Ultraviolet insolation and the tropical rainforest: Altitudinal variations, Quaternary and recent change, extinctions, and the evolution of biodiversity

Chapter
Part of the Springer Praxis Books book series (PRAXIS)

Abstract

Ultraviolet light occurs in three wavebands. UV-A is the longest waveband (>315 nm) which is close to visible light and is of limited biological significance. UV-B (280–315 nm) is damaging and mutagenic to living organisms. UV-C (<280 nm) is lethal to all life, but is fortunately absorbed in the stratosphere, so does not reach the surface of the Earth in sunlight. It is therefore toUV-B that we must turn our chief attention. This, like UV-C, is also partly absorbed by ozone in the stratosphere, but some reaches the Earth’s surface. Recent concerns about the ‘‘Ozone Hole’’ have focussed attention on polar regions, but in fact tropical regions have fairly low ozone concentrations in the stratosphere above them (Smith and Warr, 1991). The result is that, given their high overall insolation resulting from the low latitude, tropical regions have rather high UV-B levels.

Keywords

Tropical Rainforest Tropical Rain Forest Mean Annual Temperature Allopatric Speciation Altitudinal Variation 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Ahmad, I., Day, J. P., MacDonald, M. V., and Ingram, D. S. (1991) Haploid culture and UV mutagenesis in rapid-cycling Brassica napus for the generation of resistance to chlorsulfuron and Alternaria brassicicola. Annals of Botany, 67, 519–521.Google Scholar
  2. Atwell, B. J., Kriedemann, P. E., and Turnbull, C. G. N. (Eds.) (1999) Plants in Action: Adaptation in Nature, Performance in Cultivation. Macmillan, South Yarra, Australia.Google Scholar
  3. Aubry, M.-P., Lucas, S. G., and Berggren, W. A. (Eds.) (1998) Late Paleocene–Early Eocene Climatic and Biotic Events in the Marine and Terrestrial Records. Columbia University Press, New York.Google Scholar
  4. Austin, J., Butchart, N., and Shine, K. P. (1992) Possibility of an Arctic ozone hole in a doubled- CO2 climate. Nature, 360, 221–225.CrossRefGoogle Scholar
  5. Bennett, K. D. (1990) Milankovitch Cycles and their effects on species in ecological and evolutionary time. Paleobiology, 16, 11–21.Google Scholar
  6. Bennett, K. D. (2004) Continuing the debate on the role of Quaternary environmental change for macroevolution. Philosophical Trans. Royal Society London B, 359, 295–303.CrossRefGoogle Scholar
  7. Bjorn, L. O. and McKenzie, R. L. (2007) Attempts to probe the ozone layer and the ultraviolet- B levels of the past. Ambio, 36, 366–371.CrossRefGoogle Scholar
  8. Blaustein, A. R., Belden, L. K., Olson, D. H., Green, D. M., Root, T. L., and Kiesecker, J. M. (2001) Amphibian breeding and climate change. Conservation Biology, 15, 1804–1809.CrossRefGoogle Scholar
  9. Blaustein, A. R., Romansic, J. M., Kiesecker, J. M., and Hatch, A. C. (2003) Ultraviolet radiation, toxic chemicals and amphibian population declines. Diversity and Distributions, 9, 123–140.CrossRefGoogle Scholar
  10. Blumthaler, M., Ambach, W., and Ellinger, R. (1997) Increase in solar UV radiation with altitude. J. Photochemistry and Photobiology B, Biology, 39, 130–134.Google Scholar
  11. Brass, L. J. (1941) The 1938–39 Expedition to the Snow Mountains, Netherlands New Guinea. J. Arnold Arbor. 22, 271–342.Google Scholar
