The McCree-de Wit-Penning de Vries-Thornley respiration paradigms: 30 years later.

Amthor, J

doi:10.1006/anbo.2000.1175

Cited by 824Plant nutrient uptake and metabolismPhotosynthetic Processes and MechanismsPlant Water Relations and Carbon Dynamics

The McCree-de Wit-Penning de Vries-Thornley respiration paradigms: 30 years later.

Amthor, J·2000·Annals of Botany

DOI 10.1006/anbo.2000.1175

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Abstract

To grow, an organism must respire substrates to produce C-skeleton intermediates, usable energy (i.e. ATP), and reducing power [i.e. NAD(P)H] to support biosynthesis and related processes such as active transport of substrates. Respiration is also needed—mainly as a supplier of ATP—to maintain existing biomass in a functional state. As a result, quantifying links between respiration, growth, and maintenance are needed to assess potential plant productivity, to understand plant responses to environmental factors, and as the basis of cost-benefit analyses of alternative uses of photosynthate. Beginning 30 years ago, and continuing for about 5 years, rapid advances were made in understanding and quantifying relationships between respiration and the processes it supports. Progress has continued since then, though often as refinements rather than novel advances. The simplest framework (i.e. paradigm) for relating respiration to other processes divides respiration into growth and maintenance fractions. This often involves a combination of empiricism and mechanism. A three-component framework (growth, maintenance and wastage) has also been considered, although quantifying wastage (theoretically or empirically) remains problematic. The more general and flexible framework, called the general paradigm (GP, herein), relates respiration to any number of individual processes that it supports. The most important processes (from C and energy balance perspectives) identified to date that require respiration are: biosynthesis of new structural biomass, translocation of photosynthate from sources to sinks, uptake of ions from the soil solution, assimilation of N (including N 2 ) and S into organic compounds, protein turnover, and cellular ion-gradient maintenance. In addition, some part of respiration may be associated with wastage (e.g. futile cycles and mitochondrial electron transport uncoupled from oxidative phosphorylation). Most importantly, the GP can (semi-)mechanistically relate respiration to underlying physiology and biochemistry. The GP is more complicated than other approaches to describing or modelling respiration because it is more realistic, complete and mechanistic. This review describes a history of the GP and its present state. Future research questions are suggested. Copyright 2000 Annals of Botany Company

