Skip to main content
Log in

Can CO2 assimilation in maize leaves be predicted accurately from chlorophyll fluorescence analysis?

  • Minireview
  • Published:
Photosynthesis Research Aims and scope Submit manuscript

Abstract

Analysis is made of the energetics of CO2 fixation, the photochemical quantum requirement per CO2 fixed, and sinks for utilising reductive power in the C4 plant maize. CO2 assimilation is the primary sink for energy derived from photochemistry, whereas photorespiration and nitrogen assimilation are relatively small sinks, particularly in developed leaves. Measurement of O2 exchange by mass spectrometry and CO2 exchange by infrared gas analysis under varying levels of CO2 indicate that there is a very close relationship between the true rate of O2 evolution from PS II and the net rate of CO2 fixation. Consideration is given to measurements of the quantum yields of PS II (φ PS II) from fluorescence analysis and of CO2 assimilation (\(\phi _{CO_2 } \)) in maize over a wide range of conditions. The\({{\phi _{PSII} } \mathord{\left/ {\vphantom {{\phi _{PSII} } {\phi _{CO_2 } }}} \right. \kern-\nulldelimiterspace} {\phi _{CO_2 } }}\) ratio was found to remain reasonably constant (ca. 12) over a range of physiological conditions in developed leaves, with varying temperature, CO2 concentrations, light intensities (from 5% to 100% of full sunlight), and following photoinhibition under high light and low temperature. A simple model for predicting CO2 assimilation from fluorescence parameters is presented and evaluated. It is concluded that under a wide range of conditions fluorescence parameters can be used to predict accurately and rapidly CO2 assimilation rates in maize.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

A:

measured rate of CO2 assimilation

A* (=A+RL):

the rate of CO2 assimilation corrected for dark-type mitochondrial respiration

Fm′:

maximal yield of PS II chlorophylla fluorescence resulting from a saturating flash of white light under a given steady-state photosynthesis

Fs :

variable yield of fluorescence under steady-state photosynthesis

IL :

light absorbed by the leaf

IPS II :

light absorbed by PS II

Jc :

rate of whole chain electron transport

JO2 :

rate of O2 evolution from PS II

PPFD:

photosynthetic photon flux density

RD :

rate of mitochondrial respiration in the dark

RL :

rate of respiration in the light (independent of photorespiration)

Rubisco:

ribulose 1,5-bisphosphate carboxylase/oxygenase

vc :

velocity of Rubisco carboxylase

vo :

velocity of Rubisco oxygenase

vpr :

velocity of CO2 release by photorespiration

\(\phi _{CO_2 } \) :

apparent quantum yield of CO2 assimilation (A/absorbed PPFD)

\(\phi _{CO_2 ^ \cdot } \) :

quantum yield of CO2 assimilation corrected for dark-type respiration [(A+RL)/absorbed PPFD]

\(\phi _{O_2 ^ \cdot } \) :

quantum yield for photosynthetic O2 evolution

Φ PS II :

quantum yield of PS II photochemistry (electron flux through PS II/rate of photon absorption by PS II antennae)

α:

\({{\alpha - \phi _{PSII} } \mathord{\left/ {\vphantom {{\alpha - \phi _{PSII} } {\phi _{CO_2 ^ \cdot } }}} \right. \kern-\nulldelimiterspace} {\phi _{CO_2 ^ \cdot } }}\) ratio

References

  • Andrews JR, Bredenkamp GJ and Baker NR (1993) Evaluation of the role of state transitions in determining the efficiency of light utilization of CO2 assimilation in leaves. Photosynth Res (submitted)

  • Badger MR (1985) Photosynthetic oxygen exchange. Ann Rev Plant Physiol 36: 27–53

    Google Scholar 

  • Badger MR and Canvin DT (1981) Oxygen uptake during photosynthesis in C3 and C4 plants. In: Akoyunoglou G (ed) Proc. 5th Intl Cong Photosynth, Vol IV, pp 151–161. Balaban Intl Sci Serv, Philadelphia

    Google Scholar 

  • Baker NR and Leech RM (1977) Development of Photosystem I and Photosystem II activities in leaves of light-grown maize (Zea mays). Plant Physiol 60: 640–644

    Google Scholar 

  • Baker NR and Ort DR (1993) Light and crop photosynthetic performance. In: Baker NR and Thomas H (eds) Crop Photosynthesis: Spatial and Temporal Determinants. Vol 12, Topics in Photosynthesis, pp 289–312, Elsevier, London

    Google Scholar 

  • Brooks A and Farquhar GD (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: 397–406

    Google Scholar 

  • Byrd GT, Sage RF and Brown RH (1992) A comparison of dark respiration between C3 and C4 plants. Plant Physiol 100: 191–198

    Google Scholar 

  • Collatz GJ, Ribas-Carbo M and Berry JA (1992) Coupled photosynthesis-stomatal conductance model for leaves of C4 plants. Aust J Plant Physiol 19: 519–538

    Google Scholar 

  • Demmig B and Björkman O (1987) Comparison of the effect of excessive light on chlorophyll fluorescence (77K) and photon yield of O2 evolution in leaves of higher plants. Planta 171: 171–184

    Google Scholar 

  • De Veau EJ and Burris JE (1989) Photorespiratory rates in wheat and maize as determined by18O-labeling. Plant Physiol 90: 500–511

