Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

The inhibition of photosynthesis under water deficit conditions is more severe in flecked than uniform irradiance in rice (Oryza sativa) plants

Jiali Sun A , Qiangqiang Zhang A , Muhammad Adnan Tabassum A , Miao Ye A , Shaobing Peng A and Yong Li A B
+ Author Affiliations
- Author Affiliations

A Ministry of Agriculture Key Laboratory of Crop Ecophysiology and Farming System in the Middle Reaches of the Yangtze River, College of Plant Science and Technology, Huazhong Agricultural University, No.1, Shizishan Street, Wuhan, Hubei 430 070, China.

B Corresponding author. Email: liyong@mail.hzau.edu.cn

Functional Plant Biology 44(4) 464-472 https://doi.org/10.1071/FP16383
Submitted: 16 April 2016  Accepted: 22 December 2016   Published: 3 February 2017

Abstract

Water deficit is considered the major environmental factor limiting leaf photosynthesis, and the physiological basis for decreased photosynthesis under water deficit has been intensively studied with steady irradiance. Leaves within a canopy experience a highly variable light environment in magnitude and time, but the effect of water deficit on photosynthesis in fluctuating irradiance is not well understood. Two rice cultivars with different drought tolerance, Champa and Yangliangyou 6 (YLY6), were hydroponically grown under well-watered, 15% (m/v) and 20% PEG (polyethylene glycol, 6000 Da) induced water deficit conditions. The inhibition of steady-state photosynthesis in Champa is more severe than YLY6. The maximum Rubisco carboxylation capacity (Vcmax) and maximum electron transport capacity (Jmax) were decreased under 20% PEG treatment in Champa, whereas less or no effect was observed in YLY6. The induction state (IS%, which indicates photosynthesis capacity after exposure of low-light period) of both leaf photosynthetic rate (A) and stomatal conductance (gs) was highly correlated, and was significantly decreased under water deficit conditions in both cultivars. Water deficit had no significant effect on the time required to reach 50 or 90% of the maximum photosynthetic rate (T50%,A and T90%,A) after exposure to high-light level, but significantly led to a greater decrease in photosynthetic rate in the low-light period under flecked irradiance (Amin-fleck) relative to photosynthetic rate in the same light intensity of continuously low-light period (Ainitial). The lower IS% of A and more severe decrease in Amin-fleck relative to Ainitial will lead to a more severe decrease in integrated CO2 fixation under water deficit in flecked compared with uniform irradiance.

Additional keywords: dynamic photosynthesis, induction state, simulated sunflecks, steady-state photosynthesis, stomatal conductance, water deficit.


References

Allen MT, Pearcy RW (2000) Stomatal versus biochemical limitations to dynamic photosynthetic performance in four tropical rainforest shrub species. Oecologia 122, 479–486.
Stomatal versus biochemical limitations to dynamic photosynthetic performance in four tropical rainforest shrub species.Crossref | GoogleScholarGoogle Scholar |

Banaś AK, Aggarwal C, Łabuz J, Sztatelman O, Gabryś H (2012) Blue light signalling in chloroplast movements. Journal of Experimental Botany 63, 1559–1574.
Blue light signalling in chloroplast movements.Crossref | GoogleScholarGoogle Scholar |

Bernacchi CJ, Portis AR, Nakano H, von Caemmerer S, Long SP (2002) Temperature response of mesophyll conductance. Implications for the determination of Rubisco enzyme kinetics and for limitations to photosynthesis in vivo. Plant Physiology 130, 1992–1998.
Temperature response of mesophyll conductance. Implications for the determination of Rubisco enzyme kinetics and for limitations to photosynthesis in vivo.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXktlOj&md5=1a29283064c28fa71fde6bd9c92cb31dCAS |

