Sorbus pohuashanensis (Hance) Hedl. is an important forestry species valued for its ornamental, medicinal, and ecological properties. Polyploidy breeding is an important method of germplasm innovation; however, polyploidy induction and phenotypic variation caused by chromosome doubling in S. pohuashanensis are poorly understood. In this study, S. pohuashanensis seeds were used to explore the effects of different colchicine concentrations, cold stratification times, and seeds from different sources on polyploidy induction. Ploidy levels of the regenerated plants were determined by flow cytometry. The results showed that the tetraploid induction effect of S. pohuashanensis seeds was significantly affected by colchicine concentration, and the highest tetraploid induction rate of 24.75% was achieved by immersion in 0.2% (w/v) colchicine for 48 h. After 2 years of induction, 77 tetraploid plants were obtained. Compared to diploids, tetraploid plants showed significant variations in plant height, leaf morphology (apical leaflet width, middle leaflet width), and diameter of the middle petiole. The stomatal size and chloroplast number increased with chromosome doubling whereas the stomatal number and density decreased. In addition, significant differences in the percentage of sunburn associated with ploidy changes were observed. This study provides a technique for tetraploid induction of S. pohuashanensis seeds, showing the variation in traits caused by polyploidization and the effect of chromosome doubling on sunburn resistance. Tetraploidy induction provides a new direction for S. pohuashanensis germplasm innovation.

Populus wulianensis mainly grows in hilly and sloped areas and has strong resistance to adversity. Previous transcriptome studies have shown that a WRKY gene PwuWRKY48 is expression-induced under drought stress. In this study, we aim to characterize the gene’s structure and investigate its role in plant drought resistance. The results show that PwuWRKY48 (1113 bp) belongs to a class IIc WRKY subfamily and it was determined as a nuclear localization protein. The gene promoter region contains a variety of cis-elements in relation to stress resistance. Under drought stress, PwuWRKY48 was expression-induced in leaves and stems, 29.7 and 16.6 times those before treatment, respectively. Overexpressing PwuWRKY48 lines were associated with increased activities of peroxidase (POD) and superoxide dismutase (SOD), 2.5 and 1.6 times higher than those of the wild type. While malondialdehyde content (MDA), superoxide anion radical (O₂^·−), and relative conductivity were decreased by 20%, 30%, and 21.3%, proline and chlorophyll contents increased by 37.5% and 11.2%, respectively. This indicates that PwuWRKY48 efficiently improved the drought tolerance of transgenic plants. PwuWRKY48 can be used as a gene resource for molecular breeding of plant drought resistance.

Flower color serves as a vital ornamental feature of landscape plants; Sophora japonica L. mutant ‘AM’ exhibits the different colors from the common S. japonica. ‘AM’, presenting with a light purple-red wing and keel and yellowish-white flag petals, while common S. japonica is yellow and white. The metabolites contributing to this color specificity in red-flowered S. japonica ‘AM’ are not yet fully understood. In this study, the flag, wing, and keel petals were collected from ‘AM’ at various phases, including the flower bud phase, initial flowering phase, full bloom phase, and final flowering phase, for conducting the metabolic assays targeting anthocyanins. Subsequently, we identified 45 anthocyanin-related metabolites, including nine flavonoids and 36 anthocyanins. Ten major floral chromoside metabolites were found to affect the coloration differences among the petals, where the most abundant anthocyanin was cyanidin-3-O-glucoside (Cy3G), which was much higher in the keel petal (LGB) and wing petal (YB) than in the flag petal (QB), and similarly, during the four periods of different petal types, the Cy3G content was higher in the initial flowering stage (S2), the full bloom stage (S3), and the final flowering stage (S4) than the flower bud stage (S1), which was in accordance with the trend of the observed petal floral color phenotypic difference measurement correlation. This suggested that the Cy3G accumulation was the primary factor driving the distinct coloration of varying types of petals. These findings could contribute to the understanding of the biochemical mechanisms underlying S. japonica petal coloration and may support future efforts in flower color improvement.