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The substrate carbon conversion efficiency (+) varies between 0 and 0.85 in non-growing plants/tissues and rapidly growing vegetative plants and tissues, respectively.
“According to previous studies, the value of + varies between 0 and 0.85 in non-growing plants/tissues and rapidly growing vegetative plants and tissues, respectively (Amthor, 2000; Hansen et al., 2005).”
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Processes Controlling Blue Grama Production on the Shortgrass Prairie
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Ontogenetic Changes in the Respiration Coefficients of Grain Sorghum
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Differentiating Day from Night Effects of High Ambient [CO2] on the Gas Exchange and Growth ofXanthium strumariumL. Exposed to Salinity Stress
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A Comparison of the Rate of Maintenance Respiration in Some Crop Legumes and Tobacco Determined by Three Methods
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Growth and Assimilate Conversion of Cotton Bolls (Gossypium hirsutum L.) 1. Growth of Fruits
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Metabolism : organic nutrition and nitrogen metabolism
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A global overview of drought and heat-induced tree mortality reveals emerging climate change risks for forests
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Mechanisms of plant survival and mortality during drought: why do some plants survive while others succumb to drought?
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Rice yields decline with higher night temperature from global warming
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Elevated CO2 effects on plant carbon, nitrogen, and water relations: six important lessons from FACE
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Crop Yield Gaps: Their Importance, Magnitudes, and Causes
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On the variability of respiration in terrestrial ecosystems: moving beyond Q 10
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Salinity tolerance of crops – what is the cost?
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What is the maximum efficiency with which photosynthesis can convert solar energy into biomass?
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CO 2 balance of boreal, temperate, and tropical forests derived from a global database
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Global covariation of carbon turnover times with climate in terrestrial ecosystems
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Understanding the roles of nonstructural carbohydrates in forest trees – from what we can measure to what we want to know
Hartmann, H., & Trumbore, S. E. (2016) · New Phytologist · doi:10.1111/nph.13955 · Cited by 903 · see citing works
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Wright, I. J., Reich, P. B., & Westoby, M. (2001) · Functional Ecology · doi:10.1046/j.0269-8463.2001.00542.x · Cited by 869 · see citing works
Handbook of Photosynthesis
Pessarakli, M. (2005) · CRC Press eBooks · doi:10.1201/9781420027877 · Cited by 837 · see citing works
Tree and forest functioning in response to global warming
Saxe, H., Cannell, M. G. R., Johnsen, Ø., Ryan, M. G., & Vourlitis, G. L. (2001) · New Phytologist · doi:10.1046/j.1469-8137.2001.00057.x · Cited by 826 · see citing works
Evaluation of MODIS NPP and GPP products across multiple biomes
Turner, D. P., Ritts, W. D., Cohen, W. B., Gower, S. T., Running, S. W., Zhao, M., Costa, M. H., Kirschbaum, A. A., Ham, J. M., SALESKA, S. R., et al. (2006) · Remote Sensing of Environment · doi:10.1016/j.rse.2006.02.017 · Cited by 718 · see citing works
Carbon respired by terrestrial ecosystems – recent progress and challenges
Trumbore, S. E. (2006) · Global Change Biology · doi:10.1111/j.1365-2486.2006.01067.x · Cited by 579 · see citing works
Global Convergence in the Temperature Sensitivity of Respiration at Ecosystem Level
Mahecha, M. D., Reichstein, M., Carvalhais, N., Lasslop, G., Lange, H., Seneviratne, S. I., Vargas, R., Ammann, C., Arain, M. A., Cescatti, A., et al. (2010) · Science · doi:10.1126/science.1189587 · Cited by 543 · see citing works
A plant's perspective of extremes: terrestrial plant responses to changing climatic variability
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Linking leaf and root trait syndromes among 39 grassland and savannah species
Tjoelker, M. G., Craine, J. M., Wedin, D. A., Reich, P. B., & Tilman, D. G. (2005) · New Phytologist · doi:10.1111/j.1469-8137.2005.01428.x · Cited by 524 · see citing works
Energy costs of salt tolerance in crop plants
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Mechanistic scaling of ecosystem function and dynamics in space and time: Ecosystem Demography model version 2
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The Functional Organization and Control of Plant Respiration
Plaxton, W. C., & Podestá, F. E. (2006) · Critical Reviews in Plant Sciences · doi:10.1080/07352680600563876 · Cited by 506 · see citing works
Carbon isotopes in terrestrial ecosystem pools and CO 2 fluxes
Bowling, D. R., Pataki, D. E., & Randerson, J. T. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2007.02342.x · Cited by 507 · see citing works
