Scaling of respiration to nitrogen in leaves, stems and roots of higher land plants.

Using a database of 2510 measurements from 287 species, we assessed whether general relationships exist between mass-based dark respiration rate and nitrogen concentration for stems and roots, and if they do, whether they are similar to those for leaves. The results demonstrate strong respiration-nitrogen scaling relationships for all observations and for data averaged by species; for roots, stems and leaves examined separately; and for life-forms (woody, herbaceous plants) and phylogenetic groups (angiosperms, gymnosperms) considered separately. No consistent differences in the slopes of these log-log scaling relations were observed among organs or among plant groups, but respiration rates at any common nitrogen concentration were consistently lower on average in leaves than in stems or roots, indicating that organ-specific relationships should be used in models that simulate respiration based on tissue nitrogen concentrations. The results demonstrate both common and divergent aspects of tissue-level respiration-nitrogen scaling for leaves, stems and roots across higher land plants, which are important in their own right and for their utility in modelling carbon fluxes at local to global scales.

[1]  I. Terashima,et al.  Effects of Light and Nitrogen Nutrition on the Organization of the Photosynthetic Apparatus in Spinach , 1988 .

[2]  T. Tsujimori,et al.  Balancing the Global Carbon Budget , 2007 .

[3]  J. H. M. Thornley,et al.  Modelling the Components of Plant Respiration: Some Guiding Principles , 2000 .

[4]  M. G. Ryan,et al.  Effects of Climate Change on Plant Respiration. , 1991, Ecological applications : a publication of the Ecological Society of America.

[5]  W. Post,et al.  Plant Respiration in a Warmer World , 2006, Science.

[6]  Mark G Tjoelker,et al.  The hot and the cold: unravelling the variable response of plant respiration to temperature. , 2005, Functional plant biology : FPB.

[7]  J. Amthor Terrestrial higher plant respiration and net primary production , 2001 .

[8]  M. Tjoelker,et al.  Response of plant respiration to changes in temperature: mechanisms and consequences of variations in Q(10) values and acclimation , 2005 .

[9]  P. Reich,et al.  Linking leaf and root trait syndromes among 39 grassland and savannah species. , 2005, The New phytologist.

[10]  Peter A. Jones,et al.  Epigenetics in human disease and prospects for epigenetic therapy , 2004, Nature.

[11]  Louise H. Comas,et al.  Linking fine root traits to maximum potential growth rate among 11 mature temperate tree species , 2004 .

[12]  B. Osmond,et al.  Effects of Nitrogen Nutrition on Nitrogen Partitioning between Chloroplasts and Mitochondria in Pea and Wheat. , 1991, Plant physiology.

[13]  J. Amthor The McCree-de Wit-Penning de Vries-Thornley Respiration Paradigms: 30 Years Later , 2000 .

[14]  P. Reich,et al.  Photosynthesis and respiration rates depend on leaf and root morphology and nitrogen concentration in nine boreal tree species differing in relative growth rate , 1998 .

[15]  J. Amthor Plant respiratory responses to the environment and their effects on the carbon balance , 1994 .

[16]  J. Seemann,et al.  The allocation of protein nitrogen in the photosynthetic apparatus: costs, consequences, and control. , 1989 .

[17]  M. G. Ryan,et al.  Seasonal respiration of foliage, fine roots, and woody tissues in relation to growth, tissue N, and photosynthesis , 2002 .

[18]  P. Reich,et al.  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 .

[19]  R. Teskey,et al.  Measurement of stem respiration of sycamore (Platanus occidentalis L.) trees involves internal and external fluxes of CO2 and possible transport of CO2 from roots. , 2007, Plant, cell & environment.

[20]  P. Reich,et al.  Dark respiration rate increases with plant size in saplings of three temperate tree species despite decreasing tissue nitrogen and nonstructural carbohydrates. , 2006, Tree physiology.

[21]  A. Fitter,et al.  Impact of temperature on the relationship between respiration and nitrogen concentration in roots: an analysis of scaling relationships, Q10 values and thermal acclimation ratios. , 2007, The New phytologist.

[22]  Mark G. Tjoelker,et al.  Modelling respiration of vegetation: evidence for a general temperature‐dependent Q10 , 2001 .

[23]  Mark G Tjoelker,et al.  Thermal acclimation and the dynamic response of plant respiration to temperature. , 2003, Trends in plant science.

[24]  P. Reich,et al.  From tropics to tundra: global convergence in plant functioning. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[25]  M. Ribas-Carbó,et al.  Plant respiration : from cell to ecosystem , 2005 .

[26]  Mark G. Tjoelker,et al.  Universal scaling of respiratory metabolism, size and nitrogen in plants , 2006, Nature.

[27]  P. Reich,et al.  Coupling of respiration, nitrogen, and sugars underlies convergent temperature acclimation in Pinus banksiana across wide‐ranging sites and populations , 2008 .

[28]  Christopher B. Field,et al.  photosynthesis--nitrogen relationship in wild plants , 1986 .

[29]  R. Lemeur,et al.  Stem respiration and carbon dioxide efflux of young Populus deltoides trees in relation to temperature and xylem carbon dioxide concentration , 2007, Oecologia.

[30]  P. Reich,et al.  Extrapolating leaf CO2 exchange to the canopy: a generalized model of forest photosynthesis compared with measurements by eddy correlation , 1996, Oecologia.

[31]  R. Ruess,et al.  Root respiration in North American forests: effects of nitrogen concentration and temperature across biomes , 2002, Oecologia.

[32]  Sean C. Thomas,et al.  The worldwide leaf economics spectrum , 2004, Nature.

[33]  S S I T C H,et al.  Evaluation of Ecosystem Dynamics, Plant Geography and Terrestrial Carbon Cycling in the Lpj Dynamic Global Vegetation Model , 2022 .

[34]  H. Owen,et al.  New Phytol , 2008 .

[35]  S. Zarnoch,et al.  Effects of temperature and tissue nitrogen on dormant season stem and branch maintenance respiration in a young loblolly pine (Pinus taeda) plantation. , 1998, Tree physiology.

[36]  Roger M. Gifford,et al.  Plant respiration in productivity models: conceptualisation, representation and issues for global terrestrial carbon-cycle research. , 2003, Functional plant biology : FPB.

[37]  Veronica C. Lessard,et al.  Variation in sugar maple root respiration with root diameter and soil depth. , 1998, Tree physiology.

[38]  R. Betts,et al.  Acceleration of global warming due to carbon-cycle feedbacks in a coupled climate model , 2000, Nature.

[39]  R. Rosenfeld Nature , 2009, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.