  12. Brass, L. J. (1964) Results of the Archbold Expeditions No. 86: Summary of the Sixth Archbold Expedition to New Guinea. Bulletin of the American Museum of Natural History, 127, 145–215.Google Scholar
  13. Brookfield, H. C. (1964) The ecology of highland settlement: Some suggestions. American Anthropologist, 66, 20–38.CrossRefGoogle Scholar
  14. Bruijnzeel, L. A. and Proctor, J. (1993) Hydrology and biogeochemistry of tropical montane cloud forests: What do we really know? In: L. S. Hamilton, J. O. Juvik, and F. N. Scatena (Eds.), Tropical Montane Cloud Forests, p. 264. East–West Center, HI.Google Scholar
  15. Bruijnzeel, L. A., Waterloo, M. J., Proctor, J. et al. (1993) Hydrological observations in montane forests on Gunung Silam, Sabah, Malaysia, with special reference to the “Massenerhebung” effect. J. Ecology, 81, 145–167.CrossRefGoogle Scholar
  16. Bush, M. B. (1994) Amazonian speciation: A necessarily complex model. J. Biogeography, 21, 5–17.CrossRefGoogle Scholar
  17. Bush, M. B., Piperno, D. R., Colinvaux, C. A., De Oliveira, P. E., Krissek, L. A., Miller, M. C., and Rowe, W. L. (1992) A 14,300-year palaeoecological profile of a lowland tropical lake in Panama. Ecological Monographs, 62, 251–275.CrossRefGoogle Scholar
  18. Caldwell, M. M. (1971) Solar UV irradiation and the growth and development of higher plants. In: A. C. Giese (Ed.) Photophysiology, pp. 131–177. Academic Press, New York.Google Scholar
  19. Caldwell, M.M. (1981) Plant response to solar ultraviolet radiation. In: O. L. Lange, P. S. Nobel, C. B. Osmond, and H. Ziegler (Eds.), Physiological Plant Ecology, I: Encyclopedia of Plant Physiology (New Series, Vol. 12A, pp. 169–197). Springer-Verlag, Berlin.Google Scholar
  20. Caldwell, M. M., Robberecht, R., and Billings, W. D. (1980) A steep latitudinal gradient of solar ultraviolet-B radiation in the Arctic-alpine life zone. Ecology, 61, 600–611.CrossRefGoogle Scholar
  21. Caldwell, M., Teramura, A. H., Tevini, M., Bornman, J. F., Bjorn, L. O., and Kulandaivelu, G. (1995) Effects of increased ultraviolet-radiation on terrestrial plants. Ambio, 24, 166–173.Google Scholar
  22. Caldwell, M. M., Bjorn, L. O., Bornman, J. F., Flint, S. D., Kulandaivelu, G., Teramura, A. H., and Tevini, M. (1998) Effects of increased solar ultraviolet radiation on terrestrial ecosystems. J. Photochemistry and Photobiology B—Biology, 46, 40–52.Google Scholar
  23. Carey, C. and Alexander, M. A. (2003) Climatic change and amphibian declines: Is there a link? Diversity and Distributions, 9, 111–121.CrossRefGoogle Scholar
  24. Carvalho, S. M. P., Heuvelink, E., Cascais, R., and van Korten, O. (2002) Effect of day and night temperature on internode and stem length in Chrysanthemum: Is everything explained by DIF? Annals of Botany, 90, 111–118.CrossRefGoogle Scholar
  25. Collins, J. P. and Storfer, A. (2003) Global amphibian declines: Sorting the hypotheses. Diversity and Distributions, 9, 89–98.CrossRefGoogle Scholar
  26. Corlett, R. T. (1984) Human impact on the subalpine vegetation of Mt. Wilhelm, Papua New Guinea. J. Ecology, 72, 841–854.Google Scholar
  27. Daszak, P., Cunningham, A. A., and Hyatt, A. D. (2003) Infectious disease and amphibian population declines. Diversity and Distributions, 9, 141–150.CrossRefGoogle Scholar
