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Contrasting mechanisms of secondary metabolite accumulation during leaf development in two tropical tree species with different leaf expansion strategies

  • Plant Animal Interactions
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Abstract

Young leaves of most species experience remarkably higher herbivore attack rates than mature leaves. Considerable theoretical effort has focused on predicting optimal defense and tradeoffs in defense allocation during leaf expansion. Among others, allocation to secondary chemistry may be dependent on growth constraints. We studied flavanoid production during leaf development in two species of Inga (Fabaceae: Mimosoideae) with different expansion strategies: Inga goldmanii, a species with slowly expanding young leaves, and Inga umbellifera, a species with fast-expanding young leaves. In these two species, the most abundant and toxic class of defensive compounds is flavanoids (which include tannins). We measured their concentration by leaf dry weight, their total content per leaf, their HPLC chemical profile and their toxicity to a generalist herbivore at different expansion levels. Although in both species the flavanoid concentration decreased with increasing leaf expansion, that decrease was twice as pronounced for I. umbellifera as it was for I. goldmanii. I. umbellifera leaves produced flavanoids only during the first half of their development while I. goldmanii leaves continued production throughout. The changes in flavanoid HPLC profiles and toxicity were also more dramatic for I. umbellifera, which had different flavanoids in young than in mature leaves. Relative to I. umbellifera, I. goldmanii showed smaller changes in both flavanoid composition and toxicity in the transition from young to mature leaves. These results indicate that, even though young leaves suffer higher rates of attack and are predicted to have better chemical defenses than mature leaves, growth constraints may modulate defense allocation and thus, evolution of defense strategies.

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References

  • Ayres MP, Clausen TP, MacLean SF Jr, Redman AM, Reichardt PB (1997) Diversity of structure and antiherbivore activity in condensed tannins. Ecology 78:1696–1712

    Article  Google Scholar 

  • Baldwin IT, Karb MJ (1995) Plasticity in allocation of nicotine to reproductive parts in Nicotiana attenuata. J Chem Ecol 21:897–909

    Article  CAS  Google Scholar 

  • Brooks JS, Feeny PP (2004) Seasonal variation in Daucus carota leaf-surface and leaf-tissue chemical profiles. Biochem Syst Ecol 32:769–782

    Article  CAS  Google Scholar 

  • Coley PD (1983) Herbivory and defensive characteristics of tree species in a lowland tropical forest. Ecol Monogr 53:209–233

    Article  Google Scholar 

  • Coley PD (1988) Effects of plant growth rate and leaf lifetime on the amount and type of anti-herbivore defense. Oecologia 74:531–536

    Article  Google Scholar 

  • Coley PD, Aide MT (1991) Comparison of herbivory and plant defenses in temperate and tropical broad-leaved forests. In: Price PW, Lewinson TM, Fernandes GW, Benson WW (eds) Plant–animal interactions: evolutionary ecology and temperate regions. Wiley, New York, pp 25–49

    Google Scholar 

  • Coley PD, Kursar TA (1996) Anti-herbivore defenses of young tropical leaves: physiological constrains and ecological tradeoffs. In: Mulkey SS, Chazdon RL (eds) Tropical forest plant ecophysiology. Chapman & Hall, New York, pp 305–336

    Google Scholar 

  • Coley PD, Lokvam J, Rudolph K, Bromberg K, Wright L, Brenes-Arguedas T, Dvorett D, Ring S, Ponge A, Baptiste C, Pennington TR, Kursar TA (2005) Divergent defensive strategies of young leaves in two Neotropical species of Inga. Ecology 86:2633–2643

    Article  Google Scholar 

  • Cornelissen TG, Fernandes GW (2001) Defence, growth and nutrient allocation in the tropical shrub Bauhinia brevipes (Leguminosae). Aust Ecol 26:246–253

    Article  Google Scholar 

  • Crankshaw DR, Langenheim JH (1981) Variation in terpenes and phenolics through leaf development in Hymenaea and its possible significance to herbivory. Biochem Syst Ecol 9:115–124

    Article  CAS  Google Scholar 

  • Croat TB (1978) Flora of Barro Colorado Island. Stanford University Press, Stanford

