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Plant and Soil

, Volume 273, Issue 1–2, pp 279–289 | Cite as

Decomposition patterns of leaf litter of seven common canopy species in a subtropical forest: N and P dynamics

  • Xiaoniu XuEmail author
  • Eiji Hirata
Article

Abstract

Litter decomposition, governing nutrient and C cycling, is strongly influenced by the chemical litter quality. In order to determine the interspecific variation in leaf decomposition rates and to understand the chemical basis for such variation, decomposition dynamics of seven common canopy species was investigated over 2 year using the litterbag technique in a subtropical evergreen broad-leaved forest on Okinawa Island, Japan. The species studied are representatives of the vegetation in the study area and differed significantly in their chemical litter quality. Dry mass loss at the end of study varied in the order: Distylium racemosum< Quercus miyagii< Rapanea neriifolia< Symplocos confusa< Castanopsis sieboldii< Schima wallichii< Daphniphyllum glaucescens. All species showed a pattern characterized by a rapid initial decomposition followed by lower rates except for D. glaucescenswhich decomposition rate appeared to be rather constant. In the late phase, decomposition rates were correlated positively to initial N and ash contents and negatively to lignin content, lignin:N, C:N, and C:P ratios. The effects of N and lignin content or lignin:N ratio were stronger than other quality parameters. There was a wide range in patterns of N and P concentrations, from a net accumulation to a rapid loss in decomposition. The correlation between N and P release suggests that N and P dynamics may have influenced each other during litter decomposition. Analysis of initial quality for species showed that the C:P ratios were extremely high (range 1639–3811) but the N:P ratios were from 28 to 56, indicating a likely P-limitation for this forest. Our results suggest that P is an important control of litter decomposition and N and P dynamics.

Keywords

canopy species leaf decomposition lignin content litter quality nutrient release subtropical ecosystem 