  28. Dave, J. V. and Halpern, P. (1976) Effect of changes in ozone amount on the ultraviolet radiation received at sea level of a model atmosphere. Atmospheric Environment, 10, 547–555.CrossRefGoogle Scholar
  29. Du Puy, D. and Cribb, P. (1988) The Genus Cymbidium. Helm, Bromley, U.K. Eldredge, N. and Gould, S. J. (1972) Punctuated equilibria: An alternative to phyletic gradualism. In: T. M. Schopf (Ed.) Models in Paleobiology. Freeman, Cooper & Co., SanGoogle Scholar
  30. Francisco.Google Scholar
  31. Farrera, I., Harrison, S. P., Prentice, I. C., Bartlein, P. J., Bonnefille, R., Bush, M., Cramer, W., von Grafenstein, U., Holmgren, K., Hooghiemstra, H. et al. (1999) Tropical climates of the Last Glacial Maximum: A new synthesis of terrestrial palaeoclimate data. 1. Vegetation, lake levels and geochemistry. Climate Dynamics, 15, 823–856.Google Scholar
  32. Flenley, J. R. (1979) The Equatorial Rain Forest: A Geological History. Butterworths, London.Google Scholar
  33. Flenley, J. R. (1993) The origins of diversity in tropical rain forests. Trends in Ecology and Evolution, 8, 119–120.CrossRefGoogle Scholar
  34. Flenley, J. R. (2005) Palynological richness and the tropical rain forest. In: E. Bermingham, E. C. Dick, and C. Moritz (Eds.), Tropical Rainforests: Past, Present, and Future. Chicago University Press, Chicago.Google Scholar
  35. Flenley, J. R. (2007) Ultraviolet insolation and the tropical rain forest. In: M. B. Bush and J. R. Flenley (Eds.), Tropical Rain Forest Responses to Climatic Change (First Edition, pp. 219–235). Springer/Praxis, Heidelberg, Germany/Chichester, U.K.Google Scholar
  36. Flenley, J. R. (2008) Why is pollen yellow? And what explains the high biodiversity of the tropical rain forest? Terra Nostra, 2, 82.Google Scholar
  37. Flenley, J. R. (2011) Why is pollen yellow? And why are there so many species in the tropical rain forest? J. Biogeography, 38, 809–816.CrossRefGoogle Scholar
  38. Flenley, J. R. and Richards, K. (Eds.) (1982) The Krakatoa Centenary Expedition: Final Report (Miscellaneous Series No. 25). Geography Department, University of Hull, U.K.Google Scholar
  39. Forster, R. M. (1982) A study of the spatial distribution of bryophytes on Rakata. In: J. R. Flenley and K. Richards (Eds.), The Krakatoa Centenary Expedition, Final Report (Miscellaneous Series No. 25, pp. 103–126). Geography Department, University of Hull, U.K.Google Scholar
  40. Gentry, A. H. (1989) Speciation in tropical forests. In: L. B. Holm-Nielsen, I. C. Nielsen, and H. Balslev (Eds), Tropical Forests: Botanical Dynamics, Speciation and Diversity, pp. 113– 134. Academic Press, London.Google Scholar
  41. Gleason, D. F. (2001) Ultraviolet radiation and coral communities. In: C. S. Cockell and A. R. Blaustein (Eds.), Ecosystems, Evolution and Ultraviolet Radiation, pp. 118–149. Springer-Verlag, New York.Google Scholar
  42. Gleason, J. F., Bhartia P. K., Herman J. R., McPeters, R., Newman, P., Stolarski, S., Flynn, I., Labow, G., Larko, D., Seftor, C. et al. (1993) Record low global ozone in 1992. Science, 260, 523–526.CrossRefGoogle Scholar
  43. Gould, K. S. and Lister, C. (2006). Flavonoid functions in plants. In: O. M. Andersen and K. R. Markham (Eds.), Flavonoids, Chemistry, Biochemistry and Applications, pp. 397–441. Taylor & Francis, Boca Raton, FL.Google Scholar
