Zihao Liu, Yakov Kuzyakov, Jie Fang, Yucheng He, Bin Song, Bahar S. Razavi, Jonathan M. Adams
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引用次数: 0
Abstract
Background and aims
While intensive fertilization has wide-ranging impact on microbial communities, its effects on microbial recolonization of soil niches and associated enzyme activities as well as hotspots distribution remain underexplored.
Methods
Using soil zymography and high-throughput sequencing, we investigated the hotspots and activities of C-, N- and P-acquiring hydrolases, as well as bacterial community dynamics across hotspots, coldspots, and root endosphere within rice rhizosphere in sterilized and non-sterilized soils following NPK fertilization.
Results
Bacterial community reassembly after sterilization was primarily governed by compartment niches rather than by fertilization, although fertilization accelerated bacterial recovery by increasing diversity and network complexity. Specifically, the dominant taxa and major contributor of genes encoding hydrolases in the rhizosphere of non-sterilized soil shifted from Actinomycetota (K-strategists) to Pseudomonadota and Bacillota (r-strategists). In contrast, root endosphere communities had greater resilience during recolonization and likely supported rice growth by expanding enzyme hotspots area. Higher enzyme activities in hotspots, compared to coldspots, correlated strongly with increased bacterial network complexity, and less with differences in diversity and overall community composition. Fertilization triggered a trade-off between enzyme activities and hotspots area, with increased activities for β-glucosidase and leucine aminopeptidase but reduced hotspots area, whereas acid phosphatase had the opposite trend.
Conclusion
The trade-offs between enzyme activities and hotspots area highlight the micro-scale spatial heterogeneity in nutrient mobilization in paddy soils, suggesting adaptive strategies that plants and microorganisms use to regulate nutrient investment. These findings provide valuable insights for optimizing fertilization management to accelerate microbial processes and enzyme-mediated nutrient cycling.
期刊介绍:
Plant and Soil publishes original papers and review articles exploring the interface of plant biology and soil sciences, and that enhance our mechanistic understanding of plant-soil interactions. We focus on the interface of plant biology and soil sciences, and seek those manuscripts with a strong mechanistic component which develop and test hypotheses aimed at understanding underlying mechanisms of plant-soil interactions. Manuscripts can include both fundamental and applied aspects of mineral nutrition, plant water relations, symbiotic and pathogenic plant-microbe interactions, root anatomy and morphology, soil biology, ecology, agrochemistry and agrophysics, as long as they are hypothesis-driven and enhance our mechanistic understanding. Articles including a major molecular or modelling component also fall within the scope of the journal. All contributions appear in the English language, with consistent spelling, using either American or British English.