Summary
According to gas exchange measurements, mitochondrial oxygen consumption in the light is always fast, while respiratory CO2 evolution is markedly decreased (compared with rates in darkness). We analyze the metabolic events that lead to such contrasting responses. In the light, the generation of NADH in mitochondria, both in the glycine decarboxylase reaction and in the tricarboxylic acid cycle, leads to increased NAD(P)H levels, which may increase the activity of the rotenone-insensitive NAD(P)H dehydrogenases. The resulting increase of the reduction level of ubiquinone activates the alternative oxidase. Stabilization of (photo)respiratory flux during the transition from darkness to light takes place at higher NADH/NAD+ and ATP/ADP ratios. Maintenance of fast rates of mitochondrial electron transport in the light is facilitated by the import of oxaloacetate (OAA) from the cytosol to remove NADH, and by the export of citrate to the cytosol. This reduces the flow of metabolites in the tricarboxylic acid cycle, decreasing decarboxylation rates, while the rate of oxygen consumption reactions remain fast.
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
Amthor JS (2000) Direct effect of elevated CO2 on nocturnal in situ leaf respiration in nine temperate deciduous tree species is small. Tree Physiol 20: 139–144
Atkin OK, Westbeek MHM, Cambridge ML, Lambers H and Pons TL (1997) Leaf respiration in light and darkness: A comparison of slow-and fast-growing Poa species. Plant Physiol 113: 961–965
Atkin OK, Evans JR and Siebke K (1998a) Relationship between the inhibition of leaf respiration by light and enhancement of leaf dark respiration following light treatment. Aust J Plant Physiol 25: 437–443
Atkin OK, Schortemeyer M, McFarlane N and Evans JR (1998b) Variation in the components of relative growth rate in ten Acacia species from contrasting environments. Plant Cell Environ 21: 1007–1017
Atkin OK, Evans JR, Ball MC, Lambers H and Pons TL (2000a) Leaf respiration of snow gum in the light and dark. Interactions between temperature and irradiance. Plant Physiol 122: 915–923
Atkin OK, Millar AH, Garderström P and Day DA (2000b) Photosynthesis, carbohydrate metabolism and respiration in leaves of higher plants. In: RC Leegood, TD Sharkey, S von Caemmerer (eds) Photosynthesis: Physiology and Metabolism, pp 153–175. Kluwer Academic Publishers, Dordrecht
Avelange MH, Thiery JM, Sarrey F, Gans P and Rebeille F (1991) Mass-spectrometric determination of O2 and CO2 gas exchange in illuminated higher plant cells—evidence for light inhibition of substrate decarboxylations. Planta 183: 150–157
Bauwe H, Keerberg O, Bassuner R, Pärnik T and Bassuner B (1987) Reassimilation of carbon dioxide by Flaveria (Asteraceae) species representing different types of photosynthesis. Planta 172: 214–218
Bergmann A, Garderström P and Ericson I (1981) Release and refixation of ammonia during photorespiration. Physiol Plant 53: 528–532
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. Estimates from gas exchange measurements on spinach. Planta 165: 397–406
Bruhn D, Mikkelsen TN and Atkin OK (2002) Does the direct effect of atmospheric CO2 concentration on leaf respiration vary with temperature? Responses in two species of Plantago that differ in relative growth rate. Physiol Plant 114: 57–64
Budde RJA and Randall DD (1990) Pea leaf mitochondrial pyruvate dehydrogenase complex is inactivated in vivo in a light-dependent manner. Proc Natl Acad Sci USA 87: 673–676
Bykova NV and Møller IM (2001) Involvement of matrix NADP turnover in the oxidation of NAD+-linked substrates by pea leaf mitochondria. Physiol Plant 111: 448–456