Forest carbon use efficiency: is respiration a constant fraction of gross primary production?
DeLucia, E. H., Drake, J. E., Thomas, R. B., & Gonzàlez‐Meler, M. A. (2007) · Global Change Biology · doi:10.1111/j.1365-2486.2007.01365.x · Cited by 494 · see citing works
Evans Review No. 2: The hot and the cold: unravelling the variable response of plant respiration to temperature
Atkin, O. K., Bruhn, D., Hurry, V., & Tjoelker, M. G. (2005) · Functional Plant Biology · doi:10.1071/fp03176 · Cited by 491 · see citing works
Scaling of respiration to nitrogen in leaves, stems and roots of higher land plants
Reich, P. B., Tjoelker, M. G., Pregitzer, K. S., Wright, I. J., Oleksyn, J., & Machado, J. (2008) · Ecology Letters · doi:10.1111/j.1461-0248.2008.01185.x · Cited by 463 · see citing works
Rhizoeconomics: Carbon costs of phosphorus acquisition
Lynch, J. P., Ho, M. D., & phosphorus, L. (2005) · Plant and Soil · doi:10.1007/s11104-004-1096-4 · Cited by 453 · see citing works
RESPIRATION FROM A TROPICAL FOREST ECOSYSTEM: PARTITIONING OF SOURCES AND LOW CARBON USE EFFICIENCY
Chambers, J. Q., Tribuzy, E. S., Toledo, L. C., Crispim, B. F., Higuchi, N., dos SANTOS, J., de Araújo, A. C., Kruijt, B., Nobre, A. D., & Trumbore, S. E. (2004) · Ecological Applications · doi:10.1890/01-6012 · Cited by 439 · see citing works
Global variability in leaf respiration in relation to climate, plant functional types and leaf traits
Atkin, O. K., Bloomfield, K. J., Reich, P. B., Tjoelker, M. G., Asner, G. P., Bonal, D., Bönisch, G., Bradford, M., Cernusak, L. A., Cosio, E. G., et al. (2015) · New Phytologist · doi:10.1111/nph.13253 · Cited by 430 · see citing works
Plant respiration in productivity models: conceptualisation, representation and issues for global terrestrial carbon-cycle research
Gifford, R. M. (2003) · Functional Plant Biology · doi:10.1071/fp02083 · Cited by 409 · see citing works
Agriculture and the new challenges for photosynthesis research
Murchie, E. H., Pinto, M. E., & Horton, P. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02705.x · Cited by 395 · see citing works
Tropical forests and the changing earth system
Lewis, S. L. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1711 · Cited by 383 · see citing works
Fertile forests produce biomass more efficiently
Vicca, S., Luyssaert, S., Peñuelas, J., Campioli, M., Chapin, F. S., Ciais, P., Heinemeyer, A., Högberg, P., Kutsch, W. L., Law, B. E., et al. (2012) · Ecology Letters · doi:10.1111/j.1461-0248.2012.01775.x · Cited by 372 · see citing works
Global pattern of NPP to GPP ratio derived from MODIS data: effects of ecosystem type, geographical location and climate
Zhang, Y., Xu, M., Chen, H., & Adams, J. M. (2009) · Global Ecology and Biogeography · doi:10.1111/j.1466-8238.2008.00442.x · Cited by 362 · see citing works
The productivity, metabolism and carbon cycle of tropical forest vegetation
Malhi, Y. S. (2011) · Journal of Ecology · doi:10.1111/j.1365-2745.2011.01916.x · Cited by 356 · see citing works
Least‐Cost Input Mixtures of Water and Nitrogen for Photosynthesis
Wright, I. J., Reich, P. B., & Westoby, M. (2003) · The American Naturalist · doi:10.1086/344920 · Cited by 348 · see citing works
Decelerating growth in tropical forest trees
Feeley, K. J., Wright, S. J., Supardi, M. N. N., Kassim, A. R., & Davies, S. J. (2007) · Ecology Letters · doi:10.1111/j.1461-0248.2007.01033.x · Cited by 340 · see citing works
How can we make plants grow faster? A source–sink perspective on growth rate
White, A. C., Rogers, A., Rees, M., & Osborne, C. P. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv447 · Cited by 335 · see citing works
Site‐level evaluation of satellite‐based global terrestrial gross primary production and net primary production monitoring
Turner, D. P., Ritts, W. D., Cohen, W. B., Maeirsperger, T. K., Gower, S. T., Kirschbaum, A. A., Running, S. W., Zhao, M., Wofsy, S. C., Dunn, A. L., et al. (2005) · Global Change Biology · doi:10.1111/j.1365-2486.2005.00936.x · Cited by 333 · see citing works
Scaling Gross Primary Production (GPP) over boreal and deciduous forest landscapes in support of MODIS GPP product validation
Turner, D. P., Ritts, W. D., Cohen, W. B., Gower, S. T., Zhao, M., Running, S. W., Wofsy, S. C., Urbanski, S. P., Dunn, A. L., & Munger, J. W. (2003) · Remote Sensing of Environment · doi:10.1016/j.rse.2003.06.005 · Cited by 328 · see citing works
Modelling carbon sources and sinks in terrestrial vegetation
Fatichi, S., Pappas, C., Jakob Zscheischler, A., & Leuzinger, S. (2018) · New Phytologist · doi:10.1111/nph.15451 · Cited by 313 · see citing works
Root anatomical phenes associated with water acquisition from drying soil: targets for crop improvement
Lynch, J. P., Chimungu, J. G., & Brown, K. M. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru162 · Cited by 310 · see citing works
No growth stimulation of Canada’s boreal forest under half-century of combined warming and CO <sub>2</sub> fertilization
Girardin, M. P., Bouriaud, O., Hogg, E. H., Kurz, W., Zimmermann, N. E., Metsaranta, J. M., de Jong, R., Frank, D. C., Esper, J., Büntgen, U., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610156113 · Cited by 298 · see citing works
Plant allometry, stoichiometry and the temperature‐dependence of primary productivity
