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Variation in longevity and traits of leaves among co-occurring understorey plants in a tropical montane forest

Published online by Cambridge University Press:  01 March 2008

Satomi Shiodera ,
Joeni S. Rahajoe  and
Takashi Kohyama
Satomi Shiodera*
Affiliation:
Faculty of Environmental Earth Science, Hokkaido University, Sapporo 060-0810, Japan
Joeni S. Rahajoe
Affiliation:
Research Center for Biology, The Indonesian Institute of Sciences, Jalan Juanda 22, Bogor 16122, Indonesia
Takashi Kohyama
Affiliation:
Faculty of Environmental Earth Science, Hokkaido University, Sapporo 060-0810, Japan
*
1Corresponding author. Email: shiodera@ees.hokudai.ac.jp
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Abstract:

The relationship between leaf longevity and other leaf traits was compared among different life-form categories (trees, herbs, climbers and epiphytes) of 101 plant species in a tropical montane forest on Mt. Halimun, West Java, Indonesia. We applied the Cox proportional hazards regression to estimate the leaf longevity of each species from 30 mo of census data. We examined whether estimated longevity was explained by either species life-form categories, taxonomic groupings (eudicots, monocots, magnoliids and chloranthales, and ferns) or such leaf traits as leaf area, leaf mass per area (LMA), mass-based leaf nitrogen, penetrometer reading, condensed-tannin-free total phenolics and condensed tannin. There was a wide-ranged interspecific variation in leaf longevity, mostly 10–50 mo, similarly across life-form categories. LMA showed a strong positive influence on leaf longevity. We found that relationships between leaf longevity and some leaf traits were different among various life forms. Trees tended to have high LMA, while climbers tended to have low LMA at the same leaf longevity. We hypothesize that such difference among life forms reflects shoot architecture characteristics. Multi-shoot trees with branching architecture need to have self-supporting leaves, whereas semi-epiphytic climbers can maintain relatively low biomass investment to leaves hanging or relying upon the mechanical support from host plants.

Keywords

Cox proportional hazards regressionIndonesiaJavaleaf life spanlife form
Type
Research Article
Information
Journal of Tropical Ecology , Volume 24 , Issue 2 , March 2008 , pp. 121 - 133
Copyright
Copyright © Cambridge University Press 2008

