Summary
Leaves have a considerable flexibility that enables them to perform effectively in a range of light environments or where the supply of mineral nutrients is limiting. This requires coordination of the many processes associated with photosynthesis within the leaf. Leaves respond to the irradiance during growth by changing the allocation of nitrogen between proteins. An analysis is presented which allows determination of the allocation that maximizes daily photosynthesis for a given amount of nitrogen. The leaf is faced with a trade-off between increasing light absorption or photosynthetic capacity. Absorption of light can be increased by investing more in pigment-protein complexes, which increases the quantum yield of photosynthesis. Conversely, photosynthetic capacity can be increased by allocating more nitrogen to soluble proteins. The ratio of thylakoid to soluble protein is thus highly responsive to growth irradiance for most species. Photosynthetic capacity per unit leaf area can also be increased by increasing nitrogen content per unit leaf area. This is invariably associated with increased leaf mass per unit leaf area due to elongation and/or more layers of palisade cells, such that nitrogen content per unit dry weight is independent of growth irradiance.
Plants cope with limiting nutrients primarily by altering the production of leaves such that leaves that are formed generally have a minimum content of the element. With nitrogen deficiency, both light and dark reactions are equally affected; Hill and ribulose 1,5-bisphosphate carboxylase oxygenase (Rubisco) activities are reduced in parallel. For several other nutrients, including P, Fe, Cu and Mn, deficiency reduces both Hill and Rubisco activities. With P and Fe deficiency, Hill activity is specifically affected and the excess Rubisco capacity is masked by lower activation of the enzyme to bring its activity into line with Hill activity. Stomatal conductance changes in concert with changes in CO2 assimilation capacity brought about by nutrient deficiency. Consequently, the amount of CO2 fixed per unit water transpired is remarkably constant and independent of the plants nutritional status.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Abadia J, Rao IM and Terry N (1987) Changes in leaf phosphate states have only small effects on the photochemical apparatus of sugar beet leaves. Plant Sci 50: 49–55
Aerts R (1990) Nutrient use efficiency in evergreen and deciduous species from heathlands. Oecologia 84: 391–397
Anderson JM (1980) Chlorophyll-protein complexes of higher plant thylakoids: distribution, stoichiometry and organization in the photosynthetic unit. FEBS Lett 117: 327–331
Anderson JM (1982) The role of chlorophyll-protein complexes in the function and structure of chloroplast thylakoids. Mol Cell Biochem 46: 161–172
Anderson JM (1986) Photoregulation of the composition, function and structure of thylakoid membranes. Ann Rev Plant Physiol 37: 93–136
Anderson JM and Osmond CB (1987) Shade-sun responses: compromises between acclimation and photoinhibition. In: Kyle DJ, Osmond CB and Arntzen CJ (eds) Photoinhibition, pp 1–38. Elsevier Science Publishers, Amsterdam
Andreeva TF, Thyok NT, Vlasova MP and Nichiporovich AA (1972) Effect of nitrogen nutrition on photosynthetic activity in leaves of different tiers and productivity of horse-bean plants. Soviet Plant Physiol 19: 213–220
Aoki S (1986) Interaction of light and low temperature in depression of photosynthesis in tea leaves. Japan J Crop Sci 55: 496–503
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
Aro EM, Rintamaki E, Korhonen P and Maenpaa P (1986). Relationship between chloroplast structure and O2 evolution rate of leaf discs in plants from different biotypes in Finland. Plant Cell Environ 9: 87–94
Aro EM, McCaffery S and Anderson JM (1993) Photoinhibition and D1 protein degradation in peas acclimated to different growth irradiances. Plant Physiol 103: 835–843
Ball MC, Hodges VS and Laughlin GP (1991) Cold-induced photoinhibition limits regeneration of snow gum at tree-line. Funct Ecol 5: 663–668
