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Aeroterrestrial Microalgae Growing in Biofilms on Facades—Response to Temperature and Water Stress

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Abstract

The photosynthetic performance of a microalgal biofilm colonizing a building facade was investigated between February and July 2004, with an emphasis on changing water availability and air humidity. The fluorimetric measurements of the quantum efficiency (F v/F m) indicated diurnal activity patterns. At most sampling dates the algal biofilm photosynthesized particularly in the morning and substantially less in the afternoon. As long as liquid water was present, the microalgae exhibited at least some degree of photosynthesis. However, F v/F m values never exceeded 0.4, pointing to slight photoinhibition or damage of the cells. Dried cells without photosynthesis could recover within minutes after artificial moistening.

Three microalgal strains were isolated from aeroterrestrial biofilms and established as unialgal cultures. Their photosynthesis and growth were characterized under different air humidities and temperatures. Photosynthesis and growth of strain ROS 55/3 (Stichococcus sp.) showed similar patterns with decreasing relative air humidity. Positive growth and optimum photosynthesis were recorded at 100% relative air humidity. At air humidities below 93%, both processes were strongly inhibited. All studied strains grew between 1 and 30°C with optimum rates at 20–23°C, indicating eurythermal features.

The data indicate that liquid water or 100% air humidity are the prerequisite for optimum photosynthesis and growth of aeroterrestrial microalgae. However, when dried and consequently inactive, these microorganisms can recover quickly if water is suddenly available, e.g., after rain events. These physiological capabilities explain well the ecological success of aeroterrestrial microalgae in occupying many man-made substrata such as building facades and roof tiles in urban areas.

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References

  1. Bertsch, A (1966) CO2 Gaswechsel der Grünalge Apatococcus lobatus. Planta (Berlin) 70: 46–72

    Google Scholar 

  2. Blanchard, GF, Guarini, JM, Richard, P, Gros, P, Mornet, F (1996) Quantifying the short-term temperature effect on light-saturated photosynthesis of intertidal microphytobenthos. Mar Ecol Prog Ser 134: 309–331

    Article  Google Scholar 

  3. Büchel, C, Wilhelm, C (1993) In vivo analysis of slow chlorophyll fluorescence induction kinetics in algae: progress, problems and perspectives. Photochem Photobiol 58: 137–148

    Article  Google Scholar 

  4. Cockell, CS, Knowland, J (1999) Ultraviolet radiation screening compounds. Biol Rev 74(3): 311–345

    Article  PubMed  CAS  Google Scholar 

  5. Dunlap, WC, Shick, JM (1998) Ultraviolet radiation-absorbing mycosporine-like amino acids in coral reef organisms: a biochemical and environmental perspective. J Phycol 34(3): 418–430

    Article  Google Scholar 

  6. Ehling-Schulz, M, Bilger, W, Scherer, S (1997) UV-B-induced synthesis of photoprotective pigments and extracellular polysaccharides in the terrestrial cyanobacterium Nostoc commune. J Bacteriol 179: 1940–1945

    PubMed  CAS  Google Scholar 

  7. Ettl, H, Gärtner, G (1995) Syllabus der Boden-, Luft- und Flechtenalgen. Gustav Fischer Verlag, Stuttgart

    Google Scholar 

  8. Gaylarde, CC, Morton, LHG (1999) Deteriogenic biofilms on buildings and their control: a review. Biofouling 14: 59–74

    Article  Google Scholar 

  9. Govindasamy, B, Thompson, S, Mirin, A, Wickett, M, Caldeira, K, Delire, C (2005) Increase of carbon cycle feedback with climate sensitivity: results from a coupled climate and carbon cycle model. Tellus Ser B Chem Phys Meteorol 57(2): 153–163

    Article  Google Scholar 

  10. Highsmith, RC (1981) Lime-boring algae in hermatypic coral skeletons. J Exp Mar Biol Ecol 55: 267–281

    Article  Google Scholar 

  11. Hokputsa, S, Hu, CX, Paulsen, BS, Harding, SE (2003) A physicochemical comparative study on extracellular carbohydrate polymers from five desert algae. Carbohydr Polym 54: 27–32

    Article  CAS  Google Scholar 

  12. Hoyer, K, Karsten, U, Sawall, T, Wiencke, C (2001) Photoprotective substances in Antarctic macroalgae and their variation with respect to depth distribution, different tissues and developmental stages. Mar Ecol Prog Ser 211: 117–129

    Article  CAS  Google Scholar 

  13. Karsten, U, Klimant, I, Holst, G (1996a) A new in vivo fluorimetric technique to measure growth of adhering phototrophic microorganisms. Appl Environ Microb 62(1): 237–243

    CAS  Google Scholar 

  14. Karsten, U, Koch, S, West, JA (1996b) Physiological responses of the eulittoral macroalga Stictosiphonia hookeri (Rhodomelaceae, Rhodophyta) from Argentina and Chile: salinity, light and temperature acclimation. Eur J Phycol 31(4): 361–368

    Article  Google Scholar 

  15. Karsten, U, Friedl, T, Schumann, R, Hoyer, K, Lembcke, S (2005) Mycosporine-like amino acids and phylogenies in green algae: Prasiola and its relatives from the Trebouxiophyceae (Chlorophyta). J Phycol 41(3): 557–566

    Article  CAS  Google Scholar 

  16. Khandekar, ML, Murty, TS, Chittibabu, P (2005) The global warming debate: a review of the state of science. Pure Appl Geophys 1626(8–9): 1557–1586

    Article  Google Scholar 

  17. Kromkamp, JC, Forster, RM (2003) The use of variable fluorescence measurements in aquatic ecosystems: differences between multiple and single turnover measuring protocols and suggested terminology. Eur J Phycol 38: 103–112