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References

  1. Aerts, R 1997Climate, leaf litter chemistry and leaf litter decomposition in terrestrial ecosystems: a triangular relationshipOikos79439449Google Scholar
  2. Beare, M H, Parmelee, R W, Hendrix, P F, Cheng, W, Coleman, D C, Crossley, D A 1992Microbial and faunal interactions and effects on litter nitrogen and on decomposition in agroecosystemsEcol. Monogr.62569591Google Scholar
  3. Berendse, F, Bobbink, R, Rouwenhorst, G 1989A comparative study on nutrient cycling in wet heathland ecosystems. (II) Litter decomposition and nutrient mineralizationOecologia78338348CrossRefGoogle Scholar
  4. Berg, B, McClaugherty, C 2003Plant Litter: Decomposition, Humus formation, Carbon SequestrationSpringer-VerlagBerlinGoogle Scholar
  5. Bocock, K L, Gilbert, O J, Capstick, C K, Turner, D C, Ward, J S, Woodman, M J 1960Changes in leaf litter when placed on the surface of soil with contrasting humus typesJ. Soil Sci.1119Google Scholar
  6. Brown, S, Lugo, A E 1982Storage and production of organic matter in tropical forests and their role in the global carbon cycleBiotropica14161187Google Scholar
  7. Chapin, F S,III, Matson, P A, Mooney, H A 2002Principles of Terrestrial Ecosystem EcologySpringer-VerlagNew YorkGoogle Scholar
  8. Cornelissen, J H C, Thompson, K 1997Functional leaf attributes predict litter decomposition rate in herbaceous plantsNew Phytol.135109114CrossRefGoogle Scholar
  9. Coûteaux, M M, Bottner, P, Berg, B 1995Litter decomposition, climate and litter qualityTrends Ecol. Evol.106366CrossRefGoogle Scholar
  10. Cuevas, E, Brown, S, Lugo, A E 1991Above- and below-ground organic matter storage and production in a tropical pine plantation and a paired secondary forestPlant Soil135257268Google Scholar
  11. Dziadowiec, H 1987The decomposition of plant litterfall in a oak-linden-hornbeam forest and an oak-pine mixed forest of the Bialoweza national ParkActa Soc. Bot. Pol.56169185Google Scholar
  12. Editorial Committee of Experimental Methods for Plant Nutrition, Japan1990Experimental Methods for Plant NutritionHakuyusyaTokyo(in Japanese)Google Scholar
  13. Effland, M J 1977Modified procedure to determine acid insoluble lignin in wood and pulpTAPPI60143144Google Scholar
  14. Gallardo, A, Merino, J 1993Leaf decomposition in two Mediterranean ecosystems of southwest Spain: Influence of substrate qualityEcology74152161Google Scholar
  15. Gosz, J R, Likens, G E, Bormann, F H 1973Nutrient release from decomposing leaf and branch litter in the Hubbard Brook Forest, New HampshireEcol. Monogr.43173191Google Scholar
  16. Hatushima, S, Amano, T 1994Flora of the Ryukyus, South of Amami Island2The Biological Society of OkinawaNishiharaGoogle Scholar
  17. Heal, O W, Anderson, J M, Swift, M J 1997Plant litter quality and decomposition: a historical overviewCadisch, GGiller, K E eds. Driven by Nature: Plant Litter Quality and DecompositionsCAB InternationalLondon330Google Scholar
  18. Hirata, E, Asato, I, Ikuzawa, H, Terazono, R 2001Investigation on the Sustainable Management of Evergreen Broad-leaved Forest Dominated by Castanopsis sieboldiiin OkinawaOkinawa Development BureauJapanese Government(in Japanese)Google Scholar
  19. Hobbie, S E, Vitousek, P M 2000Nutrient limitation of decomposition in Hawaiian forestsEcology8118671877Google Scholar
  20. Itô, Y 1997Diversity of forest tree species in Yanbaru, the northern part of Okinawa IslandPlant Ecol.133125133CrossRefGoogle Scholar
  21. Kira, T 1989On the subtropical forestsMiyawaki, A eds. Vegetation of JapanShinbundoTokyo119127Vol. 10: Okinawa and Ogasawara,(in Japanese)Google Scholar
  22. Kwabiah, A B, Stoskopf, N C, Voroney, R P, Palm, C A 2001Nitrogen and phosphorus release from decomposing leaves under sub-humid tropical conditionsBiotropica33229240Google Scholar
  23. Loranger, G, Ponge, J F, Imbert, D, Lavelle, P 2002Leaf decomposition in two semi-evergreen tropical forest: influence of litter qualityBiol. Fertil. Soil35247252CrossRefGoogle Scholar
  24. Lousier, J D, Parkinson, D 1978Chemical element dynamics in decomposing leaf litterCan. J. Bot.5627952812Google Scholar
  25. McGroddy, M E, Silver, W L, Oliveira, R C,Jr. 2004The effect of phosphorus availability on decomposition dynamics in a seasonal lowland Amazonian forestEcosystems7172179CrossRefGoogle Scholar
  26. Melillo, J M, Aber, J B, Muratore, J F 1982Nitrogen and lignin control of hardwood leaf litter decomposition dynamicsEcology63621626Google Scholar
  27. Mesquita, R C G, Workman, S W, Neely, C L 1998Slow decomposition in a cecropia-dominated secondary forest of central AmazoniaSoil Biol. Biochem.30167175CrossRefGoogle Scholar
  28. Moro, M J, Domingo, F 2000Litter decomposition in four woody species in a Mediterranean climate: weight loss, N and P dynamicsAnn. Bot.8610651071CrossRefGoogle Scholar
  29. Olson, J S 1963Energy storage and the balance of producers and decomposers in ecological systemsEcology44322331Google Scholar
