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Copyright of Journal of Henan Agricultural Sciences is the property of Editorial Board of Journal of Henan Agricultural Sciences and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

【Objective】The present paper aimed to investigate the important role of NAC gene in the growth and development of Cinnamomum camphora and its role in salt stress, and to clarify the response mechanism of C. camphora under salt stress. 【Method】The genome-wide NAC genes of C. camphora were identified and analyzed by bioinformatics to investigate the mode of response to abiotic stress in C. camphora. By identifying the members of NAC family of C. camphora,the paper aonducteda systematic analysis in terms of physicochemical properties, phylogenetic analysis, conserved motifs and gene structures, chromosomal localization and inter-species covariance, cis-acting element prediction and expression patterns.【Result】A total of 103 CcNAC genes were identified, the amino acid counts ranged from 137 to 1136, the isoelectric points from 4.54 to 10.00, the relative molecular masses from 15 644.40 to 129 859.29 u, and the mean hydrophobicity of all proteins was negative, indicating hydrophilicity. Subcellular localization was predicted to be in the nucleus and cytoplasm. A phylogenetic evolutionary tree was constructed with Arabidopsis thaliana NAC gene sequences, which classified CcNAC genes into 16 subfamilies. The NAM subfamily had the most members, with 17 CcNAC genes, while 25 CcNAC genes were not included. Conservative motif and gene structure analysis revealed that CcNAC genes were found to contain 2-8 introns and 10 motifs. Among these, motif3 appeared to be particularly stable in the genetic evolution of C. camphora genes, while motif9 and motif10 were distributed across the NAM subfamily. Chromosome localization and replication event analysis revealed that 103 genes were distributed across 12 chromosomes, with the highest number of genes（13） found in CcNAC genes distributed across chromosomes Chr02, with the lowest number of genes found on Chr10 and Chr11, which contained two genes each; Fragment duplication was the main mode of amplification for the CcNAC family. Multi-species co-linkage analysis revealed that CcNAC genes formed 162 pairs of co-linkage genes with CcNAC genes, indicating a closer relationship than with other species. The CcNAC genes were more closely related to the CcNAC genes and to those of other species than to any other. The CcNAC gene promoters contained several abiotic stress, growth and development, and hormone response elements. The results of the qRT-PCR showed that in leaves, the expression levels of the CcNAC058 and CcNAC092 genes were maximised under low salt stress. In roots, the expression of CcNAC007, CcNAC033, CcNAC058 and CcNAC092 genes increased with increasing salt concentration.【Conclusion】The NAC gene family may be involved in the process of salt stress response during the growth and development of C. camphora. The CcNAC092 and CcNAC058 genes exhibite significant responses in both leaves and roots under salt stress. It is hypothesised that CcNAC058 and CcNAC092 are the key genes contributing to the ability of the CcNAC to produce self-defensive behaviours under salt stress. [ABSTRACT FROM AUTHOR]

Salt stress seriously affects plant growth and is a serious factor restricting the safe production of crops. High salt can cause disturbance of ions in plants, and ultimately affect the development, growth and yield of plants. It is very important to understand and improve the salt resistance mechanism of crops to ensure the safe production of crops. In this paper, the harm of salt stress on plants, sodium ion transport, and the response mechanism of plants to salt stress were reviewed. The aim is to provide some theoretical basis for promoting the study of the responding mechanisms of salt stress in plants. [ABSTRACT FROM AUTHOR]

Copyright of Bulletin of Botanical Research is the property of Bulletin of Botanical Research Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Agro-Environment Science is the property of Journal of Agro-Environment Science Editorial Board and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

