International Crop Modelling Symposium 15-17 March 2016, Berlin MODELING WHEAT GRAIN YIELD AND PROTEIN CONTENT WITH PYG MODEL. 1 Berger, A.G. – Vazquez, D. 1 1 Rainfed Crops, INIA La Estanzuela, Ruta 50km 11 Colonia UY, [email protected] Introduction Wheat grain yield has increased constantly over time due to management and genetic improvement accompanied in some cases with high risk of reductions in grain protein content (GPC) and baking quality. This reduction in GPC may result from the imbalance between carbon assimilation and, nitrogen assimilation and remobilization during grain growth (Pask et al., 2012). The balance between these components is determines by the conditions and length of vegetative growth that determine biomass and nitrogen accumulation, and the conditions during grain fill that determine grain protein content and grain biomass accumulation (Martre et al., 2003). These components are difficult to manipulate experimentally and modeling can contribute to better understand and quantify the relevance of each component. Materials and Methods The relationship among all the components of the carbon and nitrogen balance in the crop were analyzed and simulated with the model pyG. This model is a derivative of the model GECROS (Yin and vanLaar, 2005), which uses an hourly time step, simulates photosynthesis with a biochemical type model, and assumes an optimal allocation of nitrogen and carbon between crop components, among some of the main characteristics. The model was re-written in python, and several modifications relating nitrogen demand, grain number determination, and nitrogen balance were tested in this work. The results were contrasted with field data from experiments conducted during 2012, 2013, and 2014 with 11, 15 and 7 cultivars and three contrasting treatments, low nitrogen availability (lowN-lowN), high nitrogen availability (highNhighN), and low nitrogen availability until anthesis and high nitrogen availability thereafter (lowN-highN). Results and Discussion The experimental setup allowed us to observe all the range of low-high grain yield and low-high grain protein content. The model was able to capture the variability in yield and grain protein content as well as the dynamics of growth and nitrogen accumulation (Figure 1). It contributed also to determine the relevance of pre and post anthesis nitrogen uptake and the relevance of nitrogen remobilization in grain nitrogen balance and protein formation. Allowing the capacity to have deficiency driven soil nitrogen absorption in the post anthesis period significantly improved the fit to data. 1 International Crop Modelling Symposium 15-17 March 2016, Berlin The proportion of nitrogen assimilated before anthesis was greater than after anthesis, however in the lowN-highN treatment and some cultivars of highN-highN, the amount of nitrogen assimilated in post anthesis was significant. The capacity to assimilate nitrogen in post anthesis was significantly related to leaf senescence in the field and in simulations, and contributed (as indicated by simulations) to a larger capacity to assimilate carbon during grain fill. 35 lowN-lowN highN-highN CheckHighN CheckLowN Optimum 35 30 Nitrogen in aerial biomass (g N m-2) Nitrogen in aerial biomass (gN m-2) 40 a 25 20 15 10 5 30 25 20 lowN-lowN highN-highN CheckHighN CheckLowN highN-highN_obs lowN-lowN_obs b 15 10 5 0 0 0 500 1000 1500 Aerial biomass (g m-2) 2000 2500 6-May-13 25-Jun-13 14-Aug-13 3-Oct-13 22-Nov-13 11-Jan-14 Figure 1. Acummulation of biomass and nitrogen for four contrasting simulated treatments and observed data (a). Evolution over the growing season of the same treatments and nitrogen in grain (b). Conclusions The model was able to simulate well the plant nitrogen balance, including the trajectory of leaf senescence and the response of leaf senescence to post anthesis nitrogen availability. Post anthesis nitrogen absorption from the soil significantly improved the fit to observed data, in particular for lowN-HighN and highN-highN scenarios (high proteinlow yield and high protein – high yield respectively). Acknowledgements Founding provided by INIA projects CS-13 and CS-09. We also acknowledge the field support of M.X. Morales and R. Calistro. References Martre, P., J.R. Porter, P.D. Jamieson et al. (2003). Plant Physiology, 133: 1959–1967. Pask, A.J.D., R. Sylvester-Bradley, P.D. Jamieson et al. (2012). Field Crop Research 126:104–118. Yin, X. and H.H. vanLaar (2005). Wageningen Academic Publishers, The Netherlands, 155pp. 2
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