Cano FJ, López R, Warren CR (2014) Implications of the mesophyll conductance to CO2 for photosynthesis and water-use efficiency during long–term water stress and recovery in two contrasting Eucalyptus species. Plant, Cell & Environment 37, 2470–2490.
Implications of the mesophyll conductance to CO2 for photosynthesis and water-use efficiency during long–term water stress and recovery in two contrasting Eucalyptus species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXhslOksrfM&md5=073b2e55085a03c9f0f6ed927af2c74eCAS |

Cui X, Gu S, Wu J, Tang Y (2009) Photosynthetic response to dynamic changes of light and air humidity in two moss species from the Tibetan Plateau. Ecological Research 24, 645–653.
Photosynthetic response to dynamic changes of light and air humidity in two moss species from the Tibetan Plateau.Crossref | GoogleScholarGoogle Scholar |

Farquhar GD, von Caemmerer S, Berry JA (1980) A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta 149, 78–90.
A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3cXksVWrt7w%3D&md5=6db882a9dac8dc5a797c6c3206d6450cCAS |

Flexas J, Medrano H (2002) Drought-inhibition of photosynthesis in C3 plants: stomatal and non-stomatal limitations revisited. Annals of Botany 89, 183–189.
Drought-inhibition of photosynthesis in C3 plants: stomatal and non-stomatal limitations revisited.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XkslymsLs%3D&md5=89d0952cc5dabe59e7d64a5e7ecac009CAS |

Flexas J, Bota J, Escalona JM, Sampol B, Medrano H (2002) Effects of drought on photosynthesis in grapevines under field conditions: an evaluation of stomatal and mesophyll limitations. Functional Plant Biology 29, 461–471.
Effects of drought on photosynthesis in grapevines under field conditions: an evaluation of stomatal and mesophyll limitations.Crossref | GoogleScholarGoogle Scholar |

Hubbart S, Peng SB, Horton P, Chen Y, Murchie EH (2007) Trends in leaf photosynthesis in historical rice varieties developed in the Philippines since 1966. Journal of Experimental Botany 58, 3429–3438.
Trends in leaf photosynthesis in historical rice varieties developed in the Philippines since 1966.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXht1Kmt77M&md5=7e14833e89f4edb1ab301c0e602f7c75CAS |

Kaiser E, Morales A, Harbinson J, Kromdijk J, Heuvelink E, Marcelis LF (2015) Dynamic photosynthesis in different environmental conditions. Journal of Experimental Botany 66, 2415–2426.
Dynamic photosynthesis in different environmental conditions.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC28Xhs12qtbjI&md5=310aa712a81c14cdcdaea3d60c3d6892CAS |

Kromdijk J, Glowacka K, Leonelli L, Gabilly ST, Iwai M, Niyogi KK, Long SP (2016) Improving photosynthesis and crop productivity by accelerating recovery from photoprotection. Science 354, 857–861.
Improving photosynthesis and crop productivity by accelerating recovery from photoprotection.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC28XhvFGrtLfM&md5=a099c13da50dabd8446304af03734414CAS |

Kubásek J, Urban O, Šantrůček J (2013) C4 plants use fluctuating light less efficiently than do C3 plants: a study of growth, photosynthesis and carbon isotope discrimination. Physiologia Plantarum 149, 528–539.
C4 plants use fluctuating light less efficiently than do C3 plants: a study of growth, photosynthesis and carbon isotope discrimination.Crossref | GoogleScholarGoogle Scholar |

Lawson T, Kramer DM, Raines CA (2012) Improving yield by exploiting mechanisms underlying natural variation of photosynthesis. Current Opinion in Biotechnology 23, 215–220.
Improving yield by exploiting mechanisms underlying natural variation of photosynthesis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhsFGqurg%3D&md5=2dfc0a7e1030aea7f4ece16befe13e26CAS |

Leakey ADB, Press MC, Scholes JD, Watling JR (2002) Relative enhancement of photosynthesis and growth at elevated CO2 is greater under sunflecks than uniform irradiance in a tropical rain forest tree seedling. Plant, Cell & Environment 25, 1701–1714.
Relative enhancement of photosynthesis and growth at elevated CO2 is greater under sunflecks than uniform irradiance in a tropical rain forest tree seedling.Crossref | GoogleScholarGoogle Scholar |

