Root responses along a subambient to elevated CO2 gradient in a C3–C4 grassland

Atmospheric CO2 (Ca) concentration has increased significantly during the last 20 000 years, and is projected to double this century. Despite the importance of belowground processes in the global carbon cycle, community‐level and single species root responses to rising Ca are not well understood. We measured net community root biomass over 3 years using ingrowth cores in a natural C3–C4 grassland exposed to a gradient of Ca from preglacial to future levels (230–550 μmol mol−1). Root windows and minirhizotron tubes were installed below naturally occurring stands of the C4 perennial grass Bothriochloa ischaemum and its roots were measured for respiration, carbohydrate concentration, specific root length (SRL), production, and lifespan over 2 years. Community root biomass increased significantly (P<0.05) with Ca over initial conditions, with linear or curvilinear responses depending on sample date. In contrast, B. ischaemum produced significantly more roots at subambient than elevated Ca in minirhizotrons. The lifespan of roots with five or more neighboring roots in minirhizotron windows decreased significantly at high Ca, suggesting that after dense root growth depletes soil resource patches, plants with carbon surpluses readily shed these roots. Root respiration in B. ischaemum showed a curvilinear response to Ca under moist conditions in June 2000, with the lowest rates at Ca<300 μmol mol−1 and peak activity at 450 μmol mol−1 in a quadratic model. B. ischaemum roots at subambient Ca had higher SRLs and slightly higher carbohydrate concentrations than those at higher Ca, which may be related to drier soils at low Ca. Our data emphasize that belowground responses of plant communities to Ca can be quite different from those of the individual species, and suggest that complex interactions between and among roots and their immediate soil environment influence the responses of root physiology and lifespan to changing Ca.

[1]  Charles W. Cook,et al.  Increased belowground biomass and soil CO2 fluxes after a decade of carbon dioxide enrichment in a warm-temperate forest. , 2009, Ecology.

[2]  Ram Oren,et al.  Irreconcilable Differences: Fine-Root Life Spans and Soil Carbon Persistence , 2008, Science.

[3]  D. Jones,et al.  The fate of photosynthetically-fixed carbon in Lolium perenne grassland as modified by elevated CO2 and sward management. , 2007, The New phytologist.

[4]  W. Dugas,et al.  Increasing CO2 from subambient to elevated concentrations increases grassland respiration per unit of net carbon fixation , 2006 .

[5]  M. Bahn,et al.  Root respiration in temperate mountain grasslands differing in land use , 2006 .

[6]  J. Six,et al.  Element interactions limit soil carbon storage. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[7]  R. B. Jackson,et al.  Potential nitrogen constraints on soil carbon sequestration under low and elevated atmospheric CO2. , 2006, Ecology.

[8]  R. Ceulemans,et al.  Forest response to elevated CO2 is conserved across a broad range of productivity. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[9]  J. Morgan,et al.  Root dynamics and demography in shortgrass steppe under elevated CO2, and comments on minirhizotron methodology , 2005 .

[10]  D. Eissenstat,et al.  Interactive effects of soil temperature and moisture on Concord grape root respiration. , 2005, Journal of experimental botany.

[11]  R. Sicher Interactive effects of inorganic phosphate nutrition and carbon dioxide enrichment on assimilate partitioning in barley roots , 2005 .

[12]  D. Smart,et al.  Rapid decline in nitrate uptake and respiration with age in fine lateral roots of grape: implications for root efficiency and competitive effectiveness. , 2004, The New phytologist.

[13]  J. Morgan,et al.  Root Biomass of Individual Species, and Root Size Characteristics After Five Years of CO2 Enrichment on Native Shortgrass Steppe , 2005, Plant and Soil.

[14]  J. Morgan,et al.  Root production and tissue quality in a shortgrass steppe exposed to elevated CO2: Using a new ingrowth method , 2005, Plant and Soil.

[15]  N. E. Miller,et al.  Fine-root production dominates response of a deciduous forest to atmospheric CO2 enrichment. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[16]  Michael G. Ryan,et al.  Below-ground process responses to elevated CO2 and temperature: a discussion of observations, measurement methods, and models , 2004 .

[17]  I. Burke,et al.  Longevity and turnover of roots in the shortgrass steppe: influence of diameter and depth , 2002, Plant Ecology.

[18]  L. Williamson,et al.  Root production and mortality under elevated atmospheric carbon dioxide , 1995, Plant and Soil.

[19]  R. Miller,et al.  Long-term effects of elevated atmospheric CO2 on below-ground biomass and transformations to soil organic matter in grassland , 2004, Plant and Soil.

[20]  J. Reynolds,et al.  Changes in root NH4+ and NO3− absorption rates of loblolly and ponderosa pine in response to CO2 enrichment , 2004, Plant and Soil.

[21]  R. Norby,et al.  Fine-root respiration in a loblolly pine and sweetgum forest growing in elevated CO2. , 2003, The New phytologist.

[22]  J. Derner,et al.  Increasing CO2 from subambient to superambient concentrations alters species composition and increases above-ground biomass in a C3 /C4 grassland. , 2003, The New phytologist.

[23]  L. Comas,et al.  Multiple risk factors in root survivorship: a 4-year study in Concord grape. , 2003, New Phytologist.

[24]  J. Derner,et al.  Increasing CO 2 from subambient to superambient concentrations alters species composition and increases above-ground biomass in a C 3 / C 4 grassland , 2003 .

[25]  J. Derner,et al.  Soil‐ and plant‐water dynamics in a C3/C4 grassland exposed to a subambient to superambient CO2 gradient , 2002 .

[26]  R. B. Jackson,et al.  Root production and demography in a california annual grassland under elevated atmospheric carbon dioxide , 2002 .

