UV-B and Biosphere pp 66-76 | Cite as
Uses of biological spectral weighting functions and the need of scaling for the ozone reduction problem
Abstract
In several phases of assessing implications of stratospheric ozone reduction for plants, biological spectral weighting functions (BSWF) play a key role: calculating the increase of biologically effective solar ultraviolet-B radiation (UV-BBE) due to ozone reduction, assessing current latitudinal gradients of UV-BBE, and comparing solar UV-BBE with that from lamps and filters in plant experiments. Plant UV action spectra (usually determined with monochromatic radiation in the laboratory with exposure periods on the order of hours) are used as BSWF. Yet, many complicating factors cloud the realism of such spectra for plants growing day after day in polychromatic solar radiation in the field. The uses and sensitivity of BSWF in the stratospheric ozone reduction problem are described. The need for scaling BSWF from action spectra determined with monochromatic radiation in laboratory conditions over periods of hours to polychromatic solar radiation in the field is developed. Bottom-up mechanistic and top-down polychromatic action spectrum development are considered as not satisfactory to resolve realistic BSWF. A compromise intermediate approach is described in which laboratory results are tested under polychromatic radiation in growth chambers and, especially, under field conditions. The challenge of the scaling exercise is to resolve disagreements between expected spectral responses at different scales of time and radiation conditions. Iterative experiments with feedback among the different experimental venues is designed to reduce uncertainties about realistic BSWF in the field. Sensitivity analyses are employed to emphasize characteristics of BSWF that are particularly important in assessing the ozone problem. Implications for use of realistic BSWF both for improved research design and for retrospective analysis of past research is described.
Keywords
Action spectra Global change assessment Higher plant response to UV Solar ultraviolet Stratospheric ozone layer UV-B radiationPreview
Unable to display preview. Download preview PDF.
References
- Adamse, P., Britz, S. J. & Caldwell, C. R. 1994. Amelioration of UV-B damage under high irradiance. II. Role of blue light photoreceptors. Photochem. Photobiol. 60: 110–115.CrossRefGoogle Scholar
- Ballaré, C. L., Barnes, P. W. & Flint, S. D. 1995. Inhibition of hypocotyl elongation by ultraviolet-B radiation in de-etiolating tomato seedlings. The photoreceptor. Physiol. Plant. 93: 584–592.CrossRefGoogle Scholar
- Ballaré, C. L., Barnes, P. W. & Kendrick, R. E. 1991. Photo-morphogenic effects of UV-B radiation on hypocotyl elongation in wild type and stable-phytochrome-deficient mutant seedlings of cucumber. Physiol. Plant. 83: 652–658.CrossRefGoogle Scholar
- Barnes, P. W., Flint, S. D. & Caldwell, M. M. 1987. Photosynthesis damage and protective pigments in plants from a latitudinal arctic/alpine gradient exposed to supplemental UV-B radiation in the field. Arctic Alpine Res. 19: 21–27.CrossRefGoogle Scholar
- Beggs, C. J., Schneider-Ziebert, U. & Wellmann, E. 1986. UV-B radiation and adaptive mechanisms in plants. pp. 235–250. In: Worrest, R. C & Caldwell, M. M. (eds) Stratospheric ozone reduction, solar ultraviolet radiation and plant life. Springer-Verlag, Berlin, Heidelberg.CrossRefGoogle Scholar
- Bornman, J. F. 1989. Target sites of UV-B radiation in photosynthesis of higher plants. J. Photochem. Photobiol. B: Biol. 4: 145–158.CrossRefGoogle Scholar
- Brite, S. J. & Adamse, P. 1994. UV-B-induced increase in specific leaf weight of cucumber as a consequence of increased starch content. Photochem. Photobiol. 60: 116–119.CrossRefGoogle Scholar
- Buchholz, G., Ehmann, B. & Wellmann, E. 1995. Ultraviolet light inhibition of phytochrome-induced flavonoid biosynthesis and DNA photolyase formation in mustard cotyledons (Sinapis alba L.). Plant Physiol. 108: 227–234.PubMedGoogle Scholar
- Caldwell, M. M. 1971. Solar ultraviolet radiation and the growth and development of higher plants. pp. 131–177. In: Giese, A. C. (ed) Photophysiology. Volume 6. Academic Press, New York.Google Scholar
- Caldwell, M. M. 1981. Plant response to solar ultraviolet radiation. pp. 169–197. In: Lange, O. L., Nobel, P. S., Osmond, C. B. & Ziegler, H. (eds) Encyclopedia of plant physiology, Vol. 12A. Physiological plant ecology I. Responses to the physical environment. Springer-Verlag, Berlin.Google Scholar
