Developmental changes in shoot N dynamics of lucerne (Medicago sativa L.) in relation to leaf growth dynamics as a function of plant density and hierarchical position within the canopy.

Shoot N concentration in plants decreases as they get bigger, due to the fact that N accumulates less rapidly than dry matter in plants during the plant growth process, leading to an allometric relationship between shoot N content (N(sh)) and shoot mass (W(sh)): N(sh)=a(W(sh))b. The results obtained on lucerne plants growing either under controlled low density conditions or in dense stands under field conditions show that the value of the allometric coefficient b that represents the ratio between the relative N accumulation rate in shoots [dN(sh)/(N(sh)dt)] and the relative growth rate [dW(sh)/(W(sh)dt)], decreases from 0.88 for a low plant density to 0.72 for a dense stand. Therefore, the fractional increase of shoot N per unit of shoot dry matter is lower when plants are in competition for light in dense canopies. This decrease can be entirely explained by the parallel decline in the leaf area per unit of shoot mass. Thus, a remarkably constant linear relationship can be established between N(sh) and leaf area (LA): N(sh)=1.7 g m(-2) LA, regardless of the conditions (low versus high density, controlled versus field conditions). Moreover, in a field dense stand, the comparison of plants with contrasting positions between the top and the bottom of the canopy (dominant, intermediate or suppressed plants), also shows that the difference in N(sh) at similar shoot mass is explained by the proportion of leaf mass to shoot mass. These data support the idea that leaf growth drives the dynamics of shoot N accumulation. These results also indicate that competition for light among individual plants within a dense canopy induces developmental changes in plant morphology (leaf:stem ratio) that explain the differences observed in shoot N concentration. This last observation could be extrapolated to multi-specific plant stands. Therefore, the sharing of N resources among plant species could partially be the result of the sharing of light within the canopy.

[1]  M. Werger,et al.  Canopy structure and leaf nitrogen distribution in a stand of Lysimachia vulgaris L. as influenced by stand density , 1988, Oecologia.

[2]  B. Touraine,et al.  N Demand and the Regulation of Nitrate Uptake , 1994, Plant physiology.

[3]  G. Lemaire,et al.  Partitioning of Nitrogen Derived from N2 Fixation and Reserves in Nodulated Medicago sativa L. During Regrowth , 1993 .

[4]  G. Lemaire,et al.  Effects of the previous shoot removal frequency on subsequent shoot regrowth in two Medicago sativa L. cultivars , 2004, Plant and Soil.

[5]  J. R. Kiniry,et al.  CERES-Maize: a simulation model of maize growth and development , 1986 .

[6]  G M Coruzzi,et al.  Carbon and nitrogen sensing and signaling in plants: emerging 'matrix effects'. , 2001, Current opinion in plant biology.

[7]  Graeme L. Hammer,et al.  APSIM: a novel software system for model development, model testing and simulation in agricultural systems research , 1996 .

[8]  H. Sinoquet,et al.  Ecophysiology of tropical intercropping , 1995 .

[9]  J. Weiner,et al.  Asymmetric competition in plant populations. , 1990, Trends in ecology & evolution.

[10]  M. Werger,et al.  Photosynthetic capacity and nitrogen partitioning among species in the canopy of a herbaceous plant community , 1994, Oecologia.

[11]  M. Caloin,et al.  Analysis of the Time Course of Change in Nitrogen Content in Dactylis glomerata L. Using a Model of Plant Growth , 1984 .

[12]  H. Lambers,et al.  Causes and consequences of variation in growth rate and productivity of higher plants , 1990 .

[13]  Tadaki Hirose,et al.  CO2 ELEVATION, CANOPY PHOTOSYNTHESIS, AND OPTIMAL LEAF AREA INDEX , 1997 .

[14]  D. Charles-Edwards,et al.  An Analysis of Spatial Variation in the Nitrogen Content of Leaves from Different Horizons Within a Canopy , 1987 .

[15]  B. Touraine,et al.  Nitrate Uptake and Its Regulation , 2001 .

[16]  Gilles Lemaire,et al.  Nitrogen Distribution Within a Lucerne Canopy During Regrowth: Relation With Light Distribution , 1991 .

[17]  Gilles Lemaire,et al.  Diagnosis of the Nitrogen Status in Crops , 1997, Springer Berlin Heidelberg.

[18]  H. Sinoquet,et al.  An overview of the crop model STICS , 2003 .

[19]  Gordon C. Tucker Medicago sativa L. , 2004 .

[20]  N. Anten,et al.  Biomass Allocation and Light Partitioning Among Dominant and Subordinate Individuals in Xanthium canadense Stands , 1998 .

[21]  G. Lemaire,et al.  Relationships between dynamics of nitrogen uptake and dry matter accumulation in maize crops. Determination of critical N concentration , 1999, Plant and Soil.

[22]  R. C. Hardwick The Nitrogen Content of Plants and the Self-thinning Rule of Plant Ecology: A Test of the Core-skin Hypothesis , 1987 .

[23]  Gilles Lemaire,et al.  Relation entre dynamique de croissance et dynamique de prélèvement d'azote pour un peuplement de graminées fourragères. I. — Etude de l'effet du milieu , 1984 .

[24]  Gilles Lemaire,et al.  Decline in Percentage N of C3 and C4 Crops with Increasing Plant Mass , 1990 .

[25]  G. Lemaire,et al.  N Uptake and Distribution in Plant Canopies , 1997 .

[26]  D. Ackerly,et al.  Effects of CO2 elevation on canopy development in the stands of two co-occurring annuals , 1996, Oecologia.

[27]  F. Daniel-Vedele,et al.  Molecular and functional regulation of two NO3- uptake systems by N- and C-status of Arabidopsis plants. , 1999, The Plant journal : for cell and molecular biology.

[28]  N. Anten,et al.  Interspecific differences in above‐ground growth patterns result in spatial and temporal partitioning of light among species in a tall‐grass meadow , 1999 .

[29]  P. Millard The accumulation and storage of nitrogen by herbaceous plants , 1988 .

[30]  C. J. Nelson,et al.  Nitrogen Use within the Growing Leaf Blade of Tall Fescue , 1994, Plant physiology.

[31]  H. Sinoqueta,et al.  Comparison of models for daily light partitioning in multispecies canopies , 2000 .

[32]  Brian G Forde,et al.  The role of long-distance signalling in plant responses to nitrate and other nutrients. , 2002, Journal of experimental botany.

[33]  G. Lemaire,et al.  Changes in Source-Sink Relationship for Nitrogen During Regrowth of Lucerne (Medicago sativa L.) Following Removal of Shoots , 1991 .

[34]  G. Lemaire,et al.  Etude des relations entre la dynamique de prélèvement d'azote et la dynamique de croissance en matière sèche d'un peuplement de luzerne (Medicago sativa L.) , 1985 .

[35]  K. Hikosaka,et al.  Leaf nitrogen distribution in relation to leaf age and photon flux density in dominant and subordinate plants in dense stands of a dicotyledonous herb , 1998, Oecologia.

[36]  G. Lemaire,et al.  Root protein and vegetative storage protein are key organic nutrients for alfalfa shoot regrowth , 1997 .