  44. Grubb, P. J. (1977) Control of forest growth and distribution on wet tropical mountains. Ann. Rev. Ecol. Syst., 8, 83–107.CrossRefGoogle Scholar
  45. Grubb, P. J. and Whitmore, T. C. (1966) A comparison of montane and lowland rain forest in Ecuador, 2: The climate and its effects on the distribution and physiognomy of the forests. J. Ecology, 54, 303–333.CrossRefGoogle Scholar
  46. Haffer, J. (1997) Alternative models of vertebrate speciation in Amazonia: An overview. Biodiversity and Conservation, 6, 451–476.CrossRefGoogle Scholar
  47. Haffer, J. T. and Prance, G. T. (2001) Climatic forcing of evolution in Amazonia during the Cenozoic: On the refuge theory of biotic differentiation. Amazoniana—Limnologia et Oecologia Regionalis Systemae Fluminis Amazonias, 16, 579–605.Google Scholar
  48. Hastenrath, S. (1968) Certain aspects of the three-dimensional distribution of climate and vegetation belts in the mountains of central America and southern Mexico. Colloquium Geogr., 9, 122–130.Google Scholar
  49. Hope, G. S. (1986) Development of present day biotic distributions in the New Guinea mountains. In: B. A. Barlow (Ed.), Flora and Fauna of Alpine Australasia: Ages and Origins, pp. 129–145. CSIRO, Melbourne, Australia.Google Scholar
  50. Jansen, M. A. K., Gaba, V., and Greenberg, B. M. (1998) Higher plants and UV-B radiation: Balancing damage, repair and acclimation. Trends in Plant Science, 3, 131–135.CrossRefGoogle Scholar
  51. Kats, L. B. and Ferrer R. P. (2003) Alien predators and amphibian declines: Review of two decades of science and the transition to conservation. Diversity and Distributions, 9, 99–110.CrossRefGoogle Scholar
  52. Landsberg, H. E., Lippmans, H., Paffen, K. H., and Troll, C. (1966) World Maps of Climatology, Third Edition. Springer-Verlag, Berlin.Google Scholar
  53. Leach, D. G. (1962) Rhododendrons of the World. Allen & Unwin, London.Google Scholar
  54. Leavitt, P. R., Vinebrooke, R. D., Donald, D. B., Smol, J. P., and Schindler, D. W. (1997) Past ultraviolet radiation environments in lakes derived from fossil pigments. Nature, 388, 457–459.CrossRefGoogle Scholar
  55. Lee, D. W. and Lowry, J. B. (1980a) Solar ultraviolet on tropical mountains: Can it affect plant speciation? The American Naturalist, 115, 880–883.CrossRefGoogle Scholar
  56. Lee, D. W. and Lowry J. B. (1980b) Young leaf anthocyanin and solar ultraviolet. Biotropica, 12, 75–76.CrossRefGoogle Scholar
  57. Lindoo, S. J. and Caldwell, M. M. (1978) Ultraviolet-B radiation-induced inhibition of leaf expansion and promotion of anthocyanin production. Plant Physiology, 61, 278–282.CrossRefGoogle Scholar
  58. Liu, J. Q., Gao, T. G., Chen, Z. D., and Lu, A. M. (2002) Molecular phylogeny and biogeography of the Qinghai-Tibet Plateau endemic Nannoglottis (Asteraceae). Molecular Phylogenetics and Evolution, 23, 307–325.CrossRefGoogle Scholar
  59. Liu, J. Q., Wang, Y. J., Wang, A. L., Hideaki, O., and Abbott, R. J. (2006) Radiation and diversification within the Ligularia-Cremanthodium-Parasenecio complex (Asteraceae) triggered by uplift of the Qinghai-Tibetan Plateau. Molecular Phylogenetics and Evolution, 38, 31–49.CrossRefGoogle Scholar
  60. Lodish, H., Berk, A., Zipursky, S. L., Matsudaira, P., Baltimore, D., and Darnell, J. (2000) Molecular Cell Biology. Freeman, New York.Google Scholar
