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Net production and carbon cycling in a bamboo Phyllostachys pubescens stand

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Abstract

Phyllostachys pubescens Mazel ex Houzeau de Lehaie is one of the largest bamboo species with a leptomorph root system in the world. The species originates in China and has been naturalized in the neighboring countries. It was introduced in 1746 into Japan because of the economic value of the young sprouts and culm woods. It escaped from the planted areas and expanded by invading the original vegetation. In order to clarify the basic ecological characteristics of the species, carbon fixation and cycling were determined in a stand of Phyllostachys pubescens. The standing culm density and average DBH in 1991 were 7100 ha(-1) and 11.3 cm, respectively. The above-ground biomass was 116.5 t ha(-1) for culms, 15.5 t ha(-1) for branches, 5.9 t ha(-1) for leaves and 137.9 t ha(-1) in total. The total above-ground biomass was one of the largest among the world's bamboo communities. The biomasses of rhizomes and fine roots were 16.7 t ha(-1) and 27.9 t ha(-1), respectively. Annual soil respiration was 52.3 t CO(2) ha(-1) yr(-1), the highest among those determined in Japan. The gross production was high: 32.8 t C ha(-1) yr(-1). Allocation of the products to its root system was also high: 34% to gross production and 46% to the fluxes out of the leaves into other compartments of the ecosystem. This resulted in the reduced above-ground net production of 18.1 t ha(-1) yr(-1), which fell within the average range of productivity of forests under similar climate conditions. This paper discusses the correspondence of the allocation pattern with the successful range expansion.

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References

  • Anderson, J. M. 1973. Carbon dioxide evolution from two temperate deciduous wood land soils. J. Appl. Ecol. 10: 361-378.

    Google Scholar 

  • Buol, S.W., Hole, F. D. & McCracken, R. J. 1989. Soil Genesis and Classification (3rd edition). Iowa State University Press, Ames.

    Google Scholar 

  • Canham, C. D. 1988. Growth and canopy architecture of shadetolerant trees: response to canopy gaps. Ecology 67: 786-795.

    Google Scholar 

  • Cataldo, D. A., Haroon, M., Schrader, L. E. & Youngs, V. L. 1975. Rapid colorimetric determination of nitrate in plant tissue by nitration of salicylic acid. Comm. Soil Sci. Plant Anal. 6: 71- 80.

    Google Scholar 

  • Chiba, K. 1975. Studies on the mineralization rate of organic matter in forest soils and the rate of the soil respiration of forests.Mem. Faculty Agric., Kochi Univ. 27: 1-108.

    Google Scholar 

  • Chiba, K. & Tsutsumi, T. 1967. A study on the soil respiration of forests (1) The relationships between the soil respiration and air temperature. Bull. Kyoto Univ. Forests 39: 91-99.

    Google Scholar 

  • Chiba, K., Irie, Y. & Tsutsumi, T. 1968. A study on the soil respiration of forests (2) Number of plots and days to measure the soil respiration. Bull. Kyoto Univ. Forests 40: 131-139.

    Google Scholar 

  • Denslow, J. S. 1987. Tropical rainforest gaps and tree species diversity. Ann. Rev. Ecol. Syst. 18: 431-451.

    Google Scholar 

  • Edwards, N. T. & Harris, W. F. 1977. Carbon cycling in a mixed deciduous forest floor. Ecology 58: 431-437.

    Google Scholar 

  • Edwards, N. T. & Sollins, P. 1973. Continuous measurement of carbon dioxide evolution from partitioned forest floor components. Ecology 54: 406-412.

    Google Scholar 

  • Ewel, K. C., Crooper, W. P. & Gholz, H. L. 1987. Soil CO2 evolution in Florida slash pine plantations (2) Importance of root respiration. Can. J. Forest Res. 17: 330-333.

    Google Scholar 

  • Food and Agriculture Organization of the United Nations 1990. Guidelines for Soil Profile Description. Food and Agriculture Organization of the United Nations, Rome.

