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Influence of Atmospheric and Climate Change on Tree Defence Chemicals

  • Jason Q. D. GoodgerEmail author
  • Ian E. Woodrow
Chapter
Part of the Plant Ecophysiology book series (KLEC, volume 9)

Abstract

Environmental factors associated with atmospheric and climate change can potentially modify the structure and function of the world’s forests. An important indirect effect of environmental variables such as elevated carbon dioxide (CO2), air temperature, ozone (O3), UV radiation, and water-related stress on forests results from the response of tree secondary metabolism. In particular, the concentrations of defence chemicals displayed by trees can change in response to certain climate change factors, and this may influence interactions with herbivores and pathogens, and the broader forest community. An evaluation of the literature relating to climate change effects on tree defence chemicals shows variable results in both direction and magnitude of concentration changes and a dearth of studies on chemicals other than carbon-based phenolics and terpenes. Nevertheless, some generalities are evident. Elevated CO2, O3, and UV-B tend to increase tree phenolics, while mono- and sesquiterpenes remain unchanged. Elevated temperature increases volatile terpene emissions and often foliar terpene concentrations, whereas phenolics are largely unaffected. Water stress tends to increase phenolic concentrations and mild stress can also increase terpene emissions, but the effect of excess water availability remains largely unknown. A greater understanding of the implications of global climate change factors on the defence chemistry of the world’s forest trees would benefit from increasing the classes of defence chemicals examined, expanding the diversity of tree species and biomes studied, and incorporating long-term, multi-factor experiments. Clearly much more work is required to fully understand how the complexity of factors involved in global climate change influence defence chemistry in the world’s forest trees, and how this in turn will influence future tree growth and fitness and forest ecosystem functioning.

Keywords

Condensed Tannin Phenolic Concentration Silver Birch Cyanogenic Glycoside Isoprene Emission 
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.

Notes

Acknowledgments

This work was supported by an Australian Research Council Discovery grant to JQDG & IEW (DP1094530).

