Skip to main content

Fine root chemistry and decomposition in model communities of north-temperate tree species show little response to elevated atmospheric CO2 and varying soil resource availability

Abstract

Rising atmospheric [CO2] has the potential to alter soil carbon (C) cycling by increasing the content of recalcitrant constituents in plant litter, thereby decreasing rates of decomposition. Because fine root turnover constitutes a large fraction of annual NPP, changes in fine root decomposition are especially important. These responses will likely be affected by soil resource availability and the life history characteristics of the dominant tree species. We evaluated the effects of elevated atmospheric [CO2] and soil resource availability on the production and chemistry, mycorrhizal colonization, and decomposition of fine roots in an early- and late-successional tree species that are economically and ecologically important in north temperate forests. Open-top chambers were used to expose young trembling aspen (Populus tremuloides) and sugar maple (Acer saccharum) trees to ambient (36 Pa) and elevated (56 Pa) atmospheric CO2. Soil resource availability was composed of two treatments that bracketed the range found in the Upper Lake States, USA. After 2.5 years of growth, sugar maple had greater fine root standing crop due to relatively greater allocation to fine roots (30% of total root biomass) relative to aspen (7% total root biomass). Relative to the low soil resources treatment, aspen fine root biomass increased 76% with increased soil resource availability, but only under elevated [CO2]. Sugar maple fine root biomass increased 26% with increased soil resource availability (relative to the low soil resources treatment), and showed little response to elevated [CO2]. Concentrations of N and soluble phenolics, and C/N ratio in roots were similar for the two species, but aspen had slightly higher lignin and lower condensed tannins contents compared to sugar maple. As predicted by source-sink models of carbon allocation, pooled constituents (C/N ratio, soluble phenolics) increased in response to increased relative carbon availability (elevated [CO2]/low soil resource availability), however, biosynthetically distinct compounds (lignin, starch, condensed tannins) did not always respond as predicted. We found that mycorrhizal colonization of fine roots was not strongly affected by atmospheric [CO2] or soil resource availability, as indicated by root ergosterol contents. Overall, absolute changes in root chemical composition in response to increases in C and soil resource availability were small and had no effect on soil fungal biomass or specific rates of fine root decomposition. We conclude that root contributions to soil carbon cycling will mainly be influenced by fine root production and turnover responses to rising atmospheric [CO2], rather than changes in substrate chemistry.

This is a preview of subscription content, access via your institution.

Fig. 1
Fig. 2
Fig. 3

References

  • Agrell J, Mcdonald EP, Lindroth RL (2000) Effects of CO2 and light on tree phytochemistry and insect performance. Oikos 88:259–272

    Article  CAS  Google Scholar 

  • Berg B (1984) Decomposition of root litter and some factors regulating the process: Long-term root litter decomposition in a Scots pine forest. Soil Biol Biochem 16:609–617

    Article  CAS  Google Scholar 

  • Blashke L, Forstreuter M, Sheppard LJ, Keith IK, Murray MB, Polle A (2002) Lignification in beech (Fagus sylvatica) grown at elevated CO2 concentrations: interaction with nutrient availability and leaf maturation. Tree Physiol 22:469–477

    Google Scholar 

  • Booker FL, Anttonen S, Heagle AS (1996) Catechin, proanthocyanidin and lignin contents of loblolly pine (Pinus taeda) needles after chronic exposure to ozone. New Phytol 132:483–492

    Article  CAS  Google Scholar 

  • Burton AJ, Pregitzer KS, Hendrick RL (2000) Relationships between fine root dynamics and nitrogen availability in Michigan hardwood forests. Oecologia 125:389–399

    Article  Google Scholar 

  • Burton AJ, Pregitzer KS, Crawford JN, Zogg GP, Zak DR (2004) Simulated chronic NO −3 deposition reduces soil respiration in northern hardwoods forests. Glob Change Biol 10:1–12

    Article  Google Scholar 

  • Curtis PS, Vogel CS, Wang X, Pregitzer KS, Zak DR, Lussenhop J, Kubiske M, Teeri JA (2000) Gas exchange, leaf nitrogen, and growth efficiency of Populus tremuloides in a CO2-enriched atmosphere. Ecol Appl 10:3–17

    Google Scholar 

  • Djajakirana G, Joerfensen RG, Meyer B (1996) Ergosterol and microbial biomass relationship in soil. Biol Fertil Soils 22:299–304

