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Modelling the Defensive Potential of Plants

  • S. GaylerEmail author
  • E. Priesack
  • F. Fleischmann
  • W. Heller
  • T. Rötzer
  • T. Seifert
  • R. Matyssek
Chapter
Part of the Ecological Studies book series (ECOLSTUD, volume 220)

Abstract

Many products of the phenylpropanoid pathway play an important role in plant defence against different kinds of biotic and abiotic stress. The “growth–differentiation balance theory” is a conceptual framework to predict how environmental factors can influence the level of these compounds in plant tissues. In this chapter, we unveil fundamental difficulties in testing the explanatory capacity of this theory by experiments and present the potential of mechanistic modelling to support empirical evidence in this field. In different examples, the plant growth model PLATHO is used to analyse observed patterns of plant responses to experimental treatments through simulating allocation rates between different biochemical pools from plant internal source and sink strengths of carbon and nitrogen during different phenological growth stages. It is shown that divergent responses of plants to abiotic factors such as elevated CO2 are feasible with respect to allocation to carbon-based secondary compounds, depending on ecological conditions under which plants are growing.

Keywords

Stand Density Vegetation Period Allocation Rate Sink Strength Beech Tree 
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

Acknowledgements

We are grateful to the Deutsche Forschungsgemeinschaft which funded this study within the frame of Sonderforschungsbereich 607 Growth and Parasite Defence – Competition for Resources in Economic Plants from Forestry and Agronomy. We further gratefully thank Thorsten Grams for providing growth parameters of beech and spruce trees from different experimental studies and Axel Göttlein for providing data of nutrient concentrations in organs of juvenile beech trees.

