Long‐term responses of boreal vegetation to global change: an experimental and modelling investigation

The response of boreal ecosystems to future global change is an uncertain but potentially critical component of the feedback between the terrestrial biosphere and the atmosphere. To reduce some of the uncertainties in predicting the responses of this key ecosystem, the climate change experiment (CLIMEX) exposed an entire undisturbed catchment of boreal vegetation to CO2 enrichment (560 ppmv) and climate change (+ 5 °C in winter, + 3 °C in summer) for three years (1994–96). This paper describes the leaf metabolic responses of the vegetation to the experimental treatment and model simulations of possible future changes in the hydrological and carbon balance of the site. Randomized intervention analysis of the leaf gas exchange measurements for the dominant species indicated Pinus sylvestris had significantly (P < 0.01) higher photosynthetic rates and Betula pubescens and Vaccinium myrtillus had significantly (P < 0.01) lower stomatal conductances after three years treatment compared to the controls. These responses led to sustained increases in leaf water‐use efficiency of all species of trees and ground shrubs, as determined from carbon isotope analyses. Photosynthesis (A) vs. intercellular CO2 (ci) response curves (A/ci responses), RuBisCo analysis and leaf nitrogen data together suggested none of the species investigated exhibited down‐regulation in photosynthetic capacity. At the whole ecosystem level, the improved water economy of the plants did not translate into increased catchment runoff. Modelling simulations for the site indicate this was most likely brought about by a compensatory increase in evapotranspiration. In terms of the carbon budget of the site, the ecosystem model indicates that increased CO2 and temperature would lead to boreal ecosystems of the type used in CLIMEX, and typical of much of southern Norway, acting as moderate net sinks for CO2.

[1]  Graham D. Farquhar,et al.  On the Relationship Between Carbon Isotope Discrimination and the Intercellular Carbon Dioxide Concentration in Leaves , 1982 .

[2]  T. Sharkey,et al.  Stomatal conductance and photosynthesis , 1982 .

[3]  G. Farquhar,et al.  Isotopic Composition of Plant Carbon Correlates With Water-Use Efficiency of Wheat Genotypes , 1984 .

[4]  S. Idso,et al.  Rising atmospheric carbon dioxide concentrations may increase streamflow , 1984, Nature.

[5]  T. Wigley,et al.  Influences of precipitation changes and direct CO2 effects on streamflow , 1985, Nature.

[6]  R. Wright,et al.  Reversibility of acidification shown by whole-catchment experiments , 1988, Nature.

[7]  T. Sharkey,et al.  Acclimation of Photosynthesis to Elevated CO(2) in Five C(3) Species. , 1989, Plant physiology.

[8]  Stephen R. Carpenter,et al.  Randomized Intervention Analysis and the Interpretation of Whole‐Ecosystem Experiments , 1989 .

[9]  Stephen P. Long,et al.  Modification of the response of photosynthetic productivity to rising temperature by atmospheric CO2 concentrations: Has its importance been underestimated? , 1991 .

[10]  M. Stitt Rising Co2 Levels and Their Potential Significance for Carbon Flow in Photosynthetic Cells , 1991 .

[11]  S. Long,et al.  Photosynthetic CO2 assimilation and rising atmospheric CO2 concentrations , 1992 .

[12]  Ross E. McMurtrie,et al.  Mathematical models of the photosynthetic response of tree stands to rising CO2 concentrations and temperatures , 1993 .

[13]  Robert J. Scholes,et al.  Observations and modeling of biomass and soil organic matter dynamics for the grassland biome worldwide , 1993 .

[14]  James R. Ehleringer,et al.  Carbon and Water Relations in Desert Plants: An Isotopic Perspective , 1993 .

[15]  R. Wright,et al.  RAIN Project: Results after 8 Years of Experimentally Reduced Acid Deposition to a Whole Catchment , 1993 .

[16]  Stan D. Wullschleger,et al.  Foliar gas exchange responses of two deciduous hardwoods during 3 years of growth in elevated CO2: no loss of photosynthetic enhancement , 1993 .

[17]  Stan D. Wullschleger,et al.  Biochemical Limitations to Carbon Assimilation in C3 Plants—A Retrospective Analysis of the A/Ci Curves from 109 Species , 1993 .

[18]  P. Gross,et al.  Interactive effects of elevated CO(2) and soil drought on growth and transpiration efficiency and its determinants in two European forest tree species. , 1994, Tree physiology.

[19]  F. Woodward,et al.  The Climate Change Experiment (CLIMEX): Phenology and Gas Exchange Responses of Boreal Vegetation to Global Change , 1994 .

[20]  W. Oechel,et al.  Transient nature of CO2 fertilization in Arctic tundra , 1994, Nature.

[21]  Thomas M. Smith,et al.  A global land primary productivity and phytogeography model , 1995 .

[22]  F. I. Woodward,et al.  Leaf Stable Carbon Isotope Composition Records Increased Water-Use Efficiency of C 3 Plants in Response to Atmospheric CO 2 Enrichment , 1995 .

