Skip to main content
Log in

A stronger coordination of litter decomposability between leaves and fine roots for woody species in a warmer region

  • Original Paper
  • Published:
Trees Aims and scope Submit manuscript

Abstract

Key message

There is a positive correlation between leaf and root decomposition across species, both in a warm-temperate forest in Japan, as well as globally.

Abstract

Evaluating the effects of plant species traits on litter decomposition would increase our understanding of plant–soil feedbacks in forest ecosystems. Currently, an assessment of a possible coordination between leaf and root decomposition across different species is required. However, previous studies have generated conflicting results. We hypothesized that such inconsistencies may be attributed to differences in local climatic effects on the decomposition process. We focused on the linkages between leaf and fine-root decomposition of woody species in a warm-temperate forest, which have not been addressed in previous studies. We found a significant positive correlation between leaf and root decomposition, and this linkage may be attributed to a wider range of decomposition rates across the species in our study forest. Additionally, we combined our data with those of previous studies of woody species to infer a global linkage in the decomposition process between leaves and roots. We found a positive correlation in decomposition rates between leaves and roots at the global scale, as well as a relatively strong correlation in warmer regions. These results support the importance of litter quality on biogeochemical processes and suggest that synergetic interactions between climate and plant communities could be amplified in a warmer future.

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.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Adams MB, Campbell RG, Allen HL, Davey CB (1987) Root and foliar nutrient concentrations in loblolly pine: effects of season, site, and fertilization. For Sci 33:984–996

    Google Scholar 

  • Aerts R (1990) Nutrient use efficiency in evergreen and deciduous species from heathlands. Oecologia 84:391–397

    Article  Google Scholar 

  • Aerts R (1997) Climate, leaf litter chemistry and leaf litter decomposition in terrestrial ecosystems: a triangular relationship. Oikos 79:439–449. doi:10.2307/3546886

    Article  Google Scholar 

  • Aulen M, Shipley B, Bradley R (2012) Prediction of in situ root decomposition rates in an interspecific context from chemical and morphological traits. Ann Bot 109:287–297. doi:10.1093/aob/mcr259

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bardgett RD, Wardle DA (2010) Aboveground–belowground linkages: biotic interactions, ecosystem processes, and global change. Oxford University Press, New York

    Google Scholar 

  • Berg B, McClaugherty CA (2008) Plant litter, decomposition, humus formation, carbon sequestration, second edn. Springer-Verlag, Berlin

  • Berg B et al (1993) Litter mass loss rates in pine forests of Europe and Eastern United States: some relationships with climate and litter quality. Biogeochemistry 20:127–159

    Article  Google Scholar 

  • Birouste M, Kazakou E, Blanchard A, Roumet C (2012) Plant traits and decomposition: are the relationships for roots comparable to those for leaves? Ann Bot 109:463–472. doi:10.1093/aob/mcr297

    Article  PubMed  PubMed Central  Google Scholar 

  • Chapin FS III, Matson PA, Vitousek PM (2011) Principles of terrestrial ecosystem ecology. Springer, New York

    Book  Google Scholar 

  • Cornelissen JHC (1996) An experimental comparison of leaf decomposition rates in a wide range of temperate plant species and types. J Ecol 84:573–582. doi:10.2307/2261479

    Article  Google Scholar 

  • Cornelissen JHC, Thompson K (1997) Functional leaf attributes predict litter decomposition rate in herbaceous plants. New Phytol 135:109–114

    Article  Google Scholar 

  • Cornwell WK et al (2008) Plant species traits are the predominant control on litter decomposition rates within biomes worldwide. Ecol Lett 11:1065–1071. doi:10.1111/j.1461-0248.2008.01219.x

    Article  PubMed  Google Scholar 

  • Couteaux M-M, Bottner P, Berg B (1995) Litter decomposition, climate and litter quality. Trends Ecol Evol 10:63–66

    Article  CAS  PubMed  Google Scholar 

  • Craine JM (2009) Resource strategies of wild plants. Princeton University Press, Princeton

    Book  Google Scholar 

  • Craine JM, Lee WG, Bond WJ, Williamas RJ, Johnson LC (2005) Environmental constraints on a global relationship among leaf and root traits of grasses. Ecology 86:12–19

    Article  Google Scholar 

  • Esau K (1964) Plant anatomy, 2nd edn. Wiley, New York

    Google Scholar 

  • Fan P, Guo D (2010) Slow decomposition of lower order roots: a key mechanism of root carbon and nutrient retention in the soil. Oecologia 163:509–515. doi:10.1007/s00442-009-1541-4

