Source-sink partitioning. Do we need Münch?

The simulation of phloem translocation by the Münch theory commonly uses resistances from sources to sinks: the resistances are therefore regarded as important in partitioning. Although resistance is generally a set constant, it is in fact strongly affected by viscosity, and thus the concentration of the transported solute. In this paper, the model of partitioning proposed by Minchin et al. was first corrected for variations in viscosity. The model was further modified, with the source considered as an activity of solute production rather than as a compartment concentration. When so defined, the source cannot differ from the sum of sink activities, largely outdating the source- or sink-limitation concepts. The corrected model confined the effect of resistances on the partitioning to low source activities. In the example of wheat grain filling analysed, such activities would be so low that they would correspond only to pathological conditions. In that case, the use of resistances in modelling is therefore just a mathematical burden, not even easily quantifiable since they are related to anatomical traits that are difficult to access. Leaving out resistances, it becomes easy to calculate the sink activities directly from the source activities, using an intuitive, accessible parametrization. The conditions for such a simplification are discussed.

[1]  P. Sharpe,et al.  Consequences of insufficient equations in models of the Münch hypothesis of phloem transport , 1979 .

[2]  D. Aspinall,et al.  The physiology of starch and protein deposition in the endosperm of wheat. , 1990 .

[3]  Michael A. Grusak,et al.  Cold-Inhibited Phloem Translocation in Sugar Beet: II. CHARACTERIZATION AND LOCALIZATION OF THE SLOW-COOLING RESPONSE , 1985 .

[4]  J. Thornley A Balanced Quantitative Model for Root: Shoot Ratios in Vegetative Plants , 1972 .

[5]  C. Jenner,et al.  Physiological Basis of Genetic Differences in the Growth of Grains of Six Varieties of Wheat , 1978 .

[6]  Peter Millard,et al.  An ecophysiological approach to modelling resource fluxes in competing plants , 1999 .

[7]  M. Gent Photosynthate reserves during grain filling in winter wheat , 1994 .

[8]  D. B. Fisher,et al.  Accumulation and Conversion of Sugars by Developing Wheat Grains : VII. Effect of Changes in Sieve Tube and Endosperm Cavity Sap Concentrations on the Grain Filling Rate. , 1987, Plant Physiology.

[9]  R. Gifford,et al.  Accumulation and conversion of sugars by developing wheat grains. 3. Non‐diffusional uptake of sucrose, the substrate preferred by endosperm slices , 1983 .

[10]  I. F. Wardlaw,et al.  Tansley Review No. 27 The control of carbon partitioning in plants. , 1990, The New phytologist.

[11]  R. Gifford,et al.  Accumulation and Conversion of Sugars by Developing Wheat Grains. II. Light Requirement for Kernels Cultured in vitro , 1981 .

[12]  D. Obenland,et al.  Fructan Synthesis in Excised Barley Leaves (Identification of Two Sucrose-Sucrose Fructosyltransferases Induced by Light and Their Separation from Constitutive Invertases) , 1993, Plant physiology.

[13]  J. Thornley,et al.  Shoot: Root Allocation with Respect to C, N and P: an Investigation and Comparison of Resistance and Teleonomic Models , 1995 .

[14]  J. Farrar Sink strength: What is it and how do we measure it? Introduction , 1993 .

[15]  R. C. Weast CRC Handbook of Chemistry and Physics , 1973 .

[16]  Modification and quantitative analysis of the Münch model in the integrated system of water translocation in plants. , 2001, General physiology and biophysics.

[17]  C. Offler,et al.  A Novel Experimental System for Studies of Photosynthate Transfer in the Developing Wheat Grain , 1993 .

[18]  F. Woodward,et al.  A Nitrogen-led Model of Grass Growth , 1996 .

[19]  T. A. Armstrong,et al.  Culture of Detached Spikes and the Early Development of the Fourth Floret Caryopsis in Wheat , 1987 .

[20]  C. Jenner Relationship Between Levels of Soluble Carbohydrate and Starch Synthesis in Detached Ears of Wheat , 1970 .

[21]  F. I. Woodward,et al.  Calculation of Translocation Coefficients from Phloem Anatomy for use in Crop Models , 1995 .

[22]  I. F. Wardlaw,et al.  Source, sink and hormonal control of translocation in wheat , 2004, Planta.

[23]  P. Minchin,et al.  Carbon Partitioning in Split Root Systems of Barley: Relation to Metabolism , 1991 .

[24]  E. Triboi,et al.  Temperature effect on fructan oligomer contents and fructan-related enzyme activities in stems of wheat (Triticum aestivum L.) during grain filling , 1993 .

[25]  H. Schnyder The role of carbohydrate storage and redistribution in the source‐sink relations of wheat and barley during grain filling — a review , 1993 .

[26]  Takeshi Horie,et al.  Leaf Nitrogen, Photosynthesis, and Crop Radiation Use Efficiency: A Review , 1989 .

[27]  M. Zimmermann,et al.  Transport in Plants I , 1975, Encyclopedia of Plant Physiology.

[28]  M. R. Thorpe,et al.  A Simple Mechanistic Model of Phloem Transport which Explains Sink Priority , 1993 .

[29]  B. Ney,et al.  Seed growth rate in grain legumes II. Seed growth rate depends on cotyledon cell number , 1998 .

[30]  John Philip Cooper,et al.  Photosynthesis and productivity in different environments , 1976 .

[31]  A. L. Christy,et al.  A Mathematical Treatment of Munch's Pressure-Flow Hypothesis of Phloem Translocation. , 1973, Plant physiology.

[32]  E. F. Bradley,et al.  Collection and processing of field data. , 1967 .

[33]  A. Moulin,et al.  Evaluation of the CERES and EPIC models for predicting spring wheat grain yield over time , 1993 .

[34]  U. Simmen,et al.  Sucrose:Fructan 6-Fructosyltransferase, a Key Enzyme for Diverting Carbon from Sucrose to Fructan in Barley Leaves , 1995, Plant physiology.