Bykova NV, Igamberdiev AU and Møller IM (1998) Contribution of respiratory NAD(P)H dehydrogenases to glycine and glycine plus malate oxidation by pea leaf mitochondria. In: IM Møller, P Garderström, K Glimelius and E Glaser (eds) Plant Mitochondria: From Gene to Function. Backhuys Publishers, Leiden, pp 347–351
Bykova NV, Egsgaard H and Møller IM (2003) Identification of 14 new phosphoproteins involved in important plant mitochondrial processes. FEBS Lett 540: 141–146
Byrd GT, Sage RF and Brown RH (1992) A comparison of dark respiration between C3 and C4 plants. Plant Physiol 100: 191–198
Chapman EA and Graham D (1974) The effect of light on the tricarboxylic acid cycle in green leaves. I. Relative rates of the cycle in the dark and in the light. Plant Physiol 53: 879–885
Chen RD and Gadal P (1990) Structure, functions and regulation of NAD-and NADP-dependent isocitrate dehydrogenases in higher plants and in other organisms. Plant Physiol Biochem 28: 411–427
Day D and Wiskich JT (1977) Factors limiting respiration by isolated cauliflower mitochondria. Phytochemistry 16: 1499–1502
Day D, Neuburger M and Douce R (1985) Interactions between glycine decarboxylase, the tricarboxylic acid cycle and the respiratory chain in pea leaf mitochondria. Aust J Plant Physiol 12: 119–130
De Palma A, Scalera V, Bisaccia F and Prezioso G (2003) Citrate uniport by the mitochondrial tricarboxylate carrier: A basis for a new hypothesis for the transport mechanism. J Bioenerg Biomembr 35: 133–140
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
Doman NG (1959) On the interaction between photosynthesis and respiration in plants. Biochemistry (Moscow) 24: 19–24
Drake BG, Azcon-Bieto J, Berry J, Bunce J, Dijkstra P, Farrar J, Gifford RM, Gonzalez-Meler MA, Koch G, Lambers H, Siedow J and Wullschleger S (1999) Does elevated atmospheric CO2 concentration inhibit mitochondrial respiration in green plants? Plant Cell Environ 22: 649–657
Edwards GE and Walker D (1983) C3, C4: Mechanisms, and Cellular and Environmental Regulation of Photosynthesis. Blackwell, Oxford
Fondy BR, Geiger DR and Servaites JC (1989) Photosynthesis, carbohydrate-metabolism and export in Beta vulgaris L and Phaseolus vulgaris L during square and sinusoidal light regimes. Plant Physiol 89: 396–402
Fox TC and Geiger DR (1984) Effects of decreased net carbon exchange on carbohydrate metabolism in sugar beet source leaves. Plant Physiol 76: 762–768
Gardeström P and Lernmark U (1995) The contribution of mitochondria to energetic metabolism in photosynthetic cells. J Bioenerg Biomembr 27: 415–421
Gardeström P and Wigge B (1988) Influence of photorespiration on ATP/ADP ratios in the chloroplasts, mitochondria, and cytosol, studied by rapid fractionation of barley (Hordeum vulgare) protoplasts. Plant Physiol 88: 69–76
Gardeström P, Igamberdiev AU and Raghavendra AS (2002) Mitochondrial functions in the light and significance to carbon-nitrogen interactions. In: Foyer CH and Noctor G (eds) Photosynthetic Nitrogen Assimilation and Associated Carbon and Respiratory Metabolism, pp 151–172. Kluwer Academic Publishers, Dordrecht
Gemel J and Randall DD (1992) Light regulation of leaf mitochondrial pyruvate dehydrogenase complex. Plant Physiol 100: 908–914
Gerbaud A and Andre M (1987) An evaluation of the recycling in measurements of photorespiration. Plant Physiol 83: 933–937
Gfeller RP and Gibbs M (1984) Fermentative metabolism in Chlamydomonas reinhardtii. 1. Analysis of fermentative products from starch in dark and light. Plant Physiol 75: 212–218
Goldsworthy A (1966) Experiments on the origin of CO2 released by tobacco leaf segments in the light. Phytochemistry 5: 1013–1019
Goldsworthy A (1970) Photorespiration. Bot Rev 36: 321–340
Hanning I and Heldt HW (1993) On the function of mitochondrial metabolism during photosynthesis in spinach (Spinacia oleracea L.) leaves. Plant Physiol 103: 1147–1154