    Article  PubMed  Google Scholar 

  • Fortunel C et al (2009) Leaf traits capture the effects of land use changes and climate on litter decomposability of grasslands across Europe. Ecology 90:598–611

    Article  PubMed  Google Scholar 

  • Freschet GT, Cornelissen JH, van Logtestijn RS, Aerts R (2010a) Substantial nutrient resorption from leaves, stems and roots in a subarctic flora: what is the link with other resource economics traits? New Phytol 186:879–889. doi:10.1111/j.1469-8137.2010.03228.x

    Article  CAS  PubMed  Google Scholar 

  • Freschet GT, Cornelissen JHC, van Logtestijn RSP, Aerts R (2010b) Evidence of the ‘plant economics spectrum’ in a subarctic flora. J Ecol 98:362–373. doi:10.1111/j.1365-2745.2009.01615.x

    Article  Google Scholar 

  • Freschet GT, Aerts R, Cornelissen JHC (2012) A plant economics spectrum of litter decomposability. Funct Ecol 26:56–65. doi:10.1111/j.1365-2435.2011.01913.x

    Article  Google Scholar 

  • Freschet GT et al (2013) Linking litter decomposition of above- and below-ground organs to plant–soil feedbacks worldwide. J Ecol 101:943–952. doi:10.1111/1365-2745.12092

    Article  CAS  Google Scholar 

  • Fujii S, Takeda H (2010) Dominant effects of litter substrate quality on the difference between leaf and root decomposition process above- and belowground. Soil Biol Biochem 42:2224–2230. doi:10.1016/j.soilbio.2010.08.022

    Article  CAS  Google Scholar 

  • Fujimaki R (2005) Mechanism and function of fine root production in forest ecosystems. Doctoral thesis, Kyoto University (Doctoral Thesis)

  • Goebel M et al (2011) Decomposition of the finest root branching orders: linking belowground dynamics to fine-root function and structure. Ecol Monogr 81:89–102. doi:10.1890/09-2390.1

    Article  Google Scholar 

  • Graaff M-Ad, Six J, Jastrow JD, Schadt CW, Wullschleger SD (2013) Variation in root architecture among switchgrass cultivars impacts root decomposition rates. Soil Biol Biochem 58:198–206. doi:10.1016/j.soilbio.2012.11.015

    Article  Google Scholar 

  • Hishi T (2007) Heterogeneity of individual roots within the fine root architecture: causal links between physiological and ecosystem functions. Journal of Forest Research 12:126–133. doi:10.1007/s10310-006-0260-5

    Article  Google Scholar 

  • Hobbie SE (1992) Effects of plant species on nutrient cycling. Trends Ecol Evol 7:336–339. doi:10.1016/0169-5347(92)90126-V

    Article  CAS  PubMed  Google Scholar 

  • Hobbie SE, Oleksyn J, Eissenstat DM, Reich PB (2010) Fine root decomposition rates do not mirror those of leaf litter among temperate tree species. Oecologia 162:505–513. doi:10.1007/s00442-009-1479-6

    Article  PubMed  Google Scholar 

  • Holdaway RJ, Richardson SJ, Dickie IA, Peltzer DA, Coomes DA (2011) Species- and community-level patterns in fine root traits along a 120,000-year soil chronosequence in temperate rain forest. J Ecol 99:954–963. doi:10.1111/j.1365-2745.2011.01821.x

    Article  Google Scholar 

  • IUSS Working Group WRB (2006) World reference base for soil resources 2006. FAO, Rome

    Google Scholar 

  • Kerkhoff AJ, Fagan WF, Elser JJ, Enquist BJ (2006) Phylogenetic and growth form variation in the scaling of nitrogen and phosphorus in the seed plants. Am Nat 168:E103–E122

    Article  PubMed  Google Scholar 

  • Killingbeck KT (1996) Nutrients in senesced leaves: keys to the search for potential resorption and resorption proficiency. Ecology 77:1716–1727

    Article  Google Scholar 

  • Lavelle P, Blanchart E, Martin A, Martin S, Spain A (1993) A hierarchical model for decomposition in terrestrial ecosystems: application to Soils of the Humid Tropics. Biotropica 25:130. doi:10.2307/2389178

    Article  Google Scholar 

  • Morishita K, Ando M (2002) Change in cover types of urban forests damaged by pine wilt disease in the northern part of Kyoto City. Forest Research (in Japanese) 74:35–45

    Google Scholar 

  • Norby RJ, Ledford J, Reilly CD, Miller NE, O’Neill EG (2004) Fine-root production dominates response of a deciduous forest to atmospheric CO2 enrichment. Proc Natl Acad Sci USA 101:9689–9693. doi:10.1073/pnas.0403491101

