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Ecophysiological traits of plant functional groups in forest and pasture ecosystems from eastern Amazônia, Brazil

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Abstract

The plant functional group approach has the potential to clarify ecological patterns and is of particular importance in simplifying the application of ecological models in high biodiversity ecosystems. Six functional groups (pasture grass, pasture sapling, top-canopy tree, top-canopy liana, mid canopy tree, and understory tree) were established a priori based on ecosystem inhabited, life form, and position within the forest canopy profile on eastern Amazonian region. Ecophysiological traits related to photosynthetic gas exchange were then used to characterize such groups. The ecophysiological traits evaluated showed considerable variations among groups. The pasture grass functional group (a C4 photosynthetic pathway species) showed high instantaneous water use efficiency (A max/g s@A max), high photosynthetic nitrogen use efficiency (A max/N area), and high ratio of A max to dark respiration (A max/R d). Among the species with the C3 photosynthetic pathway, the top-canopy liana group showed the highest mean of A max/g s@A max, statistically distinct from the lowest average presented by the understory tree group. Furthermore, the pasture sapling group showed the lowest average of A max/R d, statistically distinct from the high average observed for the understory tree group. Welch-ANOVAs followed by Games–Howell post hoc tests applied to ecophysiological traits produced reasonable distinctions among functional groups, although no significant distinction was detected between the groups top-canopy tree and pasture sapling. Species distribution within the functional groups was accurately reproduced by discriminant analyses based on species averages of ecophysiological traits. The present work convincingly shows that the functional groups identified have distinct ecophysiological characteristics, with the potential to respond differently to environmental factors. Such information is of great importance in modeling efforts that evaluate the effects of dynamic changes in tropical plant communities over ecosystem primary productivity.

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References

  • Ackerly DD, Dudley SA, Sultan SE, Schmitt J, Coleman JS, Linder CR, Sandquist DR et al (2000) The evolution of plant ecophysiological traits: recent advances and future directions. BioScience 50:979–995

    Article  Google Scholar 

  • Carswell FE, Meir P, Wandelli EV, Bonates LCM, Kruijt B, Barbosa EM, Nobre AD, Grace J et al (2000) Photosynthetic capacity in a central Amazonian rain forest. Tree Physiol 20:179–186

    PubMed  Google Scholar 

  • Cerling TE, Ehleringer JR, Harris JM (1998) Carbon dioxide starvation, the development of C4 ecosystems, and mammalian evolution. Philos Trans Roy Soc London B 353:159–171

    Article  CAS  Google Scholar 

  • Chazdon RL (1988) Sunflecks and their importance to forest understorey plants. In: Begon M, Fitter AH, Ford ED, MacFadyen A (eds) Advances in ecological research. Academic Press, San Diego, pp 1–63

    Google Scholar 

  • Chazdon RL, Pearcy RW, Lee DW, Fetcher N (1996) Photosynthetic responses of tropical forest plants to contrasting light environments. In: Mulkey SS, Kitajima K, Wright SJ (eds) Tropical forest plant ecophysiology. Chapman & Hall, New York, pp 5–55

    Google Scholar 

  • Cornelissen JHC, Lavorel S, Garnier E, Díaz S, Buchmann N, Gurvich DE, Reich PB, ter Steege H, Morgan HD, van der Heijden MGA, Pausas JG, Poorter H (2003) Handbook for protocols for standardised and easy measurements of plant functional traits worldwide. Aust J Bot 51:335–380

    Article  Google Scholar 

  • da Rocha HR, Goulden ML, Miller SD, Menton MC, Pinto LDVO, de Freitas HC, Figueira AMS (2004) Seasonality of water and heat fluxes over a tropical forest in eastern Amazonia. Ecol Appl 14:22–32

    Google Scholar 

  • Dawson TE, Chapin FS III (1993) Grouping plants by their form-function characteristics as an avenue for simplification in scaling between leaves and landscapes. In: Ehleringer JR, Field CB (eds) Scaling physiological processes Leaf to globe. Academic Press, San Diego, pp 313–319

    Google Scholar 

  • Denslow JS (1987) Tropical rainforest gaps and tree species diversity. Annu Rev Ecol Syst 18:431–451

    Article  Google Scholar 

  • Díaz S, Hodgson J, Thompson K, Cabido M, Cornelissen J et al (2004) The plant traits that drive ecosystems: evidence from three continents. J Veget Sci 15:295–304

