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Acquisition and Diffusion of CO2 in Higher Plant Leaves

  • Chapter
Photosynthesis

Part of the book series: Advances in Photosynthesis and Respiration ((AIPH,volume 9))

Summary

Acquisition of CO2 by higher plants involves CO2 diffusion from the air into leaves and, ultimately, into chloroplasts. There, fixation of CO2 into organic compounds creates the concentration gradient which drives CO2 diffusion. CO2 encounters many obstructions along its diffusion path toward chloroplasts. The diffusion resistances attributable to boundary layer and stomata are shared with the opposing flux of water leaving the leaf. Once in the substomatal cavities, however, CO2 faces additional resistances since it has to cross walls and membranes to reach the chloroplasts. We follow the CO2 molecule from the air through the boundary layer, stomata and, finally, the mesophyll. After providing diverse anatomical examples at each level, we review the current understanding about the subtle balance which plants maintain between water loss and CO2 acquisition.

Stomatal responses to many environmental variables are well known, despite our lack of understanding of the underlying mechanisms. Techniques areavailable that allow accurate measurements of conductances through the boundary layer and stomata. The estimation of conductance through the mesophyll, however, has not been feasible until the recent development of rapid measurements of isotopic discrimination and chlorophyll fluorescence. We discuss the principles which allow the estimation of internal conductance based on these techniques and the data available. Both stomatal conductance and internal conductance correlate strongly with photosynthetic capacity and are of similar magnitude. However, stomatal conductance can vary within minutes in response to changes in the environment. Internal conductance, on the other hand, seems to be stable over several days and depends on anatomical properties of the leaf. We close considering the special case of photosynthesis where spatial compartmentation and biochemical mechanisms of CO2 concentration add complexity to the estimation of internal conductance.

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Abbreviations

Δ, Δ1:

carbon isotope discrimination, carbon isotope discrimination predicted from P a

Γ, Γ:

CO2 compensation point, CO2 compensation point in the absence of respiration R

øPSII:

photochemical efficiency of Photosystem II

A:

rate of CO2 assimilation

E:

rate of transpiration

gb, gg, gw:

boundary layer conductance, stromatal conductance, internal conductance

J, JF:

rate of electron transport, rate of electron transport calculated from chlorophyll fluorescence

LMA:

leaf dry mass per unit area

pa, p3, p1, pc:

partial pressures of CO2 in the air surrounding the leaf, at the leaf surface, in the substomatal cavities, at the sites of carboxylation, respectively

R:

rate of non-photorespiratory CO2 evolution (rate of respiration)

Sc, Smax:

surface area of chloroplasts exposed to intercellular airspace per unit leaf area, surface area of mesophyll cells exposed to intercellular airspace/per unit leaf area

VPD:

leaf to air vapor pressure difference

References

  • Araus JL, Alegre L, Tapia L, Calafell R and Serret MD (1986) Relationships between photosynthetic capacity and leaf structure in several shade plants. Amer J Bot 73:1760–1770

    Google Scholar 

  • Balaguer L, Afif D, Dizengremel P and Dreyer E (1996) Specificity factor of ribulose carboxylase/oxygenase of Quercus robur. Plant Physiol Biochem 34:879–883

    CAS  Google Scholar 

  • Ball JT, Woodrow IE and Berry JA (1987) A model predicting stomatal conductance and its contribution to the control of photosynthesis under different environmental conditions. In: Biggins I (ed) Progress in Photosynthesis Research, pp 221–224. Martinus Nijhoff, The Netherlands

    Google Scholar 

  • Berry JA, Collate GJ, Guy RD and Fogel MD (1994) The compensation point: Can a physiological concept be applied to global cycles of carbon and oxygen? In: Tolbert NE and Preiss J (eds) Regulation of Atmospheric CO2 and O2 by Photosynthetic Carbon Metabolism, pp 234–248. Oxford University Press, Oxford

    Google Scholar 

  • Beyschlag W and Pfanz H (1990) A fast method to detect the occurrence of nonhomogeneous distribution of stomatal aperture in heterobaric plant leaves. Oecologia 82:52–55

    Google Scholar 

  • Beyschlag W, Pfanz H and Ryel RJ (1992) Stomatal patchiness in Mediterranean evergreen sclerophylls. Planta 187:546–553

    Article  Google Scholar 

  • Bolhar-Nordenkampf HR and Draxler G (1993) Functional leaf anatomy. In: Hall DO, Scurlock JMO, Bolhar-Nordenkampf HR, Leegood RC and Long SP (eds) Photosynthesis and Production in a Changing Environment: A Field and Laboratory Manual, pp 91–112. Chapman and Hall, London

    Google Scholar 

  • Bongi G and Loreto F (1989) Gas-exchange properties of salt-stressed Olive (Olea europea L). leaves. Plant Physiol 90:1408–1416