    Google Scholar 

  • Hesketh, J. D., Baker, D. N. & Duncan, W. G. 1971. Simulation of growth and yield in cotton: respiration and carbon balance. Crop Sci. 11: 394-398.

    Google Scholar 

  • Isagi, Y. 1994. Carbon stock and cycling in a bamboo Phyllostachys bambusoidesstand. Ecol. Res. 9: 47-55.

    Google Scholar 

  • Isagi, Y., Kawahara, T. & Kamo, K. 1993. Biomass and net production in a bamboo Phyllostachys bambusoides stand. Ecol. Res. 8: 123-133.

    Google Scholar 

  • Isagi, Y. & Torii, A. (in press) Range expansion and its mechanism in a naturalized bamboo species, Phyllostachys pubescensin Japan. Journal of Sustainable Forestry.

  • Kimura, M., Yokoi, Y. & Hogetsu, K. 1978. Quantitative relationships between growth and respiration (2) Evaluation of constructive and maintenance respiration in growing Helianthus tuberosusleaves. Bot. Mag. Tokyo 91: 43-56.

    Google Scholar 

  • Kira, T. 1975. Primary production of forests. Pp. 5-40. In: J. P. Cooper (ed.), Photosynthesis and productivity in different environments. Cambridge University Press, Cambridge.

    Google Scholar 

  • Kira, T. 1977. Production rates. Pp. 101-114. In: T. Shidei & T. Kira (eds.), Primary productivity of Japanese forests. University of Tokyo Press, Tokyo.

    Google Scholar 

  • Kira, T. 1978. Carbon cycling. Pp. 272-276. In: T. Kira, Y. Ono & T. Hosokawa (eds.), Biological Production in aWarm-temperate Evergreen Oak Forest of Japan. University of Tokyo Press, Tokyo.

    Google Scholar 

  • Kirita, H. 1971a. Re-examination of the observationmethod ofmeasuring soil respiration under field conditions (4). An improved absorption method using a disc of plastic sponge as absorbent holder. Jpn. J. Ecol. 21: 119-127.

    Google Scholar 

  • Kirita, H. 1971b. Studies of soil respiration in warm-temperate evergreen broadleaf forests of southwestern Japan. Jpn. J. Ecol. 21: 230-244.

    Google Scholar 

  • Kucera, C. L. & Kirkham, D. R. 1971. Soil respiration studies in tall grass prairie in Missouri. Ecology 52: 912-915.

    Google Scholar 

  • Lieth, H. 1975. Modeling the primary productivity of the world. Pp. 237-263. In: H. Lieth & R. H. Whitakker (eds), Primary Productivity of the Biosphere. Springer-Verlag, New York.

    Google Scholar 

  • McClure, F. A. 1966. The Bamboos. Harvard University Press, Massachusetts.

    Google Scholar 

  • Merino, J., Field, C. & Mooney, H. A. 1982. Construction and maintenance costs of Mediterranean-climax evergreen and deciduous leaves (1) Growth and CO2 exchange analysis. Oecologia 53: 208-213.

    Google Scholar 

  • Nakane, K. 1975. Dynamics of soil organic matter in different parts on a slope under evergreen oak forest. Jpn. J. Ecol. 25: 204-216.

    Google Scholar 

  • Nakane, K. 1980. Comparative studies of cycling of soil organic carbon in three primeval moist forests. Jpn. J. Ecol. 30: 155- 172.

    Google Scholar 

  • Nakane, K., Yamamoto, M. Tsubota, H. 1983. Estimation of root respiration rate in a mature forest ecosystem. Jpn. J. Ecol. 33: 397-408.

    Google Scholar 

  • Ogawa, H. 1977. Principles and methods of estimating primary production in forests. Pp. 29-35. In: T. Shidei & T. Kira (eds), Primary Productivity of Japanese Forests. University of Tokyo Press, Tokyo.

    Google Scholar 

  • Ogawa, H. & Kira, T. 1977. Methods of estimating forest biomass. Pp. 15-25. In: T. Shidei & T. Kira (eds), Primary Productivity of Japanese Forests. University of Tokyo Press, Tokyo.

