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 cannabinus L.) is an indispensable fiber crop that faces increasing salinity stress. In previous studies regarding the molecular mechanisms of how kenaf may respond to salt stress, no metabolic evidences have been reported. Meanwhile, studies regarding kenaf stems under adverse growth conditions have not been conducted. In the present study, multiple-layer evidences including physiological, transcriptomic, and metabolic data regarding how kenaf stems were affected by the salt stress are provided, wherein the stem growth, especially the lignification process, is retarded. Meanwhile, the transcriptomic data indicated genes involved in the photosynthesis are significantly repressed while the multiple flavonoid metabolism genes are enriched. As to the metabolic data, the content variation for the growth-promotion phytohormones such as IAA and the stress-responding ones including ABA are within or without expectations, implying these phytohormones played complicated roles when the kenaf stems encounter salt stress. However, the metabolite variations did not always agree with the expression levels of corresponding key pathway genes, possibly because the metabolite could be biosynthesized or catabolized in multiple pathways. Collectively, our data may enlighten, more specifically, downstream studies on kenaf responses against salinity and other adverse conditions.

Kenaf (Hibiscus cannabinus L.) is considered suitable for the remediation of cadmium (Cd)-contaminated farmlands, because of its large biomass and resistance to Cd stress. The addition of nitrogen (N) fertilizer is an important measure used to increase crop yields, and it may also affect Cd accumulation in plants. To clarify the effects of different forms and concentrations of N on plant growth and Cd absorption in kenaf, a hydroponic experiment was conducted using three N forms (NH₄⁺–N, NO₃⁻–N and urea–N) at four concentrations (0, 2, 4 and 8 mM, 0 mM as control) under Cd stress (30 μM). The plant growth, the antioxidant enzyme activity and the Cd contents of various parts of the kenaf seedlings were measured. The results showed that the N form had the greatest impact on the growth of the kenaf and the absorption and transport of the Cd, followed by the interaction effect between the N type and the concentration. Compared to the control, the addition of N fertilizer promoted the growth of kenaf to varying degrees. Among all the treatments, the use of 2 mM of NO₃⁻–N enhanced the biomass and Cd accumulation to the greatest extent compared to CK from 2.02 g to 4.35 g and 341.30 μg to 809.22 μg per plant, respectively. The NH₄⁺–N significantly reduced the Cd contents of different parts but enhanced the translocation factors of Cd stem to root (TF S/R) and leaf to stem (TF L/S) by 34.29~78.57% and 45.10~72.55%, respectively. The peroxidase (POD), superoxide dismutase (SOD) and catalase (CAT) enzyme activities of the kenaf increased with the N treatments, especially with NH₄⁺–N. Overall, applying low concentrations of NO₃⁻–N can better promote the extraction of Cd by 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.

To screen out excellent jute germplasm resources, improve the information of jute germplasm resources, and increase the utilization rate of jute germplasm resources, this study took 15 jute germplasm resources as the research object, measured their phenotypic traits and fiber strength, and comprehensively evaluated them by using the principal component analysis and the analysis of the value of the affiliation function.The results showed that the coefficients of variation of the phenotypic traits of jute ranged from 4.14% to 159.52%. One of the traits with the highest coefficient of variation was the number of forks, indicating the abundance of genetic variation in jute. In this study, 21 agronomic traits were synthesized into six major components using principal component analysis, and the factor with the highest loading was branching height. Further calculating the value of the affiliation function, the top three varieties are HF2-13, Zhe Xiaoyuan 1, and Fuhuangma 13, which have high potential for development and utilization. By further calculating the value of the affiliation function, the top three varieties are HF2-13 (1), Zhexiaoyuan 1, and Fu Jute 13.These three varieties possess relatively high potential for development and utilization. This study clarified the differences in fiber strength of different germplasm resources, and successfully screened out the germplasm resources with excellent comprehensive performance. This study provides data support and theoretical basis for the improvement of jute varieties, the utilization of germplasm resources and the development of related industries.