References

  1. Asthana A, McCloud ES, Berenbaum MR, Tuveson RW (1993) Phototoxicity of Cirrus jambhiri to fungi under enhanced UVB radiation: role of furanocoumarins. J Chem Ecol 19:2813–2830PubMedCrossRefGoogle Scholar
  2. Ayres MP (1993) Plant defense, herbivory, and climate change. In: Kareiva PM, Kingsolver JG, Huey RB (eds) Biotic interactions and global change. Sinauer Associates, SunderlandGoogle Scholar
  3. Ballaré CL, Caldwell MM, Flint SD, Robinson SA, Bornman JF (2011) Effects of solar ultraviolet radiation on terrestrial ecosystems. Patterns, mechanisms, and interactions with climate change. Photochem Photobiol Sci 10:226–241PubMedCrossRefGoogle Scholar
  4. Betz GA, Gerstner E, Stich S, Winkler B, Welzl G, Kremmer E, Langebartels C, Heller W, Sandermann H, Ernst D (2009a) Ozone affects shikimate pathway genes and secondary metabolites in saplings of European beech (Fagus sylvatica L.) grown under greenhouse conditions. Trees 23:539–553CrossRefGoogle Scholar
  5. Betz GA, Knappe C, Lapierre C, Olbrich M, Welzl G, Langebartels C, Heller W, Sandermann H, Ernst D (2009b) Ozone affects shikimate pathway transcripts and monomeric lignin composition in European beech (Fagus sylvatica L.). Eur J For Res 128:109–116CrossRefGoogle Scholar
  6. Bidard-Bouzat MG, Imeh-Nathaniel A (2008) Global change effects on plant chemical defenses against insect herbivores. J Integr Plant Biol 50:1339–1354CrossRefGoogle Scholar
  7. Bryant JP, Chapin FSI, Klein DR (1983) Carbon/nutrient balance of boreal plants in relation to vertebrate herbivory. Oikos 40:357–368CrossRefGoogle Scholar
  8. Caldwell MM, Bornman JF, Ballaré CL, Flint SD, Kulandaivelu G (2007) Terrestrial ecosystems, increased solar ultraviolet radiation, and interactions with other climate change factors. Photochem Photobiol Sci 6:252–266PubMedCrossRefGoogle Scholar
  9. Cole CT, Anderson JE, Lindroth RL, Waller DM (2010) Rising concentrations of atmospheric CO2 have increased growth in natural stands of quaking aspen (Populus tremuloides). Glob Chang Biol 16:2186–2197CrossRefGoogle Scholar
  10. Cseke LJ, Tsai CJ, Rogers A, Nelsen MP, White HL, Karnosky DF, Podila GK (2009) Transcriptomic comparison in the leaves of two aspen genotypes having similar carbon assimilation rates but different partitioning patterns under elevated [CO2]. New Phytol 182:891–911PubMedCrossRefGoogle Scholar
  11. Day TA, Ruhland CT, Grobe CW, Xiong F (1999) Growth and reproduction of Antarctic vascular plants in response to warming and UV radiation reductions in the field. Oecologia 119:24–35CrossRefGoogle Scholar
  12. Dury SJ, Good JEG, Perrins CM, Buse A, Kaye T (1998) The effects of increasing CO2 and temperature on oak leaf palatability and the implications for herbivorous insects. Glob Chang Biol 4:55–61CrossRefGoogle Scholar
  13. FAO (2006) Global forest resources assessment 2005. Progress towards sustainable forest management. FAO, RomeGoogle Scholar
  14. Filella I, Penuelas J (1999) Altitudinal differences in UV absorbance, UV reflectance and related morphological traits of Quercus ilex and Rhododendron ferrugineum in the Mediterranean region. Plant Ecol 145:157–165CrossRefGoogle Scholar
  15. Fritz C, Palacios-Rojas N, Feil R, Stitt M (2006) Regulation of secondary metabolism by the carbon-nitrogen status in tobacco: nitrate inhibits large sectors of phenylpropanoid metabolism. Plant J 46:533–548PubMedCrossRefGoogle Scholar
  16. Fuentes JD, Wang D, Gu L (1999) Seasonal variations in isoprene emissions from a boreal aspen forest. J Appl Meteorol 38:855–869CrossRefGoogle Scholar
  17. Ghirardo A, Koch K, Taipale R, Zimmer I, Schnitzler J-P, Rinne J (2010) Determination of de novo and pool emissions of terpenes from four common boreal/alpine trees by 13CO2 labelling and PTR-MS analysis. Plant Cell Environ 33:781–792PubMedGoogle Scholar
  18. Gleadow RM, Woodrow IE (2002) Defense chemistry of cyanogenic Eucalyptus cladocalyx seedlings is affected by water supply. Tree Physiol 22:939–945PubMedCrossRefGoogle Scholar
  19. Gleadow RM, Foley WJ, Woodrow IE (1998) Enhanced CO2 alters the relationship between photosynthesis and defence in cyanogenic Eucalyptus cladocalyx F. Muell. Plant Cell Environ 21:12–22CrossRefGoogle Scholar
  20. Grote R, Niinemets Ü (2008) Modeling volatile isoprenoid emissions – a story with split ends. Plant Biol 10:8–28PubMedCrossRefGoogle Scholar