[27]  F. Day,et al.  Abundance, production and mortality of fine roots under elevated atmospheric CO2 in an oak-scrub ecosystem , 2002 .

[28]  R. B. Jackson,et al.  Nonlinear grassland responses to past and future atmospheric CO2 , 2002, Nature.

[29]  H. Lambers,et al.  The respiratory patterns in roots in relation to their functioning , 2002 .

[30]  H. W. Polley,et al.  Gas exchange and photosynthetic acclimation over subambient to elevated CO 2 in a C 3 -C 4 grassland , 2001 .

[31]  D. Phillips,et al.  Advancing fine root research with minirhizotrons. , 2001, Environmental and experimental botany.

[32]  Christina E. Wells,et al.  MARKED DIFFERENCES IN SURVIVORSHIP AMONG APPLE ROOTS OF DIFFERENT DIAMETERS , 2001 .

[33]  R. Siegwolf,et al.  Carbon allocation in calcareous grassland under elevated CO2: a combined 13C pulse‐labelling/soil physical fractionation study , 2001 .

[34]  W. Schlesinger,et al.  Effects of elevated atmospheric CO2 on fine root production and activity in an intact temperate forest ecosystem , 2000 .

[35]  Christina E. Wells,et al.  Dynamics of root systems in native grasslands: effects of elevated atmospheric CO2 , 2000 .

[36]  Christina E. Wells,et al.  Building roots in a changing environment: implications for root longevity , 2000 .

[37]  R. B. Jackson,et al.  Root dynamics and global change : seeking an ecosystem perspective , 2000 .

[38]  L. Comas,et al.  Assessing root death and root system dynamics in a study of grape canopy pruning. , 2000 .

[39]  R. B. Jackson,et al.  Global patterns of root turnover for terrestrial ecosystems , 2000 .

[40]  H. W. Polley,et al.  Elongated chambers for field studies across atmospheric CO2 gradients. , 2000 .

[41]  J. Ward,et al.  Is atmospheric CO2 a selective agent on model C3 annuals? , 2000, Oecologia.

[42]  R. B. Jackson,et al.  THE VERTICAL DISTRIBUTION OF SOIL ORGANIC CARBON AND ITS RELATION TO CLIMATE AND VEGETATION , 2000 .

[43]  M. Theodorou,et al.  Responses of Lotus corniculatus to environmental change. 2. Effect of elevated CO2, temperature and drought on tissue digestion in relation to condensed tannin and carbohydrate accumulation , 1999 .

[44]  S. Wand,et al.  Responses of wild C4 and C3 grass (Poaceae) species to elevated atmospheric CO2 concentration: a meta‐analytic test of current theories and perceptions , 1999 .

[45]  James F. Reynolds,et al.  VALIDITY OF EXTRAPOLATING FIELD CO2 EXPERIMENTS TO PREDICT CARBON SEQUESTRATION IN NATURAL ECOSYSTEMS , 1999 .

[46]  R. Sage,et al.  Implications of Stress in Low CO2 Atmospheres of the Past , 1999 .

[47]  R. Sage,et al.  11 – Implications of Stress in Low CO2 Atmospheres of the Past: Are Today's Plants Too Conservative for a High CO2 World? , 1999 .

[48]  H. Lambers,et al.  Why do fast- and slow-growing grass species differ so little in their rate of root respiration, considering the large differences in rate of growth and ion uptake? , 1998 .

[49]  K. Pregitzer,et al.  Growth and C allocation of Populus tremuloides genotypes in response to atmospheric CO2 and soil N availability. , 1998, The New phytologist.

[50]  Hendrik Poorter,et al.  Interactive effects of growth‐limiting N supply and elevated atmospheric CO2 concentration on growth and carbon balance of Plantago major , 1998 .

[51]  A. Fitter,et al.  Root production and turnover and carbon budgets of two contrasting grasslands under ambient and elevated atmospheric carbon dioxide concentrations. , 1997, The New phytologist.

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

[53]  R. Yanai,et al.  The Ecology of Root Lifespan , 1997 .

[54]  J. H. Zar,et al.  Biostatistical Analysis, 3rd edn. , 1996 .

[55]  F. Chapin,et al.  Response of Eriophorum vaginatum to CO2 enrichment at different soil temperatures: effects on growth, root respiration and PO43− uptake kinetics , 1996 .

[56]  G. Berntson,et al.  The allometry of root production and loss in seedlings of Acer rubrum (Aceraceae) and Betula papyrifera (Betulaceae): implications for root dynamics in elevated CO2 , 1996 .

[57]  D. Ackerly,et al.  Plant growth and reproduction along CO2 gradients: non‐linear responses and implications for community change , 1995 .

[58]  P. Curtis,et al.  Atmospheric CO2, soil nitrogen and turnover of fine roots , 1995 .

[59]  P. Allison Survival analysis using the SAS system : a practical guide , 1995 .

[60]  J. Jouzel,et al.  Extending the Vostok ice-core record of palaeoclimate to the penultimate glacial period , 1993, Nature.

[61]  C. Lorius,et al.  Vostok ice core provides 160,000-year record of atmospheric CO2 , 1987, Nature.

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

[63]  Larry F. Lacey,et al.  Long-term effects of on , 1987 .

[64]  Norton Nelson,et al.  A PHOTOMETRIC ADAPTATION OF THE SOMOGYI METHOD FOR THE DETERMINATION OF GLUCOSE , 1944 .

[65]  D.,et al.  Regression Models and Life-Tables , 2022 .

[66]  J. Ward,et al.  Strain Is atmospheric CO 2 a selective agent on model C 3 annuals ? , 2022 .