Hostname: page-component-586b7cd67f-rcrh6 Total loading time: 0 Render date: 2024-11-26T01:28:01.508Z Has data issue: false hasContentIssue false

Physiological Significance of Low Atmospheric CO2 for Plant–Climate Interactions

Published online by Cambridge University Press:  20 January 2017

Sharon A. Cowling
Affiliation:
Climate Impacts Group, Institute of Ecology, Lund University, S-223 62, Lund, Sweden. E-mail: [email protected]
Martin T. Sykes
Affiliation:
Climate Impacts Group, Institute of Ecology, Lund University, S-223 62, Lund, Sweden. E-mail: [email protected]

Abstract

Methods of palaeoclimate reconstruction from pollen are built upon the assumption that plant–climate interactions remain the same through time or that these interactions are independent of changes in atmospheric CO2. The latter may be problematic because air trapped in polar ice caps indicates that atmospheric CO2 has fluctuated significantly over at least the past 400,000 yr, and likely the last 1.6 million yr. Three other points indicate potential biases for vegetation-based climate proxies. First, C3-plant physiological research shows that the processes that determine growth optima in plants (photosynthesis, mitochondrial respiration, photorespiration) are all highly CO2-dependent, and thus were likely affected by the lower CO2 levels of the last glacial maximum. Second, the ratio of carbon assimilation per unit transpiration (called water-use efficiency) is sensitive to changes in atmospheric CO2 through effects on stomatal conductance and may have altered C3-plant responses to drought. Third, leaf gas-exchange experiments indicate that the response of plants to carbon-depleting environmental stresses are strengthened under low CO2 relative to today. This paper reviews the scope of research addressing the consequences of low atmospheric CO2 for plant and ecosystem processes and highlights why consideration of the physiological effects of low atmospheric CO2 on plant function is recommended for any future refinements to pollen-based palaeoclimatic reconstructions.

