Plant biostimulants have been the subject of intense interest in recent years. The aim of this study was to assess, during the years 2021–2022, the effect of mineral nitrogen (N) fertilizer, experimental (PGPB) and commercial (G) microbial biostimulants, and humic substance product (A) on the soil microbial communities, and yield of strawberries, under field conditions. Dehydrogenase activity was significantly affected by nitrogen fertilization, but an increase occurred in the treatment N+G. The treatments N+G, N+G+A, and N+PGPB+A increased FDA hydrolysis, and phosphatase activity. All plant biostimulants increased basal as well as substrate-induced respiration. Culturable bacteria (total counts, dormant forms, actinomycetes) were not clearly affected by treatment. Based on 16S rRNA analysis, bacterial community composition was different in N+PGPB+A and N+G+A treatments. The number of cultivable fungi was significantly lower in N+PGPB and N+PGPB+A treatments. The genus of fungi Pilidium, a potential phytopathogen of strawberries, was present in the second year, but in these treatments, it was absent. In the second year, strawberry yield was shown to be 95% higher in the N+PGPB+A treatment than in the control. Microbial biostimulants in combination with humic substances represent a potential solution in increasing strawberry production.

Bark beetles (Coleoptera: Scolytinae) play a dual ecological role in forest ecosystems as disturbance agents and vectors of symbiotic fungi, including blue-stain taxa that affect wood quality and tree health. This study assessed fungal communities specific to four bark beetle species—Ips acuminatus (Gyllenhal, 1827), Ips sexdentatus (Börner, 1776), Ips typographus (Linnaeus, 1758), and Pityogenes chalcographus (Linnaeus, 1761)—colonizing Scots pine (Pinus sylvestris L.) in Slovakia. Fungal DNA was extracted from beetle surfaces and analyzed using ITS2 metabarcoding on the Illumina MiSeq platform to characterize the diversity and structure of associated mycobiota. Alpha- and beta-diversity analyses revealed a taxonomically and functionally rich fungal assemblage dominated by Ascomycota, comprising over one thousand operational taxonomic units. Fungal richness and diversity varied among beetle species: I. typographus and P. chalcographus supported the most diverse communities, I. sexdentatus harbored the least diverse assemblages, and I. acuminatus showed contrasting patterns depending on the index used. Beta-diversity analysis indicated that community composition was primarily structured by beetle species identity, with weaker effects of locality and sampling method. Ophiostomatoid fungi, particularly Geosmithia pallida (G. Sm.) M. Kolařík, Kubátová & Pažoutová, Ophiostoma distortum (R.W. Davidson) de Hoog & R.J. Scheff., and Ophiostoma minus (Hedgc.) Syd. & P. Syd., were consistently prevalent and formed the core mycobiome. Random forest classification and differential abundance analyses confirmed host-specific enrichment of several ophiostomatoid and yeast taxa. Yeasts (e.g., Kuraishia, Candida, Yamadazyma), saprotrophic molds (e.g., Penicillium, Davidiella), and the entomopathogen Beauveria bassiana (Bals.-Criv.) Vuill. also occurred frequently. These findings provide the first DNA-based evidence of host-specific fungal assemblages in Scots pine bark beetles in Slovakia and emphasize their ecological significance for beetle–fungus symbioses and pine forest health.

The application of nitrification inhibitors (Nis) with nitrogen fertilizers is increasingly used as a management strategy to improve nitrogen use efficiency in crop production systems. To evaluate the effects of Ni dicyandiamide (DCD) and 1,2,4-triazole (TZ) on the rhizosphere microbiome and strawberry yield (Fragaria × ananassa Duch.), a two-year field experiment was conducted with three treatments: unfertilized control (C), mineral nitrogen fertilizer (N) applied in two doses (40 + 40 kg N ha⁻¹ year⁻¹), and a single nitrogen application (80 kg N ha⁻¹ year⁻¹) combined with nitrification inhibitors (N + Ni). Soil microbiota were assessed using cultivation-based methods and metabarcoding of 16S rRNA and ITS2 regions. Total bacterial counts on complex media increased from 5.85 to 6.15 log CFU g⁻¹ in the N treatment, while remaining 5.89 in N + Ni. Microscopic fungi increased in fertilized treatments during spring but decreased in July of the second year. Microbial community composition differed among treatments, although sampling time explained a larger proportion of variability than fertilization. Relative abundance of Gemmatimonas decreased under N + Ni, whereas Nitrososphaera increased. Fungal Shannon diversity decreased in N + Ni, while prokaryotic diversity did not differ significantly. Despite similar levels of mineral nitrogen measured before harvest, strawberry yield increased significantly in the N + Ni treatment in the second year, reaching 109% higher values than the control and 80% higher than the N treatment. This may indicate that the fertilization regime including nitrification inhibitors influenced nitrogen availability earlier in the growing season.

Dothistroma needle blight (DNB), caused by Dothistroma septosporum , is a globally important disease of pines, yet its ecological role within native host systems remains incompletely understood. We combined species‐specific quantitative PCR (qPCR) with ITS2 metabarcoding to investigate the occurrence of D. septosporum and associated needle mycobiomes of Pinus sylvestris in natural stands in Slovakia with a pooled non‐natural positive‐reference group included for comparison. D. septosporum was detected in the Vernár natural stand (11 of 16 samples), where visible DNB symptoms were also observed, and in all samples of the non‐natural positive‐reference group (15 of 15 samples). The pathogen was not detected in the other three sampled natural stands. Fungal community analyzes revealed significant differences in community composition among sample groups, while alpha diversity patterns showed comparatively minor variation. The most abundant genus across all sites was Lophodermium , whereas Dothistroma was highly abundant only in the non‐natural positive‐reference group. Co‐occurrence network analysis indicated that fungal communities were dominated by positive associations; however, patterns involving Dothistroma primarily reflected the positive‐reference group, where the pathogen was highly abundant. Our results suggest that D. septosporum is not a consistently detectable component of needle mycobiomes in native P. sylvestris stands in Slovakia and that its high abundance in the non‐natural positive‐reference group was associated with a distinct fungal community composition.