Björkman O (1968) Further studies on differentiation of photosynthetic properties in sun and shade ecotypes of Solidago virgaurea L. Physiol Plant 21: 84–89
Björkman O (1981). Responses to different quantum flux densities. In: Lange OL, Nobel PS, Osmond CB and Ziegler H (eds) Physiological Plant Ecology I. Responses to the Physical Environment. Encyclopedia of Plant Physiology, New Series, Vol. 12A, pp. 57–107. Springer-Verlag, Berlin
Björkman O and Demmig B (1987) Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77K among vascular plants of diverse origins. Planta 170: 489–504
Björkman O, Boardman NK, Anderson JM, Thorne SW, Goodchild DJ and Pyliotus NA (1972) Effect of light intensity during growth of Atriplex patula on the capacity of photosynthetic reactions, chloroplast components and structure. Carnegie Inst Wash Yrbk 71: 115–135
Boardman NK (1977) Comparative photosynthesis of sun and shade plants. Ann Rev Plant Physiol 28: 355–377
Brooks A (1986) Effects of phosphorus nutrition on ribulose 1,5-bisphosphate carboxylase activation, photosynthetic quantum yield and amounts of some Calvin-cycle metabolites in spinach leaves. Aust J Plant Physiol 13: 221–237
Brugnoli E and Björkman O (1992) Chloroplast movements in leaves: influence on chlorophyll fluorescence and measurements of light induced absorbance changes related to ΔpH and zeaxanthin formation. Photosynth Res 32: 23–35
Burkey KO and Wells R (1991) Response of soybean photosynthesis and chloroplast membrane function to canopy development and mutual shading. Plant Physiol 97: 245–252
Chabot BF and Chabot JF (1977) Effects of light and temperature on leaf anatomy and photosynthesis in Fragaria vesca. Oecologia 26: 363–377
Chow WS and Hope AB (1987) The stoichiometries of supramolecular complexes in thylakoid membranes from spinach chloroplasts. Aust J Plant Physiol 14: 21–28
Chow WS, Qian L, Goodchild DJ and Anderson JM (1988) Photosynthetic acclimation of Alocasia macrorrhiza (L.) G. Don to growth irradiance: structure, function and composition of chloroplasts. In: Evans JR, von Caemmerer S and Adams WW III (eds) Ecology of Photosynthesis in Sun and Shade, pp 107–122. CSIRO, Melbourne
Chow WS, Anderson JM and Melis A (1990a) The photosystem stoichiometry in thylakoids of some Australian shade-adapted plant species. Aust J Plant Physiol 17: 665–674
Chow WS, Goodchild DJ, Miller C and Anderson JM (1990b) The influence of high levels of brief or prolonged supplementary far-red illumination during growth on the photosynthetic characteristics, composition and morphology of Pisum sativum chloroplasts. Plant Cell Environ 13: 135–145
Chow WS, Melis A and Anderson JM (1990c) Adjustments of photosystem stoichiometry in chloroplasts improve the quantum efficiency of photosynthesis. Proc Natl Acad Sci USA 87: 7502–7506
Chow WS, Adamson HY and Anderson JM (1991) Photosynthetic acclimation of Tradescantia albiflora to growth irradiance: Lack of adjustment of light-harvesting components and its consequences. Physiol Plant 81: 175–182
Cook MG and Evans LT (1983) Nutrient responses of seedlings of wild and cultivated Oryza species. Field Crops Res 6: 205–218
Corre WJ (1983) Growth and morphogenesis of sun and shade plants. III The combined effects of light intensity and nutrient supply. Acta Bot Neerl 32: 277–294
Cui M, Vogelmann TC and Smith WK (1991) Chlorophyll and light gradients in sun and shade leaves of Spinacia oleracea. Plant Cell Environ 14: 493–500
De la Torre RW and Burkey KO (1990) Acclimation of barley to changes in light intensity: Photosynthetic electron transport activity and components. Photosynth Res 24: 127–136
De Lucia EH, Shenoi HD, Naidu SL and Day TA (1991) Photosynthetic symmetry of sun and shade leaves of different orientations. Oecologia 87: 51–57
Demmig-Adams B, Adams WW III, Winter K, Meyer A, Schreiber U, Perreira JS, Kruger A, Czygan FC and Lange OL (1989) Photochemical efficiency of Photosystem II, photon yield of O 2 evolution, photosynthetic capacity and carotenoid composition during the midday depression of net CO 2 uptake in Arbutus unedo growing in Portugal. Planta 177: 377–387
