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.

Hemp stalk, a widely available agricultural waste, is an ideal eco-friendly raw material for biochar production. Carbonization experiments were conducted as a novel approach for the scalable and value-added utilization of hemp stalk under oxygen-exclusion conditions. The effects of feedstock types—Hibiscus cannabinus (KS), Corchorus spp. (JS), and Boehmeria spp. (RS)—and pyrolysis temperatures on biochar properties were analyzed through the measurements of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy. The pH and electrical conductivity (EC) of biochars increased with increasing pyrolysis temperature. Notably, EC was significantly higher for RS (940–2278 μS/cm) than for KS (517–879 μS/cm) and JS (583–863 μS/cm). The C content in these three biochars increased as the temperature increased, whereas the H/C atomic ratio decreased, most notably in JS (by 0.33%). According to FTIR and XRD data, with the pyrolysis temperature increasing, the acidic oxygen-containing groups on biochar surfaces reduced. KS700, with superior aromatic structure and stability, may be able to effectively adsorb heavy metal ions. RS700, with relatively high pH and EC, was suitable for alleviating soil acidification and nutrient deficiency. The feedstock and pyrolysis temperature significantly affected the element content, pore structure, and stability of biochars derived from hemp stalk.

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.

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 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 an important bast fiber crop. In order to diversify the available kenaf simple sequence repeat (SSR) molecular markers and generate markers potentially useful for kenaf breeding, we developed expression sequence tag simple sequence repeat (EST-SSR) molecular markers based on lead-stressed kenaf transcriptome sequencing data and spliced unigene sequences. Additionally, the distribution of the SSRs in the transcriptome and the potential functions of the SSR-containing genes were determined. Moreover, SSR markers in the differentially expressed genes (DEGs) of a protein–protein interaction (PPI) network were analyzed to screen for polymorphic markers, which were used to examine the genetic diversity and population structure of kenaf germplasm resources. The genetic diversity and population structure of 138 kenaf germplasm materials revealed that 22 EST-SSR markers could be used to distinguish the kenaf germplasms. The 22 EST-SSR markers enrich the kenaf molecular markers database and provide an important tool for future genetic improvement of kenaf resistance to lead stress.