    Article  CAS  Google Scholar 

  • Ekblad A, Wallander H, Nasholm T (1998) Chitin and ergosterol combined to measure total and living fungal biomass in ectomycorrhizas. New Phytol 138:143–149

    Article  CAS  Google Scholar 

  • Frey B, Vilariño A, Schüepp A, Arines J (1994) Chitin and ergosterol content of extradical and intraradical mycelium of the vesicular–arbuscular mycorrhizal fungus Glomus intraradices. Soil Biol Biochem 26:711–717

    Article  CAS  Google Scholar 

  • Godman RM, Yawney HW, Tubbs CH (1990) Acer saccharum Marsh, Sugar maple. In: Burns RM, Honkala BH (eds) Silvics of North America, vol 2. USDA Forest Service Handbook Number 654. Hardwoods, Washington, DC, pp 78–91

    Google Scholar 

  • Gordon WS, Jackson RB (2000) Nutrient concentrations in fine roots. Ecology 81:275–280

    Article  Google Scholar 

  • Hagedorn F, Blaser P, Siegwolf R (2002) Elevated atmospheric CO2 and increased N deposition effects on dissolved organic carbon-clues from δ13 C signature. Soil Biol Biochem 34:355–366

    Article  CAS  Google Scholar 

  • Hamilton JG, Zangerl AR, DeLucia EH, Berenbaum MR (2001) The carbon-nutrient balance hypothesis: its rise and fall. Ecol Lett 4:86–95

    Article  Google Scholar 

  • Hattenschwiler S (2001) Tree seedling growth in natural deep shade: functional traits related to interspecific variation in response to elevated CO2. Oecologia 129:31–42

    Article  Google Scholar 

  • Herms DA, Mattson WJ (1992) The dilemma of plants: to grow or defend. Q Rev Biol 67:283–335

    Article  Google Scholar 

  • Heyworth CJ, Iason GR, Temperton V, Jarvis PG, Duncan AJ (1998) The effect of elevated CO2 concentration and nutrient supply on carbon-based plant secondary metabolites in Pinus sylvestris L. Oecologia 115:344–350

    Article  Google Scholar 

  • Hodge A (1996) Impact of elevated CO2 on mycorrhizal associations and implications for plant growth. Biol Fertil Soils 23:388–398

    Article  CAS  Google Scholar 

  • King JS, Thomas RB, Strain BR (1996) Growth and carbon accumulation in root systems of Pinus taeda and Pinus ponderosa seedlings as affected by varying CO2, temperature and nitrogen. Tree Physiol 16:635–642

    PubMed  Google Scholar 

  • King JS, Albaugh TJ, Allen HL, Kress LW (1999a) Stand-level allometry in Pinus taeda as affected by irrigation and fertilization. Tree Physiol 19:769–778

    PubMed  Google Scholar 

  • King JS, Pregitzer KS, Zak DR (1999b) Clonal variation in above- and below-ground growth responses of Populus tremuloides Michaux: influence of soil warming and nutrient availability. Plant Soil 217:119–130

    Article  Google Scholar 

  • King JS, Pregitzer KS, Zak DR, Kubiske ME, Ashby JA, Holmes WE (2001a) Chemistry and decomposition of litter from Populus tremuloides Michaux grown at elevated atmospheric CO2 and varying N availability. Glob Change Biol 7:65–74

    Article  Google Scholar 

  • King JS, Pregitzer KS, Zak DR, Kubiske ME, Holmes WE (2001b) Correlation of foliage and litter chemistry of sugar maple, Acer saccharum, as affected by elevated CO2 and varying N availability, and effects on decomposition. Oikos 94:403–416

    Article  Google Scholar 

  • King JS, Pregitzer KS, Zak DR, Sober J, Isebrands JG, Dickson RE, Hendrey GR, Karnosky DF (2001c) Fine-root biomass and fluxes of soil carbon in young stands of paper birch and trembling aspen as affected by elevated atmospheric CO2 and tropospheric O3. Oecologia 128:237–250

    Article  Google Scholar 

  • King JS, Albaugh TJ, Allen JL, Buford M, Strain BR, Dougherty P (2002) Below-ground carbon input to soil is controlled by nutrient availability and fine root dynamics in loblolly pine. New Phytol 154:389–398

