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Mass and nutrient dynamics of decaying litter from Passiflora mollissima and selected native species in a Hawaiian montane rain forest

Published online by Cambridge University Press:  10 July 2009

Paul G. Scowcroft
Paul G. Scowcroft
Affiliation:
Institute of Pacific Islands Forestry, USDA Forest Service, Pacific Southwest Research Station, 1151 Punchbowl St., Rm. 323, Honolulu, HI 96813, USA.
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Abstract

The structure and functioning of Acacia koa-Metrosideros polymorpha forests between 1200 and 1800 m elevation on the island of Hawaii are being threatened by Passiflora mollissima, an aggressive introduced liana from South America. This study was done to evaluate the short-term decomposition dynamics of Passiflora and selected native leaf and twig litter. The nutrient-rich, non-sclerophyllous Passiflora leaves completely disappeared in less than 5 mo. The estimated time for native leaf litter to lose 95% of initial dry weight ranged from 1.65 y for N-rich Acacia phyllodes to 6.67 y for Cibotium glaucum; for woody litter, the time ranged from 4.5 y for Acacia twigs to 23 y for Acacia bark. Except for Cibotium frond litter, decay rates were significantly correlated with initial lignin-ash ratios. Passiflora litter did not accelerate decomposition of Acacia and Metrosideros leaf litter. Passiflora, Acacia, and Metrosideros leaf litter showed net mineralization of N, P, Ca, K, and Mg during the study. Cibotium frond litter showed significant accumulation of N, Ca, and Mg; P levels stayed constant and K was rapidly lost. In general, twigs experienced a net loss of most nutrients, while bark experienced either no change or a significant net gain of nutrients. Nutrient cycling has increased in P. mollissima infested forests.

Keywords

Acacia koaCibotium glaucumdecompositionHawaiilitter qualityMetrosideros polymorphanutrient cyclingPassiflora mollissima
Type
Research Article
Information
Journal of Tropical Ecology , Volume 13 , Issue 3 , May 1997 , pp. 407 - 426
Copyright
Copyright © Cambridge University Press 1997

