Modelling the Components of Plant Respiration: Representation and Realism

By J. Thornley, M. Cannell. 2000

290 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Plant Science, Soil Science

View Paper: https://www.semanticscholar.org/paper/397e1325eb9f8fc8180059c85f81a69f3d5589da

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Citations in the corpus

The McCree-de Wit-Penning de Vries-Thornley Respiration Paradigms: 30 Years Later (2000, background): “It is therefore useful to consider a gR describing growth respiration within growing organs, written gR,local, where `local' means `in the growing organ' (see Cannell and Thornley, 2000; Thornley and Cannell, 2000).”
Investigation and sensitivity analysis of a mechanistic phytoplankton model implemented in a new modular numerical tool (Eco3M) dedicated to biogeochemical modelling (2006, unknown): “(mol C) (mol C) � 1 0.25 Thornley and Cannell (2000) ”
Modelling the impact of future changes in climate, CO2 concentration and land use on natural ecosystems and the terrestrial carbon sink (2004, background): “Several recent studies have indicated that this assumption may be a good approximation of reality (Gifford,1995 ; Waring et al.,1998 ; Dewar et al.,1999 ; Thornley and Cannell,2000 ),better than the assumption that maintenance respiration is a linear function of the total carbon content of each of”
Acclimation of leaf respiration to temperature is rapid and related to specific leaf area, soluble sugars and leaf nitrogen across three temperate deciduous tree species (2005, unknown): “Thus respiration responses to temperature remain poorly characterized, yet this information is vital to represent accurately plant respiration in global carbon cycles (Amthor 2000; Thornley & Cannell 2000; Wythers et al . 2005).”
The growth respiration component in eddy CO2 flux from a Quercus ilex mediterranean forest (2004, background): “In such a context, the simple growth-maintenance respiration paradigm provides a useful approximate view of plant respiration even if it can be interpreted to explain three completely different mechanisms of plant function (Thornley & Cannell, 2000).”
Nonstructural carbon in woody plants. (2014, background): “The respiratory costs of maintenance and new growth (131) may be satisfied either before or after this transfer and mixing takes place.”
Water use trade‐offs and optimal adaptations to pulse‐driven arid ecosystems (2001, background): “…ecosystems © 2001 British Ecological Society, Journal of Ecology , 89 , 464–480 include carbon costs in the analysis, but the difficulty of assigning meaningful values to the growth and maintenance costs of roots, stems and leaves discouraged us from taking this course (Thornley & Cannell 2000).”
Chronic N deposition alters root respiration‐tissue N relationship in northern hardwood forests (2012, background): “It has been suggested that a conservative respiration to photosynthesis ratio (Gifford, 2003) or a variable, but constrained, range of this ratio (Cannell & Thornley, 2000) might work best for modeling respiration at the whole plant or ecosystem level in a global change context.”
Modelling the Components of Plant Respiration: Some Guiding Principles (2000, background): “The companion paper (Thornley and Cannell, 2000) then re-examines how respiration is represented in models and how it may be represented more mechanistically, taking into account the principles outlined below.”
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, background): “…and export of carbohydrates and pools of carbon in carbohydrate and protein in leaves, but processes incorporating pool sizes and fluxes between pools have been described in models without the need to represent complex biochemical detail (Dewar et al., 1998; Dewar, 2000; Thornley & Cannell, 2000).”
A model of biogeochemical cycles of carbon, nitrogen, and phosphorus including symbiotic nitrogen fixation and phosphatase production (2007, methodology): “In this study we assume a C cost of 6 g C (gN) 1 for SNF [Thornley and Cannell, 2000] and a N cost of 15 g N (g P) 1 for biochemical P mineralization [Treseder and Vitousek, 2001].”