Register      Login
Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

Initial observations of increased requirements for light-energy dissipation in ryegrass (Lolium perenne) when source / sink ratios become high at a naturally grazed free air CO2 enrichment (FACE) site

Jianmin Guo A C , Craig M. Trotter A and Paul C. D. Newton B
+ Author Affiliations
- Author Affiliations

A Landcare Research, Private Bag 11052, Palmerston North, New Zealand.

B AgResearch Grasslands, Private Bag 11008, Palmerston North, New Zealand.

C Corresponding author. Email: guoj@landcareresearch.co.nz

Functional Plant Biology 33(11) 1045-1053 https://doi.org/10.1071/FP06168
Submitted: 11 July 2006  Accepted: 19 September 2006   Published: 1 November 2006

Abstract

Although photosynthetic response to long-term elevated CO2 has been extensively studied, little attention has yet been directed at coordinated adjustments between the use of absorbed light for CO2 fixation, and the dissipation of potentially harmful excess light. In this study, we have performed an initial analysis of photosynthetic light use and excess light dissipation in response to grazing-induced variation in the source / sink ratio in ryegrass (Lolium perenne L.) after 6 years’ exposure to Free Air CO2 Enrichment (FACE). Before grazing, when the source / sink ratio was relatively large, significant down-regulation of photosynthetic capacity (Amax) was observed in the FACE leaves compared with control leaves at the same stage of maturity. The decrease in Amax partly offset the direct stimulation of elevated CO2 on light-saturated photosynthesis, and was accompanied by a reduction in photochemical electron flow that was accompanied by a large increase in susceptibility to photoinhibition. This was indicated by large increases in both non-photochemical quenching (NPQ) and the de-epoxidised state of xanthophyll cycle (DEPS), and also by changes in the photochemical reflectance index (PRI). However, no significant increase in the xanthophyll pool size in FACE leaves was observed, despite the apparent large increase in requirements for photodissipation in FACE leaves. After grazing, when the source / sink ratio was relatively small, the CO2 fixation rates in both the FACE and control leaves were, as expected, significantly higher compared with those before grazing, and there was no down-regulation of photosynthetic capacity in the leaves under FACE conditions. In addition, the extent of photodissipation in the FACE and control leaves was not significantly different. Overall, the profile of leaf physiological and biochemical responses supports the hypothesis that the effect of long-term elevated CO2 can be significantly influenced by short-term variation in the source / sink ratio. As the xanthophyll pool size does not change significantly, this poses the question of whether the increased photodissipative demand observed here under even moderately elevated CO2 concentrations may lead to increased plant susceptibility to photoinhibition, and thus to an increased risk of damage to plant function, under conditions of low sink demand. This question clearly deserves further study.

Keywords: chlorophyll fluorescence, elevated CO2, grazing, photochemical reflectance index, photoinhibition, photosynthesis, xanthophyll cycle.


Acknowledgments

This study is supported by a grant from the New Zealand Foundation for Research Science and Technology under contract LCRX0202 and C10X0205. We thank Ted Pinkney for technical assistance and Dr Adrian Walcroft for insightful comments.


References


Ainsworth EA, Davey PA, Hymus GJ, Osborne CP, Rogers A, Blum H, Nösberger J, Long SP (2003) Is stimulation of leaf photosynthesis by elevated carbon dioxide concentration maintained in the long term? A test with Lolium perenne grown for 10 years at two nitrogen fertilization levels under free air CO2 enrichment (FACE). Plant, Cell & Environment 26, 705–714.
Crossref | GoogleScholarGoogle Scholar | open url image1

Barker DH, Adams WW (1997) The xanthophyll cycle and energy dissipation in different oriented faces of the cactus Opuntia macrorhiza. Oecologia 109, 353–361.
Crossref | GoogleScholarGoogle Scholar | open url image1

Bowes G (1993) Facing the inevitable — plants and increasing atmospheric CO2. Annual Review of Plant Physiology and Plant Molecular Biology 44, 309–332.
Crossref | GoogleScholarGoogle Scholar | open url image1

Buchmann N (2002) Plant ecophysiology and forest response to global change. Tree Physiology 22, 1177–1184.
PubMed |
open url image1

Cotrufo MFIP, Scott A (1998) Elevated CO2 reduces the nitrogen concentration of plant tissues. Global Change Biology 4, 43–54.
Crossref | GoogleScholarGoogle Scholar | open url image1

Drake BG, Gonzalez-Meler MA, Long SP (1997) More efficient plants: a consequence of rising atmospheric CO2? Annual Review of Plant Physiology and Plant Molecular Biology 48, 609–639.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Edwards GR, Clark H, Newton PCD (2001) The effects of elevated CO2 on seed production and seedling recruitment in a sheep-grazed pasture. Oecologia 127, 383–394.
Crossref | GoogleScholarGoogle Scholar | open url image1