  61. Madronich, S., McKenzie, R. L., Caldwell, M. M., and Bjorn, L. O. (1995) Changes in ultraviolet light reaching the Earth’s surface. Ambio, 24, 143–152.Google Scholar
  62. Martin, P. S. (1963) The last 10,000 Years: A Fossil Pollen Record of the American Southwest. University of Arizona Press, Tucson, AZ.Google Scholar
  63. Monteith, J. L. (1973) Principles of Environmental Physics. Arnold, London. Morley, R. J. (2000) Origin and Evolution of Tropical Rain Forests. John Wiley & Sons, Chichester, U.K.Google Scholar
  64. Murali, N. S. and Teramura, A. H. (1986a) Intraspecific differences in Cucumis sativus sensitivity to ultraviolet-B radiation. Physiol. Plant, 68, 673–677.CrossRefGoogle Scholar
  65. Murali, N. S. and Teramura, A. H. (1986b) Effectiveness of UV-B radiation on the growth and physiology of field grown soybean modified by water stress. Photochemistry and Photobiology, 44, 215–219.CrossRefGoogle Scholar
  66. Murali, N. S. and Teramura, A. H. (1986c) Effects of supplemental ultraviolet-B radiation on the growth and physiology of field-grown soybean. Environmental and Experimental Botany, 26, 233–242.CrossRefGoogle Scholar
  67. Pearson, P. N., Ditchfield, P. W., Singano, J., Harcourt-Brown, K. G., Nicholas, C. J., Olsson, R. K., Shackleton, N. J., and Hall, M. A. (2001) Warm tropical sea surface temperatures in the Late Cretaceous and Eocene epochs. Nature, 413, 481–487.CrossRefGoogle Scholar
  68. Pietras, J. T., Carroll, A. R., Singer, B. S., and Smith, M. E. (2003) 10 Kyr depositional cyclicity in the Early Eocene: Stratigraphic and Ar-40/Ar-39 evidence from the lacustrine Green River formation. Geology, 31, 593–596.CrossRefGoogle Scholar
  69. Salomans, J. B. (1986) Paleoecology of volcanic soils in the Colombian Central Cordillera (Parque Nacional de los Nevados). Dissertationes Botanicae, 95, 1–212.Google Scholar
  70. Schroeter, C. (1908) Das Pflanzenleben der Alpen: Eine Schilderung der Hochgebirgsflora. Verlag von Albert Raustein, Zurich, Switzerland.Google Scholar
  71. Shindell, D. T., Rind, D., and Lonergan, P. (1998a) Increased polar stratospheric ozone losses and delayed eventual recovery owing to increasing greenhouse-gas concentrations. Nature, 392, 589–592.CrossRefGoogle Scholar
  72. Shindell, D. T., Rind, D., and Lonergan, P. (1998b) Climate change and the middle atmosphere, Part IV: Ozone response to doubled CO2. J. Climate, 11, 895–918.CrossRefGoogle Scholar
  73. Sleumer, H. (1966) An Account of Rhododendron in Malesia. Noordhoff, Groningen, The Netherlands.Google Scholar
  74. Smith, P. M. and Warr, K. (Eds.) (1991) Global Environmental Issues. Hodder & Stoughton, with the Open University, London (295 pp.).Google Scholar
  75. Son, K. C., Kim, H., and Park, Y. S. (2002) Effects of DIF and temperature drop on the growth and flowering of egonia_hiemalis. J. Korean Society for Horticultural Science, 43, 492–496.Google Scholar
  76. Stolarski, R., Bojkov, R., Bishop, L., Zerefos, C., Staehelin, J., and Zawodry, J. (1992) Measured trends in atmospheric ozone. Science, 256, 342–349.CrossRefGoogle Scholar
  77. Storfer, A. (2003) Amphibian declines: Future directions. Diversity and Distributions, 9, 151–163.CrossRefGoogle Scholar