    CAS  Google Scholar 

  • Brewer CA and Smith WK (1997) Patterns of leaf surface wetness for montane and subalpine plants. Plant Cell Env 20: 1–11

    Google Scholar 

  • Brewer CA, Smith WK and Vogelmann TC (1991) Functional interaction between leaf trichomes, leaf wettability and the optical properties of water droplets. Plant Cell Env 14:955–962

    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

    Article  CAS  Google Scholar 

  • Brown RH (1997) Analysis of bundle sheath conductance and C4 photosynthesis using a PEP-carboxylase inhibitor. Aust J Plant Physiol 24:549–554

    CAS  Google Scholar 

  • Brown RH and Byrd GT (1993) Estimation of bundle sheath cell conductance in C4 species and O2 insensitivity of photosynthesis. Plant Physiol 103:1183–1188

    Article  CAS  PubMed  Google Scholar 

  • Brown RH and Hattersley PW (1989) Leaf anatomy of C3-C4 species as related to evolution of C4 photosynthesis. Plant Physiol 91:1543–1550

    Google Scholar 

  • Brugnoli E, Hubick KT, von Caemmerer S, Wong SC and Farquhar GD (1988) Correlation between the carbon isotope discrimination in leaf starch and sugars of C3 plants and the ratio of intercellular and atmospheric partialpressures of carbon dioxide. Plant Physiol 88:1418–1424

    CAS  Google Scholar 

  • Brugnoli E, Scartazza A, Lauteri M, Monteverdi MC and Máguas C (1998) Carbon isotope discrimination in structural and non-structural carbohydrates in relation to productivity and adaptation to unfavourable conditions. In: Griffiths H (ed) Stable Isotopes: Integration of Biological, Ecological and Geochemical Processes, pp 133–146. BIOS, Oxford

    Google Scholar 

  • Cardon ZG, Mott KA and Berry JA (1994) Dynamics of patchy stomatal movements, and their contribution to steady-state and oscillating stomatal conductance calculated using gas-exchange techniques. Plant Cell Env 17:995–1007

    Google Scholar 

  • Chonan N, Kawahara H and Matsuda T (1977) Ultrastructural development of mesophyll cells in rice seedlings. Jpn J Crop Sci 46:147–156

    Google Scholar 

  • Constable GA and Rawson HM (1980) Effect of leaf position, expansion, and age on photosynthesis, transpiration and water use efficiency of cotton. Aust J Plant Physiol 7:89–100

    Google Scholar 

  • Cowan IR (1977) Water use in higher plants. In: McKintyre AK (ed) Water: Planets, Plants and People, pp 71–107, Aust Acad Sci, Canberra

    Google Scholar 

  • Craig S and Goodchild DJ (1977) Leaf ultrastructure of Triodia irritans: A C4 grass possessing an unusual arrangement of photosynthetic tissues.

    Google Scholar 

  • Daley PF, Raschke K, Ball JT and Berry JA (1989) Topography of photosynthetic activity of leaves obtained from video images of chlorophyll fluorescence. Plant Physiol 90:1233–1238

    CAS  Google Scholar 

  • Dawson TE and Ehleringer JR (1993) Gender-specific physiology, carbon isotopediscrimination, and habitat distribution in boxelder, Acer negundo. Ecology 74:798–815

    Google Scholar 

  • Dean C and Leech RM (1982) Genome expression during normal leaf development. 2. Direct correlation between ribulose bisphosphate carboxylase content and nuclear ploidy in a polyploid series of wheat. Plant Physiol 70:1605–1608

    CAS  Google Scholar 

  • Delfine S, Alvino A, Zacchini M and Loreto F (1998) Consequences of salt stress on conductance to CO2 diffusion, Rubisco characteristics and anatomy of spinach leaves. Aust J Plant Physiol 25:395–402

    CAS  Google Scholar 

  • Delgado E, Parry MAJ, Lawlor DW, Keys AJ and Medrano H (1993) Photosynthesis, ribulose-1,5-bisphosphate carboxylase and leaf characteristics of Nicotiana tabacum L. genotypes selected by survival at low CO2 concentrations. J Exp Bot 44:1–7

    CAS  Google Scholar 

  • Dengler NG, Dengler RE, Donelly PM and Hattersley PW (1994) Quantitative leaf anatomy of C3 and C4 grasses (Poaceae): Bundle sheath and mesophyll surface area relationships. Ann Bot 73:241–255

    Article  Google Scholar 

  • Di Marco G, Manes F, Tricoli D and Vitale E (1990) Fluorescence parameters measured concurrently with net photosynthesis to investigate chloroplastic CO2 concentration in leaves of Quercus ilex L. J Plant Physiol 136:538–543

    Google Scholar 

  • Downton WJS, Loveys BR and Grant WJR (1988) Stomatal closure fully accounts for the inhibition of photosynthesis by abscisic acid. New Phytol 108:263–266

