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      Soybean photosynthetic and biomass responses to carbon dioxide concentrations ranging from pre-industrial to the distant future

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          Abstract

          Increases in soybean photosynthesis and biomass diminish at growth CO 2 concentrations >1000 ppm, constraining the benefits of increasing atmospheric CO 2 concentration on soybean productivity.

          Abstract

          Increasing atmospheric carbon dioxide concentration ([CO 2]) directly impacts C 3 plant photosynthesis and productivity, and the rate at which [CO 2] is increasing is greater than initially predicted by worst-case scenario climate models. Thus, it is increasingly important to assess the physiological responses of C 3 plants, especially those that serve as important crops, to [CO 2] beyond the mid-range levels used in traditional experiments. Here, we grew the C 3 crop soybean ( Glycine max) at eight different [CO 2] levels spanning subambient (340 ppm) to the highest level thought plausible (~2000 ppm) in chambers for 5 weeks. Physiological development was delayed and plant height and total leaf area increased at [CO 2] levels higher than ambient conditions, with very little difference in these parameters among the elevated [CO 2] treatments >900 ppm. Daily photosynthesis initially increased with rising [CO 2] but began to level off at ~1000 ppm CO 2. Similar results occurred in biomass accumulation. Thus, as [CO 2] continues to match or exceed the worst-case emission scenarios, these results indicate that carbon gain, growth, and potentially yield increases will diminish, thereby ultimately constraining the positive impact that continuing increases in atmospheric [CO 2] could have on crop productivity and global terrestrial carbon sinks.

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          Most cited references37

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          A biochemical model of photosynthetic CO2 assimilation in leaves of C 3 species.

          Various aspects of the biochemistry of photosynthetic carbon assimilation in C3 plants are integrated into a form compatible with studies of gas exchange in leaves. These aspects include the kinetic properties of ribulose bisphosphate carboxylase-oxygenase; the requirements of the photosynthetic carbon reduction and photorespiratory carbon oxidation cycles for reduced pyridine nucleotides; the dependence of electron transport on photon flux and the presence of a temperature dependent upper limit to electron transport. The measurements of gas exchange with which the model outputs may be compared include those of the temperature and partial pressure of CO2(p(CO2)) dependencies of quantum yield, the variation of compensation point with temperature and partial pressure of O2(p(O2)), the dependence of net CO2 assimilation rate on p(CO2) and irradiance, and the influence of p(CO2) and irradiance on the temperature dependence of assimilation rate.
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            Gas exchange measurements, what can they tell us about the underlying limitations to photosynthesis? Procedures and sources of error.

            The principles, equipment and procedures for measuring leaf and canopy gas exchange have been described previously as has chlorophyll fluorescence. Simultaneous measurement of the responses of leaf gas exchange and modulated chlorophyll fluorescence to light and CO2 concentration now provide a means to determine a wide range of key biochemical and biophysical limitations on photo synthesis in vivo. Here the mathematical frameworks and practical procedures for determining these parameters in vivo are consolidated. Leaf CO2 uptake (A) versus intercellular CO2 concentration (Ci) curves may now be routinely obtained from commercial gas exchange systems. The potential pitfalls, and means to avoid these, are examined. Calculation of in vivo maximum rates of ribulose-1,5-bisphosphate (RuBP) carboxylase/oxygenase (Rubisco) carboxylation (Vc,max), electron transport driving regeneration of RuBP (Jmax), and triose-phosphate utilization (VTPU) are explained; these three parameters are now widely assumed to represent the major limitations to light-saturated photosynthesis. Precision in determining these in intact leaves is improved by the simultaneous measurement of electron transport via modulated chlorophyll fluorescence. The A/Ci response also provides a simple practical method for quantifying the limitation that stomata impose on CO2 assimilation. Determining the rate of photorespiratory release of oxygen (Rl) has previously only been possible by isotopic methods, now, by combining gas exchange and fluorescence measurements, Rl may be determined simply and routinely in the field. The physical diffusion of CO2 from the intercellular air space to the site of Rubisco in C3 leaves has long been suspected of being a limitation on photosynthesis, but it has commonly been ignored because of the lack of a practical method for its determination. Again combining gas exchange and fluorescence provides a means to determine mesophyll conductance. This method is described and provides insights into the magnitude and basis of this limitation.
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              Improved temperature response functions for models of Rubisco-limited photosynthesis

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                Author and article information

                Contributors
                Role: Editor
                Journal
                J Exp Bot
                J. Exp. Bot
                exbotj
                Journal of Experimental Botany
                Oxford University Press (UK )
                0022-0957
                1460-2431
                22 June 2020
                12 March 2020
                12 March 2020
                : 71
                : 12
                : 3690-3700
                Affiliations
                [1 ] Department of Plant Biology, University of Illinois at Urbana-Champaign , Urbana, IL, USA
                [2 ] Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign , Urbana, IL, USA
                [3 ] Institute for Sustainability, Energy, and Environment, University of Illinois at Urbana-Champaign , IL, USA
                [4 ] Global Change and Photosynthesis Research Unit, United States Department of Agriculture, Agricultural Research Service , Urbana, IL, USA
                [5 ] University of Essex , UK
                Author notes
                Author information
                http://orcid.org/0000-0002-7165-906X
                http://orcid.org/0000-0002-5435-4387
                http://orcid.org/0000-0002-2397-425X
                Article
                eraa133
                10.1093/jxb/eraa133
                7475242
                32170296
                04838c1a-3a55-48a8-b947-abd5abf12295
                © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Experimental Biology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 17 October 2019
                : 24 February 2020
                : 09 March 2020
                : 11 April 2020
                Page count
                Pages: 11
                Categories
                Research Papers
                Plant—Environment Interactions
                AcademicSubjects/SCI01210

                Plant science & Botany
                biomass,elevated co2,photosynthesis,soybean (glycine max)
                Plant science & Botany
                biomass, elevated co2, photosynthesis, soybean (glycine max)

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