  21. Guenther AB, Zimmermann PR, Harley PC, Monson RK, Fall R (1993) Isoprene and monoterpene emission rate variability: model evaluations and sensitivity analyses. J Geophys Res 98:12609–12617CrossRefGoogle Scholar
  22. Gutbrodt B, Dorn S, Mody K (2012) Drought stress affects constitutive but not induced herbivore resistance in apple plants. Arthropod-Plant Interact 6:171–179CrossRefGoogle Scholar
  23. Hale BK, Herms DA, Hansen RC, Clausen TP, Arnold D (2005) Effects of drought stress and nutrient availability on dry matter allocation, phenolic glycosides, and rapid induced resistance to two lymantriid defoliators. J Chem Ecol 31:2601–2620PubMedCrossRefGoogle Scholar
  24. Helmig D, Ortega J, Guenther A, Herrick J, Geron C (2006) Sesquiterpene emissions from loblolly pine and their potential contribution to biogenic aerosol formation in the southeastern US. Atmos Environ 40:4150–4157CrossRefGoogle Scholar
  25. Herms DA, Mattson WJ (1992) The dilemma of plants: to grow or defend. Q Rev Biol 67:283–335CrossRefGoogle Scholar
  26. Himanen SJ, Nissinen A, Auriola S, Poppy GM, Stewart CN, Holopainen JK, Nerg A (2008) Constitutive and herbivore-inducible glucosinolate concentrations in oilseed rape (Brassica napus) leaves are not affected by Bt Cry1Ac insertion but change under elevated atmospheric CO2 and O3. Planta 227:427–437PubMedCrossRefGoogle Scholar
  27. Holopainen JK, Kainulainen P (2004) Reproductive capacity of the grey pine aphid and allocation response of Scots pine seedlings across temperature gradients: a test of hypotheses predicting outcomes of global warming. Can J For Res 34:94–102CrossRefGoogle Scholar
  28. Horner JD (1990) Non-linear effects of water deficits on foliar tannin concentration. Biochem Syst Ecol 18:211–213CrossRefGoogle Scholar
  29. Jenkins GI (2009) Signal transduction in responses to UV-B radiation. Annu Rev Plant Biol 60:407–431PubMedCrossRefGoogle Scholar
  30. Kangasjärvi J, Jaspers P, Kollist H (2005) Signalling and cell death in ozone-exposed plants. Plant Cell Environ 28:1021–1036CrossRefGoogle Scholar
  31. Karnosky DF, Pregitzer KS, Zak DR, Kubiske ME, Hendrey GR, Weinstein D, Nosal M, Percy KE (2005) Scaling ozone responses of forest trees to the ecosystem level in a changing climate. Plant Cell Environ 28:965–981CrossRefGoogle Scholar
  32. Kesselmeier J, Saudt M (1999) Biogenic volatile organic compounds (VOC): an overview on emission, physiology, and ecology. J Atmos Chem 33:23–88CrossRefGoogle Scholar
  33. Kharin VV, Zwiers FW, Zhang X, Hegerl GC (2007) Changes in temperature and precipitation extremes in the IPCC ensemble of global coupled model simulations. J Climate 20:1419–1444CrossRefGoogle Scholar
  34. Koricheva J, Larsson S, Haukioja E, Keinanen M (1998) Regulation of woody plant secondary metabolism by resource availability: hypothesis testing by means of meta-analysis. Oikos 83:212–226CrossRefGoogle Scholar
  35. Körner C, Asshoff R, Bignucolo O, Hattenschwiller S, Keel SG, Pelaez-Riedl S, Pepin S, Siegwolf RTW, Zotz G (2005) Carbon flux and growth in mature deciduous forest trees exposed to elevated CO2. Science 309:1360–1362PubMedCrossRefGoogle Scholar
  36. Kreuzwieser J, Gessler A (2010) Global climate change and tree nutrition: influence of water availability. Tree Physiol 30:1221–1234PubMedCrossRefGoogle Scholar
  37. Kuokkanen K, Julkunen-Tiitto R, Keinanen M, Niemela P, Tahvanainen J (2001) The effect of elevated CO2 and temperature on the secondary chemistry of Betula pendula seedlings. Trees 15:378–384CrossRefGoogle Scholar
  38. Laothawornkitkul J, Paul ND, Vickers CE, Possell M, Taylor JE, Mullineaux PM, Hewitt CN (2008) Isoprene emissions influence herbivore feeding decisions. Plant Cell Environ 31:1410–1415PubMedCrossRefGoogle Scholar
  39. Lavola A, Julkunen-Tiitto R, Aphalo P, de la Rosa T, Lehto T (1997) The effect of U.V.-B radiation on U.V.-absorbing secondary metabolites in birch seedlings grown under simulated forest soil conditions. New Phytol 137:617–621CrossRefGoogle Scholar
  40. Leakey ADB, Ainsworth EA, Bernacchi CJ, Rogers A, Long SP, Ort DR (2009) Elevated CO2 effects on plant carbon, nitrogen, and water relations: six important lessons from FACE. J Exp Bot 60:2859–2876PubMedCrossRefGoogle Scholar