    Google Scholar 

  • Edwards GE and Walker DA (1983) C3, C4: Mechanisms, and Cellular and Environmental Regulation of Photosynthesis. Blackwell, Oxford, 542 pp

    Google Scholar 

  • Ehleringer J and Pearcy RW (1983) Variation in quantum yield for CO2 uptake among C3 and C4 plants. Plant Physiol 73: 555–559

    Google Scholar 

  • Furbank RT and Badger RT (1982) Photosynthetic oxygen exchange in attached leaves of C4 monocotyledons. Aust J Plant Physiol 9: 553–558

    Google Scholar 

  • Furbank RT and Badger RT (1983) Photorespiratory characteristics of isolated bundle sheath strands of C4 monocotyledons. Aust J Plant Physiol 10: 451–458

    Google Scholar 

  • Furbank RT, Badger MR and Osmond CB (1983) Photoreduction of oxygen in mesophyll chloroplasts of C4 plants. Plant Physiol 73: 1038–1041

    Google Scholar 

  • Furbank RT, Jenkins CLD and Hatch MD (1990) C4 photosynthesis: Quantum requirement, C4 acid overcycling and Q-cycle involvement. Aust J Plant Physiol 17: 1–7

    Google Scholar 

  • Genty B, Briantais J-M and Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990: 87–92

    Google Scholar 

  • Henderson SA, von Caemmerer S and Farquhar GD (1992) Short-term measurements of carbon isotope discrimination in several C4 species. Aust J Plant Physiol 19: 263–285

    Google Scholar 

  • Krall JP and Edwards GE (1992) Relationship between Photosystem II activity and CO2 fixation in leaves. Physiol Plant 86: 180–187

    Google Scholar 

  • Ku MSB and Edwards GE (1978) Oxygen inhibition of photosynthesis. III. Temperature dependence of quantum yield and its relation to O2/CO2 solubility ratio. Planta 140: 1–6

    Google Scholar 

  • Lawlor DW and Fock H (1978) Photosynthesis, respiration, and carbon assimilation in water-stress maize at two oxygen concentrations. J Exp Bot 29: 579–593

    Google Scholar 

  • Long SP, East TM and Baker NR (1983) Chilling damage to photosynthesis in youngZea mays. J Exp Bot 34: 177–188

    Google Scholar 

  • Miranda V, Baker NR and Long SP (1981) Limitations of photosynthesis in different regions of theZea mays leaf. New Phytol 89: 179–190

    Google Scholar 

  • Oberhuber W and Edwards GE (1993) Temperature dependence of the linkage of quantum yield of Photosystem II to CO2 fixation in C4 and C3 plants. Plant Physiol 101: 507–512

    PubMed  Google Scholar 

  • Oberhuber W, Dai Z and Edwards GE (1993) Light dependence of quantum yields of Photosystem II and CO2 fixation in C3 and C4 plants. Photosynth Res 35: 265–274

    Google Scholar 

  • Öquist G and Chow WS (1992) On the relationship between the quantum yield of Photosystem II electron transport, as determined by chlorophyll fluorescence and the quantum yield of CO2-dependent O2 evolution. Photosynth Res 33: 51–62

    Google Scholar 

  • Ortiz-Lopez A, Nie GY, Ort DR and Baker NR (1990) The involvement of photoinhibition of Photosystem II and impaired membrane energization in the reduced quantum yield of carbon assimilation in chilled maize. Planta 181: 78–84

    Google Scholar 

  • Pearcy RW and Ehleringer J (1984) Comparative ecophysiology of C3 and C4 plants. Plant Cell Environ 7: 1–13

    Google Scholar 

  • Rees D and Horton P (1990) The mechanisms of changes in Photosystem II efficiency in spinach thylakoids. Biochem Biophys Acta 1016: 219–227

    Google Scholar 

  • Seaton GR and Walker DA (1990) Chlorophyll fluorescence as a measure of photosynthetic carbon assimilation. Philos Trans R Soc Lond B 242: 29–35

    Google Scholar 

  • Seaton GR and Walker DA (1992) Validating chlorophyll fluorescence measures of efficiency: Observations on fluorimetric estimation of photosynthetic rate. Proc R Soc Lond B 249: 41–47

    Google Scholar 

  • Sharp RE, Matthews MA and Boyer JS (1984) Kok effect and the quantum yield of photosynthesis. Light partially inhibits dark respiration. Plant Physiol 75: 95–101

    Google Scholar 

  • Tobin AK (1992) Carbon and nitrogen metabolism: interactions during leaf development. In: Baker NR and Thomas H (eds) Crop Photosynthesis: Spatial and Temporal Determinants. Vol 12, Topics in Photosynthesis, pp 381–412. Elsevier, London

    Google Scholar 

  • Walker DA (1993) Polarographic measurement of oxygen. In: Hall DO, Scurlock JMO, Bolhar-Nordenkampf HR, Leegood RC and Long SP (eds) Photosynthesis and Production in a C-hanging Environment, pp 168–180. Chapman and Hall, London

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Edwards, G.E., Baker, N.R. Can CO2 assimilation in maize leaves be predicted accurately from chlorophyll fluorescence analysis?. Photosynth Res 37, 89–102 (1993). https://doi.org/10.1007/BF02187468

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02187468

Key words

Navigation