De Visser R, Spitters CJT and Bouma TJ (1992) Energy cost of protein turnover: Theoretical calculation and experimental estimation from regression of respiration on protein concentration of full-grown leaves. In: Lambers H and van der Plas LHW (eds) Molecular, Biochemical and Physiological Aspects of Plant Respiration, pp. 493–508. SPB Academic Publishing bv, The Hague
Ehleringer J (1981) Leaf absorptances of Mohave and Sonoran desert plants. Oecologia 49: 366–370
Ellsworth DS and Reich PB (1992) Leaf mass per area, nitrogen content and photosynthetic carbon gain in Acer saccharum seedlings in contrasting forest light environments. Functional Ecol 6: 423–435
Evans JR (1983) Nitrogen and photosynthesis in the flag leaf of wheat (Triticum aestivum L). Plant Physiol 72: 297–302
Evans JR (1986a) A quantitative analysis of light distribution between the two photosystems, considering variation in both relative amounts of the chlorophyll-protein complexes and the spectral quality of light. Photobiochem Photobiophys 10: 135–147
Evans JR (1986b) The relationship between carbon-dioxide-limited photosynthetic rate and ribulose 1,5-bisphosphate-carboxylase content in two nuclear-cytoplasm substitution lines of wheat and the coordination of ribulose-bisphosphate-carboxylation and electron-transport capacities. Planta 167:351–358
Evans JR (1987a) The relationship between electron transport components and photosynthetic capacity in pea leaves grown at different irradiances. Aust J Plant Physiol 14: 157–170
Evans JR (1987b) The dependence of quantum yield on wavelength and growth irradiance. Aust J Plant Physiol 14:69–79
Evans JR (1988) Acclimation by the thylakoid membranes to growth irradiance and the partitioning of nitrogen between soluble and thylakoid proteins. In: Evans JR, von Caemmerer S and Adams WW III (eds.) Ecology of Photosynthesis in Sun and Shade, pp. 93–106. CSIRO, Melbourne
Evans JR (1989a) Photosynthesis and nitrogen relationships in leaves of C3 plants. Oecologia 78: 9–19
Evans JR (1989b) Partitioning of nitrogen between and within leaves grown under different irradiances. Aust J Plant Physiol 16: 533–548
Evans JR (1993a) Photosynthetic acclimation and nitrogen partitioning within a lucerne canopy. I. Canopy characteristics. Aust J Plant Physiol 20: 55–67
Evans JR (1993b) Photosynthetic acclimation and nitrogen partitioning within a lucerne canopy. II. Stability through time and comparison with a theoretical optimum. Aust J Plant Physiol 20: 69–82
Evans JR and Seemann (1989) The allocation of protein nitrogen in the photosynthetic apparatus: Costs, consequences and control. In Briggs WR (ed.) Photosynthesis, pp. 183–205. Alan R Liss, New York
Evans JR and Terashima I (1987) Effects of nitrogen nutrition on electron transport components and photosynthesis in Spinach. Aust J Plant Physiol 14: 59–68
Evans JR and Terashima I (1988) Photosynthetic characteristics of spinach leaves grown with different nitrogen treatments. Plant Cell Physiol 29: 157–165
Evans JR, Jakobsen I and Ögren E (1993) Photosynthetic light-response curves. 2. Gradients of light absorption and photosynthetic capacity. Planta 189: 191–200
Evans JR, von Caemmerer S, Setchell BA and Hudson GS (1994) The relationship between CO 2 transfer conductance and leaf anatomy in transgenic tobacco with a reduced content of Rubisco. Aust J Plant Physiol 21: 475–495
Farage PK and Long SP (1991) The occurrence of photoinhibition in an over-wintering crop of oil-seed rape (Brassica napus L.) and its correlation with changes in crop growth. Planta 185: 279–286
Farquhar GD, von Caemmerer S and Berry JA (1980) A biochemical model of photosynthetic CO 2 assimilation in leaves of C3 species. Planta 149: 78–90
Ferrar PJ and Osmond CB (1986) Nitrogen supply as a factor influencing photoinhibition and photosynthetic acclimation after transfer of shade-grown Solanum dulcamara to bright light. Planta 168: 563–570
Field C (1983) Allocating leaf nitrogen for the maximization of carbon gain: Leafage as a control on the allocation program. Oecologia 56: 341–347