Hausler RE, Schlieben NH, Schulz B and Flugge UI (1998) Compensation of decreased triose phosphate translocator activity by accelerated starch turnover and glucose transport in transgenic tobacco. Planta 204: 366–376
Heineke D, Bykova N, Gardeström P and Bauwe H (2001) Metabolic response of potato plants to an antisense reduction of the P-protein of glycine decarboxylase. Planta 212: 880–887
Hoefnagel MHN, Atkin OK and Wiskich JT (1998) Interdependence between chloroplasts and mitochondria in the light and the dark. Biochim Biophys Acta 1366: 235–255
Hurry V, Keerberg O, Pärnik T, Öquist G and Gardeström P (1996) Effect of cold hardening on the components of respiratory decarboxylation in the light and in the dark in leaves of winter rye. Plant Physiol 111: 713–719
Igamberdiev AU (1999) Foundations of metabolic organization: Coherence as a basis of computational properties in metabolic networks. BioSystems 50: 1–16
Igamberdiev AU and Gardeström P (2003) Regulation of NAD-and NADP-dependent isocitrate dehydrogenases by reduction levels of pyridine nucleotides in mitochondria and cytosol of pea leaves. Biochim Biophys Acta 1606: 117–125
Igamberdiev AU and Kleczkowski LA (2001) Implications of adenylate kinase-governed equilibrium of adenylates on contents of free magnesium in plant cells and compartments. Biochem J 360: 225–231
Igamberdiev AU and Kleczkowski LA (2003) Membrane potential, adenylate levels and Mg2+ are interconnected via adenylate kinase equilibrium in plant cells. Biochim Biophys Acta 1607: 111–119
Igamberdiev AU and Lea PJ (2002) The role of peroxisomes in the integration of metabolism and evolution of land plants. Phytochemistry 60: 651–674
Igamberdiev AU, Bykova NV and Gardeström P (1997) Involvement of cyanide-resistant and rotenone-insensitive pathways of mitochondrial electron transport during oxidation of glycine in higher plants. FEBS Lett 412: 265–269
Igamberdiev AU, Bykova NV, Lea PJ and Gardeström P (2001) The role of photorespiration in redox and energy balance of photosynthetic plant cells: A study with a barley mutant deficient in glycine decarboxylase. Physiol Plant 111: 427–438
Ivanova H, Keerberg O and Pärnik T (1993) Influence of oxygen concentration on the rates of carbon fluxes in the biochemical system of CO2 assimilation. Proc Estonian Acad Sci Chem 42: 185–197
Jahnke S (2001) Atmospheric CO2 concentration does not directly affect leaf respiration in bean or poplar. Plant Cell Environ 24: 1139–1151
Keerberg O, Drozdova IS, Pärnik TR, Keerberg HI and Voskresenskaya NP (1989) Components of photosynthetic and respiratory CO2 exchange and photosynthetic carbon metabolism in barley seedlings grown under red and blue light. Russ J Plant Physiol 36: 642–652
Keerberg O, Ivanova H, Keerberg H and Pärnik T (1999) CO2 exchange of potato transformants with reduced activities of glycine decarboxylase. In: GE de Vries, K Metzlaff (eds) Phytosfere’ 99—Highlights in European Plant Biotechnology, pp 215–219. Elsevier, Amsterdam
Keerberg O and Viil J (1988) Quantitative characteristics of photosynthetic carbon metabolism. In: AA Nichiporovich (ed) Photosynthesis and Production Processes, pp 40–53. Nauka, Moscow
Keerberg O, Ivanova H, Keerberg H and Pärnik T (2001) Contribution of primary and stored photosynthates to photorespiration. In: PS2001 Proceedings: 12th International Congress on Photosynthesis, S15-002. CSIRO, Melbourne (CD/ROM)
Keys AJ, Bird IF, Cornelius MJ, Lea PJ, Wallsgrove RM and Miflin BJ (1978) Photorespiratory nitrogen cycle. Nature 275: 741–743
Kirschbaum MUF and Farquhar GD (1987) Investigation of the CO2 dependence of quantum yield and respiration in Eucalyptus pauciflora. Plant Physiol 83: 1032–1036
Kok B (1948) A critical consideration of the quantum yield of Chlorella photosynthesis. Enzymologia 13: 1–56