    CAS  Google Scholar 

  • Dunstone RL and Evans LT (1974) Role of changes in cell size in the evolution of wheat. Aust J Plant Physiol 1:157–165

    Google Scholar 

  • Eckstein J, Beyschlag W, Mott KA and Ryel RJ (1996) Changes in photon flux can induce stomatal patchiness. Plant Cell Env, 19:1066–1074

    Google Scholar 

  • Ehleringer JR and Björkman O (1978) A comparison of photosynthetic characteristics of Encelia species possessing glabrous and pubescent leaves. Plant Physiol 62:185–190

    CAS  Google Scholar 

  • Ellis JR and Leech RM (1985) Cell size and chloroplast size in relation to chloroplast replication in light-grown wheat leaves. Planta 165:120–125

    Article  Google Scholar 

  • Epron D, Godard D, Comic G and Genty B (1995) Limitation of net CO2 assimilation rate by internal resistances to CO2 transfer in the leaves of two tree species (Fagus sylvatica L. and Castanea sativa Mill.) Plant Cell Env 18:43–51

    Google Scholar 

  • Evans JR (1983a) Photosynthesis and nitrogen partitioning in leaves of Triticum aestivum and related species. PhD thesis, ANU, Canberra

    Google Scholar 

  • Evans JR (1983b) Nitrogen and photosynthesis in the flag leaf of wheat (Triticum aestivum L.). Plant Physiol 72: 297–302

    CAS  Google Scholar 

  • Evans JR and von Caemmerer S (1996) CO2 diffusion inside leaves. Plant Physiol 110: 339–346

    CAS  PubMed  Google Scholar 

  • Evans JR and Vellen L (1996) Wheat cultivars differ in transpiration efficiency and CO2 diffusion inside their leaves. In: Ishii R and Horie T (eds) Crop research in Asia: Achievements and perspective, pp 326–329. Asian Crop Science Association, Tokyo

    Google Scholar 

  • Evans JR, Sharkey TD, Berry JA and Farquhar GD (1986) Carbon isotope discrimination measured concurrently with gas exchange to investigate CO2 diffusion in leaves of higher plants. Aust J Plant Physiol 13: 281–292

    CAS  Google Scholar 

  • Evans JR, von Caemmerer S, Setchell BA and Hudson GS (1994) The relationship between CO2 transfer conductance and leaf anatomy intransgenic tobacco with a reduced content of Rubisco. Aust J Plant Physiol 21: 475–495

    CAS  Google Scholar 

  • Farquhar GD and Raschke K (1978) On the resistance to transpiration of sites of evaporation within the leaf. Plant Physiol 61: 1000–1005

    Google Scholar 

  • Farquhar GD and Richards RA (1984) Isotopic composition of plant carbon correlates with water-use efficiency of wheat genotypes Aust J Plant Physiol 11: 539–552

    CAS  Google Scholar 

  • Farquhar GD and Sharkey TD (1982) Stomatal conductance and photosynthesis. Ann Rev Plant Physiol 33: 317–345

    CAS  Google Scholar 

  • Farquhar GD and von Caemmerer S (1982) Modelling of photosynthetic responses to environmental conditions. In: Lange OL, Nobel PS, Osmond CB and Ziegler H, (eds) Physiological Plant Ecology II. Water Relations and Carbon Assimilation Encycl. Plant Physiol (New Ser.), Vol 12B, pp 549–587. Springer Verlag, Berlin

    Google Scholar 

  • Farquhar GD, O’Leary MH and Berry JA (1982) Onthe relationship between carbon isotope discrimination and the intercellular carbon dioxide concentration in leaves. Aust J Plant Physiol 9: 121–137

    CAS  Google Scholar 

  • Gaastra P (1959) Photosynthesis of crop plants as influenced by light, CO2 temperature and stomatal diffusion resistance. Mededelingen van de Landbouwhogeschool te Wageningen, Nederland 59: 1–68

    Google Scholar 

  • Genty B and Meyer S (1995) Quantitative mapping of leaf photosynthesis using chlorophyll fluorescence imaging. Aust J Plant Physiol 22: 277–284

    Google Scholar 

  • Genty B, Briantais JM 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

    CAS  Google Scholar 

  • Gillon JS and Griffiths H (1997) The influence of (photo)respiration on carbon isotope discrimination in plants. Plant Cell Env 20: 1217–1230

    Google Scholar 

  • Gunasekera D and Berkowitz GA (1992) Heterogeneous stomatal closure in relation to leaf water deficits is not a universal phenomenon. Plant Physiol 98: 660–665

    CAS  Google Scholar 

  • Gutknecht J, Bisson MA and Tosteson FC (1977) Diffusion of carbon dioxide through lipid bilayer membranes. J Gen Physiol 69: 779–794

    CAS  PubMed  Google Scholar 

  • Guy RD, Fogel ML and Berry JA (1993) Photosynthetic fractionation of the stable isotopes of oxygen and carbon. Plant Physiol 101: 37–47