Field C and Mooney HA (1986) The photosynthesis-nitrogen relationship in wild plants. In: Givnish TJ (ed) On the Economy of Form and Function, pp. 25–55. Cambridge University Press, Cambridge
Field C, Merino J and Mooney HA (1983) Compromises between water-use efficiency and nitrogen-use efficiency in five species of California evergreens. Oecologia 60: 384–389
Fleishhacker P and Senger H (1978) Adaptation of the photosynthetic apparatus of Scenedesmus obliqus to strong and weak light conditions. II. Differences in photochemical reactions, the photosynthetic electron transport and photo-synthetic units. Physiol Plant 43: 43–51
Fredeen AL, Gamon JA and Field CB (1991) Responses of photosynthesis and carbohydrate partitioning to limitations in nitrogen and water availability in field-grown sunflower. Plant Cell Env 14: 963–970
Goodchild DJ, Björkman O and Pyliotus NA (1972) Chloroplast ultrastructure, leaf anatomy and content of chlorophyll and soluble protein in rainforest species. Carnegie Inst Washington Yrbk 71: 102–107
Goodriaan J and van Keulen H (1979) The direct and indirect effects of nitrogen shortage on photosynthesis and transpiration in maize and sunflower. Neth J Agric Sci 27: 227–234
Grahl H and Wild A (1975) Studies on the content of P-700 and cytochromes in Sinapis alba during growth under two different light intensities. In: Marcelle R (ed) Environmental and Biological Control of Photosynthesis, pp. 107–113. W Junk, The Hague
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 Delhi
Hanson HC (1917) Leaf structure as related to environment. Amer J Bot 4: 533–560
Harley PC, Thomas RB, Reynolds JF and Strain BR (1992) Modelling photosynthesis of cotton grown in elevated CO 2 -Plant Cell Environ 15: 271–282
Haupt W (1982) Light-mediated movement of chloroplasts. Ann Rev Plant Physiol 33: 205–33
Hewitt EJ and Smith TA (1975) Plant Mineral Nutrition. The English University Press, London
Hirose T and Werger MJA (1987) Maximising daily canopy photosynthesis with respect to the leaf nitrogen allocation pattern in the canopy. Oecologia 72: 520–526
Hudson GS, Evans JR, Caemmerer S von, Arvidsson BC and Andrews TJ (1992) Reduction of ribulose-l,5-bisphosphate carboxylase/oxygenase content by antisense RNA reduces photosynthesis in transgenic tobacco plants. Plant Physiol 98: 294–302
Ida K, Koyama H and Takeda S (1992) Relation between photosynthetic activities and contents of chloroplast pigments in green and red leaves of Perilla grown under different grades of shading. In: Murata N (ed) Research in Photosynthesis, pp IV. 24.635–638. Kluwer Academic Publishers, Dordrecht
Jurik TW, Chabot JF and Chabot BF (1979) Ontogeny of photosynthetic performance in Fragaria virginiana under changing light regimes. Plant Physiol 63: 542–547
Kirchhoff WR, Hall A E and Thomson WW (1989) Gas exchange, carbon isotope discrimination, and chloroplast ultrastructure of a chlorophyll-deficient mutant of cowpea. Crop Sci 29: 109–115
Kim JH, Glick RE and Melis A (1993) Dynamics of photosystem stoichiometry adjustment by light quality in chloroplasts. Plant Physiol 102: 181–190
Kriedemann PE and Anderson JE (1988) Growth and photosynthetic responses to manganese and copper deficiencies in wheat (Triticum aestivum) and barley grass (Hordeum glaucum and H. leporinum). Aust J Plant Physiol 15: 429–446
Laisk A, Oja V and Rahi M (1970) Diffusion resistance of leaves in connection with their anatomy. Fiziol Rast 17: 40–48
Langenheim JH, Osmond CB, Brooks A and Ferrar PJ (1984) Photosynthetic responses to light in seedlings of selected Amazonian and Australian rainforest tree species. Oecologia 63: 215–224
Lauer MJ, Pallardy SG, Blevins DG and Randall DD (1989) Whole leaf carbon exchange characteristics of phosphate deficient soybeans (Glycine max L.). Plant Physiol 91: 848–854
Lauerer M, Saftie D, Quick WP, Labate C, Fichtner K, Schulze ED, Rodermel SR, Bogorad L and Stitt M (1993) Decreased ribulose-1,5-bisphosphate carboxylase-oxygenase in transgenic tobacco transformed with ‘antisense’ rbcS. VI. Effect on photosynthesis in plants grown at different irradiance. Planta 190:332–345
