The McCree-de Wit-Penning de Vries-Thornley Respiration Paradigms: 30 Years Later

By J. Amthor. 2000

790 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/4356d3fe9b57d5b79c6ea1f98cfb1c88b90b88a6

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Molecular Biology

In Plant Science

Citations in the corpus

Linking growth strategies to long‐term population dynamics in a guild of desert annuals (2007, background): “This in turn may lead to high maintenance respiration rates (Ryan 1991, 1995; Reich et al. 1997; Amthor 2000; Wright et al. 2001; Turnbull et al. 2003) and lower conversion efficiency of photosynthetic assimilates to biomass, and thus to low relative growth rates.”
Whole Plant Photosynthesis, Development, and Carbon Partitioning in Potato as a Function of Temperature (2006, background): “Seed material such as seeds from soybean plants that contain more fats and proteins than potato tubers have a higher stoichiometric conversion factor than nonseed materials (Amthor, 2000; Jones et al., 1985).”
The Functional Organization and Control of Plant Respiration (2006, background): “…by photosynthetic terrestrial plants is released back into the atmosphere by respiring plants, representing about 50 percent of the annual input of CO2 from terrestrial ecosystems (Amthor, 1997, 2000; Atkin and Tjoelker, 2003; Gifford, 2003; Gonzalez-Meler et al., 2004; Atkin et al., 2005).”
The productivity, metabolism and carbon cycle of tropical forest vegetation (2012, neutral): “…a wide range of CUE values, ranging from c. 0.2 to c. 0.8 (Litton, Raich & Ryan 2007), although theoretical calculation of growth efficiency and respiratory costs associated with maintenance, nutrient acquisition and transport suggest it should be constrained between 0.2 and 0.65 (Amthor 2000).”
Plant allometry, stoichiometry and the temperature-dependence of primary productivity (2005, methodology): “However, this lack of consensus does demonstrate that, while generalized quantitative theory exists for many of the components of productivity (Thornley, 1970; Farquhar et al ., 1980; Amthor, 2000), these have not been integrated fully into a common modelling framework.”
On the variability of respiration in terrestrial ecosystems: moving beyond Q10 (2006, background): “Models that are specific to autotrophic respiration at an organismal scale are more advanced, addressing mechanistic relationships among growth, maintenance and wastage (futile) respiration, and the synthesis and translocation of metabolites within plants (Amthor, 2000).”
Crop yield gaps: their importance, magnitudes, and causes. (2009, background): “These include the facts that about half of the light energy is in wavelengths too long to be used in photosynthesis and that all plants need to consume some of the photosynthate they fix in the mitochondrial respiration that powers construction and maintenance of plant tissues (16).”
Terrestrial higher plant respiration and net primary production (2001, background): “Penning de Vries to give it a try (Amthor, 2000).”
Response of total night‐time respiration to differences in total daily photosynthesis for leaves in a Quercus rubra L. canopy: implications for modelling canopy CO2 exchange (2004, methodology): “Alternative ‘demand-driven’ regulation of the rate of respiration includes the energy-requiring processes of phloem loading and translocation (Amthor, 2000), demand for respiratory products (Amthor, 1989), enzyme capacity (Atkin & Tjoelker, 2003) and the activity of alternative biochemical pathways…”
Growth, carbon‐isotope discrimination, and drought‐associated mortality across a Pinus ponderosa elevational transect (2010, background): “Extended periods without photosynthesis may cause mortality because, while carbon allocation to wood growth may cease temporarily without death, carbon allocation to maintenance respiration (Ryan et al., 1995; Amthor, 2000) must continue at some basal level or mortality is inevitable (Marshall & War”
Coupling of respiration, nitrogen, and sugars underlies convergent temperature acclimation in Pinus banksiana across wide‐ranging sites and populations (2008, background): “…2008 The Authors Journal compilation r 2008 Blackwell Publishing Ltd, Global Change Biology, 14, 782–797 particularly with regard to constraining the ratio of respiration to photosynthesis in leaves and plants grown in various environments (Amthor, 2000; Gifford, 2003; Whitehead et al., 2004).”
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 (2011, methodology): “A more mechanistic approach widely applied to respiration involves the concept of energy cost for growth, maintenance, and ion uptake processes (Amthor, 2000; Anderson and Domsch, 2010; Blagodatsky and Richter, 1998; Chapman and Gray, 1986; Van Bodegom, 2007).”