Published July 16, 2024 | Version v1

Data from: Source-sink relationships during grain filling in wheat in response to various temperature, water deficit and nitrogen deficit regimes

  • 1. Wageningen University & Research
  • 2. National Research Institute for Agriculture, Food and Environment

Description

Grain filling is a critical process for improving crop production under adverse conditions caused by climate change. Here, using a quantitative method, we quantified post-anthesis source-sink relationships of a large data set to assess the contribution of remobilized pre-anthesis assimilates to grain growth for both biomass and nitrogen. The data set came from 13 years' semi-controlled field experimentation, in which six bread wheat genotypes were grown at plot scale under contrasting temperature, water, and nitrogen regimes. On average, grain biomass was ~10% higher than post-anthesis aboveground biomass accumulation across regimes and genotypes. Overall, the estimated relative contribution (%) of remobilized assimilates to grain biomass became increasingly significant with increasing stress intensity, ranging from virtually nil to 100%. This percentage was altered more by water and nitrogen regimes than by temperature, indicating the greater impact of water or nitrogen regimes relative to high temperatures under our experimental conditions. Relationships between grain nitrogen demand and post-anthesis nitrogen uptake were generally insensitive to environmental conditions, as there was always significant remobilization of nitrogen from vegetative organs, which helped to stabilize the amount of grain nitrogen. Moreover, variations in the relative contribution of remobilized assimilates with environmental variables were genotype-dependent. Our analysis provides an overall picture of post-anthesis source-sink relationships and pre-anthesis assimilate contributions to grain filling across (non-)environmental factors, and highlights that designing wheat adaption to climate change should account for complex multi-factor interactions.

Methods

For the processes of data collection: plants were sampled every 2 to 9 days between anthesis and ripeness maturity. Stems, leaf laminae, chaffs, and grains of each subsample were separated, and their dry mass was determined after drying to constant mass in a forced air oven at 80℃. Total nitrogen concentration of oven-dried samples was determined by the Kjeldahl digestion method using a Kjeltec 2300 analyzer (Foss Tecator AB, Hoeganaes, Sweden) between 1991 and 2002, and by the Dumas combustion method using a FlashEA 19 1112 N/Protein analyzer (Thermo Electron Corp., Waltham, MA, USA) in 2007 and 2014. 

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