    Article  Google Scholar 

  • Domingues TF, Berry JA, Martinelli LA, Ometto JPHB, Ehleringer JR (2005) Parameterization of canopy structure and leaf-level gas exchange for an eastern Amazonian tropical rain forest (Tapajos National Forest, Para, Brazil). Earth Interact 9:17

    Article  Google Scholar 

  • Drake BG, Gonzalez-Meler MA, Long SP (1997) More efficient plants: a consequence of rising atmospheric CO2? Annu Rev Plant Physiol Plant Mol Biol 48:609–639

    Article  PubMed  CAS  Google Scholar 

  • Ehleringer JR, Björkman O (1977) Quantum yields for CO2 uptake in C3 and C4 plants: dependence on temperature, CO2 and O2 concentration. Plant Physiol 59:86–90

    Article  PubMed  CAS  Google Scholar 

  • Ehleringer JR, Cerling TE, Helliker BR (1997) C4 photosynthesis, atmospheric CO2, and climate. Oecologia 112:285–299

    Article  Google Scholar 

  • Evans JR (1989) Photosynthesis and nitrogen relationships in leaves of C3 plants. Oecologia 78:9–19

    Article  Google Scholar 

  • Farquhar GD, von Caemmerer S, Berry JA (1980) A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta 149:78–90

    Article  CAS  Google Scholar 

  • Farquhar GD, Sharkey TD (1982) Stomatal conductance and photosynthesis. Annu Rev Plant Physiol Plant Mol Biol 33:317–345

    CAS  Google Scholar 

  • Field CB, Mooney HA (1986) The photosynthesis-nitrogen relationship in wild plants. In: Givnish TJ (ed) On the economy of plant form and function. University Press, Cambridge, pp 25–55

    Google Scholar 

  • Goulden ML, Miller SD, da Rocha HR, Menton MC, de Freitas HC, Figueira AMES, de Souza CAD (2004) Diel and seasonal patterns of tropical forest CO2 exchange. Ecol Appl 14:42–54

    Article  Google Scholar 

  • Grime JP (2001) Plant strategies, vegetation processes, and ecosystem properties. Willey, New York

    Google Scholar 

  • Hobbs RJ (1997) Can we use plant functional types to describe and predict responses to environmental changes? In: Smith TM, Shugart HH, Woodward FI (eds) Plant functional types. Their relevance to ecosystem properties and global change. University Press, Cambridge, pp 66–90

    Google Scholar 

  • Hodgson JG, Wilson PJ, Hunt R, Grime JP, Thompson K (1999) Allocating C-S-R plant functional types: a soft approach to a hard problem. Oikos 85:282–294

    Article  Google Scholar 

  • Holdridge LR (1947) Determination of world plant formations from simple climatic data. Science 105:367–368

    Article  PubMed  Google Scholar 

  • Hubbell SP (2005) Neutral theory in community ecology and the hypothesis of functional equivalence. Funct Ecol 19:166–172

    Article  Google Scholar 

  • Keller M, Palace M, Hurtt G (2001) Biomass estimation in the Tapajos National Forest, Brazil. Examination of sampling and allometric uncertainties. Forest Ecol Manage 154:371–382

    Article  Google Scholar 

  • Körner C (1993) Scaling from species to vegetation: the usefulness of functional groups. In: Schulze E-D, Mooney HA (eds) Biodiversity and ecosystem function. Springer-Verlag, Heidelberg, pp 117–140

    Google Scholar 

  • Leight EG Jr (1975) Structure and climate in tropical rain forest. Annu Rev Ecol Syste 6:67–85

    Article  Google Scholar 

  • Lloyd J, Grace J, Miranda AC, Meir P, Wong SC, Miranda BS, Wright IR, Gash JHC et al (1995) A simple calibrated model of Amazon rainforest productivity based on leaf biochemical properties. Plant Cell Environ 18:1129–1145

    Article  Google Scholar 

  • Loreau M, Naeem S, Inchausti P, Bengtsson J, Grime JP, Hector A, Hooper DU, Huston MA, Raffaelli D, Schmid B, Tilman D, Wardle DA (2001) Biodiversity and ecosystem functioning. Current knowledge and future challenges. Science 294:804–808

    Article  PubMed  CAS  Google Scholar 

  • Marshall B, Biscoe PV (1980) A model for C3 leaves describing the dependence of net photosynthesis on irradiance. I. Derivation. J Exp Bot 31:29–39

