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Melilotus albus is a high-quality forage, due to its high protein content, and aboveground biomass and salt tolerance. Rab (Ras-related protein in the brain) proteins are the largest GTPase family which play a key role in intracellular membrane transport, and many Rab genes have been identified in eukaryotes. The growth and distribution of M. albus are severely hampered by soil salinization. However, little is known about candidate genes for salt tolerance in M. albus. In this study, 27 Rab family genes were identified for the first time from M. albus, and divided into eight groups (Groups A-H). The number of introns in MaRabs ranged from one to seven, with most genes containing one intron. In addition, most MaRab proteins showed similarities in motif composition. Phylogenetic analysis and structural-domain comparison indicated that Rab family genes were highly conserved in M. albus. Members of the MaRab gene family were distributed across all eight chromosomes, with the largest distribution on chromosome 1. Prediction of the protein interaction network showed that 24 Rab proteins exhibited protein–protein interactions. Analysis of the promoter cis-acting elements showed that MaRab-gene family members are extensively involved in abiotic stress responses. RNA-seq data analysis of the MaRab-gene-expression patterns suggested that the Rab gene family possesses differentially expressed members in five organs and under salt stress, drought stress, and ABA (Abscisic Acid) treatment. Differentially expressed genes under drought stress, salt stress and ABA stress were validated by quantitative real-time PCR. Furthermore, heterologous expression in yeast was used to characterize the functions of MaRab1 and MaRab17, which were upregulated in reaction to salt stress. In summary, this study provided valuable information for further research into the molecular mechanism of the response of M. albus to saline stress, as well as the possibility of developing cultivars with high salt-resistance characteristics.

Nutrients carried in upstream rivers to lakes are the main cause of eutrophication. Building near-natural estuarine wetlands between rivers and lakes is an effective way to remove pollutants and restore the ecology of estuarine areas. However, for the existing estuarine wetland ecological restoration projects, there is a lack of corresponding evaluation methods and index systems to make a comprehensive assessment of their restoration effects. By summarizing a large amount of literature and doing field research, an index system was constructed by combining the characteristics of the near-natural estuarine wetlands themselves. It covered environmental benefits, technical management and maintenance, and socio-economic functions, and contained 3 systems, 7 criteria, and 16 indicators. The analytical hierarchy process (AHP) was used to determine the weights of each indicator. The top 5 indicators in order of importance were habitat diversity, total phosphorus (TP), coverage of aquatic plants, ammonia nitrogen (NH3-N), and adaptation to the surrounding landscape. The above evaluation system was used for the comprehensive evaluation of the water purification project in the Fuhe estuarine wetland, Hebei Province, as an example. The results showed that the comprehensive score of the Fuhe estuarine wetland at this stage was 4.1492, and the evaluation grade was excellent. The effect of water purification and ecological restoration was good, and the selected technology was suitable and stable in operation. It had a greater positive impact on the surrounding economy and society and can be promoted and applied. The research results were important for clarifying the advantages and defects of the project and developing efficient and advanced restoration technologies.

Drought stress is one of the major constraints that decreases global crop productivity. Alfalfa, planted mainly in arid and semi-arid areas, is of crucial importance in sustaining the agricultural system. The family 1 UDP-glycosyltransferases (UGT) is indispensable because it takes part in the regulation of plant growth and stress resistance. However, a comprehensive insight into the participation of the UGT family in adaptation of alfalfa to drought environments is lacking. In the present study, a genome-wide analysis and profiling of the UGT in alfalfa were carried out. A total of 409 UGT genes in alfalfa (MsUGT) were identified and they are clustered into 13 groups. The expression pattern of MsUGT genes were analyzed by RNA-seq data in six tissues and under different stresses. The quantitative real-time PCR verification genes suggested the distinct role of the MsUGT genes under different drought stresses and abscisic acid (ABA) treatment. Furthermore, the function of MsUGT003 and MsUGT024, which were upregulated under drought stress and ABA treatment, were characterized by heterologous expression in yeast. Taken together, this study comprehensively analyzed the UGT gene family in alfalfa for the first time and provided useful information for improving drought tolerance and in molecular breeding of alfalfa.