Leong T and Anderson JM (1984a) Adaptation of the thylakoid membranes of pea chloroplasts to light intensities. I. Study on distribution of chlorophyll-protein complexes. Photosynth Res 5:105–115
Leong T and Anderson JM (1984b) Adaptation of the thyiakoid membranes of pea chloroplasts to light intensities. II. Study of electron transport capacities, coupling factor (CF 1 ) activity and rates of photosynthesis. Photosynth Res 5: 117–128
Lichtenthaler HK, Buschmann C, Doll M, Fietz HJ, Bach T, Kozel V, Meier D and Rahmsdorf U (1981) Photosynthesis activity, chloroplast ultrastructure, and leaf characteristics of high light and low light plants and of sun and shade leaves. Photosynth Res 2: 115–141
Lichtenthaler HK, Kuhn G, Prenzel U, Buschmann C and Meier D (1982) Adaption of chloroplast ultrastructure and of chlorophyll-protein levels to high-light and low-light growth conditions. Z Naturforsch 37c: 464–475
Long SP, Postl WF and Bolhar-Nordenkampf HR (1993) Quantum yields for uptake of carbon dioxide in C3 vascular plants of contrasting habitats and taxonomic groupings. Planta 189: 226–234
Longstreth DJ, Hartsock TL and Nobel PS (1981) Light effects on leaf development and photosynthetic capacity of Hydrocotyle bonariensis Lam. Photosynth Res 2: 95–104
Longstreth DJ and Nobel PS (1980) Nutrient influences on leaf photosynthesis. Effects of nitrogen, phosphorus and potassium for Gossypium hirsutum L. Plant Physiol 65: 541–543
Ludlow MM and Wilson GL (1971) Photosynthesis of tropical pasture plants II. Temperature and illuminance history. Aust J Biol Sci 24: 1065–1075
Makino A and Osmond CB (1991) Effects of nitrogen nutrition on nitrogen partitioning between chloroplasts and mitochondria in pea and wheat. Plant Physiol 96: 355–362
Makino A, Mae T and Ohira K (1983) Photosynthesis and ribulose 1,5-bisphosphate carboxylase in rice leaves. Plant Physiol 73: 1002–1007
Makino A, Mae T and Ohira K (1988) Differences between wheat and rice in the enzymatic properties of ribulose 1,5-bisphosphate carboxylase/oxygenase and the relationship to photosynthetic gas exchange. Planta 174: 30–38
Makino A, Sakashita H, Hidema J, Mae T, Ojima K and Osmond B (1992) Distinctive responses of ribulose-1,5-bisphosphate carboxylase and carbonic anhydrase in wheat leaves to nitrogen nutrition and their possible relationships to CO 2 -transfer resistance. Plant Physiol 100: 1737–1743
McKiernan M and Baker NR (1991) Adaption to shade of the light harvesting apparatus in Silene dioica. Plant Cell Environ 14: 205–212
Moon JW Jr, Bailey DA, Fallahi E, Jensen RG and Zhu G (1990) Effect of nitrogen application on growth and photosynthetic nitrogen use efficiency in two ecotypes of wild strawberry, Fragaria chiloensis. Physiol Plant 80: 612–618
Moss DN (1964) Optimum lighting of leaves. Crop Sci 4: 131–136
Mott KA, Gibson AC and O’Leary JW (1982) The adaptive significance of amphistomatous leaves. Plant Cell Env 5: 455–460
Mott KA and Michaelson O (1991) Amphistomaty as an adaptation to high light intensity in Ambrosia cordifolia (Compositae). Amer J Bot 78: 76–79
Nobel PS and Walker DB (1985) Structure of leaf photosynthetic tissue. In: Barber J and Baker NR (eds) Photosynthetic Mechanisms and the Environment, pp. 501–536. Elsevier Science Publishers, Amsterdam
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 Physiol 55: 1067–70
Ögren E (1988) Photoinhibition of photosynthesis in willow leaves under field conditions. Planta 175: 229–236
Ögren E and Evans JR (1992) Photoinhibition of photosynthesis in situ in six species of Eucalyptus. Aust J Plant Physiol 19: 223–232
Ögren E and Evans JR (1993) Photosynthetic light response curves. I the influence of CO 2 partial pressure and leaf inversion. Planta 189: 182–190
Öquist G and Ögren E (1985) Effects of winter stress on photosynthetic electron transport and energy distribution between the two photosystems of pine as assayed by chlorophyll fluorescence kinetics. Photosynth Res 7: 19–30
Öquist G, Brunes L and Hallgren JE (1982) Photosynthetic efficiency of Betula pendula acclimated to different quantum flux densities. Plant Cell Environ 5: 9–15