Kerkhoff, A. J., Enquist, B. J., Elser, J. J., & Fagan, W. F. (2005) · Global Ecology and Biogeography · doi:10.1111/j.1466-822x.2005.00187.x · Cited by 297 · see citing works
Changing Ecology of Tropical Forests: Evidence and Drivers
Lewis, S. L., Lloyd, J., Sitch, S. A., Mitchard, E. T. A., & Laurance, W. F. (2009) · Annual Review of Ecology Evolution and Systematics · doi:10.1146/annurev.ecolsys.39.110707.173345 · Cited by 286 · see citing works
Arabidopsis Coordinates the Diurnal Regulation of Carbon Allocation and Growth across a Wide Range of Photoperiods
Ronan Sulpice, A., Flis, A., Ivakov, A. A., Apelt, F., Krohn, N., Encke, B., Abel, C., Feil, R., Lunn, J. E., & Stitt, M. (2013) · Molecular Plant · doi:10.1093/mp/sst127 · Cited by 281 · see citing works
Improving water use efficiency in grapevines: potential physiological targets for biotechnological improvement
Flexas, J., GALMÉS, J., Galla, A., GULÍAS, J., Pou, A., Ribas‐Carbó, M., Tomás, M., & Medrano, H. (2009) · Australian Journal of Grape and Wine Research · doi:10.1111/j.1755-0238.2009.00057.x · Cited by 280 · see citing works
Fingerprinting the impacts of global change on tropical forests
Lewis, S. L., Malhi, Y. S., & Phillips, O. L. (2004) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2003.1432 · Cited by 278 · see citing works
Metabolic Origin of Carbon Isotope Composition of Leaf Dark-Respired CO2 in French Bean
Tcherkez, G. G. B., Nogués, S., Bleton, J., Cornic, G., Badeck, F., & Ghashghaie, J. (2003) · PLANT PHYSIOLOGY · doi:10.1104/pp.013078 · Cited by 277 · see citing works
OAK FOREST CARBON AND WATER SIMULATIONS: MODEL INTERCOMPARISONS AND EVALUATIONS AGAINST INDEPENDENT DATA
Hanson, P. J., Amthor, J. S., Wullschleger, S. D., Wilson, K., Grant, R. F., Hartley, A. E., Hui, D., E. R. Hunt, Jr., Johnson, D. W., Kimball, J. S., et al. (2004) · Ecological Monographs · doi:10.1890/03-4049 · Cited by 264 · see citing works
Self-citation
Determinants of terrestrial ecosystem carbon balance inferred from European eddy covariance flux sites
Reichstein, M., Papale, D., Valentini, R., Aubinet, M., Bernhofer, C., Knohl, A., Laurila, T., Lindroth, A., Moors, E. J., Kim Pilegaard, L., et al. (2007) · Geophysical Research Letters · doi:10.1029/2006gl027880 · Cited by 262 · see citing works
Effect of temperature on metabolic activity of intact microbial communities: Evidence for altered metabolic pathway activity but not for increased maintenance respiration and reduced carbon use efficiency
Dijkstra, P., Thomas, S. C., Heinrich, P. L., Koch, G. W., Schwartz, E., & Hungate, B. A. (2011) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2011.05.018 · Cited by 252 · see citing works
Root strategies for phosphorus acquisition
Lynch, J. P., & Brown, K. M. (2008) · Plant ecophysiology · doi:10.1007/978-1-4020-8435-5_5 · Cited by 253 · see citing works
Convergence in the temperature response of leaf respiration across biomes and plant functional types
Heskel, M., O’Sullivan, O. S., Reich, P. B., Tjoelker, M. G., Weerasinghe, L. K., Penillard, A., Egerton, J. J. G., Creek, D., Bloomfield, K. J., Xiang, J., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1520282113 · Cited by 253 · see citing works
The Colorful World of Extracellular Electron Shuttles
Glasser, N. R., Saunders, S. H., & Newman, D. K. (2017) · Annual Review of Microbiology · doi:10.1146/annurev-micro-090816-093913 · Cited by 244 · see citing works
Growth, carbon‐isotope discrimination, and drought‐associated mortality across a Pinus ponderosa elevational transect
McDowell, N. G., Allen, C. D., & Marshall, L. A. E. (2009) · Global Change Biology · doi:10.1111/j.1365-2486.2009.01994.x · Cited by 230 · see citing works
Adapting agriculture to climate change: a review
Anwar, M., Liu, D.-K., Macadam, I., & Kelly, G. (2013) · Theoretical and Applied Climatology · doi:10.1007/s00704-012-0780-1 · Cited by 235 · see citing works
Soil respiration across scales: The importance of a model–data integration framework for data interpretation
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Authors: Amthor, J.
Affiliations: Oak Ridge National Laboratory (US)
Corresponding author: Amthor, J
ORCID: Amthor, J
Venue: Annals of Botany
Publisher: Oxford University Press (OUP)
Published: 2000-07
Volume: 86
Issue: 1
Pages: 1-20
ISSN: 0305-7364 (ISSN-L)
DOI: 10.1006/anbo.2000.1175
OpenAlex: W2107606962
Cited by: 822
References: 154
Citations by year: 2026: 27 · 2025: 17 · 2024: 33 · 2023: 39 · 2022: 45 · 2021: 37 · 2020: 40 · 2019: 38 · 2018: 37 · 2017: 39 · 2016: 36 · 2015: 39 · 2014: 36 · 2013: 36 · 2012: 29
FWCI: 21.87
Type: journal article
Language: en
Open access: closed
Locations: Annals of Botany (publishedVersion)
Funders: National Science Foundation (DE-AC05-96OR22464)
U.S. Department of Energy (DE-AC05?, DE-AC05-96OR22464)
National Aeronautics and Space Administration
U.S. Department of Agriculture
Biological and Environmental Research
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant nutrient uptake and metabolism
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
Physical Sciences › Environmental Science › Global and Planetary Change › Plant Water Relations and Carbon Dynamics
Keywords: plant respiration, growth respiration, maintenance respiration, photosynthate translocation, ion uptake, nitrogen assimilation, sulfur assimilation, protein turnover, energy balance, carbon balance, plant productivity

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