Leakey ADB, Press MC, Scholes JD (2003) Patterns of dynamic irradiance affect the photosynthetic capacity and growth of dipterocarp tree seedlings. Oecologia 135, 184–193.
Patterns of dynamic irradiance affect the photosynthetic capacity and growth of dipterocarp tree seedlings.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3s7nvFegug%3D%3D&md5=acb05c6b885c7840bfab68792dc71e9eCAS |

Li Y, Ren BB, Yang XX, Xu GH, Shen QR, Guo SW (2012) Chloroplast downsizing under nitrate nutrition restrained mesophyll conductance and photosynthesis in rice (Oryza sativa L.) under drought conditions. Plant & Cell Physiology 53, 892–900.
Chloroplast downsizing under nitrate nutrition restrained mesophyll conductance and photosynthesis in rice (Oryza sativa L.) under drought conditions.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XntVSjsLw%3D&md5=eb5e02aa15cdd9613bbf9b954b345145CAS |

Naumburg E, Ellsworth DS (2000) Photosynthetic sunfleck utilization potential of understory saplings growing under elevated CO2 in FACE. Oecologia 122, 163–174.
Photosynthetic sunfleck utilization potential of understory saplings growing under elevated CO2 in FACE.Crossref | GoogleScholarGoogle Scholar |

Parry MAJ, Andralojc PJ, Khan S, Lea PJ, Keys AJ (2002) Rubisco activity: effects of drought stress. Annals of Botany 89, 833–839.
Rubisco activity: effects of drought stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XlsVeitLo%3D&md5=036a0b10b22290a76ede64f1c9dee6bdCAS |

Pearcy RW, Roden JS, Gamon JA (1990) Sunfleck dynamics in relation to canopy structure in a soybean (Glycine max (L.) Merr.) canopy. Agricultural and Forest Meteorology 52, 359–372.
Sunfleck dynamics in relation to canopy structure in a soybean (Glycine max (L.) Merr.) canopy.Crossref | GoogleScholarGoogle Scholar |

Perez–Martin A, Michelazzo C, Torres–Ruiz JM, Flexas J, Fernández JE, Sebastiani L, Diaz–Espejo A (2014) Regulation of photosynthesis and stomatal and mesophyll conductance under water stress and recovery in olive trees: correlation with gene expression of carbonic anhydrase and aquaporins. Journal of Experimental Botany 65, 3143–3156.
Regulation of photosynthesis and stomatal and mesophyll conductance under water stress and recovery in olive trees: correlation with gene expression of carbonic anhydrase and aquaporins.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC28Xhs1Gju7fK&md5=6c2454ba6aa4ef004b7cf5fa5eec6af7CAS |

Prinsley RT, Hunt S, Smith AM, Leegood RC (1986) The influence of a decrease in irradiance on photosynthetic carbon assimilation in leaves of Spinacia oleracea L. Planta 167, 414–420.
The influence of a decrease in irradiance on photosynthetic carbon assimilation in leaves of Spinacia oleracea L.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL28Xhs1Glt7k%3D&md5=19ff42b9cdb9c1e4d55467b2c279955fCAS |

Sassenrath-Cole GF, Pearcy RW, Steinmaus S (1994) The role of enzyme activation state in limiting carbon assimilation under variable light conditions. Photosynthesis Research 41, 295–302.
The role of enzyme activation state in limiting carbon assimilation under variable light conditions.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2cXmtVWitr0%3D&md5=ab889c544764ceea0382d4182ecce19eCAS |

Sharkey TD (2016) What gas exchange data can tell us about photosynthesis. Plant, Cell & Environment 39, 1161–1163.
What gas exchange data can tell us about photosynthesis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC28XnslWhsbk%3D&md5=8bd9bdae992131cc1948e223fe74ce69CAS |

