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The biodiversity and structure of deep agricultural soil communities are poorly understood, especially for eukaryotes. Using DNA metabarcoding and co-occurrence networks, we tested whether prokaryote, fungal, protist, and nematode biodiversity declines with increasing depth (0-0.1, 0.3-0.5, and 1.1-1.7m) in pastoral soil; whether deep soil organisms are subsets of those at the surface; and whether multi-kingdom networks become more interconnected with increasing depth. Depth-related richness declines were observed for almost all detected fungal classes, protist phyla, and nematode orders, but only 13 of 25 prokaryote phyla, of which nine had increasing richness with depth. Deep soil communities were not simply subsets of surface communities, with 3.8%-12.2% of eukaryotes and 13.2% of prokaryotes detected only in the deepest samples. Eukaryotes mainly occurred in the upper soil layers whereas prokaryotes were more evenly distributed across depths. Plant-feeding nematodes were most abundant in top soil, whereas bacteria feeders were more abundant in deep soil. Co-occurrence network structure differences suggested that deep soil communities are concentrated around scarce niches of resource availability, in contrast to more spatially homogenous and abundant resources at the surface. Together, these results demonstrate effects of depth on the composition, distribution, and structure of prokaryote and eukaryote soil communities.
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http://dx.doi.org/10.1093/femsec/fiab156 | DOI Listing |
Chembiochem
September 2025
Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology (Leibniz-HKI), Beutenbergstrasse 11a, 07745, Jena, Germany.
Soils harbor some of the most diverse microbiomes on Earth. Interactions within these microbial communities are often mediated by natural products, many functioning as chemical signals. Specialized metabolites known as arginoketides, or arginine-derived polyketides, have been linked to mediate these interactions.
View Article and Find Full Text PDFJ Adv Res
September 2025
State Key Laboratory for Quality and Safety of Agro-Products, Key Laboratory for Pesticide Residue Detection of Ministry of Agriculture and Rural Affairs, Institute of Agro-Product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China. Electronic address: tangtao@za
Introduction: Microencapsulated pyraclostrobin (PYR-CS) has gained widespread adoption in agriculture owing to its extended efficacy and reduced risks for non-target organisms. However, knowledge remains limited regarding its degradation in soil and effects on soil microorganisms.
Objectives: This study investigates the hypothesis that microencapsulation alters pyraclostrobin degradation and reshapes soil microbial communities compared with conventional formulations, including emulsifiable concentrate (PYR-EC) and technical material (PYR-TC).
J Hazard Mater
September 2025
State Key Laboratory of Environmental Criteria and Risk Assessment, and State Environmental Protection Key Laboratory of Simulation and Control of Groundwater Pollution, Chinese Research Academy of Environmental Sciences, Beijing 100012, China. Electronic address:
While humic acids (HAs) are known to modulate heavy metal behavior, their profound heterogeneity across soil aggregate fractions remains overlooked. Crucially, whether HA origin within distinct soil aggregates differentially governs heavy metal speciation and bioavailability is unknown-creating a critical knowledge gap for targeted soil remediation. This study deciphers, for the first time, how aggregate-specific HAs control cadmium (Cd) and lead (Pb) dynamics.
View Article and Find Full Text PDFJ Hazard Mater
September 2025
State Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China; Lanzhou Eco-Agriculture Experimental Research Station, Lanzhou 730000, China; Key Laboratory of Stress Physio
Microplastics are pervasive soil pollutants, yet their role in driving microbial risk in medicinal plant rhizospheres remains poorly understood. Using polyethylene microplastics (PE-MPs) as a model, this study investigated the dose-dependent effects of PE-MPs (0-1000 mg/kg) on the dynamics of antibiotic resistance genes (ARGs), biocide/metal resistance genes (BMRGs), virulence factor genes (VFGs), mobile genetic elements (MGEs), and human bacterial pathogens (HBPs) in the rhizosphere of Angelica sinensis. Results showed that PE-MPs exposure increased the abundance of these genes and pathogens while simplifying the host microbial community structure.
View Article and Find Full Text PDFPLoS One
September 2025
Department of Research, Collections and Conservation, Environmental Archaeology and Materials Science, National Museum of Denmark, Kongens Lyngby, Denmark.
During the Late Bronze Age (ca. 11th-8th century BCE), far-reaching and extensive trade and exchange networks linked communities across Europe. The area around Seddin in north-western Brandenburg, Germany, has long been considered as at the core of one such networks.
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