community in a subtropical mountain reservoir: a mesocosm study. — Lake Reserv. Manage. 15: 237–253, 2010. Mishra, V., Srivastava, G., Prasad, S.M., Abraham, G.: Growth, photosynthetic pigments and photosynthetic activity during seedling stage of cowpea (Vigna unguiculata) in response to UV-B and dimethoate. — Pestic. Biochem. Physiol. 92: 30–37, 2008. Newsham, K.K., Hodgson, D.A., Murray, A.W.A. et al.: Response of two Antarctic bryophytes to stratospheric ozone depletion. — Global Change Biol. 8: 972–983, 2002. Newsham, K.K., Robinson, S.A.: Responses of plants in polar regions to UVB exposure: a meta-analysis. — Global Change Biol. 15: 2574–2589, 2009. Niemi, R., Martikainen, P.J., Silvola, J. et al.: Responses of two Sphagnum moss species and Eriophorum vaginatum to enhanced UV-B in a summer of low UV intensity. — New Phytol. 156: 509–515, 2002. Patrick, E.: Researching crusting soils: themes, trends, recent developments and implications for managing soil and water resources in dry areas. — Prog. Phys. Geog. 26: 442–461, 2002. Peng, Q., Zhou, Q.: Influence of lanthanum on chloroplast ultrastructure of soybean leaves under ultraviolet-B stress. — J. Rare Earth 27: 304–307, 2009. Pluskota, W.E., Michalczyk, D.J., Górecki, R.J.: Control of phenylalanine ammonia-lyase gene promoters from pea by UV radiation. — Acta Physiol. Plantarum 27: 229–236, 2005. Pradhan, M.K., Nayak, L., Joshi, P.N. et al.: Developmental phase-dependent photosynthetic responses to ultraviolet-B radiation: damage, defence, and adaptation of primary leaves of wheat seedlings. — Photosynthetica 46: 370–377, 2008. Ranjbarfordoei, A., Samson, R., Van Damme, P.: Photosynthesis performance in sweet almond [Prunus dulcis (Mill) D. Webb] exposed to supplemental UV-B radiation. — Photosynthetica 49: 107–111, 2011. Reddy, K.R., Kakani, V.G., Zhao, D., Mohammed, A.R., Gao, W.: Cotton responses to ultraviolet-B radiation: experimentation and algorithm development. — Agr. Forest Meteorol. 120: 249–265, 2003. Roberts, M.R., Paul, N.D.: Seduced by the dark side: integrating molecular and ecological perspectives on the influence of light on plant defence against pest and pathogens. — New Phytol. 170: 677–699, 2006. Ryan, K.G., McMinn, A., Mitchell, K.A., Trenerry, L.: Mycosporine like amino acids in Antarctic sea ice algae, and their response to UVB radiation. — Z. Naturforsch. C. 57: 471–477, 2002. Ryan, K.G., Hunt, J.E.: The effects of UVB radiation on temperate southern hemisphere forests. — Environ. Pollut. 137: 415–427, 2005. Sangtarash, M.H., Qaderi, M.M., Chinnappa, C.C., Reid, D.M.: Differential sensitivity of canola (Brassica napus) seedlings to ultraviolet-B radiation, water stress and abscisic acid. — Environ. Exp. Bot. 66: 212–219, 2009. Schreiber, U., Bilger, W., Neubauer, C.: Chlorophyll fluorescence as a nonintrusive indicator for rapid assessment of in vivo photosynthesis. — In: Schulze, E.-D., Caldwell, M.M. (ed.): Ecophysiology of Photosynthesis. Pp. 49–70. Springer-Verlag, Berlin 1994. Shi, S.B., Zhu, W.Y., Li, H.M. et al.: Photosynthesis of Saussurea superba and Gentiana straminea is not reduced after long-term enhancement of UV-B radiation. — Environ. Exp. Bot. 51: 75–83, 2004. Su, Y.-G., Li, X.-R., Chen, Y.-W. et al.: Effects of biological soil crusts on emergence of desert vascular plants in North China. — Plant Ecol. 191: 11–19, 2007. Sullivan, J.H., Gitz, D.C., Peek, M.S., McElrone, A.J.: Response of three eastern tree species to supplemental UV-B radiation: leaf chemistry and gas exchange. — Agr. Forest Meteorol. 120: 219–228, 2003. Surabhi, G.