  30. Palm, C A, Rowland, A P 1997A minimum dataset for characterization of plant quality for decompositionCadisch, GGiller, K E eds. Driven by Nature: Plant Litter Quality and DecompositionCAB InternationalLondon379392Google Scholar
  31. Pastor, J, Stillwell, M A, Tilman, D 1987Little bluestem litter dynamics in Minnesota old fieldsOecologia72327330CrossRefGoogle Scholar
  32. Prescott, C E, Corbin, J P, Parkinson, D 1992Immobilization and availability of N and P in the forest floor of fertilized Rocky Mountain coniferous forestPlant Soil143110Google Scholar
  33. Rustad, L E 1994Element dynamics along a decay continuum in a red Spruce ecosystem, in Maine, USAEcology75867879Google Scholar
  34. Sariyildiz, T, Anderson, J M 2003aDecomposition of sun and shade leaves from three deciduous tree species, as affected by their chemical compositionBiol. Fertil. Soils37137146Google Scholar
  35. Sariyildiz, T, Anderson, J M 2003bInteractions between litter quality, decomposition and soil fertility: a laboratory studySoil Biol. Biochem.35391399CrossRefGoogle Scholar
  36. Schlesinger, W H, Hasey, M V 1981Decomposition of chaparral shrub foliage: losses of organic and inorganic constituents from deciduous and evergreen leavesEcology62762774Google Scholar
  37. Sinsabaugh, R L, Moorhead, D L, Linkins, A E 1994The enzymic basis of plant litter decomposition: emergence of an ecological processAppl. Soil Ecol.197111CrossRefGoogle Scholar
  38. Soil Survey Staff1999Soil Taxonomy: A Basic System of Soil Classification for Making and Interpreting Soil Surveys, USDA Natural Resource Conservation Service Agriculture HandbookU.S. Government Printing OfficeWashington DC869Google Scholar
  39. Songwe, N C, Okali, D U U, Fasehun, F E 1995Litter decomposition and nutrient release in a tropical rainforest, Southern Bakundu Forest Reserve: CameroonJ. Trop. Ecol.11333350Google Scholar
  40. StatSoft, Japan Inc. 1999 Statistica User’s Guide. (in Japanese).Google Scholar
  41. Sullivan, N H, Bowden, W H, McDowell, W H 1999Short-term disappearance of foliar litter in three species before and after a HurricaneBiotropica31382393Google Scholar
  42. Swift, M J, Heal, O W, Anderson, J M 1979Decomposition in Terrestrial EcosystemsBlackwellOxfordGoogle Scholar
  43. Swift, M J, Russel-Smith, A, Perfect, T J 1981Decomposition and mineral-nutrient dynamics of plant litter in a regenerating bush- fallow in sub-humid tropical NigeriaJ.␣Ecol.69981995Google Scholar
  44. Taylor, B R, Parkinson, D, Parsons, W F J 1989Nitrogen and lignin content as predictors of litter decay rates: a microcosm testEcology7097104Google Scholar
  45. Tian, G, Kang, B T, Brusaard, L 1992Biological effects of plant residues with contrasting chemical composition under humid tropical conditions: decomposition and nutrient releaseSoil Biol. Biochem.2410511060Google Scholar
  46. Vitousek, P M 2004Nutrient Cycling and Limitation: Hawaii as A Model SystemPrinceton University PressPrincetonGoogle Scholar
  47. Vitousek, P M, Turner, D R, Parton, W J, Sanford, R L 1994Litter decomposition on the Mauna Loa environmental matrix, Hawaii: patterns, mechanisms, and modelsEcology75418429Google Scholar
  48. Wardle, D A, Barker, G M, Bonner, I K, Nicholson, K S 1998Can comparative approaches based on plant ecophysiological traits predict the nature of biotic interactions and individual plant species effects in ecosystems?J. Ecol.86405420CrossRefGoogle Scholar
  49. Wedderburn, M E, Carter, J 1999Litter decomposition by four functional tree types for use in silvopastoral systemsSoil Biol. Biochem.31455461CrossRefGoogle Scholar
  50. Xu, X N, Hirata, E, Tokashiki, Y, Shinohara, T 2001aStructure and species diversity of subtropical evergreen broad-leaved forest in northern Okinawan Island, JapanJ. For. Res.6201210Google Scholar
  51. Xu, X N, Hirata, E, Tokashiki, Y, Enoki, T, Shinohara, T 2001bDifferences of soil properties between evergreen broad-leaved and pine forests in northern Okinawa IslandJapan. Jap. J. For. Environ.4318Google Scholar
  52. Xu, X N, Hirata, E, Shibata, H 2004aEffect of typhoon disturbance on fine litterfall and related nutrient input in a subtropical forest on Okinawa Island, JapanBas. Appl. Ecol.5271282CrossRefGoogle Scholar
  53. Xu, X N, Hirata, E, Enoki, T, Tokashiki, Y 2004bLeaf litter decomposition and nutrient dynamics in a subtropical forest after typhoon disturbancePlant Ecol.173161170CrossRefGoogle Scholar
  54. Xu X N, Wang Q and Hirata E 2004c Precipitation partitioning and related nutrient fluxes in a subtropical forest in Okinawa, Japan. Ann. For. Sci. (in press).Google Scholar

Copyright information

© Springer 2005

Authors and Affiliations

  1. 1.Department of ForestryAnhui Agricultural UniversityHefeiP.R. China
  2. 2.Field Science Center for Northern BiosphereHokkaido UniversityHokkaidoJapan
  3. 3.Faculty of AgricultureUniversity of the RyukyusOkinawaJapan

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