    CAS  PubMed  Google Scholar 

  • Haberlandt G (1914) Physiological Plant Anatomy. Translation of the fourth German edition by M. Drummond, reprint edition (1965) (Today and Tomorrow’s Book Agency, New Dehli)

    Google Scholar 

  • Harley PC, Loreto F, Di Marco G and Sharkey TD (1992) Theoretical considerations when estimating the mesophyll conductance to CO2 flux by analysis of the response of photosynthesis to CO2. Plant Physiol 98: 1429–1436

    CAS  Google Scholar 

  • Hatch MD and Burnell JN (1990) Carbonic anhydrase activity in leaves and its role in the first step of C4 photosynthesis. Plant Physiol 93: 825–828

    CAS  Google Scholar 

  • Hatch MD and Osmond CB (1976) Compartmentation and transport in C4 photosynthesis. In: Stocking CR and Heber U (eds) Transport in Plants III. Intracellular Interactions and Transport Processes. Encyclopedia of Plant Physiology New Series, Vol 3, pp 144–184. Springer-Verlag, Berlin

    Google Scholar 

  • Hatch MD, Agostino A and Jenkins CLD (1995) Measurement of the leakage of CO2 from bundle-sheath cells of leaves during C4 photosynthesis. Plant Physiol 108: 173–181

    CAS  PubMed  Google Scholar 

  • Hatch MD, Kagawa T and Craig S (1975) Subdivision of C4 pathway species based on differing C4 acid decarboxylating systems and ultrastructural features. Aust J Plant Physiol 2: 111–128

    CAS  Google Scholar 

  • Hattersley PW (1982) δ13 C values of C4 types in grasses. Aust J Plant Physiol 9: 139–154

    CAS  Google Scholar 

  • Hausler RE, Bailey KJ, Lea PJ and Leegood RC (1996) Control of photosynthesis in barley mutants with reduced activities of glutamine synthetase and glutamine synthase. III. Aspects of glyoxylate metabolism and effects of glyoxylate on the activation state of ribulose-1,5-bisphosphate carboxylase oxygenase. Planta 200: 388–396

    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

    CAS  Google Scholar 

  • Henderson S, Hattersley P, von Caemmerer S and Osmond CB (1994) Are C4 pathway plants threatened by global climatic change? In: Schulze ED, Caldwell MM (eds) Ecophysiology of Photosynthesis, pp 529–549. Springer-Verlag, Berlin

    Google Scholar 

  • Honda SI, Hongladarom-Honda T, Kwanyuen P and Wildman SG (1971) Interpretations on chloroplast reproduction derived from correlations between cells and chloroplasts. Planta 97: 1–15

    Article  Google Scholar 

  • Hudson GS, Evans JR, von Caemmerer S, Arvidsson YBC and Andrews TJ (1992) Reduction of ribulose-1,5-bisphosphate carboxylase/oxygenase content by antisense RNA lowers photosynthesis in transgenic tobacco plants. Plant Physiol 98: 294–302

    CAS  Google Scholar 

  • Jenkins CLD (1989) Effects of the phosphoenolpyruvate carboxylase inhibitor 3,3-dichloro-2-(dihydroxyphosphinoylmethyl) propenoate on photosynthesis. C4 selectivity and studies on photosynthesis. Plant Physiol 89: 1231–1237

    CAS  Google Scholar 

  • Jenkins CLD, Furbank RT and Hatch MD (1989) Inorganic carbon diffusion between mesophyll and bundle sheath cells. Plant Physiol 91: 1356–1363

    CAS  Google Scholar 

  • Jones HG (1987) Breeding forstomatal characters. In: Zeiger E, Farquhar GD and Cowan IR (eds) Stomatal function, pp 431–443. Stanford University Press, Stanford.

    Google Scholar 

  • Jordan DB and Ogren WL (1984) The CO2/O2 specificity of ribulose 1,5-bisphosphate carboxylase/oxygenase. Dependence on ribulose bisphosphate concentration, pH and temperature. Planta 161: 308–313

    Article  CAS  Google Scholar 

  • Kaminski A (1984) Effects of ploidy on photosynthesis and leaf structure among Triticum and related species of Hordeum vulgare. PhD thesis, Cambridge

    Google Scholar 

  • Kaminski A, Austin RB, Ford MA and Morgan CL (1990) Flag leaf anatomy of Triticum and Aegilops species in relation to photosynthetic rate. Ann Bot 66: 359–365

    Google Scholar 

  • Kane HJ, Viil J, Entsch B, Paul K, Morell MK and Andrews TJ (1994) An improved method for measuring the CO2/O2 specificity of ribulose bisphosphate carboxylase-oxygenase. Aust J Plant Physiol 21: 449–461

    CAS  Google Scholar 

  • Kirschbaum MUF, Gross LJ and Pearcy RW (1988) Observed and modelled stomatal responses to dynamic light environments in the shade plant Alocasia macrorrhiza. Plant Cell Env 11: 111–121

