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First published online October 15, 2008; 10.1104/pp.108.130153

Plant Physiology 148:2013-2020 (2008)
© 2008 American Society of Plant Biologists

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WHOLE PLANT AND ECOPHYSIOLOGY

Carbon Isotope Fractionation during Photorespiration and Carboxylation in Senecio1,[W],[OA]

Gary J. Lanigan2, Nicholas Betson3, Howard Griffiths and Ulli Seibt4,*

Physiological Ecology Group, Department of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom

The magnitude of fractionation during photorespiration and the effect on net photosynthetic 13C discrimination ({Delta}) were investigated for three Senecio species, S. squalidus, S. cineraria, and S. greyii. We determined the contributions of different processes during photosynthesis to {Delta} by comparing observations ({Delta}obs) with discrimination predicted from gas-exchange measurements ({Delta}pred). Photorespiration rates were manipulated by altering the O2 partial pressure (pO2) in the air surrounding the leaves. Contributions from 13C-depleted photorespiratory CO2 were largest at high pO2. The parameters for photorespiratory fractionation (f), net fractionation during carboxylation by Rubisco and phosphoenolpyruvate carboxylase (b), and mesophyll conductance (gi) were determined simultaneously for all measurements. Instead of using {Delta}obs data to obtain gi and f successively, which requires that b is known, we treated b, f, and gi as unknowns. We propose this as an alternative approach to analyze measurements under field conditions when b and gi are not known or cannot be determined in separate experiments. Good agreement between modeled and observed {Delta} was achieved with f = 11.6{per thousand} ± 1.5{per thousand}, b = 26.0{per thousand} ± 0.3{per thousand}, and gi of 0.27 ± 0.01, 0.25 ± 0.01, and 0.22 ± 0.01 mol m–2 s–1 for S. squalidus, S. cineraria, and S. greyii, respectively. We estimate that photorespiratory fractionation decreases {Delta} by about 1.2{per thousand} on average under field conditions. In addition, diurnal changes in {Delta} are likely to reflect variations in photorespiration even at the canopy level. Our results emphasize that the effects of photorespiration must be taken into account when partitioning net CO2 exchange of ecosystems into gross fluxes of photosynthesis and respiration.


1 This work was supported by the European Research Training Network (Network for Ecophysiology in Closing Terrestrial Carbon Budget; contract no. HPRN–CT–1999–00059), by a Marie Curie Fellowship of the European Commission to U.S. (contract no. MOIF–CT–2004–2704), and by the Department of Plant Sciences, University of Cambridge.

2 Present address: Teagasc, Johnstown Castle Environmental Research Centre, Wexford, Ireland.

3 Present address: RPS Group, Willowmere House, Compass Point Business Park, Stocks Bridge Way, St. Ives PE27 6JL, United Kingdom.

4 Present address: UMR Bioemco, 78850 Thiverval-Grignon, Université Pierre et Marie Curie, Paris 6, France.

The author responsible for the distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Ulli Seibt (useibt{at}dge.stanford.edu).

[W] The online version of this article contains Web-only data.

[OA] Open Access articles can be viewed online without a subscription.

www.plantphysiol.org/cgi/doi/10.1104/pp.108.130153

* Corresponding author; e-mail useibt{at}dge.stanford.edu.

Received September 20, 2008; accepted October 12, 2008; published October 15, 2008.




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