- Caldwell, M. M. & Flint, S. D. 1994a. Solar ultraviolet radiation and ozone layer change: Implications for crop plants. pp. 487–507. In: Boote, K., Bennett, J. M., Sinclair, T. R. & Paulsen, G. M. (eds), Physiology and determination of crop yield. ASA-CSSA-SSSA, Madison, WI.Google Scholar
- Caldwell, M. M. & Flint, S. D. 1994b. Stratospheric ozone reduction, solar UV-B radiation and terrestrial ecosystems. Climate Change 28: 375–394.CrossRefGoogle Scholar
- Caldwell, M. M. & Flint, S. D. 1995. Lighting considerations in controlled environments for nonphotosynthetic plant responses to blue and ultraviolet radiation. pp. 113–124. In: Tibbitts, T.W. (ed) Proceedings international lighting in controlled environments workshop. National Aeronautics and Space Administration, Ames Research Station, Moffett Field, CA.Google Scholar
- Caldwell, M. M., Robberecht, R., Nowak, R. S. & Billings, W. D. 1982. Differential photosynthetic inhibition by ultraviolet radiation in species from the arctic-alpine life zone. Arctic Alpine Res. 14: 195–202.CrossRefGoogle Scholar
- Caldwell, M. M., Camp, L. B., Warner, C.W. & Flint, S. D. 1986. Action spectra and their key role in assessing biological consequences of solar UV-B radiation change. pp. 87–111. In: Worrest, R. C. & Caldwell, M. M. (eds) Stratospheric ozone reduction, solar ultraviolet radiation and plant life. Springer-Verlag, Berlin.CrossRefGoogle Scholar
- Caldwell, M. M., Teramura, A. H. & Tevini, M. 1989. The changing solar ultraviolet climate and the ecological consequences for higher plants. Trends Ecol. Evol. 4: 363–367.PubMedCrossRefGoogle Scholar
- Caldwell, M. M., Flint S. D. & Searles, P. S. 1994. Spectral balance and UV-B sensitivity of soybean: a field experiment. Plant Cell Environ. 17: 267–276.CrossRefGoogle Scholar
- Cen, Y. P. & Björn, L. O. 1994. Action spectra for enhancement of ultraweak luminescence by UV radiation (270–340 nm) in leaves of Brassica napus. J. Photochem. Photobiol. B: Biol. 22: 125–129.CrossRefGoogle Scholar
- Cen, Y. P. & Bornman, J. F. 1990. The response of bean plants to UV-B radiation under different irradiances of background visible light J. Exp. Bot. 41: 1489–1495.CrossRefGoogle Scholar
- Coblentz, W. W. 1932. The Copenhagen meeting of the Second International Congress on Light. Science 76: 412–415.PubMedCrossRefGoogle Scholar
- Coohill, T. P. 1989. Ultraviolet action spectra (280 to 380 nm) and solar effectiveness spectra for higher plants. Photochem. Photobiol. 50: 451–457.CrossRefGoogle Scholar
- Coohill, T. P. 1991. Action spectra again? Photochem. Photobiol. 54: 859–870.PubMedCrossRefGoogle Scholar
- Coohill, T. P. 1992. Action speetra revisited. J. Photochem. Photobiol. B: Biol. 13: 95–98.CrossRefGoogle Scholar
- Deckmyn, G., Martens, C. & Impens, I. 1994. 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.CrossRefGoogle Scholar
- Ehleringer, J. R. & Field, C. B. (eds). 1993. Scaling physiological processes: leaf to globe. Academic Press, San Diego.Google Scholar
- Ensminger, P. A. & Schäfer, E. 1992. Blue and ultraviolet-B light photoreceptors in parsley cells. Photochem. Photobiol. 55: 437–447.CrossRefGoogle Scholar
- Fernbach, E. & Mohr, H. 1992. Photoreactivation of the UV light effects on growth of scots pine (Pinus sylvestris L.) seedlings. Trees 6: 232–235.CrossRefGoogle Scholar
- Flint, S. D. & Caldwell, M. M. 1996. Scaling plant ultraviolet spectral responses from laboratory action spectra to field spectral weighting factors. J. Plant Physiol. 148: 107–114.CrossRefGoogle Scholar
- Gaba, V. & Black, M. 1987. Photoreceptor interaction in plant photomorphogenesis: the limits of experimental techniques and their interpretations. Photochem. Photobiol. 45: 151–156.CrossRefGoogle Scholar
- Jagger, J. 1981. Near-UV radiation effects on microorganisms. Photochem. Photobiol. 34: 761–768.PubMedGoogle Scholar
- Jagger, J., Stafford, R. S. & Snow, J. M. 1969. Thymine-dimer and action-spectrum evidence for indirect photoreactivation in Escherichia coli. Photochem. Photobiol. 10: 383–395.CrossRefGoogle Scholar
- Kramer, G. F., Krizek, D. T. & Mirecki, R. M. 1992. Influence of photosynthetically active radiation and spectral quality on UV-B-induced polyamine accumulation in soybean. Phytochemistry 31: 1119–1125.CrossRefGoogle Scholar
