Trees

, Volume 22, Issue 3, pp 337–349 | Cite as

Linking multiple-level tree traits with biomass accumulation in native tree species used for reforestation in Panama

  • Sylvain Delagrange
  • Catherine Potvin
  • Christian Messier
  • Lluis Coll
Original Paper

Abstract

To improve establishment yield and carbon accumulation during reforestation, analyses of species adaptations to local environments are needed. Here we measured, at the individual scale, links between biomass accumulation and multiple-level tree traits: biomass partitioning, crown morphology and leaf physiology. The study was carried out on one- and three-year-old individuals of five tropical tree species assigned to pioneer (P) or non-pioneer (NP) functional groups. Among the species, Cedrela odorata, Luehea seemannii and Hura crepitans showed the greatest biomass accumulation. On our seasonally dry site, species performance during the first year was dependent on a greater investment in above-ground foraging, while performance after three years was mainly related to water relations. However, large biomass accumulations were not simply associated with an efficient water use but also with contrasting water uses, based on inter-specific relationships. Generally, greater carbon isotope discrimination (Δleaf) was related to greater allocation to roots. Species with high Δleaf generally showed high leaf potential nitrogen use efficiency (PNUE), suggesting that lower water use efficiency (WUE) increases the efficiency of photosynthetically active N. Also, PNUE was negatively correlated to leaf mass per area (LMA), implying that photosynthetically active N is diluted as total leaf mass increases. Finally, no distinction in measured traits, including biomass accumulation, was observed between the two functional groups.

Keywords

Biomass partitioning Crown morphology Functional groups Nitrogen use efficiency Water use efficiency 