    Article  Google Scholar 

  18. Lange, OL, Bilger, W, Schreiber, U (1989) Chlorophyll fluorescence of lichens containing green and blue-green algae during hydration by water vapor uptake and by addition of liquid water. Bot Acta 102: 306–313

    Google Scholar 

  19. Lange, OL, Meyer, A, Büdel, B (1994) Net photosynthesis activation of a desiccate cyanobacterium without liquid water in high air humidity alone. Experiments with Micrcoleus sociatus isolated from a desert soil crust. Funct Ecol 8: 52–57

    Article  Google Scholar 

  20. Lange, OL, Belnap, J, Reichenberger, H, Meyer, A (1997) Photosynthesis of green algal soil crust lichens from arid lands in southern Utah, USA: role of water content on light and temperature responses of CO2 exchange. Flora 192: 1–15

    Google Scholar 

  21. Lange, OL, Leisner, JMR, Bilger, W (1999) Chlorophyll fluorescence characteristics of the cyanobacterial lichen Peltigera rufescens under field conditions—II. Diel and annual distribution of metabolic activity and possible mechanisms to avoid photoinhibtion. Flora 194: 413–430

    Google Scholar 

  22. Lange, OL, Green, TGA (2005) Lichens show that fungi can acclimate their respiration to seasonal changes in temperature. Oecologia 142(1): 11–19

    Article  PubMed  Google Scholar 

  23. Lobban, C, Harrison, P (1997) Seaweed Ecology and Physiology. Cambridge University Press, Cambridge

    Google Scholar 

  24. Moore, LR, Chisholm, SW (1999) Photophysiology of the marine cyanobacterium Prochlorococcus: ecotypic differences among cultured isolates. Limnol Oceanogr 44(3): 628–638

    Article  Google Scholar 

  25. Ong, BL, Lim, M, Wee, YC (1992) Effects of desiccation and illumination on photosynthesis and pigmentation of an edaphic population of Trentepholia odorata (Chlorophyta). J Phycol 28: 768–772

    Article  CAS  Google Scholar 

  26. Ortega-Calvo, JJ, Arino, X, Hernandez-Marine, M, Saiz-Jimenez, C (1995) Factors affecting the weathering and colonisation of monuments by phototrophic microorganisms. Sci Tot Environ 167: 329–341

    Article  CAS  Google Scholar 

  27. Palmer Jr, RJ, Friedmann, IE (1990) Water relations and photosynthesis in the cryptoendolithic microbial habitat of hot and cold deserts. Microb Ecol 19: 111–118

    Article  PubMed  Google Scholar 

  28. Rascher, U, Lakatos, M, Büdel, B, Lu¨ttge, U (2003) Photosynthetic field capacity of cyanobacteria of a tropical inselberg of the Guiana Highlands. Eur J Phycol 38: 247–256

    Article  Google Scholar 

  29. Rhee, GY, Gotham, IJ (1981) The effect of environmental factors on phytoplankton growth: temperature and the interactions of temperature with nutrient limitation. Limnol Oceanogr 26: 635–648

    Article  CAS  Google Scholar 

  30. Schlensog, M, Pannewitz, S, Green, TGA, Schroeter, B (2004) Metabolic recovery of continental antarctic cryptogams after winter. Polar Biol 27(7): 399–408

    Article  Google Scholar 

  31. Schroeter, B (1994) Langzeitmessungen von Mikroklima und metabolischer Aktivität von Flechten in der maritimen Antarktis. Mitteilung Kieler Polarforscher 9: 15–18

    Google Scholar 

  32. Starr, RC, Zeikus, J (1993) UTEX—the culture of algae at the University of Texas at Austin. J Phycol 29(supplement): 1–106

    Article  Google Scholar 

  33. Thomas, DN, Kirst, GO (1991) Salt tolerance of Ectocarpus siliculosus (Dillw) Lyngb—comparison of gametophytes, sporophytes of different geographic origin. Bot Acta 104(1): 26–36

    Google Scholar 

  34. Tomaselli, L, Lamenti, G, Bosco, M, Tiano, P (2000) Biodiversity of photosynthetic micro organisms dwelling on stone monuments. Int Biodeterior Biodegrad 46: 251–258

    Article  Google Scholar 

  35. Viles, HA (1987) Blue-green algae and terrestrial limestone weathering on Aldabra Atoll: an SEM and light microscope study. Earth Surf Process Landf 12: 319–330

    Article  Google Scholar 

  36. Welton, RG, Cuthbert, SJ, McLean, R, Hursthouse, A, Hughes, J (2003) A preliminary study of the phycological degradation of natural stone masonry. Environ Geochem Health 25: 139–145

    Article  PubMed  CAS  Google Scholar 

  37. Winston, PW, Bates, DH (1960) Saturated solutions for the control of humidity in biological research. Ecology 41: 232–237

    Article  Google Scholar 

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Acknowledgments

We thank Evelyn Lawrenz and Manuela Görs for their assistance during algal cultivation and maintenance of our species collection. Prof. Thomas Friedl, University of Göttingen, helped with the molecular identification of all strains studied. Prof. Gunter Kirst, University of Bremen, provided the temperature aluminum blocks, and Prof. Andreas Wohltmann, University of Bremen, the air humidity chambers. We greatly appreciate the financial support by the Deutsche Forschungsgemeinschaft (Project Ka 899/13-1).

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Correspondence to U. Karsten.

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Häubner, N., Schumann, R. & Karsten, U. Aeroterrestrial Microalgae Growing in Biofilms on Facades—Response to Temperature and Water Stress. Microb Ecol 51, 285–293 (2006). https://doi.org/10.1007/s00248-006-9016-1

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