Climate controls on C 3 vs . C 4 productivity in North American grasslands from carbon isotope composition of soil organic matter

We analyzed the dC of soil organic matter (SOM) and fine roots from 55 native grassland sites widely distributed across the US and Canadian Great Plains to examine the relative production of C3 vs. C4 plants (hereafter %C4) at the continental scale. Our climate vs. %C4 results agreed well with North American field studies on %C4, but showed bias with respect to %C4 from a US vegetation database (STATSGO) and weak agreement with a physiologically based prediction that depends on crossover temperature. Although monthly average temperatures have been used in many studies to predict %C4, our analysis shows that high temperatures are better predictors of %C4. In particular, we found that July climate (average of daily high temperature and month’s total rainfall) predicted %C4 better than other months, seasons or annual averages, suggesting that the outcome of competition between C3 and C4 plants in North American grasslands was particularly sensitive to climate during this narrow window of time. Root dC increased about 1% between the A and B horizon, suggesting that C4 roots become relatively more common than C3 roots with depth. These differences in depth distribution likely contribute to the isotopic enrichment with depth in SOM where both C3 and C4 grasses are present.

[1]  S. N. Stephenson,et al.  Photosynthetic Pathways and Selective Herbivory: A Hypothesis , 1973, The American Naturalist.

[2]  G. Williams Photosynthetic adaptation to temperature in c(3) and c(4) grasses: a possible ecological role in the shortgrass prairie. , 1974, Plant physiology.

[3]  J. L. Dodd,et al.  Phenological Pattern in the Shortgrass Prairie , 1976 .

[4]  Larry L. Tieszen,et al.  The Seasonal Contribution of C"3 and C"4 Plant Species to Primary Production in a Mixed Prairie , 1980 .

[5]  Paul W. Barnes,et al.  Distribution, production, and diversity of C3- and C4-dominated communities in a mixed prairie , 1983 .

[6]  Steve Archer The Distribution of Photosynthetic Pathway Types on a Mixed-grass Prairie Hillside , 1984 .

[7]  W. Parton,et al.  Primary Production of the Central Grassland Region of the United States , 1988 .

[8]  K. H. Asay,et al.  Carbon Isotope Dicrimination: Potential in Screening Cool‐Season Grasses for Water‐Limited Environments , 1990 .

[9]  L. Tieszen,et al.  Isotopic Assessment of Vegetation Changes in Grassland and Woodland Systems , 1990 .

[10]  W. Parton,et al.  Long- and short-term effects of fire on nitrogen cycling in tallgrass prairie , 1994 .

[11]  L. Tieszen,et al.  Carbon Isotope Dynamics During Grass Decomposition and Soil Organic Matter Formation , 1995 .

[12]  J. Paruelo,et al.  Relative Abundance of Plant Functional Types in Grasslands and Shrublands of North America , 1996 .

[13]  I. Burke,et al.  PRODUCTIVITY PATTERNS OF C3 AND C4 FUNCTIONAL TYPES IN THE U.S. GREAT PLAINS , 1997 .

[14]  J. Ehleringer,et al.  C4 photosynthesis, atmospheric CO2, and climate , 1997, Oecologia.

[15]  J. Ehleringer,et al.  Global vegetation change through the Miocene/Pliocene boundary , 1997, Nature.

[16]  B. Wylie,et al.  NDVI, C3 AND C4 PRODUCTION, AND DISTRIBUTIONS IN GREAT PLAINS GRASSLAND LAND COVER CLASSES , 1997 .

[17]  James S. Clark,et al.  Effects of climate and atmospheric CO2 partial pressure on the global distribution of C4 grasses: present, past, and future , 1998, Oecologia.

[18]  David R. Anderson,et al.  Model Selection and Multimodel Inference , 2003 .

[19]  R. Bol,et al.  Molecular insight into soil carbon turnover. , 1999, Rapid communications in mass spectrometry : RCM.

[20]  I. Burke,et al.  Relationship Between Root Biomass and Soil Organic Matter Pools in the Shortgrass Steppe of Eastern Colorado , 1999, Ecosystems.

[21]  P. Haldimann How do changes in temperature during growth affect leaf pigment composition and photosynthesis in Zea mays genotypes differing in sensitivity to low temperature , 1999 .

[22]  G. Robertson,et al.  Standard soil methods for long-term ecological research , 1999 .