    Article  Google Scholar 

  • Kopper BJ, Lindroth RL (2003) Effects of elevated carbon dioxide and ozone on the phytochemistry of aspen and performance of an herbivore. Oecologia 134:95–103

    Article  PubMed  Google Scholar 

  • Koricheva J, Larsson S, Haukioja E, Keinänen M (1998) Regulation of woody plant secondary metabolism by resource availability: a hypothesis testing by means of meta-analysis. Oikos 83:212–226

    Article  CAS  Google Scholar 

  • Kubiske ME, Pregitzer KS, Zak DR, Mikan CJ (1998) Growth and C allocation of Populus tremuloides genotypes in response to atmospheric CO2 and soil N availability. New Phytol 140: 251-260

    Article  Google Scholar 

  • Lambers H (1993) Rising CO2, secondary plant metabolism, plant–herbivore interactions and litter decomposition. Vegetatio 140/105:263–271

    Article  Google Scholar 

  • Larson JL, Zak DR, Sinsabaugh RL (2002) Extracellular enzyme activity beneath temperate trees growing under elevated carbon dioxide and ozone. Soil Sci Soc Am J 66:1848–1856

    CAS  Google Scholar 

  • Lewis JD, Thomas RB, Strain BR (1994) Effect of elevated CO2 on mycorrhizal colonization of loblolly pine (Pinus taeda L.) seedlings. Plant Soil 165:81–88

    Article  CAS  Google Scholar 

  • Lindroth RL (1996) CO2-mediated changes in tree chemistry and tree-Lepidoptera interactions. In: Koch GW, Mooney HA (eds) Caron dioxide and terrestrial ecosystems. Academic, San Diego, pp 105–120

    Chapter  Google Scholar 

  • Loomis WE (1932) Growth-differentiation balance vs. carbohydrate-nitrogen ratio. Proc Am Soc Hort Sci 29:240–245

    CAS  Google Scholar 

  • Lukac M, Calfapietra C, Godbold DL (2003) Production, turnover and mycorrhizal colonization of root systems of three Populus species grown under elevated CO2 (POPFACE). Glob Change Biol 9:838–848

    Article  Google Scholar 

  • McDonald EP, Agrell J, Lindroth RL (1999) CO2 and light effects on deciduous trees: growth, foliar chemistry, and insect performance. Oecologia 119:389–399

    Google Scholar 

  • Melillo JM, Aber JD, Linkins AE, Ricca A, Fry B, Nadelhoffer KJ (1989) Carbon and nitrogen dynamics along the decay continuum: plant litter to soil organic matter. Plant Soil 115:189–198

    Article  Google Scholar 

  • Nadelhoffer KJ (2000) The potential effects of nitrogen deposition on fine-root production in forest ecosystems. New Phytol 147:131–139

    Article  CAS  Google Scholar 

  • Nambiar EKS (1987) Do nutrients retranslocate from fine roots?. Can J For Res 17:913–918

    Article  Google Scholar 

  • O’Neill EG, Luxmoore RJ, Norby RJ (1987) Increases in mycorrhizal colonization and seedling growth in Pinus echinata and Quercus alba in an enriched CO2 atmosphere. Can J For Res 17:878–883

    Article  Google Scholar 

  • Parsons WJ, Kopper BJ, Lindroth RL (2003) Altered growth and fine root chemistry of Betula papyrifera and Acer saccharum under elevated CO2. Can J For Res 33:842–846

    Article  CAS  Google Scholar 

  • Peñuelas J, Castells E, Joffre R, Tognetti R (2002) Carbon-based secondary and structural compounds in Mediterranean shrubs growing near a natural CO2 spring. Glob Change Biol 8:281–288

    Article  Google Scholar 

  • Perala DA (1990) Populus tremuloides Michx., Quaking aspen. In: Burns RM, Honkala BH (eds) Silvics of North America, vol 2. USDA Forest Service Handbook Number 654. Hardwoods, Washington, DC, pp 555–569

    Google Scholar 

  • Percy KE, Awmack CS, Lindroth RL, Kubiske ME, Kopper BJ, Isebrands JG, Pregitzer KS, Hendrey GR, Dickson RE, Zak DR, Oksanen E, Sober J, Harrington R, Karnosky DF (2002) Altered performance of forest pests under atmospheres enriched by CO2 and O3. Nature 420:403–407

