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Estimating the ages of successional stands of tropical trees from growth increments

Published online by Cambridge University Press:  10 July 2009

John Terborgh
Affiliation:
Nicholas School of the Environment and Center for Tropical Conservation, Duke University, P.O. Box 90381, Durham, NC 27708, USA
Cesar Flores N.
Affiliation:
Yale School of Forestry and Environmental Studies, Yale University, New Haven, CT 06511, USA
Peter Mueller
Affiliation:
Institute of Statistics and Decision Sciences, Duke University, P.O. Box 90251, Durham, NC 27708, USA
Lisa Davenport
Affiliation:
Duke University Center for Tropical Conservation, 3705-C Erwin Road, Durham, NC 27705, USA

Abstract

Inability to age tropical trees has imposed major limitations on the basic and applied science of tropical forests. Here advantage was taken of even-aged stands present in successional chronosequences found on Amazonian Whitewater river meanders to simplify the assumptions needed to estimate tree ages from growth measurements. Growth increments of eight common early successional species were measured in 21 0.5-ha plots evenly distributed over chronosequences from the earliest post-pioneer stage to mature Ficus-Cedrela stands representing approximately the mid-point of primary succession. Increment measurements, based on 4 or 5 y of growth, were arrayed in scatter diagrams against the midpoints of the growth intervals. A loess regression of the points, weighted for the higher mortality of slow-growing individuals, was then conducted to generate a ‘best estimate lifetime growth trajectory’ (BELGT) of a ‘typical’ individual surviving to maturity. The BELGT curves were integrated to generate a set of derived curves describing the time required by a ‘typical’ surviving individual to attain any given size up to the maximum for the species. Predictions of the ages of particular stands were derived from these latter curves and found to agree within 3 to 20% of ages independently estimated from the rate of point bar accretion.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1997