References

  1. Bahnweg G, Heller W, Stich S, Knappe C, Betz G, Heerdt C, Kehr RD, Ernst D, Langebartels C, Nunn AJ, Rothenburger J, Schubert R, Wallis P, Müller-Starck G, Werner H, Matyssek R, Jr HS (2005) Beech leaf colonization by the endophyte Apiognomonia errabunda dramatically depends on light exposure and climatic conditions. Plant Biol 7:659–669PubMedCrossRefGoogle Scholar
  2. Basey JM, Jenkins SH (1993) Production of chemical defenses in relation to plant growth rate. Oikos 68:323–328CrossRefGoogle Scholar
  3. Blodgett JT, Herms DA, Bonello P (2005) Effects of fertilization on red pine defense chemistry and resistance to Sphaeropsis sapinea. Forest Ecol Manage 208(1–3):373–382CrossRefGoogle Scholar
  4. Bloom AJ, Burger M, Asensio JSR, Cousins AB (2010) Carbon dioxide enrichment inhibits nitrate assimilation in wheat and arabidopsis. Science 328:899–903PubMedCrossRefGoogle Scholar
  5. Bossel H (1996) TREEDYN3 forest simulation model. Ecol Model 90:187–227CrossRefGoogle Scholar
  6. Bryant JP, Chapin FS, Klein DR (1983) Carbon/nutrient balance of boreal plants in relation to vertebrate herbivory. Oikos 40:357–368CrossRefGoogle Scholar
  7. Cates RG (1996) The role of mixtures and variation in the production of terpenoids in conifer-insect-pathogen interactions. In: Romeo JT, Saunders JA, Barbosa P (eds) Recent advances in phytochemistry. Plenum, New York, pp 179–216Google Scholar
  8. Coley PD (1988) Effects of plant growth rate and leaf lifetime on the amount and type of anti-herbivore defense. Oecologia 74:531–536CrossRefGoogle Scholar
  9. Coley PD, Bryant JP, Chapin FS (1985) Resource availability and plant antiherbivore defense. Science 230:895–899PubMedCrossRefGoogle Scholar
  10. Dixon RA (2001) Natural products and plant disease resistance. Nature 411:843–847PubMedCrossRefGoogle Scholar
  11. Fleischmann F, Winkler JB, Oßwald W (2009) Effects of ozone and Phytophthora citricola on non-structural carbohydrates of European beech (Fagus sylvatica) saplings. Plant Soil 323:75–84CrossRefGoogle Scholar
  12. 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
  13. Gayler S, Leser C, Priesack E, Treutter D (2004) Modelling the effect of environmental factors on the “trade-off” between growth and defensive compounds in young apple trees. Trees 18:363–371CrossRefGoogle Scholar
  14. Gayler S, Grams TEE, Kozovits A, Luedemann G, Winkler B, Priesack E (2006) Analysis of competition effects in mono- and mixed cultures of juvenile beech and spruce by means of the plant growth simulation model platho. Plant Biol 8(4):503–514PubMedCrossRefGoogle Scholar
  15. Gayler S, Grams TEE, Heller W, Treutter D, Priesack E (2008) A dynamic model of environmental effects on allocation to carbon-based secondary compounds in juvenile trees. Ann Bot 101(8):1089–1098PubMedCrossRefPubMedCentralGoogle Scholar
  16. Gayler S, Klier C, Mueller CW, Weis W, Winkler JB, Priesack E (2009) Analysing the role of soil properties, initial biomass and ozone on observed plant growth variability in a lysimeter study. Plant Soil 323:125–141CrossRefGoogle Scholar
  17. Glynn C, Herms DA, Egawa M, Hansen R, Mattson WJ (2003) Effects of nutrient availability on biomass allocation as well as constitutive and rapid induced herbivore resistance in poplar. Oikos 101(2):385–397CrossRefGoogle Scholar
  18. Glynn C, Herms DA, Orians CM, Hansen RC, Larsson S (2007) Testing the growth–differentiation balance hypothesis: dynamic responses of willows to nutrient availability. New Phytol 176(3):623–634PubMedCrossRefGoogle Scholar
  19. Häberle K-H, Nunn AJ, Reiter IM, Werner H, Heller W, Bahnweg G, Gayler S, Lütz C, Matyssek R (2009) Variation of defence-related metabolites in the foliage of adult beech and spruce – a conceptual approach to approximating trade-off carbon. Eur J Forest Res 128:99–108CrossRefGoogle Scholar
  20. Hamilton JG, Zangerl AR, DeLucia EH, Berenbaum MR (2001) The carbon-nutrient balance hypothesis: its raise and fall. Ecol Lett 4:86–95CrossRefGoogle Scholar
  21. Harmer SL, Hogenesch JB, Straume M, Chang H-S, Han B, Zhu T, Wang X, Kreps JA, Kay SA (2000) Orchestrated transcription of key pathways in Arabidopsis by the circadian clock. Sci Cult 290:2110–2113Google Scholar
  22. Herms DA (2002) Effects of fertilization on insect resistance of woody ornamental plants: reassessing an entrenched paradigm. Environ Entomol 31(6):923–933CrossRefGoogle Scholar
  23. Herms DA, Mattson WJ (1992) The dilemma of plants: to grow or defend. Q R Biol 67(3):283–335CrossRefGoogle Scholar
  24. Jones CG, Hartley SE (1999) A protein competition model of phenolic allocation. Oikos 86:27–44CrossRefGoogle Scholar
  25. Jones CA, Kiniry JR (eds) (1986) CERES-Maize. A simulation model of maize growth and development. Texas A&M University Press, College Station, TXGoogle Scholar
  26. Koricheva J (2002) Meta-analysis of sources of variation in fitness costs of plant antiherbivore defenses. Ecology 83(1):176–190CrossRefGoogle Scholar
  27. Koricheva J, Larsson S, Haukioja E, Keinänen M (1998) Regulation of woody plant secondary metabolism by resource availability: hypothesis testing by means of meta-analysis. Oikos 83:212–226CrossRefGoogle Scholar
  28. Kozovits AR, Matyssek R, Blaschke H, Göttlein A, Grams TEE (2005a) Competition increasingly dominates the responsiveness of juvenile beech and spruce to elevated CO2 and O3 levels throughout two subsequent growing seasons. Glob Change Biol 11:1387–1401CrossRefGoogle Scholar