-K., Reddy, K.R., Singh, S.K.: Photosynthesis, fluorescence, shoot biomass and seed weigh responses of three cowpea (Vigna unguiculata (L.) Walp.) cultivars with contrasting sensitivity to UV-B radiation. — Environ. Exp. Bot. 66: 160–171, 2009. Urban, O., Tůma, I., Holub, P., Marek, M.V.: Photosynthesis and growth response of Calamagrostis arundinacea and C. villosa to enhanced UV-B radiation. — Photosynthetica 44: 215–220, 2006. Vogt, T.: Phenylpropanoid biosynthesis. — Mol. Plant 3: 2–20, 2010. Wang, S.W., Xie, B.T., Yin, L.N., Duan, L.S., Li, Z.H., Eneji, A.E., Tsuji, W., Tsunekawa, A.: Increased UV-B radiation affects the viability, reactive oxygen species accumulation and antioxidant enzyme activities in maize (Zea mays L.) pollen. — Photochem. Photobiol. 86: 110–116, 2010. West, N.E.: Structure and function of microphytic soil crusts in wildland ecosystems of arid and semiarid regions. — Adv. Ecol. Res. 20: 179–223, 1990. Weichmann, J.: Postharvest physiology and secondary metabolism. — J. Appl. Bot.-Angew. Bot. 74: 126–130, 2000. Whitford, W.G.: Ecology of Desert Systems. — Academic Press, San Diego 2002. Wilson, B.C., Jacobs, D.F.: Chlorophyll fluorescence of stem cambial tissue reflects dormancy development in Juglans nigra seedlings. — New Forest. 43: 771–778, 2012. Xie, Z.M., Wang, Y.X., Liu, Y.D., Liu, Y.M.: Ultraviolet-B exposure induces photo-oxidative damage and subsequent repair strategies in a desert cyanobacterium Microcoleus vaginatus Gom. — Eur. J. Soil Biol. 45: 377–382, 2009. Xu, H., Chen, S.B., Biswas, D.K. et al.: Photosynthetic and yield responses of an old and a modern winter wheat cultivars to short-term ozone exposure. — Photosynthetica 47: 247–254, 2009. Yao, X., Chu, J., He, X., Ba, C.: Protective role of selenium in wheat seedlings subjected to enhanced UV-B radiation. — Russ. J. Plant Physiol. 58: 283–289, 2011. Yoshimura, H., Zhu, H., Wu, Y.Y., Ma, R.J.: Spectral properties of plant leaves pertaining to urban landscape design of broad-spectrum solar ultraviolet radiation reduction. — Int. J. Biometeorol. 54: 179–191, 2010. Yu, J., Tang, X.X., Zhang, P.Y. et al.: Effects of CO2 enrichment on photosynthesis, lipid peroxidation and activities of antioxidative enzymes of Platymonas subcordiformis subjected to UV-B radiation stress. — Acta Bot. Sin. 46: 682–690, 2004. Zhang, Y.M., Wang, H.L., Wang, X.Q., Yang, W.K., Zhang, D.Y.: The microstructure of microbiotic crust and its influence on wind erosion for a sandy soil surface in the Gurbantunggut Desert of Northweastern China. — Geoderma 132: 441–449, 2006. Zhao, C.-M., Wang, G.-X.: Effects of drought stress on the photoprotection in Ammopiptanthus mongolicus leaves. — Acta Bot. Sin. 44: 1309–1313, 2002. Zhao, D., Reddy, K.R., Kakani, V.G., Read, J.J., Sullivan, J.H.: Growth and physiological responses of cotton (Gossypium hirsutum L.) to elevated carbon dioxide and ultraviolet-B radiation under controlled environmental conditions. — Plant Cell Environ. 26: 771–782, 2003. Zheng, X.Q., Jin, J., Chen, H. et al.: Effect of ultraviolet B irradiation on accumulation of catechins in tea (Camellia sinensis (L.) O. Kuntze). — Afr. J. Biotechnol. 7: 3283–3287, 2008. Zu, Y.G., Pang, H.H., Yu, J.H., Li, D.W., Wei, X.X., Gao, Y.X., Tong, L.: Responses in the morphology, physiology and biochemistry of Taxus chinensis var. mairei grown under supplementary UV-B radiation. — J. Photochem. Photobiol. B 98: 152–158, 2010. Zu, Y.G., Wei, X.X., Yu, J.H. et al.: Responses in the physiology and biochemistry of Korean pine (Pinus koraiensis) under supplementary UV-B radiation. — Photosynthetica 49: 448–458, 2011.