  41. Li FR, Peng SL, Chen BM, Hou YP (2010) A meta-analysis of the responses of woody and herbaceous plants to elevated ultraviolet-B radiation. Acta Oecol 36:1–9CrossRefGoogle Scholar
  42. Lindroth RL (2010) Impacts of elevated atmospheric CO2 and O3 on forests: phytochemistry, trophic interactions, and ecosystem dynamics. J Chem Ecol 36:2–21PubMedCrossRefGoogle Scholar
  43. Loreto F, Ciccioli P, Cecinato A, Brancaleoni E, Frattoni M, Tricoli D (1996) Influence of environmental factors and air composition on the emission of a-pinene from Quercus ilex leaves. Plant Physiol 110:267–275PubMedCentralPubMedGoogle Scholar
  44. Lower SS, Kirshenbaum S, Orians CM (2003) Preference and performance of a willow-feeding leaf beetle: soil nutrient and flooding effects on host quality. Oecologia 136:402–411PubMedCrossRefGoogle Scholar
  45. Lukac M, Calfapietra C, Lagomarsino A, Loreto F (2010) Global climate change and tree nutrition: effects of elevated CO2 and temperature. Tree Physiol 30:1209–1220PubMedCrossRefGoogle Scholar
  46. McKenzie RL, Aucamp PJ, Bais AF, Bjorn LO, Ilyas M, Madronich S (2011) Ozone depletion and climate change: impacts on UV radiation. Photochem Photobiol Sci 10:182–198PubMedCrossRefGoogle Scholar
  47. Min S-K, Zhang X, Zwiers FW, Hegerl GC (2011) Human contribution to more-intense precipitation extremes. Nature 470:378–381PubMedCrossRefGoogle Scholar
  48. Mott KA (2009) Stomatal responses to light and CO2 depend on the mesophyll. Plant Cell Environ 32:1479–1486PubMedCrossRefGoogle Scholar
  49. Neilson EH, Goodger JQD, Woodrow IE, Møller BL (2013) Plant chemical defense: at what cost? Trends Plant Sci 18:251–258Google Scholar
  50. Novick KA, Katul GG, McCarthy HR, Oren R (2012) Increased resin flow in mature pine trees growing under elevated CO2 and moderate soil fertility. Tree Physiol 32:752–763PubMedCrossRefGoogle Scholar
  51. O’Gorman PA, Schneider T (2009) The physical basis for increases in precipitation extremes in simulations of 21st-century climate change. Proc Natl Acad Sci U S A 106:14773–14777PubMedCentralPubMedCrossRefGoogle Scholar
  52. Paajanen R, Julkunen-Tiitto R, Nybakken L, Petrelius M, Tegelberg R, Pusenius J, Rousi M, Kellomaki S (2011) Dark-leaved willow (Salix myrsinifolia) is resistant to three-factor (elevated CO2, temperature and UV-B-radiation) climate change. New Phytol 190:161–168PubMedCrossRefGoogle Scholar
  53. Pall P, Allen MR, Stone DA (2007) Testing the Clausius-Clapeyron constraint on changes in extreme precipitation under CO2 warming. Climate Dynam 28:351–363CrossRefGoogle Scholar
  54. Pall P, Aina T, Stone DA, Stott PA, Nozawa T, Hilberts AGJ, Lohmann D, Allen MR (2011) Anthropogenic greenhouse gas contribution to flood risk in England and Wales in autumn 2000. Nature 470:382–386PubMedCrossRefGoogle Scholar
  55. Pegoraro E, Rey A, Barron-Gafford G, Monson RK, Malhi Y, Murthy R (2005) The interacting effects of elevated atmospheric CO2 concentration, drought and leaf-to-air vapour pressure deficit on ecosystem isoprene fluxes. Oecologia 146:120–129PubMedCrossRefGoogle Scholar
  56. Peltonen PA, Vapaavuori E, Julkunen-Tiitto R (2005) Accumulation of phenolic compounds in birch leaves is changed by elevated carbon dioxide and ozone. Glob Chang Biol 11:1305–1324CrossRefGoogle Scholar
  57. Raisanen T, Ryyppo A, Julkunen-Tiitto R, Kellomaki S (2008) Effects of elevated CO2 and temperature on secondary compounds in the needles of Scots pine (Pinus sylvestris L.). Trees 22:121–135CrossRefGoogle Scholar
  58. Rennenberg H, Loreto F, Polle A, Brilli F, Fares S, Beniwal RS, Gessler A (2006) Physiological responses of forest trees to heat and drought. Plant Biol 8:556–571PubMedCrossRefGoogle Scholar
  59. Rosenstiel TN, Potosnak MJ, Griffin KL, Fall R, Monson RK (2003) Increased CO2 uncouples growth from isoprene emission in an agriforest ecosystem. Nature 421:256–259PubMedCrossRefGoogle Scholar
  60. Roth S, McDonald EP, Lindroth RL (1997) Atmospheric CO2 and soil water availability: consequences for tree insect interactions. Can J For Res 27:1281–1290CrossRefGoogle Scholar
  61. Sallas L, Luomala EM, Utriainen J, Kainulainen P, Holopainen JK (2003) Contrasting effects of elevated carbon dioxide concentration and temperature on rubisco activity, chlorophyll fluorescence, needle ultrastructure and secondary metabolites in conifer seedlings. Tree Physiol 23:97–108PubMedCrossRefGoogle Scholar