  29. Kozovits AR, Matyssek R, Winkler JB, Göttlein A, Blaschke H, Grams TEE (2005b) Above-ground space sequestration determines competitive success in juvenile beech and spruce trees. New Phytol 167:181–196PubMedCrossRefGoogle Scholar
  30. Le Bot J, Benard C, Robin C, Bourgaud F, Adamowicz S (2009) The ‘trade-off’ between synthesis of primary and secondary compounds in young tomato leaves is altered by nitrate nutrition: experimental evidence and model consistency. J Exp Bot 60(15):4301–4314. doi: 10.1093/jxb/erp271 PubMedCrossRefGoogle Scholar
  31. Leser C, Treutter D (2005) Effects of nitrogen supply on growth, contents of phenolic compounds and pathogen (scab) resistance of apple trees. Physiol Plant 123:49–56CrossRefGoogle Scholar
  32. Lindroth RL, Kinney KK, Platz CL (1993) Responses of deciduous trees to elevated atmospheric CO2: productivity, phytochemistry, and insect performance. Ecology 74(3):763–777CrossRefGoogle Scholar
  33. Loomis WE (1932) Growth differentiation balance vs. carbohydrate-nitrogen ratio. Proc Am Soc Hortic Sci 29:240–245Google Scholar
  34. Lötscher M, Gayler S (2005) Contribution of current photosynthates to root respiration of non-nodulated Medicago sativa: effects of light and nitrogen supply. Plant Biol 7(6):601–610PubMedCrossRefGoogle Scholar
  35. Luedemann G, Matyssek R, Fleischmann F, Grams TEE (2005) Acclimation to ozone affects, host/pathogen interaction, and competitiveness for nitrogen in juvenile Fagus sylvatica and Picea abies trees infested with Phytophthora citricola. Plant Biol 7:640–649PubMedCrossRefGoogle Scholar
  36. Mattson WJ, Julkunen-Tiitto R, Herms DA (2005) CO2 enrichment and carbon partitioning to phenolics: do plant responses accord better with the protein competition or the growth-differentiation balance model? Oikos 111:337–347CrossRefGoogle Scholar
  37. Matyssek R, Schnyder H, Elstner E-F, Munch J-C, Pretzsch H, Sandermann H (2002) Growth and parasite defence in plants: the balance between resource sequestration and retention. Plant Biol 4(2):133–136CrossRefGoogle Scholar
  38. Matyssek R, Agerer R, Ernst D, Munch JC, Osswald W, Pretzsch H, Priesack E, Schnyder H, Treutter D (2005) The plant’s capacity in regulating resource demand. Plant Biol 7:560–580PubMedCrossRefGoogle Scholar
  39. Mittelstraß K, Treutter D, Pleßl M, Heller W, Elstner EF, Heiser I (2006) Modification of primary and secondary metabolism of potato plants by nitrogen application differentially affects resistance to Phytophthora infestans and Alternaria solani. Plant Biol 8(5):653–661PubMedCrossRefGoogle Scholar
  40. Pizarro LC, Bisigato AJ (2010) Allocation of biomass and photoassimilates in juvenile plants of six Patagonian species in response to five water supply regimes. Ann Bot 106:297–307CrossRefGoogle Scholar
  41. Pretzsch H, Biber P (2010) Size-symmetric versus size-asymmetric competition and growth partitioning among trees in forest stands along an ecological gradient in central Europe. Can J Forest Res 40:370–385CrossRefGoogle Scholar
  42. Ros B, Thümmler F, Wenzel G (2004) Analysis of differentially expressed genes in a susceptible and moderately resistant potato cultivar upon Phytophthora infestans infection. Mol Plant Pathol 5:191–201PubMedCrossRefGoogle Scholar
  43. Rühmann S, Leser C, Bannert M, Treutter D (2002) Relationship between growth, secondary metabolism, and resistance of apple. Plant Biol 4(2):137–143CrossRefGoogle Scholar
  44. Schwinning S, Weiner J (1998) Mechanisms determining the degree of size asymmetry in competition among plants. Oecologia 113:447–455CrossRefGoogle Scholar
  45. Stamp N (2003a) Out of the quagmire of plant defense-hypotheses. Q R Biol 78:23–55CrossRefGoogle Scholar
  46. Stamp N (2003b) Theory of plant defensive level: example of process and pitfalls in development of ecological theory. Oikos 102(3):672–678CrossRefGoogle Scholar
  47. Stamp N (2004) Can the growth-differentiation hypothesis be tested rigorously. Oikos 107:439–448CrossRefGoogle Scholar
  48. Stefanelli D, Goodwin I, Jones R (2010) Minimal nitrogen and water use in horticulture: effects on quality and content of selected nutrients. Food Res Int. doi: 10.1016/j.foodres.2010.04.022
  49. van Ittersum MK, Leffelaar PA, van Keulen H, Kropff MJ, Bastiaans L, Goudriaan J (2003) On approaches and applications of the Wageningen crop models. Eur J Agron 18:201–234CrossRefGoogle Scholar
  50. Winkler JB, Lang H, Graf W, Reth S, Munch JC (2009) Experimental setup of field lysimeters for studying effects of elevated ozone and below-ground pathogen infection on a plant-soil-system of juvenile beech (Fagus sylvatica L.). Plant Soil 323:7–19CrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2012

Authors and Affiliations

  • S. Gayler
    • 1
    • 2
    Email author
  • E. Priesack
    • 1
  • F. Fleischmann
    • 3
  • W. Heller
    • 4
  • T. Rötzer
    • 5
  • T. Seifert
    • 6
  • R. Matyssek
    • 7
  1. 1.Institute of Soil EcologyHelmholtz Zentrum MünchenNeuherbergGermany
  2. 2.Water & Earth System Science (WESS) Competence Clusterc/o University of TübingenTübingenGermany
  3. 3.Pathology of Woody PlantsTechnische Universität MünchenFreisingGermany
  4. 4.Institute of Biochemical Plant PathologyHelmholtz Zentrum MünchenNeuherbergGermany
  5. 5.Chair for Forest Growth and Yield ScienceTechnische Universität MünchenFreisingGermany
  6. 6.Department of Forest and Wood ScienceStellenbosch UniversityStellenboschSouth Africa
  7. 7.Chair of Ecophysiology of PlantsTechnische Universität MünchenFreisingGermany

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