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References

LITERATURE CITED

Aber, J. D., Melillo, J. M. & Mcclaugherty, C. A. 1990. Predicting long-term patterns of mass loss, nitrogen dynamics, and soil organic matter formation from initial fine litter chemistry in temperate forest ecosystems. Canadian Journal of Botany 68:2201–2208.CrossRefGoogle Scholar
Association of Official Analytical Chemists. 1980. Official methods of analysis. (13th edition). Association of Official Analytical Chemists, Washington, DC. 1018 pp.Google Scholar
Balakrishnan, N. & Mueller-Dombois, D. 1983. Nutrient studies in relation to habitat types and canopy dieback in the montane rain forest ecosystem, Island of Hawaii. Pacific Science 37:339–359.Google Scholar
Blair, J. M., Parmelee, R. W. & Beare, M. H. 1990. Decay rates, nitrogen fluxes, and decomposer communities of single- and mixed-species foliar litter. Ecology 71:1976–1985.CrossRefGoogle Scholar
JrChapin, F. S., Vitousek, P. M. & Van Cleve, K. 1986. The nature of nutrient limitation in plant communities. American Naturalist 127:48–58.CrossRefGoogle Scholar
Chapman, K., Whittaker, J. B. & Heal, O. W. 1988. Metabolic and faunal activity in litters of tree mixtures compared with pure stands. Agriculture, Ecosystems and Environment 24:33–40.CrossRefGoogle Scholar
Constantinides, M. & Fownes, J. H. 1994. Nitrogen mineralization from leaves and litter of tropical plants: relationship to nitrogen, lignin and soluble polyphenol concentrations. Soil Biology and Biochemistry 26:49–55.CrossRefGoogle Scholar
Crews, T. E., Kitayama, K., Fownes, J. H., Riley, R. H., Herbert, D. A., Mueller-Dombois, D. & Vitousek, P. M. 1995. Changes in soil phosphorus fractions and ecosystem dynamics across a long chronosequence in Hawaii. Ecology 76:1407–1424.CrossRefGoogle Scholar
Escobar, L. K. 1980. Interrelationships of the edible species of Passiflora centering around Passiflora mollissima (H.B.K.) Bailey subgenus Tacsonia. Unpublished Ph.D. dissertation. University of Texas, Austin.Google Scholar
Fogel, R. & JrCromack, K. 1977. Effect of habitat and substrate quality on Douglas fir litter decomposition in western Oregon. Canadian Journal of Botany 55:1632–1640.CrossRefGoogle Scholar
Freund, R. J., Littell, R. C., & Spector, P. C. 1986. SAS system for linear models. SAS Institute Inc., Cary, North Carolina. 210 pp.Google Scholar
Gerrish, G. & Mueller-Dombois, D. 1980. Behavior of native and non-native plants in two tropical rainforests on Oahu, Hawaiian Islands. Phytocoenologia 8:237–295.CrossRefGoogle Scholar
Gerrish, G., Mueller-Dombois, D. & Bridges, K. W. 1988. Nutrient limitation and Metrosideros forest dieback in Hawaii. Ecology 69:723–727.CrossRefGoogle Scholar
Giambelluca, T. W., Nullet, M. A. & Schroeder, T. A. 1986. Rainfall atlas of Hawaii. Water Resources Research Center Rep. R76. State of Hawaii, Department of Land and Natural Resources, Division of Water and Land Development, Honolulu, HI. 267 pp.Google Scholar
Gilbert, L. E. 1975. Ecological consequences of a coevolved mutualism between butterflies and plants. Pp. 210–224 in Gilbert, L. E. and Raven, D. H. (eds). Coevolution of animals and plants. University of Texas Press, Austin, TX. 263 pp.CrossRefGoogle Scholar
Goering, H. K., & Van Soest, P. J. 1970. Forage fiber analysis: apparatus, reagents, procedures, and some applications. Agricultural Handbook No. 379. U.S. Department of Agriculture, Agricultural Research Service, Washington, DC.20 pp.Google Scholar
Hegarty, E. E. 1991. Leaf litter production by lianes and trees in a sub-tropical Australian rain forest. Journal Tropical Ecology 7:201–214.CrossRefGoogle Scholar
Heanes, D. L. 1984. Determination of total organic C in soils by improved chromic acid digestion and spectrophotometric procedure. Communications in Soil Science and Plant Analysis 15:1191–1213.CrossRefGoogle Scholar
Hladik, A. 1974. Importance des lianes dans la production foliaire de la foret équatoriale du Nord-Est du Gabon. Comptes Rendus de l'Académie des Sciences, Paris, 278 (série D):2527–2530.Google Scholar
Isaac, R. A. & Johnson, W. C. 1976. Determination of total nitrogen in plant tissue using a block digestor. Journal of the Association of Official Analytical Chemists 59:98–100.Google Scholar