Sharkey TD, Seemann JR, Pearcy RW (1986) Contribution of metabolites of photosynthesis to postillumination CO2 assimilation in response to lightflecks. Plant Physiology 82, 1063–1068.
Contribution of metabolites of photosynthesis to postillumination CO2 assimilation in response to lightflecks.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2sXpvFGqsA%3D%3D&md5=e8756d0ad132666563afe7f142cbb8ddCAS |

Sharkey TD, Bernacchi CJ, Farquhar GD, Singsaas EL (2007) Fitting photosynthetic carbon dioxide response curves for C3 leaves. Plant, Cell & Environment 30, 1035–1040.
Fitting photosynthetic carbon dioxide response curves for C3 leaves.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVeiur3F&md5=6e09ee70f54fef63acd184d4920e8411CAS |

Sun JL, Ye M, Peng SB, Li Y (2016) Nitrogen can improve the rapid response of photosynthesis to changing irradiance in rice (Oryza sativa L.) plants. Scientific Reports 6, 31305
Nitrogen can improve the rapid response of photosynthesis to changing irradiance in rice (Oryza sativa L.) plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC28XhtlCisbfL&md5=bddd4e3c93d8ddb62da99a4402a8a378CAS |

Tausz M, Warren CR, Adams MA (2005) Dynamic light use and protection from excess light in upper canopy and coppice leaves of Nothofagus cunninghamii in an old growth, cool temperate rainforest in Victoria, Australia. New Phytologist 165, 143–156.
Dynamic light use and protection from excess light in upper canopy and coppice leaves of Nothofagus cunninghamii in an old growth, cool temperate rainforest in Victoria, Australia.Crossref | GoogleScholarGoogle Scholar |

Timm HC, Stegemann J, Küppers M (2002) Photosynthetic induction strongly affects the light compensation point of net photosynthesis and coincidentally the apparent quantum yield. Trees 16, 47–62.
Photosynthetic induction strongly affects the light compensation point of net photosynthesis and coincidentally the apparent quantum yield.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XmsVKks70%3D&md5=69d351bf40202a02b6e8cdbeac34bc75CAS |

Valentini R, Epron D, Deangelis P, Matteucci G, Dreyer E (1995) In situ estimation of net CO2 assimilation, photosynthetic electron flow and photorespiration in turkey oak (Q. cerris L.) leaves. Diurnal cycles under different levels of water-supply. Plant, Cell & Environment 18, 631–640.
In situ estimation of net CO2 assimilation, photosynthetic electron flow and photorespiration in turkey oak (Q. cerris L.) leaves. Diurnal cycles under different levels of water-supply.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXmvFKks70%3D&md5=41edb41469ff1b6c31851f2fee2efe26CAS |

Valladares F, Allen MT, Pearcy RW (1997) Photosynthetic responses to dynamic light under field conditions in six tropical rainforest shrubs occurring along a light gradient. Oecologia 111, 505–514.
Photosynthetic responses to dynamic light under field conditions in six tropical rainforest shrubs occurring along a light gradient.Crossref | GoogleScholarGoogle Scholar |

Wada M (2013) Chloroplast movement. Plant Science 210, 177–182.
Chloroplast movement.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXhtV2rtrzO&md5=99ed8fc5bd76c518b466c9d91a5f828cCAS |

Way DA, Pearcy RW (2012) Sunflecks in trees and forests: from photosynthetic physiology to global change biology. Tree Physiology 32, 1066–1081.
Sunflecks in trees and forests: from photosynthetic physiology to global change biology.Crossref | GoogleScholarGoogle Scholar |

Wong SL, Chen CW, Huang HW, Weng JH (2012) Using combined measurements for comparison of light induction of stomatal conductance, electron transport rate and CO2 fixation in woody and fern species adapted to different light regimes. Tree Physiology 32, 535–544.
Using combined measurements for comparison of light induction of stomatal conductance, electron transport rate and CO2 fixation in woody and fern species adapted to different light regimes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhtFCkt77P&md5=cf6873cb4a1ae02f2dfd5ccd3e17f55cCAS |