- Krizek, D. T., Kramer, G. F., Upadhyaya, A. & Mirecki, R. M. 1993. UV-B response of cucumber seedlings grown under metal halide and high pressure sodium deluxe lamps. Physiol. Plant. 88: 350–358.CrossRefGoogle Scholar
- Krizek, D. T., Mirecki, R. M. & Kramer, G. F. 1994. Growth analysis of UV-B-irradiated cucumber seedlings as influenced by photosynthetic photon flux source and cultivar. Physiol. Plant. 90: 593–599.CrossRefGoogle Scholar
- Kumagai, T. & Sato, T. 1992. Inhibitory effects of increase in near-UV radiation on the growth of Japanese rice cultivars (Oryza sativa L.) in a phytotron and recovery by exposure to visible radiation. Jpn. J. Breeding 42: 545–552.Google Scholar
- Langer, B. & Wellmann, E. 1990. Phytochrome induction of photore-activating enzyme in Phaseolus vulgaris L. seedlings. Photochem. Photobiol. 52: 861–863.CrossRefGoogle Scholar
- Menezes, S. & Tyrrell, R. M. 1982. Damage by solar radiation at defined wavelengths: involvement of inducible repair systems. Photochem. Photobiol. 36: 313–318.PubMedCrossRefGoogle Scholar
- Middleton, E. M. & Teramura, A. H. 1993. The role of flavonol glycosides and carotenoids in protecting soybean from ultraviolet-B damage. Plant Physiol. 103: 741–752.PubMedGoogle Scholar
- Middleton, E. M. & Teramura, A. H. 1994. Understanding photosynthesis, pigment and growth responses induced by UV-B and UV-A irradiances. Photochem. Photobiol. 60: 38–45.CrossRefGoogle Scholar
- Mirecki, R. M. & Teramura, A. H. 1984. Effects of ultraviolet-B irradiance on soybean. V. the dependence of plant sensitivity on the photosynthetic photon flux density during and after leaf expansion. Plant Physiol. 74: 475–480.PubMedCrossRefGoogle Scholar
- Mohr, H. 1986. Coaction between pigment systems. pp. 547–564. In: Kendrick, R. E. & Kronenberg, G. H. M. (eds) Photomorpho-genesis in plants. Martinus Nijhoff/Dr. W. Junk, DordrechtGoogle Scholar
- Panagopoulos, I., Bornman, J. F. & Björn, L. O. 1990. Effects of ultraviolet radiation and visible light on growth, fluorescence induction, ultraweak luminescence and peroxidase activity in sugar beet plants. J. Photochem. Photobiol. B: Biol. 8: 73–87.CrossRefGoogle Scholar
- Pang, Q. & Hays, J. B. 1991. UV-B-inducible and temperature-sensitive photoreactivation of cyclobutane pyrimidine dimers in Arabidopsis thaliana. Plant Physiol. 95: 536–543.PubMedCrossRefGoogle Scholar
- Quaite, F. E., Sutherland, B. M. & Sutherland, J. C. 1992. Action spectrum for DNA damage in alfalfa lowers predicted impact of ozone depletion. Nature 358: 576–578.CrossRefGoogle Scholar
- Robberecht, R., Caldwell, M. M. & Billings, W. D. 1980. Leaf ultraviolet optical properties along a latitudinal gradient in the arctic-alpine life zone. Ecology 61: 612–619.CrossRefGoogle Scholar
- Rundel, R. D. 1983. Action spectra and estimation of biologically effective UV radiation. Physiol. Plant. 58: 360–366.CrossRefGoogle Scholar
- Searles, P. S., Caldwell, M. M. & Winter, K. 1995. The response of five tropical dicotyledon species to solar ultraviolet-B radiation. Am. J. Bot. 82: 445–453.CrossRefGoogle Scholar
- Setlow, R. B. 1974. The wavelengths in sunlight effective in producing skin cancer: a theoretical analysis. Proc. Nat Acad. Sci. USA 71: 3363–3366.PubMedCrossRefGoogle Scholar
- Steinmüller, D. 1986. Zur Wirkung ultravioletter Strahlung (UV-B) auf die Struktur von Blattoberflächen und zu Wirkungsmechanismen bei der Akkumulation und Biosynthese der Kutikularlipide einiger Nutzpflanzen. PhD Dissertation, University of Karlsruhe.Google Scholar
- Takayanagi, S., Trunk, J. G., Sutherland, J. C. & Sutherland, B. M. 1994. Alfalfa seedlings grown outdoors are more resistant to UV-induced DNA damage than plants grown in a UV-frcc environmental chamber. Photochem. Photobiol. 60: 363–367.CrossRefGoogle Scholar
- Tevini, M. & Teramura, A. H. 1989. UV-B effects on terrestrial plants. Photochem. Photobiol. 50: 479–487.CrossRefGoogle Scholar
- Warner, C. W. & Caldwell, M. M. 1983. Influence of photon flux density in the 400–700 nm waveband on inhibition of photosynthesis by UV-B (280–320 nm) irradiation in soybean leaves: separation of indirect and immediate effects. Photochem. Photobiol. 38: 341–346.CrossRefGoogle Scholar
- Webb, R. B. 1977. Lethal and mutagenic effects of near-ultraviolet radiation. Photochem. Photobiol. Rev. 2: 169–261.CrossRefGoogle Scholar
- Wilson, M. I. & Greenberg, B. M. 1993. Specificity and photo-morphogenic nature of ultraviolet-B-induced cotyledon curling in Brassica napus L. Plant Physiol. 102: 671–677.PubMedCrossRefGoogle Scholar