    Google Scholar 

  • Körner C, Scheel JA and Bauer H (1979) Maximum leaf diffusive conductance in vascular plants. Photosynthetica 13: 45–82

    Google Scholar 

  • Laisk AK (1977) Kinetics of photosynthesis and photorespiration in C3 plants (In Russian) Nauka, Moscow

    Google Scholar 

  • Laisk A and Loreto F (1996) Determining photosynthetic parameters from leaf CO2 exchange and chlorophyll fluorescence. Plant Physiol 110: 903–912

    CAS  PubMed  Google Scholar 

  • Laisk A and Sumberg A (1994) Partitioning of the leaf CO2 exchange into components using CO2 exchange and fluorescence measurements. Plant Physiol 106: 689–695

    CAS  PubMed  Google Scholar 

  • Laisk A, Oja V and Rahi M (1970) Diffusion resistance of leaves in connection with their anatomy. Fiziologiya Rastenii 17, 40–48

    Google Scholar 

  • Lauteri M, Scartazza A, Guido MC and Brugnoli E (1997) Genetic variation in photosynthetic capacity, carbon isotope discrimination and mesophyll conductance in provenances of Castanea sativa adapted to different environments. Funct Ecol 11: 675–683

    Article  Google Scholar 

  • Leuning R (1995) A critical appraisal of a combined stomatal-photosynthesis model for C3 plants. Plant Cell Env 18: 339–355

    CAS  Google Scholar 

  • Lloyd J, Syvertsen JP, Kriedemann PE and Farquhar GD (1992) Low conductances for CO2 diffusion from stomata to the sites of carboxylation in leaves of woody species. Plant Cell Env 15: 873–899

    CAS  Google Scholar 

  • Long SP, Farage PK, Bolhar-Nordenkampf HR and Rohrhofer U (1989) Separating the contribution of the upper and lower mesophyll to photosynthesis in Zea mays L. leaves. Planta 177: 207–216

    Article  Google Scholar 

  • Longstreth DJ, Hartsock TL and Nobel PS (1980) Mesophyll cell properties for some C3 and C4 species with high photosynthetic rates. Plant Physiol 48: 494–498

    Google Scholar 

  • Loreto F and Sharkey TD (1990) Low humidity can cause uneven photosynthesis inolive (Olea europaea L.) leaves. Tree Physiol 6: 409–415

    PubMed  Google Scholar 

  • Loreto F, Harley PC, Di Marco G and Sharkey TD (1992) Estimation of mesophyll conductance to CO2 flux by three different methods. Plant Physiol 98: 1437–1443

    Google Scholar 

  • Loreto F, Di Marco G, Tricoli D and Sharkey TD (1994) Measurements of mesophyll conductance, photosynthetic electron transport and alternative electron sinks of field grown wheat leaves. Photosyn Res 41: 397–403

    CAS  Google Scholar 

  • McWilliam JR and Mison K (1974) Significance of the pathway in Triodia irritans (spinifex), a grass adapted to arid environments. Aust J Plant Physiol 1: 171–175

    CAS  Google Scholar 

  • Makino A, Nakano H and Mae T (1994) Effects of growth temperature on the responses of ribulose-1,5-bisphosphate carboxylase, electront ransport components, and sucrose synthesis enzymes to leaf nitrogen in rice, and their relationships to photosynthesis. Plant Physiol 105: 1231–1238

    CAS  PubMed  Google Scholar 

  • Maxwell K, von Caemmerer S and Evans JR (1997) Is a low internal conductance to CO2 diffusion a consequence of Crassulacean Acid Metabolism? Aust J Plant Physiol 24: 777–786

    CAS  Google Scholar 

  • Meinzer FC and Zhu J (1998) Nitrogen stress reduces the efficiency of the C4 CO2 concentrating system, and there fore quantum yield, in Saccharum (sugarcane) species. J Exp Bot 49: 1227–1234

    Article  CAS  Google Scholar 

  • Molin WT, Meyers SP, Baer GR and Schrader LE (1982) Ploidy effects in isogenic populations of alfalfa. II. Photosynthesis, chloroplast number, ribulose-1,5-bisphosphate carboxylase, chlorophyll, and DNA in protoplasts. Plant Physiol 70: 1710–1714

    CAS  Google Scholar 

  • Morison JIL and Gifford RM (1983) Stomatal sensitivity to carbon dioxide and humidity. A comparison of two C3 and C4 grass species. Plant Physiol 71: 789–796

    CAS  Google Scholar 

  • Mott KA (1988) Do stomata respond to CO2 concentrations other than intercellular? Plant Physiol 86: 200–203

    CAS  Google Scholar 

  • Mott KA and O’Leary JW (1984) Stomatal behaviour and CO2 exchange characteristics in amphistomatous leaves. Plant Physiol 74: 47–51

