Adventitious roots (ARs) are crucial for grafted watermelon seedlings, playing vital roles in nutrient absorption, stress resistance, and grafting efficacy. However, the way in which scions regulate endogenous hormones to influence AR formation remains poorly understood. In this study, we constructed watermelon seedlings (WP) using "HXX" as the scion and "Tie Zhen No. 3" as the rootstock. Scion cotyledons removal (WP-1) significantly promoted AR development. In contrast, true leaf removal (WP-2) had minimal effect, while simultaneous removal of both (WP-3) elicited intermediate responses. Endogenous hormone dynamics showed that WP-1 maintained progressively increasing indole-3-acetic acid (IAA) with lower abscisic acid (ABA) and jasmonic acid (JA) levels, whereas both WP-2 and WP-3 exhibited divergent hormonal profiles in ARs during later development stages. Transcriptome sequencing revealed that differentially expressed genes (DEGs) are enriched in various hormone signaling pathways. On the fourth day, when the number of differential genes was the highest, the DEGs significantly expressed in all three treatment groups were enriched in the activation signaling pathways and responses of JA, auxin, ethylene, and cytokinins. Transcription factors such as bHLH, ERF, MYB, and NAC were significantly expressed during the development of ARs, playing a key regulatory role. The Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis identified 82 DEGs across five hormone signal transduction pathways. The weighted gene co-expression network analysis (WGCNA) identified modules positively correlated with AR hormones, highlighting hub genes such as ethylene transcription factors (CRF4, ABR1, ERF054, ERF098), auxin response factors (SAUR21 and SAUR32), and other regulators (CSA, HSP, bHLH93, ZAT5, ZAT13, NAC, MYB, and C3H). These findings provide preliminary evidence of the scion's regulatory role in AR development through hormones, offering a foundation for improving watermelon grafting practices.

Adventitious roots (ARs) are crucial for grafted seedlings, playing vital roles in nutrient absorption, stress resistance, and grafting efficacy. However, how scions regulate endogenous hormones to influence AR formation remains poorly understood. In this study, we constructed watermelon seedlings (WP) using “HXX” as the scion and “Tie Zhen No. 3” as the rootstock. Removing scion cotyledons (WP-1) significantly promoted AR development, while removing true leaves (WP-2) had minimal effect. Simultaneous removal of both (WP-3) increased endogenous levels of IAA (Indole-3-Acetic Acid), abscisic acid (ABA), and jasmonic acid (JA). Transcriptome sequencing revealed that differentially expressed genes (DEGs) are enriched in various hormone signaling pathways. On the fourth day, when the number of differential genes was the highest, the DEGs significantly expressed in all three treatment groups were enriched in the activation signaling pathways and responses of JA, auxin, ethylene, and cytokinins. Transcription factors such as bHLH, ERF, MYB, and NAC were significantly expressed during the development of ARs, playing a key regulatory role. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis identified 82 DEGs across five hormone signal transduction pathways. Weighted gene co-expression network analysis (WGCNA) identified modules positively correlated with AR hormones, highlighting hub genes such as ethylene transcription factors (CRF4, ABR1, ERF054, ERF098), auxin response factors (SAUR21, SAUR32), and other regulators (CSA, HSP, bHLH93, ZAT5, ZAT13, NAC, MYB, C3H). These findings provide molecular insights into how scions regulate AR development through hormones, offering a foundation for improving watermelon grafting practices.

Our previous study revealed a significant effect of red and blue light on steady-state and dynamic photosynthesis in cucumber seedlings. To further investigate the mechanism by which red and blue light affect photosynthesis, cucumber (Cucumis sativus L. cv. Jinyou 365) seedlings were exposed to white light (W), monochromatic red light (R), monochromatic blue light (B), and mixed red–blue light with red:blue photon flux ratios of 9:1 (9R1B), 7:3 (7R3B), 5:5 (5R5B), 3:7 (3R7B), and 1:9 (1R9B). We measured photosynthetic pigment contents, induction curves of photosynthetic gas exchange and chlorophyll fluorescence parameters during low-to-high-light transition, as well as the activities and gene expression of key Calvin cycle enzymes. The results showed that B yielded higher photosynthetic pigment contents than R, although both remained lower than W. Mixed red–blue light with a blue-light ratio above 50% produced significantly higher pigment contents than W. Under low light, blue light exhibited negligible effects on photosynthesis. In contrast, under high light, 7R3B, 5R5B, 3R7B and 1R9B elevated net photosynthetic rate (A) and stomatal conductance (Gs). Among these, 7R3B, 5R5B and 3R7B also accelerated photoinduction, as reflected by a shorter time to reach 90% steady-state net photosynthetic rate (T_90%A). Chlorophyll fluorescence parameters changed rapidly and attained a steady state within 5 min during light induction. During photoinduction, biochemical limitation was severe in the early stage but declined rapidly, while stomatal limitation appeared in mid-induction and persisted into the late stage; photochemical limitation remained minor, and the severity of these limitations was modified by light quality. Red and blue light exerted negligible effects on chlorophyll fluorescence parameters under low light. However, blue light enhanced the relative electron transport rate of PSII under high light by elevating the fraction of open PSII centers. Furthermore, blue light significantly increased the activities and gene expression of key Calvin cycle enzymes. Correlation analysis revealed that higher chlorophyll contents were positively associated with A and Gs under high light but showed no significant correlation with photoinduction. Higher A and Gs under both low- and high-light intensities were associated with faster photoinduction.