    Google Scholar 

  • Feeny PP (1970) Seasonal changes in oak leaf tannins and nutrients as a cause of spring feeding by winter moth caterpillars. Ecology 51:565–581

    Article  Google Scholar 

  • Forkner RE, Marquis RJ, Lill JT (2004) Feeny revisited: condensed tannins as anti-herbivore defences in leaf-chewing herbivore communities of Quercus. Ecol Entomol 29:174–187

    Article  Google Scholar 

  • Haukioja E (2003) Putting the insect into the birch–insect interaction. Oecologia 136:161–168

    Article  PubMed  Google Scholar 

  • Herms DA, Mattson WJ (1992) The dilemma of plants: to grow or defend. Q Rev Biol 67:283–335

    Article  Google Scholar 

  • Jones CG, Hartley SE (1999) A protein competition model of phenolic allocation. Oikos 86:27–44

    Article  CAS  Google Scholar 

  • Kleiner KW, Ellis DD, McCown BH, Raffa KF (2003) Leaf ontogeny influences leaf phenolics and the efficacy of genetically expressed Bacillus thuringiensis cry1A(a) δ-endotoxin in hybrid poplar against gypsy moth. J Chem Ecol 29:2585–2602

    Article  PubMed  CAS  Google Scholar 

  • Koptur S (1984) Experimental evidence of defense of Inga (Mimosoidead) saplings by ants. Ecology 65:1787–1793

    Article  Google Scholar 

  • Koricheva J (1999) Interpreting phenotypic variation in plant allelochemistry: problems with the use of concentrations. Oecologia 119:467–473

    Article  Google Scholar 

  • Kursar TA, Coley PD (1991) Nitrogen content and expansion rate of young leaves of rain forest species implications for herbivory. Biotropica 23:141–150

    Article  Google Scholar 

  • Kursar TA, Coley PD (1992a) Delayed development of the photosynthetic apparatus in tropical rain forest species. Funct Ecol 6:411–422

    Article  Google Scholar 

  • Kursar TA, Coley PD (1992b) Delayed greening in tropical leaves an antiherbivore defense? Biotropica 24:256–262

    Article  Google Scholar 

  • Kursar TA, Coley PD (2003) Convergence in defense syndromes of young leaves in tropical rainforests. Biochem Syst Ecol 31:929–949

    Article  CAS  Google Scholar 

  • Laitinen ML, Julkunen-Tiitto R, Rousi M (2002) Foliar phenolic composition of European white birch during bud unfolding and leaf development. Physiol Plant 114:450–460

    Article  PubMed  CAS  Google Scholar 

  • Lambdon PW, Hassall M, Boar RR, Mithen R (2003) Asynchrony in the nitrogen and glucosinolate leaf-age profiles of Brassica: is this a defensive strategy against generalist herbivores? Agric Ecosyst Environ 97:205–214

    Article  CAS  Google Scholar 

  • Langenheim JH, Macedo CA, Ross MK, Stubblebine WH (1986) Leaf development in the tropical leguminous tree Copaifera in relation to microlepidopteran herbivory. Biochem Syst Ecol 14:51–59

    Article  Google Scholar 

  • Leigh EGJ, Rand AS, Windsor DM (1996) The ecology of a tropical forest: seasonal rhythms and long-term changes, 2nd edn. Smithsonian Institution Press, Washington, D.C.

    Google Scholar 

  • Lokvam J, Kursar TA (2005) Divergence in structure and function of phenolic defenses in young leaves of two co-occurring Inga species. J Chem Ecol

  • Lokvam J, Coley PD, Kursar TA (2004) Cinnamoyl glucosides of catechin and dimeric procyanidins from young leaves of Inga umbellifera (Fabaceae). Phytochemistry 65:351–358

    Google Scholar 

  • Lokvam J, Brenes-Arguedas T, Lee SJ, Coley PD, Kursar TA (2006) Allelochemic function for a primary metabolite: the case of L-tyrosine hyper-production in Inga umbellifera (Fabaceae). Am J Bot (in press)

  • Loomis WE (1932) Growth-differentiation balance versus carbohydrate ratio. Proc Am Soc Hortic Sci 29:240–245

