ISME J 14:757–770ĭai Z, Su W, Chen H, Barberan A, Zhao H, Yu M et al (2018) Long-term nitrogen fertilization decreases bacterial diversity and favors the growth of Actinobacteria and Proteobacteria in agro-ecosystems across the globe.

Pedobiologia 49:479–497ĭai Z, Liu G, Chen H, Chen C, Wang J, Ai S et al (2020) Long-term nutrient inputs shift soil microbial functional profiles of phosphorus cycling in diverse agroecosystems. Ecology 87:492–503Ĭolemana DC, Whitmanb WB (2005) Linking species richness, biodiversity and ecosystem function in soil systems. Glob Change Biol 20:3814–3822Ĭleveland CC, Reed SC, Townsend AR (2006) Nutrient regulation of organic matter decomposition in a tropical rain forest. Environ Microbiol 12:1842–1854Ĭeulemans T, Stevens CJ, Duchateau L, Jacquemyn H, Gowing DJ, Merckx R et al (2014) Soil phosphorus constrains biodiversity across European grasslands. Nat Methods 12:59–60Ĭampbell BJ, Polson SW, Hanson TE, Mack MC, Schuur EA (2010) The effect of nutrient deposition on bacterial communities in Arctic tundra soil. Nat Methods 12:59īuchfink B, Xie C, Huson DH (2015) Fast and sensitive protein alignment using DIAMOND. J Agric Sci 55:11–33īuchfink B, Xie C, Huson DH (2014) Fast and sensitive protein alignment using DIAMOND. Soil Biol Biochem 36:1785–1792īremner J (1960) Determination of nitrogen in soil by the Kjeldahl method. 1–55īending GD, Turner MK, Rayns F, Marx M-C, Wood M (2004) Microbial and biochemical soil quality indicators and their potential for differentiating areas under contrasting agricultural management regimes. In: Advances in ecological research: Elsevier. Environ Microbiol 8:1–10īeals EW (1984) Bray-Curtis ordination: an effective strategy for analysis of multivariate ecological data. Ecology 94:714–724Īrtursson V, Finlay RD, Jansson JK (2006) Interactions between arbuscular mycorrhizal fungi and bacteria and their potential for stimulating plant growth. This study provides valuable information that improves our understanding on the effects of N and P input on the belowground soil microbial community and functional characteristics in plantations of different stand ages.Īllision SD, Lu Y, Weihe C, Goulden ML, Msrtiny AC, Treseder KK, Martiny JBH (2013) Microbial abundance and composition influence litter decomposition response to environmental change. Moreover, the functional differences in the soil microbiomes were identified between the 6YMP and 24YMP soil. The P addition could impact the genes involved in inorganic P-solubilization and organic P-mineralization by increasing soil AP and TP. glyptostroboides plantation land (5 years of experimental treatment) significantly enriched microbes (e.g., Lysobacter, Luteimonas, and Rhodanobacter) involved in nitrification, denitrification, and P-starvation response regulation, which might further lead to the decreasing in alpha diversity (especially in 6YMP soil). In this study, we designed three N additions and three P levels (5 years of experimental treatment) at two Metasequoia glyptostroboides plantations of different ages (young, 6 years old middle mature, 24 years old) to understand how different addition levels of N and P affect the soil microbiome. Also, trees of different life stages have different fertilization requirements. Nitrogen (N) and phosphorus (P) have significant effects on soil microbial community diversity, composition, and function.

Metasequoia le 2.4