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References

LITERATURE CITED

ACKERLY, D. 1999. Self-shading, carbon gain and leaf dynamics: a test of alternative optimality models. Oecologia 119:300–310.CrossRefGoogle ScholarPubMed
ACKERLY, D. D. & BAZZAZ, F. A. 1995. Seedling crown orientation and interception of diffuse radiation in tropical forest gaps. Ecology 76:1134–1146.CrossRefGoogle Scholar
ALLISON, P. D. 1995. Survival analysis using SAS: a practical guide. SAS publishing, North Carolina. 304 pp.Google Scholar
ANDERSON, L. J., COMAS, L. H., LAKSO, A. N. & EISSENSTAT, D. M. 2003. Multiple risk factors in root survivorship: a 4-year study in Concord grape. New Phytologist 158:489–501.CrossRefGoogle ScholarPubMed
BATE-SMITH, E. C. 1977. Astringent tannins of Acer species. Phytochemistry 16:1421–1426.CrossRefGoogle Scholar
BONGERS, F. & POPMA, J. 1988. Is exposure-related variation in leaf characteristics of tropical rain forest species adaptive? Pp. 191–200 in Werger, M. J. A., van der Aart, P. J. M., During, H. J. & Verhoeven, J.T.A. (eds.). Plant form and vegetation structure. SPB Academic Publishing, The Hague.Google Scholar
BRYANT, J. P., HEITKONIG, I., KUROPAT, P. & OWEN-SMITH, N. 1991. Effects of severe defoliation on the long-term resistance to insect attack and on leaf chemistry in six woody species of the southern African savanna. American Naturalist 137:50–63.CrossRefGoogle Scholar
BURNHAM, K. P. & ANDERSON, D. R. 1998. Model selection and multimodel inference: a practical information-theoretic approach. Springer, New York. 353 pp.CrossRefGoogle Scholar
CHABOT, B. F. & HICKS, D. J. 1982. The ecology of leaf life spans. Annual Review of Ecology and Systematics 13:229–259.CrossRefGoogle Scholar
CHAZDON, R. L. & FETCHER, N. 1984. Photosynthetic light environments in a lowland tropical rain forest in Costa Rica. Journal of Ecology 72:553–564.CrossRefGoogle Scholar
COLEY, P. D. 1983. Herbivory and defensive characteristics of tree species in a lowland tropical forest. Ecological Monographs 53:209–233.CrossRefGoogle Scholar
COLEY, P. D. 1986. Costs and benefits of defense by tannins in a neotropical tree. Oecologia 70:238–241.CrossRefGoogle Scholar
COLEY, P. D. & AIDE, T. M. 1991. Comparison of herbivory and plant defenses in temperate and tropical broad-leaved forests. Pp. 25–49 in Price, P. W., Lewinsohn, T. M., Fernandes, G. W. & Benson, W. W. (eds.). Plant-animal interactions: evolutionary ecology in tropical and temperate regions. John Wiley & Sons, New York.Google Scholar
COX, D. R. 1972. Regression models and life-tables. Journal of the Royal Statistical Society B 34:187–220.Google Scholar
CRAINE, J. M., BERIN, D. M., REICH, P. B., TILMAN, D. G. & KNOPS, J. M. H. 1999. Measurement of leaf longevity of 14 species of grasses and forbs using a novel approach. New Phytologist 142:475–481.CrossRefGoogle Scholar
ELLSWORTH, D. S. & REICH, P. B. 1992. Leaf mass per area, nitrogen content and photosynthetic carbon gain in Acer saccharum seedlings in contrasting forest light environments. Functional Ecology 6:423–435.CrossRefGoogle Scholar
FOLIN, O. & CIOCALTEU, V. 1927. On tyrosine and tryptophane determinations in proteins. Journal of Biological Chemistry 73:627–650.CrossRefGoogle Scholar
GENTRY, A. H. 1988. Changes in plant community diversity and floristic composition on environmental and geographical gradients. Annals of the Missouri Botanical Garden 75:1–34.CrossRefGoogle Scholar
HIKOSAKA, K. 1996. Effects of leaf age, nitrogen nutrition and photon flux density on the organization of the photosynthetic apparatus in leaves of a vine (Ipomoea tricolor Cav.) grown horizontally to avoid mutual shading of leaves. Planta 198:144–150.CrossRefGoogle Scholar
HIKOSAKA, K., TERASHIMA, I. & KATOH, S. 1994. Effects of leaf age, nitrogen nutrition and photon flux density on the distribution of nitrogen among leaves of a vine (Ipomoea tricolor Cav.) grown horizontally to avoid mutual shading of leaves. Oecologia 97:451–457.CrossRefGoogle ScholarPubMed
HIKOSAKA, K., HANBA, Y. T., HIROSE, T. & TERASHIMA, I. 1998. Photosynthetic nitrogen-use efficiency in leaves of woody and herbaceous species. Functional Ecology 12:896–905.CrossRefGoogle Scholar
JULKUNEN-TIITTO, R. 1985. Phenolic constituents in the leaves of northern willows: methods for the analysis of certain phenolics. Journal of Agricultural and Food Chemistry 33:213–217.CrossRefGoogle Scholar
KIKUZAWA, K. 1991. A cost-benefit analysis of leaf habit and leaf longevity of trees and their geographical pattern. American Naturalist 138:1250–1263.CrossRefGoogle Scholar
KIKUZAWA, K. 1995. Leaf phenology as an optimal strategy for carbon gain in plants. Canadian Journal of Botany 73:158–163.CrossRefGoogle Scholar
MAGNUSSEN, S., ALFARO, R. I. & BOUDEWYN, P. 2005. Survival-time analysis of white spruce during spruce budworm defoliation. Silva Fennica 39:177–189.CrossRefGoogle Scholar
NAKAMURA, K., NOERDJITO, W. A. & HASYIM, A. 1994. Regional difference and seasonality of rainfall in Java, with special reference to Bogor. Tropics 4:93–103.CrossRefGoogle Scholar