    CAS  Google Scholar 

  • Nichols-Orians CM, Schultz JC (1990) Interactions among leaf toughness, chemistry, and harvesting by attine ants. Ecol Entomol 15:311–320

    Article  Google Scholar 

  • Numata S, Kachi N, Okuda T, Manokaran N (2004) Delayed greening, leaf expansion, and damage to sympatric Shorea species in a lowland rain forest. J Plant Res 117:19–25

    Article  PubMed  Google Scholar 

  • Orians GH, Janzen DH (1974) Why are embryos so tasty? Am Nat 108:581–592

    Article  Google Scholar 

  • Read J, Gras EK, Sanson GD, Clissold F, Brunt C (2003) Does chemical defence decline more in developing leaves that become strong and tough at maturity? Aust J Bot 51:489–496

    Article  CAS  Google Scholar 

  • Rhoades DF (1979) Evolution of plant chemical defense against herbivores. In: Rosenthal GA, Janzen DH (eds) Herbivores: their interaction with secondary plant metabolites, 1st edn. Academic Press, New York, pp 1–54

    Google Scholar 

  • Riipi M, Ossipov V, Lempa K, Haukioja E, Koricheva J, Ossipova S, Pihlaja K (2002) Seasonal changes in birch leaf chemistry: are there trade-offs between leaf growth, and accumulation of phenolics? Oecologia 130:380–390

    Article  Google Scholar 

  • Ruusila V, Morin JP, van Ooik T, Saloniemi I, Ossipov V, Haukioja E (2005) A short-lived herbivore on a long-lived host: tree resistance to herbivory depends on leaf age. Oikos 108:99–104

    Article  Google Scholar 

  • Salminen JP, Ossipov V, Haukioja E, Pihlaja K (2001) Seasonal variation in the content of hydrolysable tannins in leaves of Betula pubescens. Phytochemistry 57:15–22

    Article  PubMed  CAS  Google Scholar 

  • Salminen JP, Roslin T, Karonen M, Sinkkonen J, Pihlaja K, Pulkkinen P (2004) Seasonal variation in the content of hydrolyzable tannins, flavonoid glycosides, and proanthocyanidins in oak leaves. J Chem Ecol 30:1693–1711

    Article  PubMed  CAS  Google Scholar 

  • Tikkanen OP, Julkunen-Tiitto R (2003) Phenological variation as protection against defoliating insects: the case of Quercus robur and Operophtera brumata. Oecologia 136:244–251

    Article  PubMed  Google Scholar 

  • Turner IM (1995) Foliar defences and habitat adversity of three woody plant communities in Singapore. Funct Ecol 9:279–284

    Article  Google Scholar 

  • Valkama E, Salminen JP, Koricheva J, Pihlaja K (2004) Changes in leaf trichomes and epicuticular flavonoids during leaf development in three birch taxa. Ann Bot 94:233–242

    Article  PubMed  CAS  Google Scholar 

  • Waterman PG, Mole S (1994) Analysis of phenolic plant metabolites. Blackwell, Oxford

    Google Scholar 

Download references

Acknowledgements

We acknowledge financial support from the NSF (DEB 0108150 and DEB 0234936 to P. D. Coley and T. A. Kursar). Also, the Autoridad Nacional del Ambiente of Panama and Oris Acevedo of the Smithsonian Tropical Research Institute for facilitating sample collections. We are grateful to Jenny Burns, Leslie Wright, David Victor and Tobin Biesele for help with the bioassays, to Kathleen Rudolph and Keryn Bromberg, for the sample collection and to Franz Goller, Fred Adler, Collin Nichols-Orians, and three anonymous reviewers for valuable comments on the manuscript. The sample collections and export for this analysis were done in compliance with the laws of the Republic of Panama.

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Correspondence to Tania Brenes-Arguedas.

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Communicated by Colin Orians

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Brenes-Arguedas, T., Horton, M.W., Coley, P.D. et al. Contrasting mechanisms of secondary metabolite accumulation during leaf development in two tropical tree species with different leaf expansion strategies. Oecologia 149, 91–100 (2006). https://doi.org/10.1007/s00442-006-0423-2

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  • DOI: https://doi.org/10.1007/s00442-006-0423-2

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