    Article  CAS  Google Scholar 

  • 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 Rondonia, Brazil. Oecologia 114:170–179

    Article  Google Scholar 

  • McWilliam A-LC, Cabral OMR, Gomes BM, Esteves JL, Roberts JM (1996) Forest and pasture leaf-gas exchange in south-west Amazonia. In: Gash JHC, Nobre CA, Roberts JM, Victoria RL (eds) Amazonian deforestation and climate. John Wiley & Sons, West Sussex, pp 265–286

    Google Scholar 

  • Meir P, Grace J, Miranda AC (2001) Leaf respiration in two tropical rainforests: constraints on physiology by phosphorus, nitrogen and temperature. Funct Ecol 15:378–387

    Article  Google Scholar 

  • Miller SD, Goulden ML, Menton MC, da Rocha HR, de Freitas HC, Figueira AMES, de Souza CAD (2004) Biometric and micrometeorological measurements of tropical forest carbon balance. Ecol Appl 14:114–126

    Article  Google Scholar 

  • Nepstad DC, Moutinho P, Dias-Filho MB, Davidson E, Cardinot G, Markewitz D, Figueiredo R, Vianna N et al (2002) The effects of partial throughfall exclusion on canopy processes, aboveground production, and biogeochemistry of an Amazon forest. J Geophys Res 107(D20):8085, doi:10.1029/2001JD000360

    Article  CAS  Google Scholar 

  • Ometto JPH, Flanagan LB, Martinelli LA, Moreira MZ, Higuchi N, Ehleringer JR (2002) Carbon isotope discrimination in forest and pasture ecosystems of the Amazon Basin, Brazil. Global Biogeochem Cycles 16(4):1109, doi:10.1029/2001GB001462

    Article  CAS  Google Scholar 

  • Pearcy RW (1990) Sunflecks and photosynthesis in plant canopies. Annu Rev Plant Physiol Plant Mol Biol 41:421–453

    Article  CAS  Google Scholar 

  • Pearcy RW, Ehleringer JR (1984) Comparative ecophysiology of C3 and C4 plants. Plant Cell Environ 7:1–13

    Article  CAS  Google Scholar 

  • Peng C (2000) From static biogeographical model to dynamic global vegetation model: a global perspective on modelling vegetation dynamics. Ecol Modell 135:33–54

    Article  CAS  Google Scholar 

  • Phillips OL, Vásquez Martínez R, Arroyo L, Baker TR, Killeen T, Lewis SL, Malhi Y, Mendoza et al (2002) Increasing dominance of large lianas in Amazonian forests. Nature 418:770–774

    Article  PubMed  CAS  Google Scholar 

  • Phillips OL, Baker TR, Arroyo L, Higuchi N, Killeen TJ, Laurance WF, Lewis SL, Lloyd J et al (2004) Pattern and process in Amazon tree turnover, 1976–2001. Philos Trans Roy Soc London B 359:381–407

    Article  CAS  Google Scholar 

  • Putz FE (1983) Liana biomass and leaf area of a “Tierra Firme” forest in the Rio Negro Basin, Venezuela. Biotropica 15:185–189

    Article  Google Scholar 

  • Raunkiaer C (1934) The life forms of plants and statistical plant geography. Clarendon Press, Oxford

    Google Scholar 

  • Reich PB, Walters MB, Ellsworth DS (1997) From tropics to tundra. Global convergence in plant functioning. Proc Natl Acad Sci 94:13730–13734

    Article  PubMed  CAS  Google Scholar 

  • Reich PB, Uhl C, Walters MB, Ellsworth DS (1991) Leaf lifespan as a determinant of leaf structure and function among 23 amazonian tree species. Oecologia 86:16–24

    Article  Google Scholar 

  • Roberts J, Cabral OMR, de Aguiar LF (1990) Stomatal and boundary-layer conductances in an Amazonian Terra Firme Rain Forest. J Appl Ecol 27:336–353

    Article  Google Scholar 

  • Sá TD de A, da Costa J de PR, Roberts JM (1996) Forest and pasture conductances in southern Pará, Amazonia. In: Gash JHC, Nobre CA, Roberts JM, Victoria RL (eds) Amazonian deforestation and climate. John Wiley & Sons, West Sussex, pp 241–264

