Net soil carbon input under ambient and elevated CO2 concentrations: isotopic evidence after 4 years

Elevation of atmospheric CO2 concentration is predicted to increase net primary production, which could lead to additional C sequestration in terrestrial ecosystems. Soil C input was determined under ambient and Free Atmospheric Carbon dioxide Enrichment (FACE) conditions for Lolium perenne L. and Trifolium repens L. grown for four years in a sandy‐loam soil. The 13C content of the soil organic matter C had been increased by 5‰ compared to the native soil by prior cropping to corn (Zea mays) for > 20 years. Both species received low or high amounts of N fertilizer in separate plots. The total accumulated above‐ground biomass produced by L. perenne during the 4‐year period was strongly dependent on the amount of N fertilizer applied but did not respond to increased CO2. In contrast, the total accumulated above‐ground biomass of T. repens doubled under elevated CO2 but remained independent of N fertilizer rate. The C:N ratio of above‐ground biomass for both species increased under elevated CO2 whereas only the C:N ratio of L. perenne roots increased under elevated CO2. Root biomass of L. perenne doubled under elevated CO2 and again under high N fertilization. Total soil C was unaffected by CO2 treatment but dependent on species. After 4 years and for both crops, the fraction of new C (F‐value) under ambient conditions was higher (P= 0.076) than under FACE conditions: 0.43 vs. 0.38. Soil under L. perenne showed an increase in total soil organic matter whereas N fertilization or elevated CO2 had no effect on total soil organic matter content for both systems. The net amount of C sequestered in 4 years was unaffected by the CO2 concentration (overall average of 8.5 g C kg−1 soil). There was a significant species effect and more new C was sequestered under highly fertilized L. perenne. The amount of new C sequestered in the soil was primarily dependent on plant species and the response of root biomass to CO2 and N fertilization. Therefore, in this FACE study net soil C sequestration was largely depended on how the species responded to N rather than to elevated CO2.

[1]  David Harris,et al.  Carbon‐13 input and turn‐over in a pasture soil exposed to long‐term elevated atmospheric CO2 , 2000 .

[2]  P. Ineson,et al.  Elevated CO2 reduces the nitrogen concentration of plant tissues , 1998 .

[3]  H. A. Torbert,et al.  Effects of elevated atmospheric CO2 in agro‐ecosystems on soil carbon storage , 1997 .

[4]  A. Lüscher,et al.  Using stable isotopes to determine soil carbon input differences under ambient and elevated atmospheric CO2 conditions , 1997 .

[5]  R. B. Jackson,et al.  The fate of carbon in grasslands under carbon dioxide enrichment , 1997, Nature.

[6]  A. Lüscher,et al.  Growth response of Trifolium repens L. and Lolium perenne L. as monocultures and bi‐species mixture to free air CO2 enrichment and management , 1997 .

[7]  A. Lúscher,et al.  Stimulation of Symbiotic N2 Fixation in Trifolium repens L. under Elevated Atmospheric pCO2 in a Grassland Ecosystem , 1996, Plant physiology.

[8]  MICHAEL B. Jones,et al.  The effects of elevated CO2 concentrations on the root growth of Lolium perenne and Trifolium repens grown in a FACE* system , 1995 .

[9]  J. Roy,et al.  The influence of elevated CO2 on community structure, biomass and carbon balance of mediterranean old-fleld microcosms , 1995 .

[10]  H. Weigel,et al.  Effects of CO2 enrichment and intraspecific competition on biomass partitioning, nitrogen content and microbial biomass carbon in soil of perennial ryegrass and white clover , 1995 .

[11]  J. Amthor Terrestrial higher‐plant response to increasing atmospheric [CO2] in relation to the global carbon cycle , 1995 .

[12]  C. W. Wood,et al.  Free-air CO2 enrichment effects on soil carbon and nitrogen , 1994 .

[13]  H. Rogers,et al.  Effects of free-air CO2 enrichment on cotton root growth , 1994 .

[14]  J. Nagy,et al.  Carbon isotope dynamics of free-air CO2-enriched cotton and soils , 1994 .

[15]  C. Kessel,et al.  Carbon‐13 and Nitrogen‐15 Natural Abundance in Crop Residues and Soil Organic Matter , 1994 .

[16]  J. P. Grime,et al.  Evidence of a feedback mechanism limiting plant response to elevated carbon dioxide , 1993, Nature.

[17]  J. Morel,et al.  Use ofr 13C variations at natural abundance for studying the biodegradation of root mucilage, roots and glucose in soil , 1992 .

[18]  C. E. Powell,et al.  Effect of Elevated CO2 on the Photosynthesis, Respiration and Growth of Perennial Ryegrass , 1992 .

[19]  L. Lekkerkerk,et al.  Carbon Fluxes in Plant-Soil Systems at Elevated Atmospheric CO2 Levels. , 1991, Ecological applications : a publication of the Ecological Society of America.

[20]  P. Sánchez,et al.  Decomposition and nutrient release patterns of the leaves of three tropical legumes , 1990 .

[21]  P. Brookes,et al.  The Soil Microbial Biomass : Its Measurement, Properties and Role in Soil Nitrogen and Carbon Dynamics Following Substrate Incorporation , 1990 .

[22]  W. Parton,et al.  Analysis of factors controlling soil organic matter levels in Great Plains grasslands , 1987 .

[23]  R. Norby,et al.  Carbon allocation, root exudation and mycorrhizal colonization of Pinus echinata seedlings grown under CO(2) enrichment. , 1987, Tree physiology.

[24]  R. H. Fox,et al.  Interactions between fertilizer nitrogen and soil nitrogen—the so‐called ‘priming’ effect , 1985 .

[25]  D. Jenkinson STUDIES ON THE DECOMPOSITION OF PLANT MATERIAL IN SOIL. V. THE EFFECTS OF PLANT COVER AND SOIL TYPE ON THE LOSS OF CARBON FROM14C LABELLED RYEGRASS DECOMPOSING UNDER FIELD CONDITIONS , 1977 .

[26]  D. Jenkinson Studies on the decomposition of plant material in soil .IV. The effect of rate of addition , 1977 .

[27]  J. Balesdent,et al.  Measurement of soil organic matter turnover using 13C natural abundance. , 1996 .

[28]  A. Lüscher,et al.  Stimulation of Symbiotic N, Fixation in Trifolium repens 1. under Elevated Atmospheric pC0, in a Grassland Ecosystem' , 1996 .

[29]  K. Paustian,et al.  Management Impacts on Carbon Storage and Gas Fluxes (C0 2 , CH.Jin Mid-Latitude Cropland , 1995 .

[30]  S V Krupa,et al.  Plant responses to atmospheric CO2 enrichment with emphasis on roots and the rhizosphere. , 1994, Environmental pollution.

[31]  T. Boutton 11 – Stable Carbon Isotope Ratios of Natural Materials: II. Atmospheric, Terrestrial, Marine, and Freshwater Environments , 1991 .

[32]  R. Prebble,et al.  Turnover of Soil Organic Matter under Pasture as Determined by 13C Natural Abundance , 1990 .

[33]  J. Houghton,et al.  Climate change : the IPCC scientific assessment , 1990 .

[34]  J. Balesdent,et al.  Soil Organic Matter Turnover in Long-term Field Experiments as Revealed by Carbon-13 Natural Abundance , 1988 .

[35]  J. Goudriaan,et al.  Plant growth in response to CO2 enrichment, at two levels of nitrogen and phosphorus supply. 1. Dry matter, leaf area and development , 1983 .

[36]  D. Jenkinson The fate of plant and animal residues in soil , 1981 .