    Google Scholar 

  • Mott KA and Parkhurst DF (1991) Stomatal responses to humidity in air and Helox. Plant Cell Env 14: 509–515

    Google Scholar 

  • Mott KA, Gibson AC and O’Leary JW (1982) The adaptive significance of amphistomatic leaves. Plant Cell Env 5: 455–460

    Google Scholar 

  • Nishio JN, Sun J and Vogelmann TC (1993) Carbon fixation gradients across spinach leaves do not follow internal light gradients. Plant Cell 5: 953–961

    Article  CAS  PubMed  Google Scholar 

  • Nobel PS (1991) Physicochemical and Environmental Plant Physiology. Academic Press, New York

    Google Scholar 

  • Nobel PS, Zaragoza LJ and Smith WK (1975). Relation between mesophyll surface area, photosynthetic rate and illumination level during development for leaves of Plectranthus parviflorus Henkel. Plant Physiology 55, 1067–70.

    Google Scholar 

  • Ntefidou M and Manetas Y (1996) Optical properties of hairs during the early stages of leaf development in Platanus orientalis. Aust J Plant Physiol 23: 535–538

    Google Scholar 

  • Parker ML and Ford MA (1982) The structure of the mesophyll of flag leaves in three Triticum species Ann Bot 49: 165–176

    Google Scholar 

  • Parkhurst DF (1994) Diffusion of CO2 and other gases in leaves. New Phytol 126: 449–479

    CAS  Google Scholar 

  • Parkhurst DF and Mott K (1990) Intercellular diffusion limits to CO2 uptake in leaves. Plant Physiol 94: 1024–1032

    CAS  Google Scholar 

  • Parkhurst DF, Wong SC, Farquhar GD and Cowan IR (1988) Gradients of intercellular CO2 levels across the leaf mesophyll. Plant Physiol 86: 1032–1037

    CAS  Google Scholar 

  • Parry MAJ, Keys AJ and Gutteridge S (1989) Variation in the specificity factor of C3 higher plant RubisCOs determined by the total consumption of ribulose-P2. J Exp Bot 40: 317–320

    CAS  Google Scholar 

  • Pearcy RW, Osteryoung K and Randall D (1982) Carbon dioxide exchange characteristics of C4 Hawaiian Euphorbia species native to diverse habitats. Oecologia 55: 333–341

    Article  Google Scholar 

  • Peat HJ and Fitter AH (1994) A comparative study of the distribution and density of stomata in the British flora. Biol J Linnean Soc 52: 377–393

    Google Scholar 

  • Peltier G, Cournac L, Despaux V, Dimon B, Fina L, Genty B and Rumeau D (1995) Carbonic anhydrase activity in leaves as measured in vivo by 18O exchange between carbon dioxide and water. Planta, 196: 732–739

    CAS  Google Scholar 

  • Peterson RB (1990) Effects of irradiance on the in vivo CO2∶O2 specificity factor of tobacco using simultaneous gas exchange and fluorescence techniques. Plant Physiol 94:892–898

    Google Scholar 

  • Pfeffer M and Peisker M (1995) In vivo Km for CO2 (Kp of phosphoenolpyruvate carboxylase (PEPC) and mesophy ll CO2 transport resistance (rm) in leaves of Zea mays L. In: Mathis P (ed) Photosynthesis: From Light to Biosphere, Vol V, pp 547–550. Kluwer Academic Publishers, Dordrecht

    Google Scholar 

  • Price GD, von Caemmerer S, Evans JR, Yu J-W, Lloyd J, Oja V, Kell P, Harrison K, Gallagher A and Badger MR (1994) Specific reduction of chloroplast carbonic anhydrase activity by antisense RNA in transgenic tobacco plants has a minor effect on photosynthetic CO2 assimilation. Planta, 193:331–340

    Article  CAS  Google Scholar 

  • Price G D, Evans JR, von Caemmerer S, Yu J-W and Badger MR (1995) Specific reduction of chloroplast glyceraldehyde-3-phosphate dehydrogenase activity by antisense RNA reduces CO2 assimilation via a reduction in RuBP regeneration in transgenic tobacco plants. Planta, 195: 369–378

    Article  CAS  PubMed  Google Scholar 

  • Price GD, von Caemmerer S, Evans JR, Siebke K, Anderson JM and Badger M (1998) Photosynthesis is strongly reduced by antisense suppression of chloroplastic cytochrome bf complex in transgenic tobacco. Aust J Plant Physiol 25: 445–452

    CAS  Google Scholar 

  • Psaras GK (1986) Chloroplast arrangement along intercellular spaces in the leaves of a Mediterranean subshrub. J Plant Physiol 126: 189–193

    Google Scholar 

  • Psaras GK, Diamantopoulos GS and Makrypoulias CP (1996) Chloroplast arrangement along intercellular air spaces. Israel J Plant Sci 44: 1–9

