The role of plant-specific rhizosphere bacterial biomarkers in enhancing soil nutrient cycling in Pb–Zn waste slag
摘要
This study aimed to investigate the specific effects of native plants on soil microbial diversity and functional gene expression in Pb–Zn slag environments. Bacterial biomarkers were analyzed to address the challenge posed by the vast diversity within soil bacterial communities, which can obscure the contributions of key species to soil nutrient cycling.
MethodsWe utilized 16S rRNA gene sequencing and multivariate statistical analysis to examine the influence of three herbaceous plants—Artemisia annua, Buddleja davidii, and Carex breviculmis—on rhizosphere bacterial biomarkers and the overall bacterial community structure.
ResultsThe presence of these plants significantly improved soil nutrient levels and enhanced microbial metabolic functions compared to non-vegetated soils (CK). Specifically, A. annua and B. davidii increased the abundance of genes associated with nitrogen (N) and phosphorus (P) cycling, such as the nar and nir gene families involved in N cycling and the ugp gene family involved in P transport. All three plants increased the abundance of genes (czcABD) encoding ABC transporter proteins, with C. breviculmis showing the highest abundance of metal resistance genes, including ZnuB and ZnuC. Key biomarkers, such as Bradyrhizobium, Bryobacter, and Rokubacteriales, played critical roles. Bradyrhizobium was linked to nitrogen fixation in the rhizosphere of A. annua and B. davidii, while Bryobacter and Rokubacteriales contributed to carbon cycling in the rhizosphere of C. breviculmis. Network analysis demonstrated that plant species significantly reshaped microbial interaction networks, fostering more efficient microbial interactions within the rhizosphere.
ConclusionsThese findings highlight that the enhancement of soil nutrient cycling is primarily driven by increased biomarker abundance and diversity, emphasizing the critical role of bacterial biomarkers in improving soil nutrients in metal-contaminated environments.