    Article  PubMed  CAS  Google Scholar 

  • Phillips RL, Zak DR, Holmes WE, White DC (2002) Microbial community composition and function beneath temperate trees exposed to elevated carbon dioxide and ozone. Oecologia 131:236–244

    Article  Google Scholar 

  • Pregitzer KS (2002) Fine roots of trees—a new perspective. New Phtyol 154:267–273

    Article  Google Scholar 

  • Pregitzer KS, Zak DR, Curtis PS, Kubiske ME, Teeri JA, Vogel CS (1995) Atmospheric CO2, soil nitrogen and turnover of fine roots. New Phytol 129:579–585

    Article  Google Scholar 

  • Pregitzer KS, Zak DR, Maziasz J, DeForest J, Curtis PS, Lussenhop J (2000) Interactive effects of atmospheric CO2 and soil-N availability on fine roots of Populus tremuloides. Ecol Appl 10:18–33

    Google Scholar 

  • Runion GB, Entry JA, Prior SA, Mitchell RJ, Rogers HH (1999) Tissue chemistry and carbon allocation in seedlings of Pinus palustris subjected to elevated atmospheric CO2 and water stress. Tree Physiol 19:329–335

    PubMed  CAS  Google Scholar 

  • Sanders IR, Streitwolf-Engel R, van der Heijden MGA, Boller T, Wieken A (1998) Increased allocation to external hyphae of arbuscular mycorrhizal fungi under elevated CO2 enrichment. Oecologia 117:496–503

    Article  Google Scholar 

  • Schlesinger WH (1997) Biogeochemistry: an analysis of global change. Academic Press, San Diego

    Google Scholar 

  • Schmidt K (2000) Effects of elevated CO2 and soil fertility on fungal biomass and root litter in decomposing fine roots of trembling aspen (Populus tremuloides Michaux) and sugar maple (Acer saccharum Marsh.). MS thesis, Michigan Technological University, Houghton, MI, USA

  • Smith SE, Read DJ (1997) Mycorrhizal symbiosis. Academic Press, San Diego

    Google Scholar 

  • Stahl PD, Parkin TB (1996) Relationship of soil ergosterol concentration and fungal biomass. Soil Biol Biochem 28:847–855

    Article  CAS  Google Scholar 

  • Taiz L, Zeiger E (1991) Plant physiology. Benjamin/Cummings, Redwood City, CA

    Google Scholar 

  • Vogt KA, Grier CC, Vogt DJ (1986) Production, turnover, and nutrient dynamics of above- and belowground detritus of world forests. Adv Ecol Res 15:303–377

    Article  Google Scholar 

  • Zak DR, Pregitzer KS, Curtis PS, Vogel CS, Holmes WE, Lussenhop JL (2000a) Atmospheric CO2, soil N-availability, and allocation of biomass and nitrogen by Populus tremuloides. Ecol Appl 10:34–46

    Google Scholar 

  • Zak DR, Pregiter KS, Curtis PS, Holmes WE (2000b) Atmospheric CO2 and the composition and function of soil microbial communities. Ecol Appl 10:47–59

    Google Scholar 

Download references

Acknowledgements

This research was supported by DOE Program of Ecosystem Research (PER) grant number DE-FG02-93ER6166, the USDA Forest Service Northern Global Change Program, and USDA NRI Competitive Grants Program No. 2001-35107-11262. Logistical support for this project was provided by The University of Michigan Biological Station and is gratefully acknowledged. Dr. Chris Vogel helped install and maintain the CO2 control hardware, and Paul Higgins managed the field site and final harvest with a high level of efficiency and professionalism. Finally, we thank the many students who helped with various aspects of the project over the years.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to J. S. King.

Additional information

Communicated by Jim Ehleringer

Rights and permissions

Reprints and Permissions

About this article

Cite this article

King, J.S., Pregitzer, K.S., Zak, D.R. et al. Fine root chemistry and decomposition in model communities of north-temperate tree species show little response to elevated atmospheric CO2 and varying soil resource availability. Oecologia 146, 318–328 (2005). https://doi.org/10.1007/s00442-005-0191-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00442-005-0191-4

Keywords

  • Trembling aspen
  • Sugar maple
  • Carbon-based secondary compounds
  • Soil C cycling