    Google Scholar 

  • Pyke KA and Leech RM (1987) Cellular levels of ribulose 1,5-bisphosphate carboxylase and chloroplast compartment size in wheat mesophyll cells. J Exp Bot 38:1949–1956

    CAS  Google Scholar 

  • Pyke KA and Leech RM (1992) Chloroplast division and expansion is radically altered bynuclear mutations in Arabidopsis thaliana. Plant Physiol 99:1005–1008

    CAS  Google Scholar 

  • Pyke KA and Leech RM (1994) A genetic analysis of chloroplast division and expansion in Arabidopsis thaliana. Plant Physiol 104:201–207

    CAS  PubMed  Google Scholar 

  • Pyke KA, Rutherford SM, Robertson EJ and Leech RM (1994) arc6, a fertile Arabidopsis mutant with only two mesophyll cell chloroplasts. Plant Physiol 106:1169–1177

    CAS  PubMed  Google Scholar 

  • Raschke K (1987) Action of abscisic acid onguard cells. In: Zeiger E, Farquhar GD and Cowan IR (eds) Stomatal Function, pp 253–279. Stanford University Press, Stanford.

    Google Scholar 

  • Renou JL, Gerbaud A, Just D and Andre M (1990) Differing substomataland chloroplastic CO2 concentrations in waterstressed wheat. Planta 182:415–419

    CAS  Google Scholar 

  • Ridolfi M and Dreyer E (1997) Responses to water stress in an ABA-unresponsive hybrid poplar (Populus koreana x trichocarpa cv. Peace). III. Consequences for photosynthetic carbon assimilation. New Phytol 135: 31–40

    Article  CAS  Google Scholar 

  • Roeske CA and O’Leary MH (1984) Carbon isotope effects on the enzyme-catalyzed carboxylation of ribulose bisphosphate. Biochemistry 23: 6275–6284

    Article  CAS  Google Scholar 

  • Rooney MA (1988) Short-term carbon isotope fractionation by plants. Ph.D. thesis, University of Wisconsin, Madison, WI.

    Google Scholar 

  • Roupsard O, Gross P and Dreyer E (1996) Limitation of photosynthetic activity by CO2 availability in the chloroplasts of oak leaves from different species and during drought. Ann Sci For 53:243–254

    Google Scholar 

  • Rumeau D, Cuine S, Fina L, Gault N, Nicole M and Peltier G (1996) Subcellular distribution of carbonic anhydrase in Solanum tuberosum L. leaves. Characterisation of two compartment-specific isoforms. Planta, 199:79–88

    Article  CAS  PubMed  Google Scholar 

  • Sasahara T (1982) Influence of genome on leaf anatomy of Triticum and Aegilops. Ann Bot 50:491–497

    Google Scholar 

  • Sasaki H, Samejima M and Ishii, R (1996) Analysis by δ13C measurement on mechanism of cultivar difference in leaf photosynthesis of rice (Oryza sativa L.). Plant Cell Physiol 37: 1161–1166

    CAS  Google Scholar 

  • Schmidt-Nielsen K (1991) Animal physiology: adaptation and environment. Cambridge University Press, Cambridge.

    Google Scholar 

  • Sharkey TD and Raschke K (1981) Effect of light quality on stomatal opening in leaves of Xanthium strumarium L. Plant Physiol 68: 1170–1174

    CAS  Google Scholar 

  • Sharkey TD, Imai K, Farquhar GD and Cowan IR (1982) A direct confirmation of the standard method of estimating intercellular partial pressure of CO2. Plant Physiol 69: 657–659

    CAS  Google Scholar 

  • Sharkey TD, Vassey TL, Vanderveer PJ and Vierstra RD (1991) Carbon metabolism enzymes and photosynthesis in transgenic tobacco (Nicotiana tabacum L.) having excess phytochrome. Planta 185: 287–296

    Article  CAS  Google Scholar 

  • Siebke K and Weis E (1995a) Assimilation images of leaves of Glechoma hederacea: Analysis of non-synchronous stomata related oscillations. Planta, 196:155–165

    Article  CAS  Google Scholar 

  • Siebke K and Weis E (1995b) Imaging of chlorophyll-a-fluorescence in leaves: Topography of photosynthetic oscillations in leaves of Glechoma hederacea. Photosynth Res 45:225–237

    Article  CAS  Google Scholar 

  • Solomon AK (1974) Apparent viscosity of human red blood cell membranes. Biochim Biophys Acta 373: 145–149

    CAS  PubMed  Google Scholar 

  • Sultemeyer D and Rinast KA (1996) The CO2 permeability of the plasma membrane of Chlamydomonas reinhardtii: massspectrometric 18O-exchange measurements from 13C18O2 in suspensions of carbonic anhydrase-loaded plasma-membrane vesicles. Planta 200:358–368

