To investigate the quantitative response of tomato yield and fruit quality to deficit irrigation applied at different growth stages, greenhouse experiments were conducted in 2017 and 2018. Three irrigation treatments (full irrigation and two-thirds or one-third of full irrigation) were applied to greenhouse-grown tomato plants at flowering and fruit development (stage 2) and at fruit maturation stage (stage 3). Grey relational analysis (GRA), the technique for order preference by similarity to an ideal solution (TOPSIS), and principal components analysis (PCA) were used to calculate the comprehensive fruit quality indexes, and combinatorial evaluation method was determined. The results showed that deficit irrigation significantly reduced evapotranspiration (ET) and tomato yield and that relative yield had a negative linear correlation with relative seasonal water deficit (1−ETi/ETc). However, deficit irrigation improved fruit quality, especially at stage 2. Total soluble solids, the total soluble sugar concentration, the sugar-to-acid ratio, and vitamin C in the tomatoes all increased significantly in plants that were deficit irrigated compared with fully irrigated plants, while organic acids and lycopene decreased in both years. There were linear correlations between fruit quality parameters and 1−ETi/ETc. The comprehensive quality index derived from GRA and PCA is reliable, and the comprehensive quality indexes given by GRA, PCA, and a combination of GRA and PCA showed positive linear correlation with 1−ETi/ETc. The comprehensive quality ranking showed that in both years, F2/3M1 (two-thirds full irrigation at stage 2) gave a better result and CK (full irrigation) the worst. An appropriate water deficit at the flowering and fruit development stage, which results in a trade-off between acceptable yield and improved fruit quality, is recommended. Our results provide a sound basis for tomato production that has a desirable balance between high yield and high fruit quality.
Xuelian Jiang, Yueling Zhao, Ling Tong, Rui Wang and Sheng Zhao
Yu-Xiong Zhong, Jian-Ye Chen, Hai-Ling Feng, Jian-Fei Kuang, Ruo Xiao, Min Ou, Hui Xie, Wang-Jin Lu, Yue-Ming Jiang and He-Tong Lin
Fresh fruit of longan (Dimocarpus longan Lour.) are susceptible to pericarp browning and aril breakdown. Aril breakdown in longan fruit is regarded as one of the most important factors reducing quality and shortening storage life of the fruit. To better understand the molecular mechanism of aril breakdown, the expression patterns of three expansin (EXP) and three xyloglucan endotransglucosylase (XET) genes in relation to the aril breakdown of longan fruit stored at room temperature (25 °C) or low temperature (4 °C) were investigated. The results showed that aril breakdown index increased progressively during storage at 25 and at 4 °C. Northern blotting analysis revealed that the accumulations of three EXP and three XET genes exhibited differential characteristics with the occurrence of aril breakdown. During storage at 25 °C, the accumulations of Dl-XET3 increased after 1 day, suggesting that Dl-XET3 correlated well with the early aril breakdown, while Dl-EXP3 together with Dl-XET1 and Dl-XET2 was involved in later aril breakdown. However, expression of Dl-XET1 and Dl-XET2 could be mainly involved in aril breakdown of longan fruit stored at 4 °C. In addition, Dl-EXP2, whose accumulation increased sharply when longan fruit were transferred from low temperature to room temperature within 12 hours, was related to the aril breakdown in this storage period. These data indicated that Dl-EXPs and Dl-XETs were closely related to aril breakdown in longan fruit.