Krömer S (1995) Respiration during photosynthesis. Annu Rev Plant Physiol Plant Mol Biol 46: 47–70
Krömer S and Heldt HW (1991) Respiration of pea leaf mitochondria and redox transfer between the mitochondrial and extramitochondrial compartment. Biochim Biophys Acta 1057: 42–50
Krömer S and Scheibe R (1996) Function of the chloroplastic malate valve for respiration during photosynthesis. Biochem Soc Trans 24: 761–766
Krömer S, Malmberg G and Gardeström P (1993) Mitochondrial contribution to photosynthetic metabolism—a study with barley (Hordeum vulgare L) leaf protoplasts at different light intensities and CO2 concentrations. Plant Physiol 102: 947–955
Krömer S, Gardeström P and Samuelsson G (1996) Regulation of the supply of oxaloacetate for mitochondrial metabolism via phosphoenolpyruvate carboxylase in barley leaf protoplasts. II. Effects of metabolites on PEPC activity at different activation states of the protein. Biochim Biophys Acta 1289: 351–361
Kruger NJ, Bulpin PV and ap Rees T (1983) The extent of starch degradation in the light is pea leaves. Planta 157: 271–273
Kumarasinghe KS, Keys AJ and Whittingham CP (1977) The flux of carbon through the glycolate pathway during photosynthesis in leaves. J Exp Bot 28: 1247–1257
Laisk A and Oja V (1998) Dynamics of Leaf Photosynthesis. CSIRO Publishing, Collingwood
Laisk AH (1977) Equipment and methods for the measurement of PCW curves. In: AA Nichiporovich, ed, Kinetika Fotosinteza i Fotodykhaniya u C3 Rastenij (Kinetics of photosynthesis and Photorespiration of C3 Plants). Nauka, Moscow, pp 48–71
Ligeza A, Tikhonov AN and Subczynski WK (1997) In situ measurements of oxygen production and consumption using paramagnetic fusinite particles injected into a bean leaf. Biochim Biophys Acta 1319: 133–137
Loreto F, Delfine S and Di Marco G (1999) Estimation of photorespiratory carbon dioxide recycling during photosynthesis. Aust J Plant Physiol 26: 733–736
Loreto F, Velikova V and Di Marco G (2001) Respiration in the light measured by (CO2)-C12 emission in (CO2)-C13 atmosphere in maize leaves. Aust J Plant Physiol 28: 1103–1108
Luethy MH, Gemel J, Johnston ML, Mooney BP, Miernyk JA and Randall DD (2001) Developmental expression of the mitochondrial pyruvate dehydrogenase complex in pea (Pisum sativum) seedlings. Physiol Plant 112: 559–566
Mahon JD, Fock H and Canvin DT (1974) Changes in specific radioactivities of sunflower leaf metabolites during photosynthesis in 14CO2 and 12CO2 at normal and low oxygen. Planta 120: 123–134
Marsh HVJ, Galmiche JM and Gibbs M (1965) Effect of light on the tricarboxylic acid cycle in Scenedesmus. Plant Physiol 40: 1913–1922
Maxwell DP, Wang Y and McIntosh L (1999) The alternative oxidase lowers mitochondrial reactive oxygen production in plant cells. P Natl Acad Sci USA 96: 8271–8276
McCashin BG, Cossins EA and Canvin DT (1988) Dark respiration during photosynthesis in wheat leaf slices. Plant Physiol 87: 155–161
Melo AMP, Roberts TH and Møller IM (1996) Evidence for the presence of two rotenone-insensitive NAD(P)H dehydrogenases on the inner surface of the inner membrane of potato tuber mitochondria. Biochim Biophys Acta 1276: 133–139
Melzer E and O’Leary MH (1987) Anapleurotic CO2 fixation by phosphoenolpyruvate carboxylase in C3 plants. Plant Physiol 84: 58–60
Michalecka AM, Svensson AS, Johansson FI, Agius SC, Johanson U, Brennicke A, Binder S and Rasmusson AG (2003) Arabidopsis genes encoding mitochondrial type II NAD(P)H dehydrogenases have different evolutionary origin and show distinct responses to light. Plant Physiol 133: 642–652
Møller IM (2001) Plant mitochondria and oxidative stress: electron transport, NADPH turnover, and metabolism of reactive oxygen species. Annu Rev Plant Physiol Plant Mol Biol 52: 561–591