Isaac, R. A. & Johnson, W. C. 1985. Elemental analysis of plant tissue by plasma emission spectroscopy – collaborative study. Journal of the Association of Official Analytical Chemists 68:449–505.Google Scholar
Khattree, R. & Naik, D. N. 1995. Applied multivariate statistics with SAS software. SAS Institute Inc., Cary, North Carolina. 396 pp.Google Scholar
Klemmedson, J. O. 1992. Decomposition and nutrient release from mixtures of Gambel oak and ponderosa pine leaf litter. Forest Ecology and Management 47:349–361.CrossRefGoogle Scholar
Laishram, I. D. & Yadava, P. S. 1988. Lignin and nitrogen in the decomposition of leaf litter in a sub-tropical forest ecosystem at Shiroy hills in northeastern India. Plant and Soil 106:59–64.CrossRefGoogle Scholar
La Caro, F. & Rudd, R. L. 1985. Leaf litter disappearance rates in Puerto Rican montane rain forest. Biotropica 17:269–276.CrossRefGoogle Scholar
La Rosa, A. M. 1984. The biology and ecology of Passiflora mollissima in Hawaii. Hawaii Cooperative National Park Resources Studies Unit Technical Report 50. University of Hawaii, Honolulu, HI. 168 pp.Google Scholar
Lavelle, P., Blanchart, E., Martin, A., Martin, S., Spain, A., Toutain, F., Barois, I. & Schaefer, R. 1993. A hierarchical model for decomposition in terrestrial ecosystems: application to soils of the humid tropics. Biotropica 25:130–150.CrossRefGoogle Scholar
Lisanework, N. & Michelsen, A. 1994. Litterfall and nutrient release by decomposition in three plantations compared with a natural forest in the Ethiopian highland. Forest Ecology and Management 65:149–164.CrossRefGoogle Scholar
Meentemeyer, V. 1978. Macroclimate and lignin control of litter decomposition rates. Ecology 59:465–472.CrossRefGoogle Scholar
Melillo, J. M., Aber, J. D. & Muratore, J. F. 1982. Nitrogen and lignin control of hardwood leaf litter decomposition dynamics. Ecology 63:621–626.CrossRefGoogle Scholar
Mooney, H. A., Field, C. & Vasquez-Yanes, C. 1984. Photosynthetic characteristics of wet tropical forest plants. Pp. 113–128 in Medina, E., Mooney, H. A. & Vazquez-Yanes, C. (eds). Physiological ecology of plants of the wet tropics. Dr. W. Junk, The Hague. 254 pp.CrossRefGoogle Scholar
Olson, J. S. 1963. Energy storage and the balance of producers and decomposers in ecological systems. Ecology 44:322–331.CrossRefGoogle Scholar
Perry, D. A. 1994. Forest ecosystems. Johns Hopkins University Press, Baltimore. 649 pp.Google Scholar
SAS Institute. 1985. SAS user's guide: Statistics, version 5 edition. SAS Institute Inc., Cary, North Carolina. 956 pp.Google Scholar
SAS Institute. 1992. SAS technical report P-229, SAS/STAT software: Changes and enhancements, release 6.07. SAS Institute Inc., Cary, North Carolina.Google Scholar
Scowcroft, P. G. 1986. Fine litterfall and leaf decomposition in a montane Acacia-Metrosideros rain forest. Pp. 66–82 in Smith, C. W. & Stone, C. P. (eds). Proceedings 6th conference in natural sciences, Hawaii Volcanoes National Park; 1986 06 13; Hawaii National Park, HI. University of Hawaii Cooperative National Park Resources Studies Unit, Honolulu, HI. 98 pp.Google Scholar
Scowcroft, P. G. & Nelson, R. E. 1976. Disturbance during logging stimulates regeneration of koa. Res. Note PSW-306. U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station, Berkeley, CA. 7 pp.Google Scholar
Seastedt, T. R. 1984. The role of microarthropods in decomposition and mineralization processes. Annual Review of Entomology 29:25–46.CrossRefGoogle Scholar
Shuman, G. E., Stanley, M. A. & Knudsen, D. 1973. Automated total nitrogen analysis of soil and plant materials. Soil Science Society of America Proceedings 37:480–481.CrossRefGoogle Scholar
Soil Survey Staff. 1994. Keys to soil taxonomy, 6th ed.U.S. Department of Agriculture, Soil Conservation Service, Washington, D.C.306 pp.Google Scholar
Staaf, H. 1980. Influence of chemical composition, addition of raspberry leaves, and nitrogen supply on decomposition rate and dynamics of nitrogen and phosphorus in beech leaf litter. Oikos 35:55–62.CrossRefGoogle Scholar