References

  1. Ares A, Fownes JH (1999) Water supply regulates structure, productivity, and water use efficiency of Acacia koa in Hawaii. Oecologia 121:458–466CrossRefGoogle Scholar
  2. Bazzaz FA (1979) The physiological ecology of plant succession. Ann Rev Ecol Syst 10:351–371CrossRefGoogle Scholar
  3. Bonal D, Sabatier D, Montpied P, Tremeaux D, Guehl J-M (2000) Interspecific variability of δ13C among trees in rainforests of French Guiana: functional groups and canopy integration. Oecologia 124:454–468CrossRefGoogle Scholar
  4. Brienen RJW, Zuidema PA (2005) Relating tree growth to rainfall in Bolivian rain forests: a test for six species using tree ring analysis. Oecologia 146:1–12PubMedCrossRefGoogle Scholar
  5. Brodribb TJ, Holbrook NM, Guttiérez MV (2002) Hydraulic and photosynthetic co-ordination in seasonally dry tropical forest trees. Plant Cell Environ 25:1435–1444CrossRefGoogle Scholar
  6. Canham CD, Denslow JS, Platt WJ, Runkle JR, Spies T, White PS (1990) Light regimes beneath closed canopies and tree-fall gaps in temperate and tropical forests. Can J For Res 20:620–631CrossRefGoogle Scholar
  7. Carpenter FL, Nichols JD, Pratt RT, Young KC (2004a) Methods of facilitating reforestation of tropical degraded land with the native timber tree, Terminalia amazonia. For Ecol Manage 202:281–291CrossRefGoogle Scholar
  8. Carpenter FL, Nichols JD, Sandi E (2004b) Early growth of native and exotic trees planted on degraded tropical pasture. For Ecol Manage 196:367–378CrossRefGoogle Scholar
  9. Casper BB, Forseth IN, Wait DA (2005) Variation in carbon isotope discrimination in relation to plant performance in a natural population of Cryptantha flava. Oecologia 145:541–548PubMedCrossRefGoogle Scholar
  10. Casper BB, Jackson RB (1997) Plant competition underground. Ann Rev Ecol Syst 28:545–570CrossRefGoogle Scholar
  11. Chapin III FS, Zavaleta ES, Eviner VT, Naylor RL, Vitousek PM, Reynolds HL, Hooper DU, Lavorel S, Sala OE, Hobbie SE, Mack MC, Diaz S (2000) Consequences of changing biodiversity. Nature 405:234–242PubMedCrossRefGoogle Scholar
  12. Chave J, Riéra B, Dubois M-A (2001) Estimation of biomass in a neotropical forest of French Guiana: spatial and temporal variability. J Trop Ecol 17:79–96CrossRefGoogle Scholar
  13. Condit R, Hubbell SP, Foster RB (1995) Mortality rates of 205 Neotropical tree and shrub species and the impact of a severe drought. Ecol Monogr 65:419–539CrossRefGoogle Scholar
  14. Condit R, Hubbell SP, Foster RB (1996) Assessing the response of plant functional types to climatic change in tropical forest. J Veg Sci 7:405–416CrossRefGoogle Scholar
  15. Coomes DA, Grubb PJ (2000) Impacts of root competition in forests and woodlands: a theoretical framework and review of experiments. Ecol Monogr 70:171–207Google Scholar
  16. Cornelissen JHC, Lavorel S, Garnier E, Diaz S, Buchmann N, Gurvich DE, Reich PB, ter Steege H, Morgan HD, van der Heijden MGA, Pausas JG, Poorter H (2003) A handbook of protocols for standardised and easy measurement of plant functional traits worldwide. Aust J Bot 51:335–380CrossRefGoogle Scholar
  17. Croat TR (1978) Flora of Barro Colorado Island. Stanford University, StanfordGoogle Scholar
  18. Davidson EA, Reis de Carvalho CJ, Vieira ICG, Figueiredo RO, Moutinho P, Ishida FY, dos Santos MTP, Guerrero JB, Kalif K, Sabá RT (2004) Nitrogen and phosphorus limitation of biomass growth in a tropical secondary forest. Ecol Appl 14:S150–S163CrossRefGoogle Scholar
  19. Delagrange S, Messier C, Lechowicz MJ, Dizengremel P (2004) Physiological, morphological and allocational plasticity in understory deciduous trees: Importance of individual size and light availability. Tree Physiol 24:775–784PubMedGoogle Scholar
  20. Denslow JS, Schultz JC, Vitousek PM, Strain BR (1990) Growth responses of tropical shrubs to treefall gap environments. Ecology 71:165–179CrossRefGoogle Scholar
  21. Drake PL, Franks PJ (2003) Water resource partitioning, stem xylem hydraulic properties, and plant water use strategies in a seasonally dry riparian tropical rainforest. Oecologia 137:321–329PubMedCrossRefGoogle Scholar
  22. Elias M, Potvin C (2003) Assessing inter- and intra-specific variation in trunk carbon concentration for 32 neotropical tree species. Can J For Res 33:1039–1045CrossRefGoogle Scholar
  23. Ellis AR, Hubbell SP, Potvin C (2000) In situ field measurements of photosynthetic rates of tropical tree species: a test of the functional group hypothesis. Can J Bot 78:1336–1347CrossRefGoogle Scholar
  24. Farquhar GD, Hubick KT, Condon AG, Richards RA (1989) Carbon isotope fractionation and plant water-use efficiency. In: Rundel PW, Ehleringer JR, Nagy KA (eds) Stable isotopes in ecological research. Springer, New York, pp 21–40Google Scholar
