Skip to main content
Log in

Autumn leaf colours as indicators of decomposition rate in sycamore (Acer pseudoplatanus L.)

  • Published:
Plant and Soil Aims and scope Submit manuscript

Abstract

We tested the hypothesis that there is a causal connection between autumn colour, nutrient concentration and decomposibility of fresh leaf litter. Samples from patches of different autumn colours within the leaves of the deciduous tree sycamore (Acer pseudoplatanus) were sealed into litter bags and incubated for one winter in an outdoor leaf mould bed. Green leaf patches were decomposed faster than yellow or brown patches and this corresponded with the higher N and P concentrations in the former. Black patches, indicating colonisation by the tar spot fungus Rhytisma acerinum, were particularly high in P, but were decomposed very slowly, owing probably to resource immobilisation by the fungus. The results supported the hypothesis and were consistent with a previous study reporting an interspecific link between autumn coloration and decomposition rate. Autumn leaf colour of deciduous woody plants may serve as a useful predictor of litter decomposibility in ecosystem or biome scale studies where extensive direct measurements of litter chemistry and decomposition are not feasible.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Aerts R 1995 The advantages of being evergreen. Trends Ecol. Evol. 10, 402–407.

    Article  Google Scholar 

  • Aerts R 1997 Climate, leaf litter chemistry and leaf litter decomposition in terrestrial ecosystems: A triangular relationship. Oikos 79, 439–449.

    Google Scholar 

  • Aerts R and De Caluwe H 1997 Nutritional and plant-mediated controls on leaf litter decomposition of Carex species. Ecology 78, 244–260.

    Article  Google Scholar 

  • Ahmad I, Farrar J F and Whitbread R 1984 Fluxes of phosphorus in leaves of barley infected with brown rust. New Phytol. 98, 361–375.

    Article  CAS  Google Scholar 

  • Anderson J M 1991 The effects of climate change on decomposition processes in grassland and coniferous forests. Ecol. Appl. 1, 326–347.

    Google Scholar 

  • Berendse F 1994 Litter decomposability - a neglected component of plant fitness. J. Ecol. 82, 187–190.

    Article  Google Scholar 

  • Berg B and Ekbohm G 1991 Litter mass-loss rates and decomposition patterns in some needle and leaf litter types. Long-term decomposition in a Scots pine forest. VII. Can. J. Bot. 69, 1449–1456.

    Google Scholar 

  • Berg B, Ekbohm G, Johansson M B, McClaugherty C, Rutigliano F and De Santo A V 1996 Maximum decomposition limits of forest litter types: A synthesis. Can. J. Bot. 74, 659–672.

    Article  Google Scholar 

  • Broadfoot W M and Pierre W H 1939 Forest soil studies. I. Relation of rate of decomposition of tree leaves to their acidic-base balance and other chemical properties. Soil Sci. 48, 329–348.

    CAS  Google Scholar 

  • Cadisch G and Giller K E 1997 Driven by nature. Plant litter quality and decomposition. CAB International, Wallingford, UK. 409 p.

    Google Scholar 

  • Choong M F, Lucas P W, Ong J S Y, Pereira B, Tan H T W and Turner I M 1992 Leaf fracture toughness and sclerophylly: Their correlations and ecological implications. New Phytol. 121, 597–610.

    Article  Google Scholar 

  • Coley P D 1988 Effects of plant growth rate and leaf lifetime on the amount and type of antiherbivore defense. Oecologia 74, 531–536.

    Article  Google Scholar 

  • Cornelissen J H C 1996 An experimental comparison of leaf decomposition rates in a wide range of temperate plant species and types. J. Ecol. 84, 573–582.

    Article  Google Scholar 

  • Cornelissen J H C, Pérez-Harguindeguy N, Díaz S, Grime, J P, Marzano B, Cabido M and Cerabolini B 1999 Leaf structure and defence control litter decomposition rate across species and life forms in regional floras on two continents. New Phytol. 143, 191–200.

    Article  Google Scholar 

  • Cornelissen J H C and Thompson K 1997 Functional leaf attributes predict litter decomposition rate in herbaceous plants. New Phytol. 135, 109–114.

    Article  Google Scholar 

  • Cotrufo M F, Ineson P and Rowland A P 1994 Decomposition of tree leaf litters grown under elevated CO2: effect of litter quality. Plant Soil 163, 121–130.

    Google Scholar 

  • Coû teaux M-M, Bottner P and Berg B 1995 Litter decomposition, climate and litter quality. Trends Ecol. Evol. 10, 63–66.

    Article  Google Scholar 

  • Dighton J and Boddy L 1989 Role of fungi in nitrogen, phosphorus and sulphur cycling in temperate forest ecosystems. In Nitrogen, Phosphorus and Sulphur Utilization by Fungi. Eds. L Boddy, R Marchant and DJ Read. pp 269–298.Cambridge University Press, Cambridge.

    Google Scholar 

  • Ellis M B and Ellis J P 1997 Microfungi on land plants. The Richmond Publishing Co. Ltd.

  • Evans J R 1983 Nitrogen and photosynthesis in the flag leaf of wheat (Tricitum aestivum L.). Plant Physiol. 72, 297–302.

    Article  PubMed  CAS  Google Scholar 

  • Field C and Mooney H A 1986 The photosynthesis-nitrogen relationship in wild plants. In On the Economy of Plant Form and Function. Ed. TJ Givnish, pp 25–55. Cambridge University Press, Cambridge.