Swift, M. J., Heal, O. W. & Anderson, J. M. 1979. Decomposition in terrestrial ecosystems. Studies in ecology. Vol. 5. Blackwell Scientific Publications, Oxford UK. 372 pp.CrossRefGoogle Scholar
Tanner, E. V. J. 1981. The decomposition of leaf litter in Jamaican montane rain forests. Journal of Ecology 69:263–275.CrossRefGoogle Scholar
Tanner, E. V. J., Kapos, V. & Franco, W. 1992. Nitrogen and phosphorus fertilization effects on Venezuelan montane forest trunk growth and litterfall. Ecology 73:78–86.CrossRefGoogle Scholar
Tanner, E. V. J., Kapos, V., Freskos, S., Healey, J. & Theobold, A. M. 1990. Nitrogen and phosphorus fertilization of Jamaican montane forest trees. Journal of Tropical Ecology 6:231–238.CrossRefGoogle Scholar
Taylor, B. R., Parkinson, D. & Parsons, W. F. J. 1989a. Nitrogen and Iignin content as predictors of litter decay rates: a microcosm test. Ecology 70:97–104.CrossRefGoogle Scholar
Taylor, B. R., Parsons, W. F. J. & Parkinson, D. 1989b. Decomposition of Populus tremuloides leaf litter accelerated by addition of Alnus crispa litter. Canadian Journal of Forestry Research 19:674–679.CrossRefGoogle Scholar
Thaiutsa, B. & Granger, O. 1979. Climate and the decomposition rate of tropical forest litter. Unasylva 31:28–35.Google Scholar
Thomas, W. A. 1968. Decomposition of loblolly pine needles with and without addition of dogwood leaves. Ecology 49:568–571.CrossRefGoogle Scholar
Thompson, M. V. & Vitousek, P. M. In Press. Asymbiotic nitrogen fixation and litter decomposition on a long soil-age gradient in Hawaiian montane rain forest. Biotropica.Google Scholar
Tian, G., Kang, B. T. & Brussaard, L. 1992. Biological effects of plant residues with contrasting chemical compositions under humid tropical conditions – decomposition and nutrient release. Soil Biology and Biochemistry 24:1051–1060.CrossRefGoogle Scholar
Vitousek, P. M. 1982. Nutrient cycling and nutrient use efficiency. American Midland Naturalist 119:553–572.CrossRefGoogle Scholar
Vitousek, P. M. & Walker, L. R. 1989. Biological invasion by Myrica faya in Hawai'i: plant demography, nitrogen fixation, ecosystem effects. Ecological Monographs 59:247–265.CrossRefGoogle Scholar
Vttousek, P. M., Loope, L. L. & Stone, C. P. 1987. Introduced species in Hawaii: biological effects and opportunities for ecological research. Trends in Ecology and Evolution 2:224–229.CrossRefGoogle Scholar
Vitousek, P. M., Matson, P. A. & Turner, D. R. 1988. Elevation and age gradients in Hawaiian montane rainforest: foliar and soil nutrients. Oecologia 77:565–570.CrossRefGoogle ScholarPubMed
Vitousek, P. M., Turner, D. R. & Kitayama, K. 1995. Foliar nutrients during long-term soil development in Hawaiian montane rain forest. Ecology 76:712–720.CrossRefGoogle Scholar
Vitousek, P. M., Turner, D. R., Parton, W. J. & Sanford, R. L. 1994. Litter decomposition on the Mauna Loa environmental matrix, Hawai'i: Patterns, mechanisms, and models. Ecology 75:418–429.CrossRefGoogle Scholar
Vitousek, P. M., Walker, L. R., Whiteaker, L. D. & Matson, P. A. 1993. Nutrient limitations to plant growth during primary succession in Hawaii Volcanoes National Park. Biogeochemistry 23:197–215.CrossRefGoogle Scholar
Warschauer, F. R., Jacobi, J. D., La Rosa, A. M., Scott, J. M. & Smith, C. W. 1983. The distribution, impact and potential management of the introduced vine Passiflora mollissima (Passifloraceae) in Hawai'i. Hawaii Cooperative National Park Resources Studies Unit Technical Report 48. University of Hawaii, Honolulu, HI.39 pp.Google Scholar
White, D. L., Haines, B. L. & Boring, L. R. 1988. Litter decomposition in southern Appalachian black locust and pine-hardwood stands: litter quality and nitrogen dynamics. Canadian Journal of Forestry Research 18:54–63.CrossRefGoogle Scholar
Wieder, R. K. & Lang, G. E. 1982. A critique of the analytical methods used in examining decomposition data obtained from litter bags. Ecology 63:1636–1642.CrossRefGoogle Scholar
Wiegert, R. G. 1970. Effects of ionizing radiation on leaf fall, decomposition and litter microarthropods of a montane rain forest. Pp. H89–H100 in Odum, H. T. & Pigeon, R. F. (eds). A tropical rain forest: a study of irradiation and ecology at El Verde, Puerto Rico. U.S. Atomic Energy Commission, Oak Ridge, TN.Google Scholar