Soil salinization in arid and coastal areas poses a significant threat to crop production, which is further aggravated by climate change and the over-exploitation of aquifers. Cultivation of salt and drought-tolerant crops such as quinoa represents a promising adaptation pathway for agriculture in saline soils. Quinoa (Chenopodium quinoa Willd.) is a salt-loving plant, known for its tolerance to drought and salinity using complex stress responses. However, available models of quinoa growth are limited, particularly under salinity stress. The objective of this study was to calibrate the crop growth, and salinity and drought stress parameters of the SWAP - WOFOST model and evaluate whether this model can represent quinoa's stress tolerance mechanisms. Field experimental data were used from two quinoa varieties: ICBA-Q5 grown under saline conditions in Laayoune, Morocco, in 2021, and Bastille grown under rainfed, non-saline conditions in Merelbeke, Belgium, from 2018 to 2023. Calibration and parameter uncertainty was performed using the DiffeRential Evolution Adaptive Metropolis (DREAMzs) algorithm on key parameters identified via sensitivity analysis using the Morris method. The resulting crop parameters provide insights into the stress tolerance mechanisms of quinoa, including reduction of transpiration and uptake of solutes. The salinity stress function of SWAP effectively represents these tolerance mechanisms and accurately predicts the impact on yield, under arid conditions. Under Northwestern European climate, the model replicates the impact of drought stress on yield. The calibrated model offers perspectives for evaluating practices to reduce soil salinization in arid conditions and for modeling crop performance under water-limited conditions or future salinization in temperate regions.
Rising soil salinity hinders global crop yields by damaging plants, threatening food security. This study assessed glycine betaine (GB) application methods (foliar, seed priming) and salinity levels (0, 60, 120, 180 mM NaCl) on quinoa over two seasons. For ionic homeostasis, seed priming improved K+/Na+ ratio by 10-15 % at low salinity, while foliar was 12-18 % more effective at high salinity. Seed priming remained 10-15 % superior for roots. Foliar enhanced osmolytes by 12-16 % at low salinity, but seed priming had 16-20 % stronger effects at high salinity. Under low salinity, seed priming provided 8-12 % better protection for chlorophyll and photosynthetic efficiency. At high salinity, foliar GB was 10-15 % best for chlorophyll, seed priming 12-16 % more effective for photosynthetic rate, and foliar GB had an 8-10 % edge for Fv/Fm. GB reduced MDA by 8-12 % at low salinity, 12-16 % with seed priming at medium salinity in 2023, and 16-20 % with foliar in 2024. At high salinity, seed priming decreased MDA by 20-25 % in 2023, while foliar showed a 24-28 % reduction. GB moderately enhanced antioxidants by 8-12 % under mild stress, but seed priming and foliar differed 16-20 % in effectiveness under severe stress. For nutrients, seed priming had a 12-16 % advantage for nitrogen at medium salinity in 2023, while foliar excelled with a 16-20 % increase under high stress in 2024. Seed priming was 16-20 % better for phosphorus at high salinity in 2023, but foliar had 20-25 % superior results in 2024. These findings highlight complex plant responses to GB-salinity interactions, with optimal methods varying by trait, stress level, and environmental conditions. (c) 2024 SAAB. Published by Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.