  78. Stuart, S. N., Chanson, J. S., Cox, N. A., Young, B. E., Rodrigues, A. S. L., Fischman, D. L., and Waller, R. W. (2004) Status and trends of amphibian declines and extinctions worldwide. Science, 306, 1783–1786.CrossRefGoogle Scholar
  79. Sullivan, J. H., Teramura, A. H., and Ziska, L. H. (1992) Variation in UV-B sensitivity in plants from a 3,000-m elevational gradient in Hawaii. Amer. J. Botany, 79, 737–743.Google Scholar
  80. Teramura, H. (1983) Effects of ultraviolet-B radiation on the growth and yield of crop plants. Physiol. Plant, 58, 415–427.CrossRefGoogle Scholar
  81. Troll, C. (1959) Die tropischen Gebirge: Ihre dreidimensionale klimatische und pflanzengeogra ¨phische Zonierung. Dummlers, Bonn, Germany (93 pp.) [in German].Google Scholar
  82. van der Hammen, T. (1974) The Pleistocene changes of vegetation and climate in tropical South America. J. Biogeography, 1, 3–26.CrossRefGoogle Scholar
  83. van der Staaij, J. W. M., Bolink, E., Rozema, J., and Ernst, W. H. O. (1997) The impact of elevated UV-B (280–320 nm) radiation on the reproduction biology of a highland and a lowland population of Silene vulgaris. Plant Ecology, 128, 172–179.Google Scholar
  84. van Steenis, C. G. G. J. (1934–1936) On the origin of the Malaysian mountain flora. Bulletin du Jardin Botanique Buitenzorg Series III, Part I, 13: 135–262; Part II, 13: 289–417, Part III, 14, 56–72.Google Scholar
  85. van Steenis, C. G. G. J. (1972) The Mountain Flora of Java. E. J. Brill, Leiden, The Netherlands. Visscher, H., Looy, C. V., Collinson, M. E., Brinkhuis, H., Cittert, J. H. A. V. K. V., KurschnerGoogle Scholar
  86. W. M., and Sephton, M. A. (2004) Environmental mutagenesis during the end-Permian ecological crisis. Proceedings of the National Academy of Sciences U.S.A, 101, 12952–12956.Google Scholar
  87. Walker, D. and Flenley, J. R. (1979) Late Quaternary vegetational history of the Enga District of upland Papua New Guinea. Philosophical Trans. Royal Society London B, 286, 265–344.CrossRefGoogle Scholar
  88. Wang, Y. J., Pan, J. T., Liu, S. V., and Liu, J. Q. (2005) A new species of Saussurea (Asteraceae) from Tibet and its systematic position based on ITS sequence analysis. Botanical J. Linnean Society, 147, 349–356.CrossRefGoogle Scholar
  89. Wilf, P., Cuneo, N. R., Johnson, K. R., Hicks, J. F., Wing, S. L., and Obradovich, J. D. (2003) High plant diversity in Eocene South America: Evidence from Patagonia. Science, 300, 122–125.CrossRefGoogle Scholar
  90. Willis, K. J. and Niklas, K. J. (2004) The role of Quaternary environmental change in plant macroevolution: The exception or the rule? Philosophical Trans. Royal Society London B, 359, 159–172.CrossRefGoogle Scholar
  91. Willis, K. J., Bennett, K. D., and Birks, H. J. B. (2009) Variability in thermal and UV-B energy fluxes through time and their influence on plant diversity and speciation. J. Biogeography, 36, 1630–1644.CrossRefGoogle Scholar
  92. Zachos, J., Pagani, M., Sloan, L., Thomas, E., and Billups, K. (2001) Trends, rhythms and aberrations in global climate 65Ma to present. Science, 292, 686–693.CrossRefGoogle Scholar

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Authors and Affiliations

  1. 1.Geography Programme, School of People, Environment and PlanningMassey UniversityPalmerston NorthNew Zealand

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