Oya V and Laisk AK (1976) Adaptation of the photosynthetic apparatus to the light profile in the leaf. Soviet Plant Physiol 23: 381–386
Park RB and Pon NG (1963) Chemical composition and substructure of lamellae isolated from Spinacea oleracea chloroplasts. J Mol Biol 6: 105–114
Pearcy RW (1987) Photosynthetic gas exchange responses of Australian tropical forest trees in canopy, gap and understory micro-environments. Funct Ecol 1: 169–178
Pearcy RW and Franceschi VR (1986) Photosynthetic characteristics and chloroplast ultrastructure of C 3 and C 4 tree species grown in high-and low-light environments. Photosynth Res 9: 317–331
Pons TL, Schieving F, Hirose T and Werger MJA (1989) Optimization of leaf nitrogen allocation for canopy photosynthesis in Lysimachia vulgaris. In: Lambers H, Cambridge ML, Konings H and Pons TL (eds) Causes and Consequences of Variation in Growth Rate and Productivity of Higher Plants, pp. 175–186. SPB Academic Publishing, The Hague
Pons TL, van der Werf A and Lambers H (1993) Photosynthetic nitrogen use efficiency of inherently slow-and fast-growing species: Possible explanations for observed differences. In: Roy J and Garnier E (eds) A Whole Plant Perspective on Carbon-nitrogen Interactions, pp. 51–67. SPB Academic Publishing bv, The Hague
Pugnaire FI and Chapin FS II (1993) Controls over nutrient resorption from leaves of evergreen mediterranean species. Ecology 74: 124–129
Radin JW and Boyer JS (1981) Control of leaf expansion by nitrogen nutrition in sunflower plants. Plant Physiol 69: 771–775
Sage RF, Pearcy RW and Seemann JR (1987) The nitrogen use efficiency of C 3 and C 4 plants. III. Leaf nitrogen effects on the activity of carboxylating enzymes in Chenopodium album (L.) and Amaranthus retroflexus (L.). Plant Physiol 85: 355–359
Sage RF, Sharkey TD and Pearcy RW (1990) The effect of leaf nitrogen and temperature on the CO 2 response of photosynthesis in the C 3 dicot Chenopodium album L. Aust J Plant Physiol 17: 135–148
Sampath P and Kulandaivelu G (1983) Photochemical activities and organization of photosynthetic apparatus of C 3 and C 4 plants grown under different light intensities. Photosynth Res 4: 351–360
Sheriff DW (1992) Roles of carbon gain and allocation in growth at different nitrogen nutrition in Eucalyptus camaldulensis and Eucalyptus globulus seedlings. Aust J Plant Physiol 19: 637–652
Sims DA and Pearcy RW (1989) Photosynthetic acclimation to sun and shade conditions by a tropical forest understorey herb, Alocasia macrorrhiza, and a related crop species Colocasia esculenta. Oecologia 79: 53–59
Spiller S and Terry N (1980) Limiting factors in photosynthesis. II. Iron stress diminishes photochemical capacity by reducing the number of photosynthetic units. Plant Physiol 65: 121–125
Strauss-Debenedetti S and Bazazz FA (1991) Plasticity and acclimation to light in tropical Moraceae of different successional positions. Oecologia 87: 377–387
Taylor SE and Terry N (1984) Limiting factors in photosynthesis. V. Photochemical energy supply colimits photosynthesis at low values of intercellular CO 2 concentration. Plant Physiol 75: 82–86
Terashima I (1986) Dorsiventrality in photosynthetic light response curves of a leaf. J Exp Bot 37: 399–405
Terashima I and Evans JR (1988) Effects of light and nitrogen nutrition on the organization of the photosynthetic apparatus in spinach. Plant Cell Physiol 29: 143–155
Terashima I and Inoue Y (1984) Comparative photosynthetic properties of palisade tissue chloroplasts and spongy tissue chloroplasts of Camellia japonica L.: Functional adjustment of photosynthetic apparatus to light environment within a leaf. Plant Cell Physiol 25: 555–563
Terashima I and Inoue Y (1985a) Palisade tissue chloroplasts and spongy tissue chloroplasts in spinach: Biochemical and ultrastructural differences. Plant Cell Physiol 26: 781–785
Terashima I and Inoue Y (1985b) Vertical gradients in photosynthetic properties of spinach chloroplasts dependent on intraleaf light environment. Plant Cell Physiol 26:781–785