    Google Scholar 

  • Syvertsen JP, Lloyd J, McConchie C, Kriedemann PE and Farquhar GD (1995) On the site of biophysical constraints to CO2 diffusion through the mesophyll of hypostomatous leaves. Plant Cell Env 18: 149–157

    Google Scholar 

  • Tenney SM and Remmers JE (1963) Comparative quantitative morphology of the mammalian lung: Diffusing area. Nature, 197: 54–56

    CAS  PubMed  Google Scholar 

  • Terashima I (1992) Anatomy of non-uniform leaf photosynthesis. Photosynth Res 31:, 195–212

    Article  CAS  Google Scholar 

  • Terashima I, Wong SC Osmond CB and Farquhar GD (1988) Characterisation of non-uniform photosynthesis induced by abscisic acid in leaves having different mesophyll anatomies. Plant Cell Physiol 29:385–394

    CAS  Google Scholar 

  • Turrell FM (1936) The area of the internal exposed surface of dicotyledon leaves. Amer J Bot 23: 255–263

    Google Scholar 

  • Utsunomiya E and Muto S (1993) Carbonic anhydrase in the plasma membranes from leaves of C3 and C4 plants. Physiol Plant 88: 413–19

    Article  CAS  Google Scholar 

  • Villar R, Held AA and Merino J (1994) Comparison of methods to estimate dark respiration in the light in leaves of two woody species. Plant Physiol 105:167–172

    CAS  PubMed  Google Scholar 

  • Vitousek PM, Field CB and Matson PA (1990) Variation in foliar δ13C in Hawaiian Metrosideros polymorpha: a case of internal resistance? Oecologia 84: 362–370

    Google Scholar 

  • Vogel JC (1993) Variability of carbon isotope fractionation during photosynthesis. In: Ehleringer JR, Hall AE and Farquhar GD (eds) Stable Isotopes and Plant Carbon-Water Relations, pp 29–46. Academic Press, San Diego

    Google Scholar 

  • von Caemmerer S and Evans JR (1991) Determination of the average partial pressure of CO2 in chloroplasts from leaves of several C3 plants. Aust J Plant Physiol 18: 287–305

    Google Scholar 

  • von Caemmerer S and Farquhar GD (1981) Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves. Planta 153: 376–387

    Article  Google Scholar 

  • von Caemmerer S, Evans JR, Hudson GS and Andrews TJ (1994) The kinetics of ribulose-1,5-bisphosphate carboxylase/oxygenase in vivo inferred from measurements of photosynthesis in leaves of transgenic tobacco. Planta, 195:88–97

    Article  Google Scholar 

  • von Caemmerer S, Ludwig M, Millgate A, Farquhar GD, Price D, Badger M and Furbank RT (1997) Carbon isotope discrimination during C4 photosynthesis: insights from transgenic plants. Aust J Plant Physiol 24: 487–494

    Google Scholar 

  • Watanabe N, Evans JR and Chow WS (1994) Changes in the photosynthetic properties of Australian wheat cultivars over the last century. Aust J Plant Physiol 21: 169–183

    CAS  Google Scholar 

  • Williams TG, Flanagan LB and Coleman JR (1996) Photosynthetic gas exchange and discriminationagainst 13CO2 and C18O16O in tobacco plants modified by an antisense construct to have low chloroplastic carbonic anhydrase. Plant Physiol 112:319–326

    CAS  PubMed  Google Scholar 

  • Willmer C and Flicker M (1996) Stomata. Chapman and Hall, London

    Google Scholar 

  • Wong SC, Cowan IR and Farquhar GD (1979) Stomatal conductance correlates with photosynthetic capacity. Nature 282:424–426

    Article  Google Scholar 

  • Wong SC, Cowan IR and Farquhar GD (1985a) Leaf conductance in relation to rate of CO2 assimilation. I. Influence of nitrogen nutrition, phosphorus nutrition, photon flux density, and ambient partial pressure of CO2 during ontogeny. Plant Physiol 78: 821–825

    Google Scholar 

  • Wong SC, Cowan IR and Farquhar GD (1985b) Leaf conductance in relation to rate of CO2 assimilation. II. Effects of short-term exposures to different photon flux densities. Plant Physiol 78: 826–829

    CAS  Google Scholar 

  • Yoshie F (1986) Intercellular CO2 concentration and water-use efficiency of temperate plants with different life-forms and from different microhabitats. Oecologia 68: 370–374

    Article  Google Scholar 

  • Zeiger E, Farquhar GD and Cowan IR (1987) Stomatal function. Stanford University Press, Stanford

    Google Scholar 

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Evans, J.R., Loreto, F. (2000). Acquisition and Diffusion of CO2 in Higher Plant Leaves. In: Leegood, R.C., Sharkey, T.D., von Caemmerer, S. (eds) Photosynthesis. Advances in Photosynthesis and Respiration, vol 9. Springer, Dordrecht. https://doi.org/10.1007/0-306-48137-5_14

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