[23]  P. Ciais,et al.  A Large Northern Hemisphere Terrestrial CO2 Sink Indicated by the 13C/12C Ratio of Atmospheric CO2 , 1995, Science.

[24]  S. Carpenter,et al.  Ecosystem experiments. , 1995, Science.

[25]  P. Polglase,et al.  Carbon balance in the tundra, boreal forest and humid tropical forest during climate change: scaling up from leaf physiology and soil carbon dynamics , 1995 .

[26]  Temperature effects on the photosynthetic response of C3 plants to long-term CO2 enrichment , 1995 .

[27]  S. Kellomäki,et al.  Effects of needle age, long-term temperature and CO(2) treatments on the photosynthesis of Scots pine. , 1995, Tree physiology.

[28]  Lawrence E. Band,et al.  Modelling temporal variability in the carbon balance of a spruce/moss boreal forest , 1996 .

[29]  Martin Heimann,et al.  Global and hemispheric CO2 sinks deduced from changes in atmospheric O2 concentration , 1996, Nature.

[30]  J. Guehl,et al.  Growth dynamics, transpiration and water-use efficiency in Quercus robur plants submitted to elevated CO2 and drought , 1996 .

[31]  J. Houghton,et al.  Climate change 1995: the science of climate change. , 1996 .

[32]  G. Farquhar,et al.  The CO 2 Dependence of Photosynthesis, Plant Growth Responses to Elevated Atmospheric CO 2 Concentrations and Their Interaction with Soil Nutrient Status. I. General Principles and Forest Ecosystems , 1996 .

[33]  Peter D. Blanken,et al.  Annual cycles of water vapour and carbon dioxide fluxes in and above a boreal aspen forest , 1996 .

[34]  Yadvinder Malhi,et al.  The use of eddy covariance to infer the net carbon dioxide uptake of Brazilian rain forest , 1996 .

[35]  S. Kellomäki,et al.  Acclimation of photosynthetic parameters in Scots pine after three years exposure to elevated temperature and CO2 , 1996 .

[36]  Kai-yun Wang Canopy CO2 exchange of Scots pine and its seasonal variation after four-year exposure to elevated CO2 and temperature , 1996 .

[37]  S. Kellomäki,et al.  Photosynthetic responses to needle water potentials in Scots pine after a four-year exposure to elevated CO(2) and temperature. , 1996, Tree physiology.

[38]  D. Tissue,et al.  Growth and photosynthesis of loblolly pine (Pinus taeda) after exposure to elevated CO(2) for 19 months in the field. , 1996, Tree physiology.

[39]  J. Ehleringer,et al.  Carbon isotope discrimination during photosynthesis and the isotope ratio of respired CO2 in boreal forest ecosystems , 1996 .

[40]  J. Buwalda,et al.  Photosynthetic Activity of Leaves of Pinus radiata and Nothofagus fusca After 1 Year of Growth at Elevated CO2 , 1996 .

[41]  David C. Lowe,et al.  Variability in the O2/N2 ratio of southern hemisphere air, 1991–1994: Implications for the carbon cycle , 1996 .

[42]  F. Woodward,et al.  In situ Gas Exchange Responses of Boreal Vegetation to Elevated CO 2 and Temperature: First Season Results , 1996 .

[43]  John M. Norman,et al.  Root mass, net primary production and turnover in aspen, jack pine and black spruce forests in Saskatchewan and Manitoba, Canada. , 1997, Tree physiology.

[44]  B. Drake,et al.  MORE EFFICIENT PLANTS: A Consequence of Rising Atmospheric CO2? , 1997, Annual review of plant physiology and plant molecular biology.

[45]  R. Norby,et al.  Temperature‐controlled open‐top chambers for global change research , 1997 .

[46]  Peter E. Thornton,et al.  Simulating forest productivity and surface-atmosphere carbon exchange in the BOREAS study region. , 1997, Tree physiology.

[47]  Carbon isotope discrimination and stomatal responses of mature Pinus sylvestris L. trees exposed in situ for three years to elevated CO2 and temperature , 1997 .

[48]  S. Zarnoch,et al.  Seasonal trends of light‐saturated net photosynthesis and stomatal conductance of loblolly pine trees grown in contrasting environments of nutrition, water and carbon dioxide , 1997 .

[49]  J. Heath,et al.  Effects of elevated CO2 on leaf gas exchange in beech and oak at two levels of nutrient supply: Consequences for sensitivity to drought in beech , 1997 .

[50]  Mark R. Lomas,et al.  Testing the Responses of a Dynamic Global Vegetation Model to Environmental Change: A Comparison of Observations and Predictions , 1997 .

[51]  D. Tissue,et al.  Atmospheric CO2 enrichment increases growth and photosynthesis of Pinus taeda: a 4 year experiment in the field , 1997 .

[52]  Richard Betts,et al.  The science of climate change , 2010 .