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References

LITERATURE CITED

Ashton, P. S. 1981. The need for information regarding tree age and growth in tropical forests. Pp. 36 in Borman, F. H. & Berlyn, G. (eds). Age and growth rate of tropical trees: new directions for research. Yale University: School of Forestry and Environmental Studies. Bulletin No. 94.Google Scholar
Baas, P. & Vetter, R. E. (eds). 1989. Growth rings in tropical woods. Rijksherbarium, Leiden, The Netherlands.Google Scholar
Clark, D. A. 1994. Plant demography. Pp. 90105 in McDade, L. A., Bawa, K. S., Hespenheide, H. A. & Hartshorn, G. S. (eds). La Selva: ecology and natural history of a Neotropical rain forest. University of Chicago Press, Chicago.Google Scholar
Clark, D. A. & Clark, D. B. 1992. Life history diversity of canopy and emergent trees in a Neotropical rain forest. Ecological Monographs 62:315344.CrossRefGoogle Scholar
Condit, R., Hubbell, S. P. & Foster, R. B. 1993. Identifying fast-growing native trees from the Neotropics using data from a large, permanent census plot. Forest Ecology and Management 62:123143.CrossRefGoogle Scholar
Condit, R., Hubbell, S. P. & Foster, R. B. 1995. Mortality rates of 205 neotropical tree species and the responses to a severe drought. Ecological Monographs 65:419439.CrossRefGoogle Scholar
Efron, B. & Tibshirani, R. 1991. Statistical data analysis in the computer age. Science 253:390395.CrossRefGoogle ScholarPubMed
Foster, R. B. 1990. Long-term change in the successional forest community of the Rio Manu floodplain. Pp. 565572 in Gentry, A. H. (ed.). Four Neotropical rainforests. Yale University Press, New Haven, Connecticut.Google Scholar
Foster, R. B., Arce, B. J. & Wachter, T. S. 1986. Dispersal and the sequential plant communities in Amazonian Peru floodplain. Pp. 357369 in Fleming, T. H. & Estrada, A. (eds). Frugivores and seed dispersal. Dr. W. Junk, Dordrecht.CrossRefGoogle Scholar
Gentry, A. H., (ed.) 1990. Four Neotropical rainforests. Yale University Press, New Haven.Google Scholar
Gentry, A. H. & Terborgh, J. 1990. Composition and dynamics of the Cocha Cashu ‘mature’ floodplain forest. Pp. 542564 in Gentry, A. H. (ed.). Four Neotropical rainforests. Yale University Press, New Haven.Google Scholar
Groenendael, J. M. Van, Bullock, S. H. & Perez-Jemenez, L. A. 1996. Aspects of the population biology of the gregarious tre. Cordia elaeagnoides in Mexican tropical deciduous forest. Journal of Tropical Ecology 12:1124.Google Scholar
Hartshorn, G. S. 1975. A matrix model of tree population dynamics. Pp. 4151 in Golley, F. B. & Medina, E. (eds). Tropical ecological systems. Springer Verlag, New York.CrossRefGoogle Scholar
Kalliola, R., Salo, J. & Makinen, Y. 1987. Reneración natural de selvas en la Amazonia Peruana 1: dinamica fluvial y sucesión reberena. Memorias del Museo de Historia Natural ‘Javier Prado’(hima) 19A:1102.Google Scholar
Kalliola, R., Salo, J., Puhakka, M. & Rajasilta, M. 1991. New site formation and colonizing vegetation in primary succession on the western Amazon floodplains. fournal of Ecology 79:877901.Google Scholar
King, D. A. 1993. Growth history of a Neotropical tree inferred from the spacing of leaf scars. Journal of Tropical Ecology 9:525532.Google Scholar
Korning, J. & Balslev, H.. 1994. Growth rates and mortality patterns of tropical lowland tree species and the relation to forest structure in Amazonian Ecuador. Journal of Tropical Ecology 10:151166.CrossRefGoogle Scholar
Lieberman, D., Hartshorn, G., Lieberman, M. & Peralta, R. 1990. Forest dynamics at La Selva Biological Station, 1969–1985. Pp. 509521 in Gentry, A. H. (ed.). Four Neotropical rainforests. Yale University Press, New Haven, Connecticut.Google Scholar
Lieberman, D., Lieberman, M., Hartshorn, G. & Peralta, R. 1985a. Growth rates and age-size relationships of tropical wet forest trees in Costa Rica. Journal of Tropical Ecology 1:97109.CrossRefGoogle Scholar
Lieberman, D., Lieberman, M., Peralta, R. & Hartshorn, G. 1985b. Mortality patterns and stand turnover rates in a wet tropical forest in Costa Rica. Journal of Ecology 73:915924.Google Scholar
Lieberman, M. & Lieberman, D. 1985. Simulation of growth curves from periodic increment data. Ecology 66:632635.Google Scholar
Lieberman, M. & Lieberman, D. 1987. Forest tree growth and dynamics at La Selva, Costa Rica. Journal of Tropical Ecology 3:347359.Google Scholar
Mervart, J. 1972. Growth and mortality rates in the natural high forest of western Nigeria. Nigeria Forestry Information Bulletin (n.s.) No. 22.Google Scholar
Oyama, K. 1993. Are age and height correlated i. Chamaedorea tepejilote (Palmae)? Journal of Tropical Ecology 9:381385.CrossRefGoogle Scholar
Pinard, M. 1993. Impacts of stem harvesting on populations o. Iriartea deltoidea (Palmae) in an extractive reserve in Acre, Brazil. Biotropica 25:214.Google Scholar
Pinero, D., Martínez-Ramos, M. & Sarukhán, J. 1984. A population model o. Astrocaryum mexicanum and a sensitivity analysis of its finite rate of increase. Journal of Ecology 72:977990.Google Scholar
Putz, F. E. & Milton, K. 1982. Tree mortality rates on Barro Colorado Island. Pp. 95100 in Leigh, E. G. Jr., Rand, A. S. & Windsor, D. M. (eds). The ecology of a tropical forest: seasonal rhythms and long-term changes. Smithsonian Institution Press, Washington, D.C.Google Scholar
Sarukhán, J. 1978. Studies on the demography of tropical trees. Pp. 163184 in Tomlinson, P. B. & Zimmermann, H. (eds). Tropical trees as living systems. Cambridge University Press, Cambridge, England.Google Scholar
Swaine, M. D., Hall, J. B. & Alexander, I. J. 1987a. Tree population dynamics at Kade, Ghana (1968–1982). Journal of Tropical Ecology 3:331345.Google Scholar
Swaine, M. D., Lieberman, D. & Putz, F. E. 1987b. The dynamics of tree populations in tropical forest: a review. Journal of Tropical Ecology 3:359367.CrossRefGoogle Scholar
Terborgh, J., Foster, R. B. & Nunez, V. P. 1996. Tropical tree communities: a test of the nonequilibrium hypothesis. Ecology 77:561567.Google Scholar
Terborgh, J. & Petren, K., 1991. Development of habitat structure through succession in an Amazonian floodplain forest. Pp. 2846 in Bell, S. S., McCoy, E. D. & Mushinsky, H. R. (eds). Habitat structure: the physical arrangement of objects in space. Chapman & Hall, New York.Google Scholar
Valen, L. Van. 1975. Life, death, and energy of a tree. Biotropica 7:260269.CrossRefGoogle Scholar
Walker, L. R., Zasada, J. C. & Chapin, F. S. III 1986. The role of life history processes in primary succession on an Alaskan floodplain. Ecology 67:12431253.Google Scholar