Farquhar GD, von Caemmerer S, Berry JA (1980) A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta 149, 78–90.
Crossref | GoogleScholarGoogle Scholar | open url image1

Foyer CH (1988) Feedback inhibition of photosynthesis through source–sink regulation in leaves. Plant Physiology and Biochemistry 26, 483–492. open url image1

Furbank RT, Taylor WC (1995) Regulation of photosynthesis in C3 and C4 plants: a molecular approach. The Plant Cell 7, 797–807.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Gamon JA, Serrano L, Surfus JS (1997) The photochemical reflectance index: an optical indicator of photosynthetic radiation use efficiency across species, functional types, and nutrient levels. Oecologia 112, 492–501.
Crossref | GoogleScholarGoogle Scholar | open url image1

Genty B, Briantais JM, Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochimica et Biophysica Acta 990, 87–92. open url image1

Gilmore AM, Yamamoto HY (1991) Resolution of lutein and zeaxanthin using a non-endcapped lightly carbon-loaded C18 high-performance liquid chromatographic column. Journal of Chromatography 543, 137–145.
Crossref | GoogleScholarGoogle Scholar | open url image1

Griffin KL, Seemann JR (1996) Plants, CO2 and photosynthesis in the 21st century. Chemistry & Biology 3, 245–254.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Guo JM, Trotter CM (2004) Estimating photosynthetic light-use efficiency using the photochemical reflectance index: variations among species. Functional Plant Biology 31, 255–265.
Crossref | GoogleScholarGoogle Scholar | open url image1

Habash DZ, Paul MJ, Parry MAJ, Keys AJ, Lawlor DW (1995) Increased capacity for photosynthesis in wheat grown at elevated CO2: the relationship between electron transport and carbon metabolism. Planta 197, 482–489.
Crossref | GoogleScholarGoogle Scholar | open url image1

Herold A (1980) Regulation of photosynthesis by sink activity: the missing link. New Phytologist 86, 131–144.
Crossref | GoogleScholarGoogle Scholar | open url image1

Hogan KP, Fleck I, Bungard R, Cheeseman JM, Whitehead D (1997) Effect of elevated CO2 on the utilization of light energy in Nothofagus fusca and Pinus radiata. Journal of Experimental Botany 48, 1289–1297. open url image1

Hymus GJ, Ellsworth DS, Baker NR, Long SP (1999) Does free-air carbon dioxide enrichment affect photochemical energy use by evergreen trees in different seasons? A chlorophyll fluorescence study of mature loblolly pine. Plant Physiology 120, 1183–1191.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Hymus GJ, Baker NR, Long SP (2001) Growth in elevated CO2 can both increase and decrease photochemistry and photoinhibition of photosynthesis in a predictable manner. Dactylis glomerata grown in two levels of nitrogen nutrition. Plant Physiology 127, 1204–1211.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Isopp H, Frehner M, Almeida JPF, Blum H, Daepp M, Hartwig UA, Lüscher A, Suter D, Nösberger J (2000) Nitrogen plays a major role in leaves when source–sink relationships change: C and N metabolism in Lolium perenne growing under free air CO2 enrichment. Australian Journal of Plant Physiology 27, 851–858. open url image1

Jones M, Clifton BG, Raschi A, Miglietta F (1995) the effects on Arbutus unedo L. of long term exposure to elevated CO2. Global Change Biology 1, 295–302.
Crossref | GoogleScholarGoogle Scholar | open url image1

Kicklighter DW, Bondeau A, Schloss AL, Kaduk J, McGuire AD (1999) Comparing global models of terrestrial net primary productivity (NPP): global patterns and differentiation by major biomass. Global Change Biology 5, 16–24.
Crossref | GoogleScholarGoogle Scholar | open url image1

Kurasova I, Kalina J, Stroch M, Urban O, Spunda V (2003) Response of photosynthetic apparatus of spring barley (Hordeum vulgare L.) to combined effect of elevated CO2 concentration and different growth irradiance. Photosynthetica 41, 209–219.
Crossref | GoogleScholarGoogle Scholar | open url image1

Luo Y, Sims DA, Thomas RB, Tissue DT, Ball JT (1998) Nonlinearity of photosynthetic responses to growth in rising atmospheric CO2: an experimental and modelling study. Global Change Biology 4, 173–183.
Crossref | GoogleScholarGoogle Scholar | open url image1

Medlyn BE (1996) The optimal allocation of nitrogen within the C3 photosynthetic system at elevated CO2. Australian Journal of Plant Physiology 23, 593–603. open url image1