    Google Scholar 

  • Gallardo A and Merino J 1993 Leaf decomposition in two mediterranean ecosystems of Southwest Spain - influence of substrate quality. Ecology 74, 152–161.

    Article  Google Scholar 

  • Gange A C 1996 Positive effects of endophyte infection on sycamore aphids. Oikos 75, 500–510.

    Google Scholar 

  • Gillon D, Joffre R and Ibrahima A 1999 Can litter decomposability be predicted by near-infrared reflectance spectroscopy? Ecology 80, 175–186.

    Article  Google Scholar 

  • Gunnarsson T 1987 Selective feeding on a maple leaf by Oniscus asellus (Isopoda). Pedobiologia 30, 161–165.

    Google Scholar 

  • Hawksworth D L, Kirk P M, Sutton B C and Pegler D N 1995 Ainsworth and Bisby's dictionary of the fungi. 8th Edn. CAB International, Wallingford, UK.

    Google Scholar 

  • Herms D A and Mattson WJ 1992 The dilemma of a plant: To grow or defend? The Quarterly Review of Biology 67, 283–335.

    Article  Google Scholar 

  • Hobbie S E 1992 Effects of plants on nutrient cycling. Trends Ecol. Evol. 7, 336–339.

    Article  Google Scholar 

  • Huffaker R C 1982 Biochemistry and physiology of leaf proteins. In Encyclopedia of Plant Physiology, Vol. 14 A. Nucleic Acids and Proteins in Plants I: Structure, biochemistry and physiology of proteins. Eds. D Boulter and B Parthier pp 370–400. Springer, Berlin, Germany.

    Google Scholar 

  • Jones EW1944 Biological Flora of the British Isles: Acer L. J. Ecol. 32, 215–252.

    Google Scholar 

  • Leith I D and Fowler D 1988 Urban distribution of Rhytisma acerinum (Pers) Fries (tar-spot) on sycamore. New Phytol. 108, 175–181.

    Article  Google Scholar 

  • Meentemeyer V 1978 Macroclimate and lignin control over litter decomposition rates. Ecology 59, 465–472.

    Article  CAS  Google Scholar 

  • Melillo J M, Aber J D and Muratore J F 1982 Nitrogen and lignin control of hardwood leaf litter decomposition dynamics. Ecology 63, 571–584.

    Article  Google Scholar 

  • Ohlson M 1987 Spatial variation in decomposition rate of Carex rostrata leaves on a Swedish mire. J. Ecol. 75, 1191–1197.

    Article  Google Scholar 

  • Pastor J, Aber J D and McClaugherty C A 1984 Aboveground production and N and P cycling along a nitrogen mineralization gradient on Blackhawk island, Wisconsin. Ecology 65, 256–268.

    Article  CAS  Google Scholar 

  • Sanger J E 1971 Quantitative investigations of leaf pigments from their inception in buds through autumn coloration to decomposition in fallen leaves. Ecology 52, 1075–1089.

    Article  CAS  Google Scholar 

  • Stevens F L 1925 Plant disease fungi. The Macmillan Company, New York, USA.

    Google Scholar 

  • Swift M J, Heal O W and Anderson J M 1979 Decomposition in terrestrial ecosystems. Blackwell Scientific Publishers, Oxford, UK.

    Google Scholar 

  • Taylor B, Parkinson D and Parsons W J F 1989 Nitrogen and lignin content as predictors of litter decay rates: a microcosm test. Ecology 70, 97–104.

    Article  Google Scholar 

  • Taylor B R, Prescott C E, Parsons W J F and Parkinson D 1991 Substrate control of litter decomposition in four Rocky Mountain coniferous forests. Can. J. Bot. 69, 2242–2250.

    Google Scholar 

  • Upadhyay V P, Singh J S and Meentemeyer V 1989 Dynamics and weight loss of leaf litter in central Himalayan forests: Abiotic versus litter quality influences. J. Ecol. 77, 147–161.

    Article  Google Scholar 

  • Walters D R 1989 Phosphorus and nitrogen fluxes between plant and fungus in parasitic associations. In Nitrogen, Phosphorus and Sulphur Utilization by Fungi. Eds. L Boddy, R Marchant and DJ Read pp 131–153. Cambridge University Press, Cambridge, UK.

    Google Scholar 

  • Wessman C A, Aber J D, Peterson D L and Melillo J M 1988 Remote sensing of canopy chemistry and nitrogen cycling in temperate forest ecosystems. Nature 335, 154–156.

    Article  Google Scholar 

  • Wright W and Illius A W 1995 A comparative study of the fracture properties of five grasses. Funct. Ecol. 9, 269–278.

    Article  Google Scholar 

  • Yamashita T and Fujino A 1987 Change in content of ribulose 1,5-biphosphate carboxylase during senescence of mulberry (Morus alba L.) leaves. Soil Sci. Plant Nutr. 33, 431–438.

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cornelissen, J., Pérez-Harguindeguy, N., Gwynn-Jones, D. et al. Autumn leaf colours as indicators of decomposition rate in sycamore (Acer pseudoplatanus L.). Plant and Soil 225, 33–38 (2000). https://doi.org/10.1023/A:1026530214258

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1026530214258

Navigation