Møller IM (2002) A new dawn for plant mitochondrial NAD(P)H dehydrogenases. Trends Plant Sci 7: 235–237
Møller IM and Lin W (1986) Membrane-bound NAD(P)H dehydrogenases in higher plant cells. Annu Rev Plant Physiol 37: 309–334
Nakamura Y and Miyachi S (1982) Effect of temperature on starch degradation in Chlorella vulgaris 11h cells. Plant Cell Physiol 23: 333–341
Ogren WL (1984) Photorespiration: Pathways, regulation, and modification. Annu Rev Plant Physiol 35: 415–442
Oliver DJ (1994) The glycine decarboxylase complex from plant mitochondria. Annu Rev Plant Physiol Plant Mol Biol 45: 323–337
Osmond CB and Grace SC (1995) Perspectives on photoinhibition and photorespiration in the field—quintessential inefficiencies of the light and dark reactions of photosynthesis. J Exp Bot 46: 1351–1362
Pärnik T and Keerberg O (1995) Decarboxylation of primary and end-products of photosynthesis at different oxygen concentrations. J Exp Bot 46: 1439–1447
Pärnik T, Keerberg O and Viil J (1976) Estimation of photorespiration in bean and maize leaves. Newslett Appl Nucl Meth Biol Agr 6: 5–7
Pärnik TR, Voronin PY, Ivanova HN and Keerberg OF (2002) Respiratory CO2 fluxes in photosynthesizing leaves of C3 species varying in rates of starch synthesis. Russ J Plant Physiol 49: 821–827
Pascal N, Dumas R and Douce R (1990) Comparison of the kinetic behavior toward pyridine nucleotides of NAD+-linked dehydrogenases from plant mitochondria. Plant Physiol 94: 189–193
Picault N, Palmieri L, Pisano I, Hodges M and Palmieri F (2002) Identification of a novel transporter for dicarboxylates and tricarboxylates in plant mitochondria—bacterial expression, reconstitution, functional characterization, and tissue distribution. J Biol Chem 277: 24204–24211
Pinelli P and Loreto F (2003) (CO2)-C12 emission from different metabolic pathways measured in illuminated and darkened C3 and C4 leaves at low, atmospheric and elevated CO2 concentration. J Exp Bot 54: 1761–1769
Pons TL and Welschen RAM (2002) Overestimation of respiration rates in commercially available clamp-on leaf chambers. Complications with measurement of net photosynthesis. Plant Cell Environ 25: 1367–1372
Purvis AC (1997) Role of the alternative oxidase in limiting superoxide production by plant mitochondria. Physiol Plant 100: 165–170
Raghavendra AS, Padmasree K and Saradadevi K (1994) Interdependence of photosynthesis and respiration in plant cells—interactions between chloroplasts and mitochondria. Plant Sci 97: 1–14
Rasulov BH (1986) Photosynthetic parameters of cotton leaves at various source-sink relations within the whole plant system. Russ J Plant Physiol 33: 922–929
Rasulov BH and Oja V (1982) Estimation of components of respiration in the light considering the presence of residual oxygen. Russ J Plant Physiol 30: 616–622
Rasulov BH, Laisk AH and Asrorov KA (1983) Photosynthesis and photorespiration in some cotton species during ontogeny. Russ J Plant Physiol 30: 616–645
Raven JA and Farquhar GD (1990) The influence of N-metabolism and organic acid synthesis on the natural abundance of isotopes of carbon in plants. New Phytol 116: 505–529
Ribas-Carbo M, Lennon AM, Robinson SA, Giles L, Berry JA and Siedow JN (1997) The regulation of electron partitioning between the cytochrome and alternative pathways in soybean cotyledon and root mitochondria. Plant Physiol 113: 903–911
Ribas-Carbo M, Robinson SA, Gonzalez-Meler MA, Lennon AM, Giles L, Siedow JN and Berry JA (2000) Effects of light on respiration and oxygen isotope fractionation in soybean cotyledons. Plant Cell Environ 23: 983–989
Robinson JM (1988) Does O2 photoreduction occur within chloroplasts in vivo? Physiol Plant 72: 666–680
Sharkey TD (1988) Estimating the rate of photosynthesis in leaves. Physiol Plant 73: 147–152