    Google Scholar 

  • Oshima, Y. 1961. Ecological studies of Sasacommunities I. Productive structure of some of the Sasacommunities in Japan. Bot. Mag. Tokyo 74: 199-210.

    Google Scholar 

  • Phillipson, J., Putman, R. J., Steel, J. & Woodell, S. R. J. 1975. Litter input, litter decomposition and the evolution of carbon dioxide in beech, woodland-wytham wood, Oxford. Oecologia 20: 203-217.

    Google Scholar 

  • Raich, J. W. & Nadelhoffer, K. J. 1989. Belowground carbon allocation in forest ecosystems: Global trends. Ecology 70: 1346- 1354.

    Google Scholar 

  • Sakai, M. & Tsutsumi, T. 1987. Carbon cycles of two different soils in a cool-temperate forest in Japan (2) Seasonal variations of soil respiration rates under the effects of soil environmental factors. J. Jpn. Forestry Soc. 69: 41-48.

    Google Scholar 

  • Simono T., Takeda, H., Iwatsubo, G. & Tsutsumi, T. (1989) Seasonal changes in soil respiration rates from the floor of Chamaecyparis obtusaand Cryptomeria japonicaplantations. Bull. Kyoto Univ. Forests 61: 46-59.

    Google Scholar 

  • Suzuki, S. 1978. Index to Japanese Bambusaceae. Gakken, Tokyo.

    Google Scholar 

  • Suzuki, T. 1989. Biomass and productivity of bamboo stands. Reports of the Tropical Agriculture Research Center, Japan 65: 94-97.

    Google Scholar 

  • Schlesinger, W. H. 1977. Carbon balance in terrestrial detritus. Ann. Rev. Ecol. System. 8: 51-81.

    Google Scholar 

  • Uchimura, E. 1978. Ecological studies on cultivation of tropical bamboo forest in the Philippines. Bull. Forestry Forest Products Res. Inst. 301: 79-118.

    Google Scholar 

  • Ueda, K. 1960. Studies on the physiology of bamboo. Bull. of the Kyoto Univ. Forests 30: 1-69.

    Google Scholar 

  • Veblen, T. T., Schlegel, F. M. & Escobar, R. (1980) Dry-matter production of two species of bamboo (Chesquea culeouand C. tenuiflora) in South-Central Chile. J. Ecol. 68: 397-404.

    Google Scholar 

  • Walter, H. 1952. —Eine einfache Methode zur ökologischen Erfassung des CO2-Factors am Standort. Ber. Deutschen Bot. Sesellschaft 65: 175-182.

    Google Scholar 

  • Williams, K., Percival, F., Merino, J. & Mooney, H. A. 1987. Estimation of tissue construction cost from heat of combustion and organic nitrogen content. Plant, Cell Envir. 10: 725-734.

    Google Scholar 

  • Witkamp, M. & Frank, M. L. 1969. Evolution of CO2 from litter, humus and subsoil of a pine stand. Pedobiologia 9: 358-365.

    Google Scholar 

  • Yamamoto, S. 1992. The gap theory in forest dynamics. Bot. Mag. Tokyo 105: 375-383.

    Google Scholar 

  • Yokoi, Y., Kimura, M. & Hogetsu, K. 1978. Quantitative relationships between growth and respiration (1) Components of respiratory loss and growth efficiencies of etiolated red bean seedlings. Bot. Mag. Tokyo 91: 31-41.

    Google Scholar 

  • Yoneda, T. & Okata, H. 1987. An assessment of root respiration in a Solidago altissimacommunity. Mem. of the Osaka Kyoiku Univ. Series III 36: 147-158.

    Google Scholar 

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Isagi, Y., Kawahara*, T., Kamo*, K. et al. Net production and carbon cycling in a bamboo Phyllostachys pubescens stand. Plant Ecology 130, 41–52 (1997). https://doi.org/10.1023/A:1009711814070

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