NIINEMETS, U. 1999. Components of leaf dry mass per area – thickness and density – alter leaf photosynthetic capacity in reverse directions in woody plants. New Phytologist 144:35–47.CrossRefGoogle Scholar
OSADA, N., TAKEDA, H., FURUKAWA, A. & AWANG, M. 2001. Leaf dynamics and maintenance of tree crowns in a Malaysian rain forest stand. Journal of Ecology 89:774–782.CrossRefGoogle Scholar
POORTER, L., KWANT, R., HERNÁNDEZ, R., MEDINA, E. & WERGER, M. J. A. 2000. Leaf optical properties in Venezuelan cloud forest trees. Tree Physiology 20:519–526.CrossRefGoogle ScholarPubMed
REICH, P. B. 1993. Reconciling apparent discrepancies among studies relating life span, structure and function of leaves in contrasting plant life forms and climates: ‘the blind men and the elephant retold’. Functional Ecology 7:721–725.CrossRefGoogle Scholar
REICH, P. B., UHL, C., WALTERS, M. B. & ELLSWORTH, D. S. 1991. Leaf lifespan as a determinant of leaf structure and function among 23 amazonian tree species. Oecologia 86:16–24.CrossRefGoogle ScholarPubMed
REICH, P. B., WALTERS, M. B. & ELLSWORTH, D. S. 1992. Leaf life-span in relation to leaf, plant, and stand characteristics among diverse ecosystems. Ecological Monographs 62:365–392.CrossRefGoogle Scholar
REICH, P. B., WALTERS, M. B. & ELLSWORTH, D. S. 1997. From tropics to tundra: global convergence in plant functioning. Proceedings of the National Academy of Sciences of the United States of America 94:13730–13734.CrossRefGoogle ScholarPubMed
REICH, P. B., UHL, C., WALTERS, M. B., PRUGH, L. & ELLSWORTH, D. S. 2004. Leaf demography and phenology in Amazonian rain forest: a census of 40 000 leaves of 23 tree species. Ecological Monographs 74:3–23.CrossRefGoogle Scholar
ROSSITER, M., SCHULTZ, J. C. & BALDWIN, I. T. 1988. Relationships among defoliation, red oak phenolics, and gypsy moth growth and reproduction. Ecology 69:267–277.CrossRefGoogle Scholar
ROZENDAAL, D. M. A., HURTADO, V. H. & POORTER, L. 2006. Plasticity in leaf traits of 38 tropical tree species in response to light; relationships with light demand and adult stature. Functional Ecology 20:207–216.CrossRefGoogle Scholar
SIMBOLON, H., WIRADINATA, H. & YONEDA, M. 1998. Plant diversity in Gunung Halimun National Park, West Java, Indonesia: inventorying activities. Pp. 1–11 in Simbolon, H., Yoneda, M. & Sugarjito, J. (eds.). Research and conservation of biodiversity in Indonesia, Vol. IV. Gunung Halimun: the last submontane tropical forest in West Java. LIPI, PHPA & JICA, Bogor.Google Scholar
SUZUKI, E., YONEDA, M., SIMBOLON, H., MUHIDIN, A. & WAKIYAMA, S. 1997. Establishment of two 1-ha permanent plots in Gn. Halimun National Park for study of vegetation structure and forest dynamics. Pp. 36–55 in Yoneda, M., Sugarjito, J. & Simbolon, H. (eds.). Research and conservation of biodiversity in Indonesia, Vol. II. The inventory of natural resources in Gunung Halimun National Park. LIPI, PHPA & JICA, Bogor.Google Scholar
SUZUKI, E., YONEDA, M., SIMBOLON, H., FANANI, Z., NISHIMURA, T. & KIMURA, M. 1998. Monitoring of vegetational changes on permanent plots in Gunung Halimun National Park. Pp. 60–81 in Simbolon, H., Yoneda, M. & Sugarjito, J. (eds.). Research and conservation of biodiversity in Indonesia, Vol. IV. Gunung Halimun: the last submontane tropical forest in West Java. LIPI, PHPA & JICA, Bogor.Google Scholar
TURNER, I. M. 1994. Sclerophylly: primarily protective? Functional Ecology 8:669–675.CrossRefGoogle Scholar
TURNER, I. M. 2001. The ecology of trees in the tropical rain forest. Cambridge University Press, Cambridge. 312 pp.CrossRefGoogle Scholar
VENABLES, W. N. & RIPLEY, B. D. 2002. Modern applied statistics with S. (Fourth edition). Springer, New York. 512 pp.CrossRefGoogle Scholar
VINCENT, G. 2006. Leaf life span plasticity in tropical seedlings grown under contrasting light regimes. Annals of Botany 97:245–255.CrossRefGoogle ScholarPubMed
WATERMAN, P. G. & MOLE, S. 1994. Analysis of phenolic plant metabolites. Blackwell, Oxford. 248 pp.Google Scholar
WELLS, C. E. & EISSENSTAT, D. M. 2001. Marked differences in survivorship among apple roots of different diameters. Ecology 82:882–892.CrossRefGoogle Scholar
WRIGHT, I. J., REICH, P. B., WESTOBY, M., ACKERLY, D. D., BARUCH, Z., BONGERS, F., CAVENDER-BARES, J., CHAPIN, T., CORNELISSEN, J. H. C., DIEMER, M., FLEXAS, J., GARNIER, E., GROOM, P. K., GULIAS, J., HIKOSAKA, K., LAMONT, B. B., LEE, T., LEE, W., LUSK, C., MIDGLEY, J. J., NAVAS, M. -L., NIINEMETS, U., OLEKSYN, J., OSADA, N., POORTER, H., POOT, P., PRIOR, L., PYANKOV, V. I., ROUMET, C., THOMAS, S. C., TJOELKER, M. G., VENEKLAAS, E. J. & VILLAR, R. 2004. The worldwide leaf economics spectrum. Nature 428:821–827.CrossRefGoogle ScholarPubMed
WRIGHT, I. J., REICH, P. B., CORNELISSEN, J. H. C., FALSTER, D. S., GARNIER, E., HIKOSAKA, K., LAMONT, B. B., LEE, W., OLEKSYN, J., OSADA, N., POORTER, H., VILLAR, R., WARTON, D. I. & WESTOBY, M. 2005. Assessing the generality of global leaf trait relationships. New Phytologist 166:485–496.CrossRefGoogle ScholarPubMed