  25. Givnish TJ (1988) Adaptation to sun and shade: a whole plant perspective. Aust J Plant Physiol 15:63–92CrossRefGoogle Scholar
  26. Haggar JP, Briscoe CB, Butterfield RP (1998) Native species: a resource for the diversification of forestry production in the lowland humid tropics. For Ecol Manage 106:195–203CrossRefGoogle Scholar
  27. Hartshorn GS (1989) Application of gap theory to tropical forest management: natural regeneration on strip clear-cuts in the Peruvian Amazon. Ecology 70:567–576CrossRefGoogle Scholar
  28. Healey C (2007) The biodiversity-ecosystem functioning relationship: separating the effects of species richness, from those of species identity and environmental heterogeneity in a tropical tree plantation. M.Sc. thesis, Department of Biology, McGill University, Montreal, QCGoogle Scholar
  29. Hikosaka K, Hirose T (2000) Photosynthetic nitrogen-use efficiency in evergreen broad-leaved woody species coexisting in a warm-temperate forest. Tree Physiol 20:1249–1254PubMedGoogle Scholar
  30. Hintze JL (2002) NCSS 2001 User’s guide-1. Number cruncher statistical systems. Kaysville, UT, USA, p 570 Google Scholar
  31. Hiremath AJ (2000) Photosynthetic nutrient-use efficiency in three fast-growing tropical trees with differing leaf longevities. Tree Physiol 20:937–944PubMedGoogle Scholar
  32. Hiremath AJ, Ewel JJ (2001) Ecosystem nutrient use efficiency, productivity, and nutrient accrual in model tropical communities. Ecosystems 4:669–682CrossRefGoogle Scholar
  33. Hooper ER, Condit R, Legendre P (2002) Responses of 20 native tree species to reforestation strategies for abandoned farmland in Panama. Ecol Appl 12:1626–1641CrossRefGoogle Scholar
  34. Ketterings QM, Coe R, van Noordwijk M, Ambagau Y, Palm CA (2001) Reducing uncertainty in the use of allometric biomass equations for predicting above-ground tree biomass in mixed secondary forests. For Ecol Manage 146:199–209CrossRefGoogle Scholar
  35. Kitayama K, Aiba S-I, Takyu M, Majalap N, Wagai R (2004) Soil phosphorus fractionation and phosphorus-use efficiency of a Bornean tropical montane rain forest during soil aging with podozolization. Ecosystems 7:259–274CrossRefGoogle Scholar
  36. Kraenzel M, Castillo A, Moore T, Potvin C (2003) Carbon storage of harvest-age teak (Tectona grandis) plantations, Panama. For Ecol Manage 173:213–225CrossRefGoogle Scholar
  37. Lamb D (1998) Large-scale ecological restoration of degraded tropical forest lands: the potential role of timber plantations. Res Ecol 6:271–279CrossRefGoogle Scholar
  38. Lewis SL, Tanner EVJ (2000) Effects of above- and belowground competition on growth and survival of rain forest tree seedlings. Ecology 81:2525–2538Google Scholar
  39. Martinelli LA, Almeida S, Brown IF, Moreira MZ, Victoria RL, Sternberg LSL, Ferreira CAC, Thomas WW (1998) Stable carbon isotope ratio of tree leaves, boles and fine litter in a tropical forest in Rondônia, Brazil. Oecologia 114:170–179CrossRefGoogle Scholar
  40. Martinez-Garza C, Pena V, Ricker M, Campos A, Howe HF (2005) Restoring tropical biodiversity: Leaf traits predict growth and survival of late-successional trees in early-successional environments. For Ecol Manage 217:365–379CrossRefGoogle Scholar
  41. Meinzer FC (2003) Functional convergence in plant responses to the environment. Oecologia 134:1–11PubMedCrossRefGoogle Scholar
  42. Nabuurs GJ, Mohren GMJ (1995) Modelling analysis of potential carbon sequestration in selected forest types. Can J For Res 25:1157–1172Google Scholar
  43. Nelson BW, Mesquita R, Pereira JLG, Souza SGA, Batista GT, Couto LB (1999) Allometric regressions for improved estimate of secondary forest biomass in the central Amazon. For Ecol Manage 117:147–169CrossRefGoogle Scholar
  44. Onoda Y, Hikosaka K, Hirose T (2004) Allocation to cell walls decreases photosynthetic nitrogen-use efficiency. Funct Ecol 18:419–425CrossRefGoogle Scholar
  45. Pearcy RW, Muraoka H, Valladares F (2005) Crown architecture in sun and shade environments: assessing function and trade-offs with a three-dimensional simulation model. New Phytol 166:791–800PubMedCrossRefGoogle Scholar
  46. Piotto D, Viquez E, Montagnini F, Kanninen M (2004) Pure and mixed forest plantations with native species of the dry tropics of Costa Rica: a comparison of growth and productivity. For Ecol Manage 190:359–372CrossRefGoogle Scholar
  47. Poorter H, Evans JR (1998) Photosynthetic nitrogen-use efficiency of species that differ inherently in specific leaf area. Oecologia 116:26–37CrossRefGoogle Scholar
  48. Poorter L, Bongers F (2006) Leaf traits are good predictors of plant performance across 53 rain forest species. Ecology 87:1733–1743PubMedCrossRefGoogle Scholar
  49. Porté A, Loustau D (2001) Seasonal and interannual variations in carbon isotope discrimination in a maritime pine (Pinus pinaster) stand assessed from the isotopic composition of cellulose in annual rings. Tree Physiol 21:861–868PubMedGoogle Scholar