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Olson JS (1963) Energy storage and the balance of producers and decomposers in ecological systems. Ecology 44:322–331

    Article  Google Scholar 

  • Park BB, Yanai RD (2009) Nutrient concentrations in roots, leaves and wood of seedling and mature sugar maple and American beech at two contrasting sites. For Ecol Manage 258:1153–1160. doi:10.1016/j.foreco.2009.06.003

    Article  Google Scholar 

  • Perez-Harguindeguy N, Dıaz S, Cornelissen JHC, Vendramini F, Cabido M, Castellanos A (2000) Chemistry and toughness predict leaf litter decomposition rates over a wide spectrum of functional types and taxa in central Argentina. Plant Soil 218:21–30

    Article  CAS  Google Scholar 

  • Pregitzer KS, DeForest JL, Burton AJ, Allen MF, Ruess RW, Hendrick RL (2002) Fine root architecture of nine North American trees. Ecol Monogr 72:293–309. doi:10.2307/3100029

    Article  Google Scholar 

  • Rasse DP, Rumpel C, Dignac M-F (2005) Is soil carbon mostly root carbon? Mechanisms for a specific stabilisation. Plant Soil 269:341–356. doi:10.1007/s11104-004-0907-y

    Article  CAS  Google Scholar 

  • Silver WL, Miya RK (2001) Global patterns in root decomposition: comparisons of climate and litter quality effects. Oecologia 129:407–419. doi:10.1007/s004420100740

    Article  Google Scholar 

  • Smith MD, Knapp AK, Collins SL (2009) A framework for assessing ecosystem dynamics in response to chronic resource alterations induced by global change. Ecology 90:3279–3289

    Article  PubMed  Google Scholar 

  • Swift MJ, Heal OW, Anderson JM (1979) Decomposition in terrestrial ecosystems. Blackwell Scientific Publications, Oxford, London

    Google Scholar 

  • Takeda H, Ishida Y, Tsutsumi T (1987) Decomposition of leaf litter in relation to litter quality and site conditions. Memoirs of the College of Agriculture, Kyoto Univ 130:17–38

    Google Scholar 

  • Tjoelker MG, Craine JM, Wedin D, Reich PB, Tilman D (2005) Linking leaf and root trait syndromes among 39 grassland and savannah species. New Phytol 167:493–508. doi:10.1111/j.1469-8137.2005.01428.x

    Article  CAS  PubMed  Google Scholar 

  • Tsutsumi T (1973) Nutrient Production in terrestrial plant community, vol 1b. Lectures of Ecology, Kyoritsu Shuppan, Tokyo (in Japanese)

    Google Scholar 

  • Wang H, Liu S, Mo J (2010) Correlation between leaf litter and fine root decomposition among subtropical tree species. Plant Soil 335:289–298. doi:10.1007/s11104-010-0415-1

    Article  CAS  Google Scholar 

  • Withington JM, Reich PB, Oleksyn J, Eissenstat DM (2006) Comparisons of structure and life span in roots and leaves among temperate trees. Ecol Monogr 76:381–397

    Article  Google Scholar 

  • Zhang D, Hui D, Luo Y, Zhou G (2008) Rates of litter decomposition in terrestrial ecosystems: global patterns and controlling factors. J Plant Ecol 1:85–93. doi:10.1093/jpe/rtn002

    Article  Google Scholar 

Download references

Author contribution statement

SF and NM designed and conducted the experiment. SF and ASM analyzed the data. SF and ASM wrote the manuscript with critical inputs from NM and HT.

Acknowledgments

We thank Dr. Noriyuki Osada, Ms. Ayumi Kawamura Ms. Shoko Oguchi, and the staff of the Kamigamo Experimental Station, Field Science Education and Research Center of Kyoto University for their support of this study. This study was supported by the Fujiwara Natural History Foundation and by the Japan Society for the Promotion of Science (JSPS) Grant-in-Aid for Young Scientists (No. 25850115 to S.F.). We thank Dr. Ulrich Lüttge, guest Editor and anonymous reviewers for their helpful comments.

Conflict of interest

The authors declare that they have no conflict of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Saori Fujii.

Additional information

Communicated by T. Koike and K. Noguchi.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOCX 364 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Fujii, S., Makita, N., Mori, A.S. et al. A stronger coordination of litter decomposability between leaves and fine roots for woody species in a warmer region. Trees 30, 395–404 (2016). https://doi.org/10.1007/s00468-015-1221-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00468-015-1221-4

Keywords

Navigation