Svensson AS and Rasmusson AG (2001) Light-dependent gene expression for proteins in the respiratory chain of potato leaves. Plant J 28: 73–82
Tovar-Méndez A, Miernyk JA and Randall DD (2003) Regulation of pyruvate dehydrogenase complex activity in plant cells. Eur J Biochem 270: 1043–1049
Turpin DH, Botha FC, Smith RG, Feil R, Horsey AK and Vanlerberghe GC (1990) Regulation of carbon partitioning to respiration during dark ammonium assimilation by the green alga Selenastrum minutum. Plant Physiol 93: 166–175
Vanlerberghe GC and McIntosh L (1996) Signals regulating the expression of the nuclear gene encoding alternative oxidase of plant mitochondria. Plant Physiol 111: 589–595
Vanlerberghe GC, Day DA, Wiskich JT, Vanlerberghe AE and McIntosh L (1995) Alternative oxidase activity in tobacco leaf mitochondria — dependence on tricarboxylic acid cycle-mediated redox regulation and pyruvate activation. Plant Physiol 109: 353–361
Villar R, Held AA and Merino J (1994) Comparison of methods to estimate dark respiration in the light in leaves of 2 woody species. Plant Physiol 105: 167–172
Villar R, Held AA and Merino J (1995) Dark leaf respiration in light and darkness of an evergreen and a deciduous plant species. Plant Physiol 107: 421–427
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
Wallsgrove RM, Turner JC, Hall NP, Kendall AC and Bright SWJ (1987) Barley mutants lacking chloroplast glutamine synthetase. Biochemical and genetic analysis. Plant Physiol 83: 155–158
Weger HG, Birch DG, Elrifi IR and Turpin DH (1988) Ammonium assimilation requires mitochondrial respiration in the light—a study with the green alga Selenastrum minutum. Plant Physiol 86: 688–692
Wigge B, Krömer S and Gardeström P (1993) The redox levels and subcellular distribution of pyridine nucleotides in illuminated barley leaf protoplasts studied by rapid fractionation. Physiol Plant 88: 10–18
Wingler A, Lea PJ and Leegood RC (1999a) Photorespiratory metabolism of glyoxylate and formate in glycine-accumulating mutants of barley and Amaranthus edulis. Planta 207: 518–526
Wingler A, Quick WP, Bungard RA, Bailey KJ, Lea PJ and Leegood RC (1999b) The role of photorespiration during drought stress: An analysis utilizing barley mutants with reduced activities of photorespiratory enzymes. Plant Cell Environ 22: 361–373
Winter H, Robinson DG and Heldt HW (1993) Subcellular volumes and metabolite concentrations in barley leaves. Planta 191: 180–190
Winter H, Robinson DG and Heldt HW (1994) Subcellular volumes and metabolite concentrations in spinach leaves. Planta 193: 530–535
Wiskich JT and Dry IB (1985) The tricarboxylic acid cycle in plant mitochondria: Its operation and regulation. In: R Douce, D Day (eds) Higher Plant Cell Respiration, Vol 18, pp 281–313. Springer-Verlag, Berlin
Yamauchi M and Yamada Y (1985) Glycolate synthesis in tomato leaf disks: Involvement of storage material in photorespiration. J Fac Agr Kyushu Univ 30: 135–147
Zalensky OV, Voznesensky VL, Ponomaryeva MM and Shtanko TP (1955) Effect of temperature on the metabolism of carbon fixed in the process of photosynthesis. Bot J (Russia) 40: 347–358
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2005 Springer
About this chapter
Cite this chapter
Hurry, V. et al. (2005). Respiration in Photosynthetic Cells: Gas Exchange Components, Interactions with Photorespiration and the Operation of Mitochondria in the Light. In: Lambers, H., Ribas-Carbo, M. (eds) Plant Respiration. Advances in Photosynthesis and Respiration, vol 18. Springer, Dordrecht. https://doi.org/10.1007/1-4020-3589-6_4
Download citation
DOI: https://doi.org/10.1007/1-4020-3589-6_4
Publisher Name: Springer, Dordrecht
Print ISBN: 978-1-4020-3588-3
Online ISBN: 978-1-4020-3589-0
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)