[Objective] The paper aimed to study the effects of spraying different concentrations of CO donors on processed tomato seedlings under salt stress, and provided a theoretical basis for exploring the role of CO in areas such as improving salt tolerance in tomato. [Method] Processed tomato line KT-32 was used as the experimental material, and four treatments of exogenous CO donors (0, 0.05, 0.10, 0.15, 0.25 mmol/L) were set up by hydroponic culture with Hoagland nutrient solution culture (CK) and salt stress (100 mmol/L NaCl) + spraying, the root morphology, osmoregulatory substance content, reactive oxygen species (ROS), membrane lipid activity degree and cell membrane permeability of each treatment were measured. Combining analysis of variance and principal component analysis, the optimal concentration of exogenous CO donors under 100 mmol/L NaCl stress was analyzed. [Result]] Salt stress inhibited root growth of processed tomato seedlings, causing a decrease in total root length, root volume, and average root diameter, an increase in reactive oxygen species content in leaves, degradation of chlorophyll and proteins, and damaged to cell membrane structure and activation of protective enzyme systems. The injury of salt stress on processed tomatoes was alleviated when CO donors were exogenously applied, with the best effect at a concentration of 15 µmol/L (H3), and at 9 days of salt treatment, total root length, root projected area, root surface area, root mean diameter, and root volume were increased by 24. 22%, 38.16%, 38. 16%, 24.51%, 24.51%, and 53.97%, chlorophyll a, chlorophyll b, and total chlorophyll content increased by 29. 04%, 34.73%, and 30.75%, respectively, and osmoregulatory substance proline content, soluble sugar content, and relative water content of leaves increased by 40.68%, 55.20%, and 117.34%, respectively, and the rate of reactive oxygen species (ROS) O2- production and H2O2 content in leaves decreased by 47.34% and 20.91%, respectively; The activities of protective enzymes SOD, POD and APX increased by 36. 19%, 97.23% and 135.35%, respectively; MDA content and relative conductivity decreased by 57.82% and 19.35%, respectively; 21 indicators of root morphology and physiology of processed tomato seedlings were normalized by the principal component analysis showed that the overall score of H3 treatment was higher than that of other treatments subjected to salt stress, ranking second among all treatments at 2. 25. [Conclusion] Exogenous CO increases the antioxidant enzyme activity and osmoregulatory substances of processed tomato seedlings under salt stress, reduces membrane lipid peroxidation, increases photosynthetic pigment content, maintains the relative stability of the antioxidant enzyme system and reactive oxygen species in the internal and external membrane environment, and has a concentration effect, with the best alleviation effect at 15 µmol/L. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Irrigation & Drainage is the property of Journal of Irrigation & Drainage Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

【Objective】The present paper aimed to enrich the salt tolerance gene resources of Arundo donax and provide help for molecular breeding.【Method】The ‘LZ＿ No.1’ A. donax with consistent growth were treated with 0, 50, 100, 150 and 200 mmol/L NaCl salt solutions for 36 hours, and each treatment consisted of 3 replicates. Stems from the same site were collected for transcriptome sequencing and bioinformatics analysis. 5 differentially expressed genes were randomly selected for qRT-PCR to verify the expression pattern.【Result】De novo assembly was performed on the sequencing data after quality control, and a total of 971 309 transcripts were generated, with a GC content of 47.14%, and the N50 of Unigene contigs reached 1126 bp, indicating a good assembly effect. The 7305 differentially expressed genes identified were subjected to GO and KEGG enrichment analysis, and the results showed that stems of ‘LZ＿ No.1’ responded to salt stress mainly through nitrogen metabolism, ion transport, terpenoid synthesis, zeatin synthesis, linoleic acid metabolism, salicylic acid biosynthesis and osmotic regulator substances. The differentially expressed genes were screened, and a total of 104 core differentially expressed genes were obtained, of which 88315＿c0＿g1＿i1, 1200＿c2＿g1＿i1, 13330＿c0＿g1＿i8, 46571＿c0＿g1＿i7, 3434＿c0＿g1＿i11 and 713＿c0＿g1＿i32 genes with large differential multiples may play an important role in the response to the salt. The identification of transcription factors indicated that AP2/ERF-ERF family, MYB-related family and WRKY family were the most important gene families in salt response, and most of these three transcription factor family members were up-regulated in response to salt stress, indicating that they mainly worked by increasing the expression of genes. The detection results of the five differentially expressed genes by qRT-PCR were basically consistent with the RNA-seq results, which also demonstrated the reliability of the transcriptome data.【Conclusion】The study identifies important genes and transcription factors of A.donax in response to salt stress, which can lay a solid foundation for its future genetic improvement work. [ABSTRACT FROM AUTHOR]

Copyright of Acta Agriculturae Zhejiangensis is the property of Acta Agriculturae Zhejiangensis Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Agricultural Science & Technology (1008-0864) is the property of Journal of Agricultural Science & Technology and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Mycosystema is the property of Mycosystema Editorial Board and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)