    Google Scholar 

  • Sakai RK, Fitzjarrald DR, Moraes OLL, Staebler RM, Acevedo OC, Czikowsky MJ, da Silva R, Brait E et al (2004) Land-use change effects on local energy, water, and carbon balances in an Amazonian agricultural field. Global Change Biol 10:895–907

    Article  Google Scholar 

  • Schnitzer SA, Bongers F (2002) The ecology of lianas and their role in forests. Trends Ecol Evol 17:223–230

    Article  Google Scholar 

  • Shuttleworth WJ (1989) Micrometeorology of temperate and tropical forest. Philos Trans Roy Soc London B 324:299–334

    Article  Google Scholar 

  • Silver WL, Neff J, McGroddy M, Veldkamp E, Keller M, Cosme R (2000) Effects of soil texture on belowground carbon and nutrient storage in a lowland Amazonian forest ecosystem. Ecosystems 3:193–209

    Article  CAS  Google Scholar 

  • Solbrig OT (1993) Plant traits and adaptative strategies: Their role in ecosystem function. In: Schulze E-D, Mooney HA (eds) Biodiversity and ecosystem function. Springer-Verlag, Heidelberg, pp 97–116

    Google Scholar 

  • Smith TM, Shugart HH, Woodward FI (1997) Plant functional types. Their relevance to ecosystem properties and global change. University Press, Cambridge

    Google Scholar 

  • Telles E de CC, de Camargo PB, Martinelli LA, Trumbore S, da Costa ES, Santos J, Higuchi N, Oliveira RC Jr (2003) Influence of soil texture on carbon dynamics and storage potential in tropical forest soils of Amazonia. Global Biogeochem Cycles 17(2):1040, doi:10.1029/2002GB001953

    Article  CAS  Google Scholar 

  • Vieira S, de Camargo PB, Selhorst D, da Silva R, Hutyra L, Chambers JQ, Brown IF, Higuchi N et al (2004) Forest structure and carbon dynamics in Amazonian tropical rain forests. Oecologia 140:468–479

    Article  PubMed  Google Scholar 

  • von Caemmerer S, Farquhar GD (1981) Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves. Planta 153:376–387

    Article  Google Scholar 

  • von Caemmerer S (2000) Biochemical models of leaf photosynthesis. CSIRO Publishing, Collingwood

    Google Scholar 

  • Weiher E, van der Werf A, Thompson K, Roderick M, Garnier E, Eriksson O (1999) Challenging Theophrastus: a common core list of plant traits for functional ecology. J Veget Sci 10:609–620

    Article  Google Scholar 

  • Wright IJ, Reich PB, Cornelissen JHC, Falster DS, Garnier E, Hikosaka K, Lamont BB, Lee W et al (2005) Assessing the generality of global leaf trait relationships. New Phytologist 166:485–496

    Article  PubMed  Google Scholar 

  • Würth MKR, Winter K, Körner C (1998) In situ responses to elevated CO2 in tropical forest understorey plants. Funct Ecol 12:886–895

    Article  Google Scholar 

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Acknowledgments

We are thankful to the assistance provided by our friends at the LBA-ECO Santarém regional office. We are also in debt to J. Ometto and A. Calil for a great work on sample analyses. Financial support for this work was provided partially by a research grant from NASA LBA-Ecology to J.R.E., L.B.F., and L.A.M and partially by a research grant from NASA LBA-Ecology to J.R.E., J.A.B., and L.A.M.

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Authors and Affiliations

  1. University of Utah, 1400 East 257 South, Salt Lake City, UT, 84112-0840, USA

    Tomas F. Domingues & James R. Ehleringer

  2. Centro de Energia Nuclear na Agricultura, Universidade de São Paulo - Avenida Centenário, 303 Piracicaba, Sao Paulo, SP, 13416-000, Brazil

    Luiz A. Martinelli

  3. Institute of Geography, School of GeoSciences, The University of Edinburgh, Drummond Street, Edinburgh, EH8 9XP, Scotland, UK

    Tomas F. Domingues

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  1. Tomas F. Domingues
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Correspondence to Tomas F. Domingues.

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Domingues, T., Martinelli, L. & Ehleringer, J. Ecophysiological traits of plant functional groups in forest and pasture ecosystems from eastern Amazônia, Brazil. Plant Ecol 193, 101–112 (2007). https://doi.org/10.1007/s11258-006-9251-z

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