Type
Research Article
Copyright
University of Washington

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Anklin, M., Schwander, J., Stauffer, B., Tschumi, J., Fuchs, A. (1997). CO2 record between 40 and 8 kyr B.P. from the Greenland Ice Core Project ice core. Journal of Geophysical Research. 102, 2653926545.Google Scholar
Araus, J.L., Buxo, R. (1993). Changes in carbon isotope discrimination in grain cereals from the north-western Mediterranean basin during the past seven millennia. Australian Journal of Plant Physiology. 20, 117128.Google Scholar
Bartlein, P.J., Prentice, I.C., Webb, T. III. (1986). Climatic response surfaces from pollen data for some eastern North American taxa. Journal of Biogeography. 13, 3557.Google Scholar
Bert, D., Leavitt, S.W., Dupouey, J.L. (1997). Variations of wood delta C-13 and water-use efficiency of Abies alba during the last century. Ecology. 78, 15881596.Google Scholar
Brooks, A., Farquhar, G.D. (1985). Effect of temperature on the CO2/O2 specificity of ribulose-1,5-bisphosphate carboxylase/oxygenase and the rate of respiration in the light. Planta. 165, 397406.Google Scholar
Campbell, W.J., Allen, L.H., Bowes, G. (1988). Effects of CO2 concentration on Rubisco activity, amount and photosynthesis in soybean leaves. Plant Physiology. 88, 13101316.CrossRefGoogle ScholarPubMed
Cerling, T.E., Ehleringer, J.R., Harris, J.M. (1998). Carbon dioxide starvation, the development of C4 ecosystems, and mammalian evolution. Philosophical Transactions of the Royal Society, London (B). 353, 159171.Google Scholar
Chapin, F.S., Schulze, E.D., Mooney, H.A. (1990). The ecology and economics of carbon storage in plants. Annual Review of Ecology and Systematics. 21, 423447.CrossRefGoogle Scholar
Cole, D.R., Monger, H.C. (1994). Influence of atmospheric CO2 on the decline of C4 plants during the last deglaciation. Nature. 368, 533536.CrossRefGoogle Scholar
Colinvaux, P.A., De Oliveira, P.E., Moreno, J.E., Miller, M.C., Bush, M.B. (1996). A long pollen record from lowland Amazonia: forest and cooling in glacial times. Science. 274, 8588.Google Scholar
Collatz, G.J., Berry, J.A., Clark, J.S. (1998). Effects of climate and atmospheric CO2 partial pressure on the global distribution of C4 grasses: present, past and future. Oecologia. 114, 441454.Google Scholar
Cowling, S.A. in press, Simulated effects of low atmospheric CO2 on structure and composition of North American vegetation at the Last Glacial Maximum. Global Ecology and Biogeography Letters, 8.Google Scholar
Cowling, S.A., Sage, R.F. (1998). Interactive effects of low atmospheric CO2 and elevated temperature on growth, photosynthesis, and respiration in Phaseolus vulgaris . Plant, Cell and Environment. 21, 427435.Google Scholar
Cowling, S. A, Maslin, M. A and Sykes, M. T. (in review), An alternate tropical refugia hypothesis based on modelled physiological responses of Amazon vegetation to glacial climate, Science. Google Scholar
Crowley, T.J., Baum, S.K. (1997). Effect of vegetation on an ice-age climate model simulation. Journal of Geophysical Research. 102, 1646316480.Google Scholar
Davis, M.B. (1989). Insights from palaeoecology on global change. Bulletin of the Ecological Society of America. 70, 222228.Google Scholar
Ehleringer, J.R., Cerling, T.E., Helliker, B.R. (1997). C4 photosynthesis, atmospheric CO2 and climate. Oecologia. 112, 285299.Google Scholar
Farquhar, G.D. (1997). Carbon dioxide and vegetation. Science. 278, 1411.Google Scholar
Farquhar, G.D., Sharky, T.D. (1982). Stomatal conductance and photosynthesis. Annual Review of Plant Physiology. 33, 317345.Google Scholar
Farquhar, G.D., von Caemmerer, S., Berry, J.A. (1980). A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta. 149, 7890.CrossRefGoogle Scholar
Farquhar, G.D., Ehleringer, J.R., Hubrick, K.T. (1989). Carbon isotope discrimination and photosynthesis. Annual Review of Plant Physiology and Plant Molecular Biology. 40, 503537.CrossRefGoogle Scholar
Giresse, P., Maley, J., Brenac, P. (1994). Late Quaternary palaeoenvironments in the Lake Barombi Mbo (West Cameroon) deduced from pollen and carbon isotopes of organic matter. Palaeogeography, Palaeoclimatology, Palaeoecology. 107, 6578.CrossRefGoogle Scholar
Hattenschwiler, S., Körner, C. (1996). System-level adjustments to elevated CO2 in model spruce ecosystems. Global Change Biology. 2, 377387.Google Scholar
Hattenschwiler, S., Miglietta, F., Raschi, A., Körner, C. (1997). Thirty year of in situ tree growth under elevated CO2: a model for future forest responses. Global Change Biology. 3, 463471.Google Scholar
Idso, S.B. (1989). A problem for palaeoclimatology. Quaternary Research. 31, 433434.Google Scholar
Johnson, H.B., Polley, H.W., Mayeaux, H.S. (1993). Increasing CO2 and plant-plant interactions: effects on natural vegetation. Vegetatio. 104/105, 157170.CrossRefGoogle Scholar
Jolly, D., Haxeltine, A. (1997). Effect of low glacial atmospheric CO2 on tropical African montane vegetation. Science. 276, 786788.Google Scholar