Terashima I and Saeki T (1983) Light environment within a leaf. I. Optical properties of paradermal sections of Camellia leaves with special reference to differences in the optical properties of palisade and spongy tissues. Plant Cell Environ 24: 1493–1501
Terashima I and Saeki T (1985) A new model for leaf photosynthesis incorporating the gradients of light environment and of leaf photosynthetic properties of chloroplasts within a leaf. Ann Bot 56: 489–499
Terashima I, Sakaguchi S and Hara N (1986) Intra-leaf and intracellular gradients in chloropiast ultrastructure of dorsiventral leaves illuminated from the adaxial or abaxial side during their development. Plant Cell Physiol 27: 1023–1031
Thompson WA, Stocker GC and Kriedemann PE (1988) Growth and photosynthetic response to light and nutrients in Flindersia brayleyana F. Muell., a rainforest tree with a broad tolerance to sun and shade. In: Evans JR, von Caemmerer S and Adams WW III (eds) Ecology of Photosynthesis in Sun and Shade, pp. 299–315. CSIRO Melbourne
Thompson WA, Huang LK and Kriedemann PE (1992) Photosynthetic response to light and nutrients in sun-tolerant and shade-tolerant rainforest trees. II. Leaf gas exchange and component processes of photosynthesis. Aust J Plant Physiol 19: 19–42
Turnbull MH (1991) The effect of light quantity and quality during development on the photosynthetic characteristics of six Australian rainforest tree species. Oecologia 87: 110–117
Vogelmann TC, Bornman JF and Josserand S (1989) Photosynthetic light gradients and spectral regime within leaves of Medicago sativa. Phil Trans R Soc Lond B 323: 411–421
von Caemmerer S and Evans JR (1991) Determination of the average partial pressure of CO 2 in chloroplasts from leaves of several C 3 plants. Aust J Plant Physiol 18: 287–305
von Caemmerer S and Farquhar GD (1981) Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves. Planta 153: 376–87
von Caemmerer S, Evans JR, Hudson GS and Andrews TJ (1994) The kinetics of ribulose-l,5-bisphosphate carboxylase/oxygenase in vivo inferred from measurements of photo-synthesis in leaves of transgenic tobacco. Planta 195: 88–97
Walters MB and Field CB (1987) Photosynthetic light acclimation in two rainforest Piper species with different ecological amplitudes. Oecologia 72: 449–456
Wild A (1979) Physiologie der photosythese hoherer pflanzen. Die an passung an die lichtbedingungen. Ber Deutsch Bot Ges 92: 341–364
Wilhelm C and Wild A (1984) The variability of the photosynthetic unit in Chlorella. II. The effect of light intensity and cell development on photosynthesis, P 700 and cytochrome f in homocontinuous and synchronous cultures of Chlorella. J Plant Physiol 115: 125–135
Wong SC Cowan IR and Farquhar GD (1979) Stomatal conductance correlates with photosynthetic capacity. Nature 282: 424–426
Wong SC Cowan IR and Farquhar GD (1985) Leaf conductance in relation to rate of CO 2 assimilation. I. Influence of nitrogen nutrition, phosphorus nutrition, photon flux density, and ambient partial pressure of CO 2 during ontogeny. Plant Physiol 78: 821–825
Wullschleger SD (1993) Biochemical limitations to carbon assimilation in C 3 plants-a retrospective analysis of the A/C 1 curves from 109 species. J Exp Bot 44: 907–920
Yoshida S and Coronel SV (1976) Nitrogen nutrition, leaf resistance and leaf photosynthetic rate of the rice plant. Soil Sci Plant Nutr 22: 207–211
Yoshie F (1986) Intercellular CO 2 , concentration and water-use efficiency of temperate plants with different life forms and from different microhabitats. Oecologia 68: 370–374
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1996 Kluwer Academic Publishers
About this chapter
Cite this chapter
Evans, J.R. (1996). Developmental Constraints on Photosynthesis: Effects of Light and Nutrition. In: Baker, N.R. (eds) Photosynthesis and the Environment. Advances in Photosynthesis and Respiration, vol 5. Springer, Dordrecht. https://doi.org/10.1007/0-306-48135-9_11
Download citation
DOI: https://doi.org/10.1007/0-306-48135-9_11
Publisher Name: Springer, Dordrecht
Print ISBN: 978-0-7923-4316-5
Online ISBN: 978-0-306-48135-2
eBook Packages: Springer Book Archive