  50. Potvin C, Whidden E, Moore T (2004) A case study of carbon pools under three different land-uses in Panama. Clim Change 67:291–307CrossRefGoogle Scholar
  51. Reich PB, Ellsworth DS, Walters MB (1998) Leaf structure (specific leaf area) modulates photosynthesis nitrogen relations: evidence from within and across species and functional groups. Funct Ecol 12:948–958CrossRefGoogle Scholar
  52. Ricard J-P, Messier C, Delagrange S, Beaudet M (2003) Do understory sapling respond to light and below-ground competition?: a field experiment in a hardwood forest and a literature review. Ann For Sci 60:749–756CrossRefGoogle Scholar
  53. Ryan MG, Yoder BJ (1997) Hydraulic limits to tree height and tree growth. Bioscience 47:235–242CrossRefGoogle Scholar
  54. Ryan MG, Bond BJ, Law BE, Hubbard RM, Woodruff D, Cienciala E, Kucera J (2000) Transpiration and whole-tree conductance in ponderosa pine trees of different heights. Oecologia 124:553–560CrossRefGoogle Scholar
  55. Santiago LS, Kitajima K, Wright SJ, Mulkey SS (2004) coordinated changes in photosynthesis, water relations and leaf nutritional traits of canopy trees along a precipitation gradient in lowland tropical forest. Oecologia 139:495–502PubMedCrossRefGoogle Scholar
  56. Scherer-Lorenzen M, Potvin C, Koricheva J, Schmid B, Hector A, Bornik Z, Reynolds G, Schulze ED (2005) The design of experimental tree plantations for functional biodiversity research. In: Scherer-Lorenzen M, Körner C, Schulze ED (eds) The functional significance of forest diversity. Ecological studies, vol 176. Springer, Heidelberg, pp 347–376Google Scholar
  57. Sterck FJ, Martinéz-Ramos M, Dyer-Leal G, Rodriguez-Velasquez J, Poorter L (2003) The consequences of crown traits for the growth and survival of tree saplings in a Mexican lowland rainforest. Funct Ecol 17:194–200CrossRefGoogle Scholar
  58. Stier SC, Siebert SF (2002) The Kyoto Protocol: an opportunity for biodiversity restoration forestery. Conserv Biol 16:575–576CrossRefGoogle Scholar
  59. Terwilliger VJ, Kitajima K, Le Roux-Swarthout DJ, Mulkey S, Wright SJ (2001) Intrinsic water-use efficiency and heterotrophic investment in tropical leaf growth of two Neotropical pioneer tree species as estimated from δ13C values. New Phytol 152:267–281CrossRefGoogle Scholar
  60. Valladares F, Skillman JB, Pearcy RW (2002) Convergence in light capture efficiencies among tropical forest understory plants with contrasting crown architectures: a case of morphological compensation. Am J Bot 89:1275–1284CrossRefGoogle Scholar
  61. Valladares F, Wright SJ, Lasso E, Kitajima K, Pearcy RW (2000) Plastic phenotypic response to light of 16 congeneric shrubs from a Panamanian rainforest. Ecology 81:1925–1936CrossRefGoogle Scholar
  62. Vitousek PM, Field CB, Matson PA (1990) Variation in foliar (δ13C in Hawaiian Metrosideros polymorpha: a case of internal resistance? Oecologia 84:362–370Google Scholar
  63. Vitousek PM, Sanford RL Jr (1986) Nutrient cycling in moist tropical forest. Ann Rev Ecol Syst 17:137–167CrossRefGoogle Scholar
  64. Walcroft AS, Silvester WB, Grace JC, Carson SD, Waring RH (1996) Effects of branch length on carbon isotope discrimination in Pinus radiata . Tree Physiol 16:281–286PubMedGoogle Scholar
  65. Welden CW, Hewett SW, Hubbell SP, Foster RB (1991) Sapling survival, growth, and recruitment: relationship to canopy height in a neotropical forest. Ecology 72:35–50CrossRefGoogle Scholar
  66. Wright IJ, Westoby M (2002) Leaves at low versus high rainfall: coordination of structure, lifespan and physiology. New Phytol 155:403–416CrossRefGoogle Scholar
  67. Würth MKR, Peláez-Riedl S, Wright SJ, Körner C (2005) Non-structural carbohydrate pools in a tropical forest. Oecologia 143:11–24PubMedCrossRefGoogle Scholar
  68. Xu ZH, Saffigna PG, Farquhar GD, Simson JA, Haines RJ, Walker S, Osborne DO, Guinto D (2000) Carbon isotope discrimination and oxygen isotope composition in clones of the F1 hybrid between slash and Caribbean pine in relation to tree growth, water-use efficiency and foliar nutrient concentration. Tree Physiol 20:1209–1218PubMedGoogle Scholar

Copyright information

© Springer-Verlag 2007

Authors and Affiliations

  • Sylvain Delagrange
    • 1
    • 4
  • Catherine Potvin
    • 2
  • Christian Messier
    • 1
  • Lluis Coll
    • 1
    • 3
  1. 1.The Centre for Forest Research (CFR)Université du Québec à MontréalMontrealCanada
  2. 2.Smithsonian Tropical Research Institute and Department of BiologyMcGill UniversityMontrealCanada
  3. 3.Centre Tecnològic Forestal de CatalunyaSolsonaSpain
  4. 4.Institut québecois d’Aménagement de la Forêt feuillueRiponCanada

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