  62. Schrope M (2000) Successes in fight to save ozone layer could close holes by 2050. Nature 408:627PubMedCrossRefGoogle Scholar
  63. Searles PS, Flint SD, Caldwell MM (2001) A meta-analysis of plant field studies simulating stratospheric ozone depletion. Oecologia 127:1–10CrossRefGoogle Scholar
  64. Sharkey TD, Singsaas EL, Vanderveer PJ, Geron C (1996) Field measurements of isoprene emission from trees in response to temperature and light. Tree Physiol 16:649–654PubMedCrossRefGoogle Scholar
  65. Sipura M, Ikonen A, Tahvanainen J, Roininen H (2002) Why does the leaf beetle Galerucella lineola F. attack wetland willow? Ecology 83:3393–3407CrossRefGoogle Scholar
  66. Solomon S, Qin D, Manning M et al (eds) (2007) Climate change 2007: the physical science basis contribution of working group I to the fourth assessment report of the Intergovernmental Panel on Climate Change. Cambridge University Press, CambridgeGoogle Scholar
  67. Stiling P, Cornellisen T (2007) How does elevated carbon dioxide (CO2) affect plant-herbivore interactions? A field experiment and meta-analysis of CO2-mediated changes on plant chemistry and herbivore performance. Glob Chang Biol 13:1823–1842CrossRefGoogle Scholar
  68. Sun Y, Solomon S, Dai A, Portmann RW (2007) How often will it rain? J Climate 20:4801–4818CrossRefGoogle Scholar
  69. Tegelberg R, Aphalo PJ, Julkunen-Tiitto R (2002) Effects of long-term, elevated ultraviolet-B radiation on phytochemicals in the bark of silver birch (Betula pendula). Tree Physiol 22:1257–1263PubMedCrossRefGoogle Scholar
  70. Tingey DT, Manning M, Grothaus LC, Burns WF (1980) Influence of light and temperature on monoterpene emission rates from slash pine. Plant Physiol 65:797–801PubMedCentralPubMedCrossRefGoogle Scholar
  71. Trenberth KE, Dai A, Rasmussen RM, Parsons DB (2003) The changing character of precipitation. Bull Am Meteorol Soc 84:1205–1217CrossRefGoogle Scholar
  72. Valkama E, Koricheva J, Oksanen E (2007) Effects of elevated O3, alone and in combination with elevated CO2, on tree leaf chemistry and insect herbivore performance: a meta-analysis. Glob Chang Biol 13:184–201CrossRefGoogle Scholar
  73. Veteli TO, Kuokkanen K, Julkunen-Tiitto R, Roininen H, Tahvanainen J (2002) Effects of elevated CO2 and temperature on plant growth and herbivore defensive chemistry. Glob Chang Biol 8:1240–1252CrossRefGoogle Scholar
  74. Veteli TO, Mattson WJ, Niemela P, Julkunen-Tiitto R, Kellomaki S, Kuokkanen K, Lavola A (2007) Do elevated temperature and CO2 generally have counteracting effects on phenolic phytochemistry of boreal trees? J Chem Ecol 33:287–296PubMedCrossRefGoogle Scholar
  75. Vingarzan R (2004) A review of surface ozone background levels and trends. Atmos Environ 38:3431–3442CrossRefGoogle Scholar
  76. Williams RS, Lincoln DE, Norby RJ (2003) Development of gypsy moth larvae feeding on red maple saplings at elevated CO2 and temperature. Oecologia 137:114–122PubMedCrossRefGoogle Scholar
  77. Wittig VE, Ainsworth EA, Naidu SL, Karnosky DF, Long SP (2009) Quantifying the impact of current and future tropospheric ozone on tree biomass, growth, physiology and biochemistry: a quantitative meta-analysis. Glob Chang Biol 15:396–424CrossRefGoogle Scholar
  78. Woodrow IE, Berry JA (1988) Enzymatic regulation of photosynthetic CO2 fixation in C3 Plants. Annu Rev Plant Physiol Plant Mol Biol 39:533–594CrossRefGoogle Scholar
  79. Woodrow IE, Slocum DJ, Gleadow RM (2002) Influence of water stress on cyanogenic capacity in Eucalyptus cladocalyx. Funct Plant Biol 29:103–110CrossRefGoogle Scholar
  80. Zhao D, Reddy KR, Kakani VG, Read JJ, Sullivan JH (2003) Growth and physiological responses of cotton (Gossypium hirsutum L) to elevated carbon dioxide and ultraviolet-B radiation under controlled environmental conditions. Plant Cell Environ 26:771–782CrossRefGoogle Scholar
  81. Zvereva EL, Kozlov MV (2006) Consequences of simultaneous elevation of carbon dioxide and temperature for plant-herbivore interactions: a metaanalysis. Glob Chang Biol 12:27–41CrossRefGoogle Scholar

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© Springer Science+Business Media Dordrecht 2014

Authors and Affiliations

  1. 1.School of BotanyThe University of MelbourneParkvilleAustralia

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