Liu, B., Phillips, F.M., Campbell, A.R. (1996). Stable carbon and oxygen isotopes of pedogenic carbonates, Ajo Mountains, southern Arizona: implications for palaeoenvironmental change. Palaeogeography, Palaeoclimatology, Palaeoecology. 124, 233246.Google Scholar
Long, S.P. (1991). Modification of the response of photosynthetic productivity to rising temperature by atmospheric CO2 concentrations: has its importance been underestimated. Plant, Cell and Environment. 14, 729739.Google Scholar
Mayeux, H.S., Johnson, H.B., Polley, H.W., Malone, S.R. (1997). Yield of wheat across a subambient carbon dioxide gradient. Global Change Biology. 3, 269278.Google Scholar
Osmond, C.B., Winter, K., Ziegler, H. (1982). Functional significance of different pathways of CO2 fixation in photosynthesis. Lange, O.L., Nobel, P.S., Osmond, C.B., Zeigler, H. Physiological Plant Ecology II: Water Relations and Carbon Assimilation. Springer-Verlag, Berlin., 479547.Google Scholar
Pearcy, R.W., Ehleringer, J. (1984). Comparative ecophysiology of C3 and C4 plants. Plant, Cell, and Environment. 7, 113.Google Scholar
Polley, H.W., Johnson, H.B., Marino, B.D., Mayeux, H.S. (1993). Increases in C3 plant water-use efficiency and biomass over glacial to present CO2 concentrations. Nature. 361, 6164.Google Scholar
Polley, H.W., Johnson, H.B., Mayeux, H.S. (1995). Nitrogen and water requirements of C3 plants grown at glacial to present carbon dioxide concentrations. Functional Ecology. 9, 8696.CrossRefGoogle Scholar
Prentice, I.C., Bartlein, P.J., Webb, T. III. (1991). Vegetation and climatic change in eastern North America since the last glacial maximum. Ecology. 72, 20382056.CrossRefGoogle Scholar
Raymo, M.E. (1992). Global climate change: a three million year perspective. Kukla, G.J., Went, E. Start of a Glacial. Springer-Verlag, Berlin., 207223.Google Scholar
Robinson, J.M. (1994). Speculations on carbon dioxide starvation, late Tertiary evolution of stomatal regulation and floristic modernisation. Plant, Cell, and Environment. 17, 345354.Google Scholar
Sage, R.F. (1995). Was low atmospheric CO2 during the Pleistocene a limiting factor for the origin of agriculture. Global Change Biology. 1, 93106.Google Scholar
Sage, R.F. (1994). Acclimation of photosynthesis to increasing atmospheric CO2: The gas exchange perspective. Photosynthetic Research. 39, 351368.Google Scholar
Sage, R.F., Cowling, S.A. (1999). Implications of stress in low CO2 atmospheres of the past: are today's plants too conservative for a high CO2 world. Lui, Y., Mooney, H.A. Carbon Dioxide and Environmental Stress. Academic Press, San Diego., 289308.CrossRefGoogle Scholar
Sage, R.F., Reid, C.D. (1994). Photosynthetic response mechanisms to environmental change in C3 plants. Wilkinson, R.E. Plant-Environment Interactions. Dekker, New York., 413499.Google Scholar
Sage, R.F., Reid, C.D. (1992). Photosynthetic acclimation to sub-ambient CO2 (20 Pa) in the C3 annual Phaseolus vulgaris L. Photosynthetica. 27, 605617.Google Scholar
Schappi, B., Körner, C. (1996). Growth responses of an alpine grassland to elevated CO2 . Oecologia. 105, 4352.Google Scholar
Sharkey, T.D. (1988). Estimating the rate of photorespiration in leaves. Physiologia Plantarum. 73, 147152.Google Scholar
Smith, H.J., Wahlen, M., Mastroianni, D. (1997). The CO2 concentration of air trapped in GISP2 ice from the Last Glacial Maximum-Holocene transition. Geophysical Research Letters. 24, 14.Google Scholar
Solomon, A.M. (1984). Forest responses to complex interacting full glacial environmental conditions. Program and Abstracts-AmQua Meeting at the University of Colorado (13–15 August). p. 120.Google Scholar
Street-Perrott, F.A., Huang, Y., Perrott, R.A., Eglinton, G., Barker, P., Khelifa, L.B., Harkness, D.D., Olago, D.O. (1997). Impact of lower atmospheric carbon dioxide on tropical mountain ecosystems. Science. 278, 14221426.Google Scholar
Sukumar, R., Suresh, H.S., Ramesh, R. (1995). Climate change and its impact on tropical montane ecosystems in southern India. Journal of Biogeography. 22, 533536.Google Scholar
Tissue, D.T., Griffin, K.L., Thomas, R.B., Strain, B.R. (1995). Effects of low and elevated CO2 on C3 and C4 annuals. II. Photosynthesis and leaf biochemistry. Oecologia. 101, 2128.Google Scholar
Webb, R.S., Anderson, K.H., Webb, T. III. (1993). Pollen response-surface estimates of late-Quaternary changes in the moisture balance of the northeastern United States. Quaternary Research. 40, 213227.Google Scholar
Woodward, F.I. (1993). Plant responses to past concentrations of CO2 . Vegetatio. 104–105, 145155.Google Scholar
Woodward, F.I., Kelly, C.K. (1995). The influence of CO2 concentration on stomatal density. New Phytologist. 131, 311327.Google Scholar
Yeoh, H., Badger, M.R., Watson, L. (1981). Variations in kinetic properties of ribulose-1,5-bisphosphate carboxylase among plants. Plant Physiology. 67, 11511155.CrossRefGoogle ScholarPubMed