[23]  A. Knapp,et al.  8 - Success of C 4 Photosynthesis in the Field: Lessons from Communities Dominated by C 4 Plants , 1999 .

[24]  J. Ehleringer,et al.  Carbon isotope ratios in belowground carbon cycle processes , 2000 .

[25]  R. Sage,et al.  Photosynthetic performance at low temperature of Bouteloua gracilis Lag., a high-altitude C4 grass from the Rocky Mountains, USA , 2000 .

[26]  J. Blair,et al.  Rainfall Variability, Carbon Cycling, and Plant Species Diversity in a Mesic Grassland , 2002, Science.

[27]  Organic carbon and carbon isotopes in modern and 100‐year‐old‐soil archives of the Russian steppe , 2002 .

[28]  G. L. Hutchinson,et al.  Response of C3 and C4 grasses to supplemental summer precipitation. , 2002 .

[29]  Y. Zhou,et al.  The effect of soil texture and roots on the stable carbon isotope composition of soil organic carbon , 2003 .

[30]  R. DeFries,et al.  Global distribution of C3 and C4 vegetation: Carbon cycle implications , 2003 .

[31]  J. Blair,et al.  Productivity responses to altered rainfall patterns in a C4-dominated grassland , 2003, Oecologia.

[32]  Georg Cadisch,et al.  Carbon isotopic fractionation during decomposition of plant materials of different quality , 2003 .

[33]  J. C. Winslow,et al.  The influence of seasonal water availability on global C3 versus C4 grassland biomass and its implications for climate change research , 2003 .

[34]  J. Berry,et al.  The contribution of C3 and C4 plants to the carbon cycle of a tallgrass prairie: an isotopic approach , 2003, Oecologia.

[35]  R. Werner,et al.  Intramolecular, compound-specific, and bulk carbon isotope patterns in C3 and C4 plants: a review and synthesis. , 2004, The New phytologist.

[36]  P. Hattersley The distribution of C3 and C4 grasses in Australia in relation to climate , 1983, Oecologia.

[37]  D. Tilman,et al.  Species effects on nitrogen cycling: a test with perennial grasses , 1990, Oecologia.

[38]  G. Farquhar,et al.  Effect of temperature on the CO2/O2 specificity of ribulose-1,5-bisphosphate carboxylase/oxygenase and the rate of respiration in the light , 1985, Planta.

[39]  R. Sage,et al.  Low‐temperature photosynthetic performance of a C4 grass and a co‐occurring C3 grass native to high latitudes , 2004 .

[40]  J. A. Teeri,et al.  Climatic patterns and the distribution of C4 grasses in North America , 1976, Oecologia.

[41]  Peter E. Thornton,et al.  VEMAP Phase 2 Bioclimatic Database. I. Gridded Historical (20th century) Climate for Modeling Ecosystem Dynamics Across the Conterminous USA , 2004 .

[42]  A. Zhisheng,et al.  δ13C variation of C3 and C4 plants across an Asian monsoon rainfall gradient in arid northwestern China , 2005 .

[43]  K. Klumpp,et al.  C-isotope composition of CO2 respired by shoots and roots: fractionation during dark respiration? , 2005 .

[44]  David Tilman,et al.  Niche differences in phenology and rooting depth promote coexistence with a dominant C4 bunchgrass , 2005, Oecologia.

[45]  J. Berry,et al.  Simulation of carbon isotope discrimination of the terrestrial biosphere , 2005 .

[46]  Ling-xi Zhou,et al.  Long‐term record of atmospheric CO2 and stable isotopic ratios at Waliguan Observatory: Background features and possible drivers, 1991–2002 , 2005 .

[47]  Franz-Werner Badeck,et al.  Post-photosynthetic fractionation of stable carbon isotopes between plant organs--a widespread phenomenon. , 2005, Rapid communications in mass spectrometry : RCM.

[48]  IN Ornithology,et al.  STABLE ISOTOPES AND THE DETERMINATION OF AVIAN MIGRATORY CONNECTIVITY AND SEASONAL INTERACTIONS , 2005 .

[49]  Jianping Pan,et al.  Regional climate model downscaling of the U.S. summer climate and future change , 2006 .

[50]  L. Tieszen,et al.  Late quaternary temperature record from buried soils of the North American Great Plains , 2007 .

[51]  Roger Jones,et al.  Regional climate projections , 2007 .