Abstract
To better understand the source–sink flow and its relationships with zinc (Zn) and other nutrients in wheat (Triticum aestivum L.) plants for biofortification and improving grain nutritional quality, the effects of reducing the photoassimilate source (through the flag leaf removal and spike shading) or sink (through the removal of all spikelets from one side of the spike, i.e., 50% spikelets removal) in the field of the accumulation of Zn and other nutrients in grains of two wheat cultivars (Jimai 22 and Jimai 44) were investigated at two soil Zn application levels. The kernel number per spike (KNPS), single panicle weight (SPW), thousand kernel weight (TKW), total grain weight (TGW) sampled, concentrations and yields of various nutrient elements including Zn, iron (Fe), manganese (Mn), copper (Cu), nitrogen (N), phosphorus (P), potassium (K), calcium (Ca) and magnesium (Mg), phytate phosphorus (phytate-P), phytic acid (PA) and phytohormones (ABA: abscisic acid, and the ethylene precursor ACC: 1-aminocylopropane-1-carboxylic acid), and carbon/N ratios were determined. Soil Zn application significantly increased the concentrations of grain Zn, N and K. Cultivars showing higher grain yields had lower grain protein and micronutrient nutritional quality. SPW, KNPS, TKW (with the exception of TKW in the removal of half of the spikelets), TGW, and nutrient yields in wheat grains were most severely reduced by half spikelet removal, secondly by spike shading, and slightly by flag leaf removal. Grain concentrations of Zn, N and Mg consistently showed negative correlations with SPW, KNPS and TGW, but positive correlations with TKW. There were general positive correlations among grain concentrations of Zn, Fe, Mn, Cu, N and Mg, and the bioavailability of Zn and Fe (estimated by molar ratios of PA/Zn, PA/Fe, PA × Ca/Zn, or PA × Ca/Fe). Although Zn and Fe concentrations were increased and Ca was decreased in treatments of half spikelet removal and spike shading, the treatments simultaneously increased PA and limited the increase in bioavailability of Zn and Fe. In general, different nutrient elements interact with each other and are affected to different degrees by source–sink manipulation. Elevated endogenous ABA levels and ABA/ACC ratios were associated with increased TKW and grain-filling of Zn, Mn, Ca and Mg, and inhibited K in wheat grains. However, the effects of ACC were diametrically opposite. These results provide a basis for wheat grain biofortification to alleviate human malnutrition.
Highlights
Zinc (Zn) is an essential micronutrient to sustain the nutritional health of plants, animals and humans [1,2]
The single panicle weight, kernel number per spike and total grain weight were highest in the control treatment, followed by flag leaf removal secondly, spike shading thirdly, and half spikelet removal lastly
Spike shading had the lowest value, which was significantly lower than the control, and half spikelet removal had the maximum thousand kernel weight, which was significantly higher than the control (Table 1)
Summary
Zinc (Zn) is an essential micronutrient to sustain the nutritional health of plants, animals and humans [1,2]. Reducing the sources of carbohydrates from photosynthesis through spike shading or defoliation or reducing the sink size of grain through partial spikelet removal has been commonly conducted to investigate the source–sink limitations of crop assimilates for grain development and dry matter accumulation [15,16]. These physical manipulations were recently applied to investigate the source–sink relationship of micronutrient accumulation in wheat grains, especially for Zn [17,18,19]. Such contradictory and inconsistent results possibly result from the different genotypes of wheat cultivars investigated or different environmental conditions, which need to be further verified across multiple location-years and more wheat varieties to better understand the source–sink relationships of grain Zn accumulation, especially regarding the impacts of artificial source–sink manipulation on grain Zn accumulation and its interaction with the photosynthate transport
Sign-in/Register to view highlights & summary 
Published Version (
Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