Niyogi KK (1999) Photoprotection revisited: genetic and molecular approaches. Annual Review of Plant Physiology and Molecular Biology 50, 333–359.
Crossref | GoogleScholarGoogle Scholar | open url image1

Radoglou KM, Jarvis PG (1990) Effects of CO2 enrichment on four poplar clones. I. Growth and leaf anatomy. Annals of Botany 65, 617–626. open url image1

Robertson EJ, Leech RM (1995) Significant changes in cell and chloroplast development in young wheat leaves (Triticum aestivum cv. Hereward) grown in elevated CO2. Plant Physiology 107, 63–71.
PubMed |
open url image1

Rogers A, Humphries SW (2000) A mechanistic evaluation of photosynthetic acclimation at elevated CO2. Global Change Biology 6, 1005–1011.
Crossref | GoogleScholarGoogle Scholar | open url image1

Rogers A, Fischer BU, Byant J, Frehner M, Blum H, Raines CA, Long SP (1998) Acclimation of photosynthesis to elevated CO2 under low-N nutrition is affected by the capacity for assimilate utilization — perennial ryegrass under free-air CO2 enrichment. Plant Physiology 118, 683–689.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Ross DJ, Newton PCD, Tate KR (2004) Elevated CO2 effects on herbage production and soil carbon and nitrogen pools and mineralization in a species-rich, grazed pasture on a seasonally dry sand. Plant and Soil 260, 183–196.
Crossref | GoogleScholarGoogle Scholar | open url image1

Sage RF (1994) Acclimation of photosynthesis to increasing atmospheric CO2: the gas exchange perspective. Photosynthesis Research 39, 351–368.
Crossref | GoogleScholarGoogle Scholar | open url image1

Saxe H, Ellsworth DS, Heath J (1998) Tree and forest functioning in an enriched CO2 atmosphere. New Phytologist 139, 395–436.
Crossref | GoogleScholarGoogle Scholar | open url image1

Scarascia-Mugnozza G, De Angelis P, Matteucci G, Valentini R (1996) Long-term exposure to elevated CO2 in a natural Quercus ilex L. community: net photosynthesis and photochemical efficiency of PSII at different levels of water stress. Plant, Cell & Environment 19, 643–654.
Crossref | GoogleScholarGoogle Scholar | open url image1

Sharkey TD (1985) Photosynthesis in intact leaves of C3 plants: physics, physiology and rate limitations. Botanical Review 51, 53–105. open url image1

Spunda V, Kalina J, Cajánek M, Pavlìcková H, Marek V (1998) Long-term exposure of Norway spruce to elevated CO2 concentration induces changes in photosystem II mimicking an adaptation to increased irradiance. Journal of Plant Physiology 152, 413–419. open url image1

Stitt M (1991) Rising CO2 levels and their potential significance for carbon flow in photosynthetic cells. Plant, Cell & Environment 14, 741–762.
Crossref | GoogleScholarGoogle Scholar | open url image1

Stylinski CD, Oechel WC, Tissue DT, Miglietta F, Raschi A (2000) Effects of lifelong [CO2] enrichment on carboxylation and light utilization of Quercus pubescens Willd. examined with gas exchange, biochemistry and optical techniques. Plant, Cell & Environment 23, 1353–1362.
Crossref | GoogleScholarGoogle Scholar | open url image1

Tissue DT, Griffin KL, Ball JT (1999) Photosynthetic adjustment in field-grown ponderosa pine trees after six years of exposure to elevated CO2. Plant Physiology 19, 221–228. open url image1

Tóth VR, Mészáros I, Veres S, Nagy J (2002) Effects of the available nitrogen on the photosynthetic activity and xanthophyll cycle pool of maize in field. Journal of Plant Physiology 159, 627–634.
Crossref | GoogleScholarGoogle Scholar | open url image1

Turnbull MH, Tissue DT, Griffin KL, Rogers GND, Whitehead D (1998) Photosynthetic acclimation to long-term exposure to elevated CO2 concentration in Pinus radiata D. Don. is related to age of needles. Plant, Cell & Environment 21, 1019–1028.
Crossref | GoogleScholarGoogle Scholar | open url image1

von Caemmerer S, Farquhar GD (1981) Some relationships between the biochemistry of photosynthesis and the gas exchange rates of leaves. Planta 153, 376–387.
Crossref | GoogleScholarGoogle Scholar | open url image1

von Caemmerer S, Ghannoum O, Conroy JP, Clark H, Newton PCD (2001) Photosynthetic responses of temperature species to free air CO2 enrichment (FACE) in a grazed New Zealand pasture. Australian Journal of Plant Physiology 28, 439–450. open url image1