The scientific management of salinized agricultural lands and the use of undeveloped saline lands to ensure food security have become one of the most urgent tasks nowadays. Biochar contains rich carbon (C) and functional groups, and processes high alkalinity, porosity, and specific surface area (SSA). Thus, it has been widely used as an effective organic conditioner in acidic or neutral soils to improve their fertility. However, so far, the impacts of biochar application on properities of saline soils and the underlying mechanisms remain unveiled. Therefore, in this study, we focus on the investigation of the impacts of biochar on the physical, chemical, and biological properties of saline soils. We found that biochar could: (1) decrease soil bulk density (BD), increase soil porosity, promote the formation of soil aggregation and enhance the leaching of soil salts; (2) increase the cation exchange capacity (CEC) of soil, decrease the salinity of soil through ion exchange and adsorption; (3) directly act as the nutrient supplements, indirectly adsorb water and nutrients or improve nutrient availability (e.g., soil organic carbon (SOC) turnover and sequestration, nutrient cycling); and (4) improve the structure and functioning of the soil microbial community and therefore indirectly impact the C, nitrogen (N) and phosphorus (P) cycling in soil systems. However, these impacts heavily depend on the properties, the concentration of the biochar added to the soil, and the type and location of the soil. In fact, some studies have shown that the addition of biochar in soil could even increase the salinity of saline soils. Another issue is the lack of long-term and large-scale field experiments regarding the impact of biochar addition on properties of saline soils. Therefore, future studies should focus on long-term field experiments with the combination of traditional soil analytical methods and mordern molecular techniques (e.g., high-throughput sequencing, macro-genomics, and metabolomics) to comprehensively reveal the response mechanism of physicochemical properties and microbial characteristics of saline soils to exogenous biochar. Our study can provide a scientific foundation for the practical agricultural production and ecological management of biochar.

WRKY gene family is one of the largest transcription factor families involved in various physiological processes of plants. Flax (Linum usitatissimum) is an important stem fiber crop, and it is also an economically important crop in natural fiber and textile industries around the world. In this study, 105 WRKY genes were obtained by screening the whole genome of flax. There were 26 in group I, 68 in group II, 8 in group III and 3 in group UN. The characteristics of the WRKY motif and gene structure in each group are similar. The promoter sequence of WRKY genes includes photoresponsive elements, core regulatory elements and 12 cis-acting elements under abiotic stress. Similar to A. thaliana and Compositae plants, WRKY genes are evenly distributed on each chromosome, with segmental and tandem repeated events, which play a major role in the evolution of WRKY genes. The flax WRKY gene family is mainly concentrated in group I and group II. This study is mainly based on genome-wide information to classify and analyze the flax WRKY gene family, laying a foundation for further understanding the role of WRKY transcription factors in species evolution and functional analysis.

Kenaf (Hibiscus cannabinu) is a grass bast fiber crop that has the ability to tolerate and accumulate heavy metals, and it has been considered as a potential heavy metal accumulator and remediation plant. Nramp is a natural resistance-related macrophage, which plays an important role in the transport of divalent metal ions, plant growth and development, and abiotic stress. In this study, the Nramp gene family of kenaf was analyzed at the whole genome level. A total of 15 HcNramp genes were identified. They are distributed unevenly on chromosomes. Phylogenetic analysis classified 15 HcNramp proteins into 3 different subfamilies. All proteins share specific motif 4 and motif 6, and the genes belonging to the same subfamily are similar in structure and motif. The promoters are rich in hormone response, meristem expression, and environmental stress response elements. Under different treatments, the expression levels of HcNramp genes vary in different tissues, and most of them are expressed in roots first. These findings can provide a basis for understanding the potential role of the Nramp gene family in kenaf in response to cadmium (Cd) stress, and are of great significance for screening related Cd tolerance genes in kenaf.

Kenaf is one of the most important natural cannabis plants. Molecular marker-assisted breeding is vital for accelerating the breeding process of kenaf. However, the number of kenaf markers is insufficient for molecular marker-assisted breeding. Using transcriptome sequencing data for salt-stressed kenaf plants, the number and distribution of simple sequence repeats (SSRs) and single nucleotide variations (SNVs) in the expressed sequences were determined. The objectives of this study were to elucidate the sequence variations in kenaf genes expressed in response to salt stress and to identify stable and dependable molecular markers. Primers were designed for SSR loci and then EST-SSR molecular markers were generated. The subsequent analyses revealed that 30.50% of the unigenes contained SSR motifs, most of which were single nucleotides followed by trinucleotides and dinucleotides. The unigenes containing SSRs were mostly associated with kenaf salt tolerance. Additionally, 10,483 SNVs were detected in contig sequences. Of the 3995 differentially expressed genes encoding interacting proteins, 1297 contained SSRs. Most of these genes were associated with metabolic pathways (e.g., 03000 transcription factors, B09132 signal transduction, and 04122 sulfur relay system). We designed 20 pairs of EST-SSR primers to genotype 30 kenaf varieties (lines), of which 9 primer pairs were ideal for genotyping (e.g., 1 highly polymorphic marker and 2 moderately polymorphic markers). The primer pairs designed for the EST-SSR markers in the kenaf genome may be useful SSR molecular markers for future research on kenaf. The verified polymorphic markers may be applicable to the molecular marker-assisted breeding of salt-tolerant kenaf varieties.